From owner-chromosomes@net.bio.net Tue Jul 01 23:00:00 1997
Path: biosci!bloom-beacon.mit.edu!ai-lab!eecs-usenet-02.mit.edu!xfer02.netnews.com!howland.erols.net!portc02.blue.aol.com!audrey02.news.aol.com!not-for-mail
From: shinrichs9@aol.com (SHinrichs9)
Newsgroups: bionet.genome.chromosomes
Subject: Cytochrome C & Lambda Repressor DNA sequences
Date: 2 Jul 1997 13:16:10 GMT
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I am interested in comparing certain DNA sequences in order to investigate
ancestral relationships. Thus, I am requesting DNA sequences from informed
people who might be able to provide references. If one can I would
appreciate them sending them to me at Shinrichs9@aol.com. Thanks.

I am most interested in the human and chimpanzee DNA sequences for the
Cytochrome C protein. Also, I am interested in the human and chimpanzee
DNA sequences for the lambda repressor.

In addition, as a second priority I am interested in the DNA sequences for
the following species for the above mentioned molecules.

Type	Species
Mammals	Man
Mammals	Rhesus monkey
Mammals	Horse
Mammals	Donkey
Mammals	Cow, Pig, Sheep
Mammals	Dog
Mammals	Rabbit
Mammals	Cal. Grey Whale
Mammals	Great gray kangaroo
Vert.	Chicken, turkey
Vert.	Pigeon
Vert.	Pekin duck
Vert.	Snapping turtle
Vert.	Rattlesnack
Vert.	Bullfrog
Vert.	Tuna
Vert.	Dogfish
	
Insects	Samia cynthia (a moth)
Insects	Tobacco hornworm moth
Insects	Screworm fly
Insects	Drosphila (fruit fly)
	
Insects	Baker's yeast
Insects	Candida krusei (a yeast)
Insects	Neurospara crassa (a mold)
	
Higher plants	Wheat germ
Higher plants	Buckwheat seed
Higher plants	Sunflower seed
Higher plants	Mung bean
Higher plants	Cauliflower
Higher plants	Pumpkin
Higher plants	Sesame seed
Higher plants	Castor bean
Higher plants	Cottonseed
Higher plants	Abutilon seed


SHinrichs9@aol.com
http://members.aol.com/SHinrichs9/
Please email me if you post so I am aware, thank-you

From owner-chromosomes@net.bio.net Tue Jul 01 23:00:00 1997
Path: biosci!agate!newsfeed.kornet.nm.kr!newsfeed.dacom.co.kr!newsfeed.direct.ca!News1.Vancouver.iSTAR.net!news.istar.net!EU.net!blackbush.xlink.net!news-ge.switch.ch!in2p3.fr!univ-lyon1.fr!news
From: robinson@evomol.univ-lyon1.fr (Marc Robinson)
Newsgroups: bionet.genome.chromosomes
Subject: Re: Cytochrome C & Lambda Repressor DNA sequences
Date: 2 Jul 1997 17:40:02 GMT
Organization: Universite Claude Bernard - Lyon 1
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In article <19970702131600.JAA04943@ladder02.news.aol.com>, shinrichs9@aol.com (SHinrichs9) writes:
>I am interested in comparing certain DNA sequences in order to investigate
>ancestral relationships. Thus, I am requesting DNA sequences from informed
>people who might be able to provide references. If one can I would
>appreciate them sending them to me at Shinrichs9@aol.com. Thanks.

http://acnuc.univ-lyon1.fr/

at this site you can query a number of sequence databases through gene
name, taxonomical units including species name, keywords, etc.

hope this helps,
Marc
_________________________________________________________________
Marc Robinson
UMR CNRS 5558 "Biometrie, Genetique, et Biologie des Populations"
Universite Claude Bernard Lyon 1
43, boulevard du 11 novembre 1918
69622 Villeurbanne cedex
France
tel : +33 4 72 44 80 00 - poste 42 59
fax : +33 4 78 89 27 19
e-mail : robinson@biomserv.univ-lyon1.fr

La liberte ne s'use que quand on ne s'en sert pas.
_________________________________________________________________



From owner-chromosomes@net.bio.net Tue Jul 01 23:00:00 1997
Path: biosci!rutgers!news.sgi.com!news-peer.gsl.net!news.gsl.net!portc01.blue.aol.com!audrey01.news.aol.com!not-for-mail
From: huntpharm@aol.com (Huntpharm)
Newsgroups: bionet.genome.chromosomes
Subject: job opportunity in bioinformatics
Date: 2 Jul 1997 22:44:49 GMT
Lines: 11
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I am looking for a person to head up bioinformatics. As a visionary you
will be responsible for leading a group of five and taking the
bioinformatics team to the next level.  You will lead this group
responsible for the application of computer technology to genomic analysis
and research. We are a leading pharmaceutical company with research
facilities in Connecticut and can provide excellent benefits (health
insurance, dental and vision plans, paid vacations and more. Excellent
compensation package. A high impact, high profile position with excellent
opportunity for advancement.  Please contact Scott Shanes by phone at
609-584-8733 EXT. 218, fax CV to 609-584-9575 or E-Mail to
SIS@diedremoire.com or Neurohunt@aol.com.

From owner-chromosomes@net.bio.net Wed Jul 02 23:00:00 1997
Path: biosci!CCVAX.SINICA.EDU.TW!bocmchen
From: bocmchen@CCVAX.SINICA.EDU.TW (cmchen)
Newsgroups: bionet.genome.chromosomes
Subject: post-doctoral position available
Date: 2 Jul 1997 23:33:17 -0700
Organization: IBAS
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Post-doctoral Research Fellow

A post-doctoral research position is available immediately.  The work
involves in situ hybridization and molecular analysis of Phalaenopsis
species and hybrids.  Candidates should have a Ph.D. degree in Genetics
or a related discipline.  The project is supported by National Science
Council of the Republic of China.  Initial appointment is for one year,
with the possibility of extension for two more years.  Send a letter of
interest, curriculum vitae and two letters of recommendation to: Prof.
Chi-Chang Chen, Department of Botany, National Taiwan University,
Taipei, Taiwan.  Tel: 886-2-3630231 ext 2371;  Fax: 886-2-3918940. or
write to the E-mail address: bocmchen@ccvax.sinica.edu.tw.

From owner-chromosomes@net.bio.net Wed Jul 02 23:00:00 1997
Path: biosci!bloom-beacon.mit.edu!eru.mt.luth.se!www.nntp.primenet.com!nntp.primenet.com!news.maxwell.syr.edu!ais.net!su-news-hub1.bbnplanet.com!news.bbnplanet.com!venus.sun.com!wnoc-sfc-news!wnoc-tyo-news!news.nc.u-tokyo.ac.jp!news
From: "Shou Serizawa" <ss77190@hongo.ecc.u-tokyo.ac.jp>
Newsgroups: bionet.genome.chromosomes
Subject: YAC library
Date: 3 Jul 1997 03:18:48 GMT
Organization: Network Operation Centre, The University of Tokyo
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 Does anybody know of YAC library of mice, having a large insert in the
clone, like 1-2Mbp. I already know of YAC library having an insert of 500Kb
on average.
Thanks in advance.

Shou Serizawa
Dept. of Biophysics and Biochemistry
The University of Tokyo


From owner-chromosomes@net.bio.net Wed Jul 02 23:00:00 1997
Path: biosci!OBZOR.BIO21.ACAD.BG!ttsonev
From: ttsonev@OBZOR.BIO21.ACAD.BG (biofac)
Newsgroups: bionet.genome.chromosomes
Subject: Help, please!
Date: 3 Jul 1997 10:23:03 -0700
Organization: Institute of Plant Physiology
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<HTML>
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<BR><TT>Faculty of Biology</TT>
<BR><TT>8, Dragan Tsankov Blvd</TT>
<BR><TT>1421 Sofia, Bulgaria</TT>
<BR><TT>Tel: (3592) 63301</TT>
<BR><TT>Fax (3592) 658079</TT><TT></TT>

<P><TT>Dear Sirs,</TT><TT></TT>

<P><TT>The&nbsp; daughter of&nbsp; a colleague&nbsp; of&nbsp; ours,&nbsp;
chief&nbsp; researcher&nbsp; in&nbsp; the</TT>
<BR><TT>"Cytology,&nbsp; Histology and&nbsp; Embriology" at&nbsp; the Biological
Faculty of</TT>
<BR><TT>the&nbsp; Sofia University&nbsp; "St Kliment&nbsp; Ohridsky" is&nbsp;
suffering from&nbsp; an</TT>
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<BR><TT>Department&nbsp; and the parents of the girl address you with the
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<BR><TT>for&nbsp; financial funds,&nbsp; necessary for&nbsp; bone marrow&nbsp;
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<BR><TT>conducted&nbsp; abroad. The&nbsp; required sum&nbsp; amounts to&nbsp;
USD 80&nbsp; 000 - 1000</TT>
<BR><TT>000.</TT>
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<BR><TT>The&nbsp; donation account&nbsp; in the&nbsp; name of Desislava
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<BR><TT>was&nbsp; opened in&nbsp; Biochim Ad,&nbsp; Sredetz Branch,&nbsp;
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<BR><TT></TT>&nbsp;
<BR>&nbsp;</HTML>


From owner-chromosomes@net.bio.net Wed Jul 02 23:00:00 1997
Path: biosci!NCGR.ORG!gas
From: gas@NCGR.ORG ("Gustavo A. Seluja")
Newsgroups: bionet.genome.chromosomes
Subject: classical genetics question
Date: 3 Jul 1997 10:06:08 -0700
Organization: NCGR
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Distribution: world
Message-ID: <33BBDBC4.1133@ncgr.org>
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NNTP-Posting-Host: net.bio.net

Perhaps I can get a definite answer to the following question.  Who is
more genetically similar: 2 brothers or father and son?  Here, I'm
thinking of nuclear material, and not mitochondrial genome.  Thanks to
anyone interested in answering this question! (references will be most
welcome)

-- 
Gustavo A. Seluja, MSc
Bioinformatics Associate
National Center for Genome Resources
1800 Old Pecos Trail, Suite A
Santa Fe, NM 87505
USA

mailto:gas@ncgr.org
http://www.ncgr.org/
ph: 505-982-7840 - operator
ph: 505-995-4453 - direct
fax: 505-982-7690

From owner-chromosomes@net.bio.net Wed Jul 02 23:00:00 1997
Path: biosci!daresbury!lyra.csx.cam.ac.uk!server1.netnews.ja.net!server5.netnews.ja.net!server3.netnews.ja.net!baron.netcom.net.uk!netcom.net.uk!dispatch.news.demon.net!demon!europa.clark.net!cpk-news-hub1.bbnplanet.com!su-news-hub1.bbnplanet.com!news.bbnplanet.com!venus.sun.com!wnoc-sfc-news!wnoc-tyo-news!news.nc.u-tokyo.ac.jp!news
From: "Shou Serizawa" <ss77190@hongo.ecc.u-tokyo.ac.jp>
Newsgroups: bionet.genome.chromosomes
Subject: YAC library
Date: 3 Jul 1997 03:22:09 GMT
Organization: Network Operation Centre, The University of Tokyo
Message-ID: <01bc8761$1917d120$c4200b85@kawauso.biochem.s.u-tokyo.ac.jp>
NNTP-Posting-Host: neuron.biochem.s.u-tokyo.ac.jp
X-Newsreader: Microsoft Internet News 4.70.1161
Lines: 9

Does anybody know of YAC library of mice, having a large insert in the
clone, like 1-2Mbp. I already know of YAC library having an insert of 500Kb
on average.
Thanks in advance.

Shou Serizawa
Dept. of Biophysics and Biochemistry
The University of Tokyo
e-mail: ss77190@hongo.ecc.u-tokyo.ac.jp

From owner-chromosomes@net.bio.net Sat Jul 05 23:00:00 1997
Path: biosci!rutgers!dziuxsolim.rutgers.edu!uunet!in3.uu.net!194.162.162.196!newsfeed.nacamar.de!howland.erols.net!news-peer.sprintlink.net!news-sea-19.sprintlink.net!news-in-west.sprintlink.net!news.sprintlink.net!Sprint!207.20.0.4!newsfeed2.aimnet.com!news.internetMCI.com!not-for-mail
From: drtpttpotgrt@elprpypspfo.com
Newsgroups: bionet.genome.chromosomes
Subject: !!!Your ONENUMBER for everything!!!!
Date: 6 Jul 1997 03:30:07 GMT
Organization: Internet MCI
Lines: 31
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NNTP-Posting-Host: usr2-dialup3.mix1.bloomington.mci.net


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From owner-chromosomes@net.bio.net Sat Jul 05 23:00:00 1997
Path: biosci!TEOSINTE.AGRON.MISSOURI.EDU!ed
From: ed@TEOSINTE.AGRON.MISSOURI.EDU (Ed Coe)
Newsgroups: bionet.genome.chromosomes
Subject: Postdoctoral:  Mutants in the Maize Genome
Date: 6 Jul 1997 10:38:46 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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Message-ID: <33BFDA7F.A31@teosinte.agron.missouri.edu>
NNTP-Posting-Host: net.bio.net

Content-Type: text/plain; charset=us-ascii
Content-Transfer-Encoding: 7bit

Maize is a species in which the incredible resource of mutants is barely
tapped.  This postdoctoral position is to oversee, conduct, and advance
novel research approaches for mapping of visible-expression genes; to
position these genes with cDNAs; and to seek evidence of biochemical
functions.  This is an opportunity to experience the wide range of
mutants in maize; high-efficiency mapping; and strategies by which to
follow molecular clues to gene functions.  Other ongoing research in the
group includes studies in quantitative trait inheritance; gene
expression and relationship to traits; and the Maize Genome database and
informatics, which are opportunities for additional experience. 
Appointee will be a participant in the University of Missouri maize
group, which has broad training and research strengths that range across
breeding, molecular pathology, entomology, physiological genetics,
organelle genetics, cytogenetics, cell biology, and gene regulation. 
Conduct of the project requires expertise in molecular genetics, and
knowledge pertinent to  plant physiology and biochemistry.  Review of
applications will begin immediately and will continue until the position
is filled.  Send a CV; brief statement of research interests; and names,
phone numbers, and email addresses of 3 references to:  Dr. Edward Coe,
210 Curtis Hall, University of Missouri, Columbia, MO 65211,
ed@teosinte.agron.missouri.edu, phone 573-882-2768, fax 573-884-7850. 
Women and minorities are encouraged to apply.  The University of
Missouri is an EEO/AA/ADA employer.

From owner-chromosomes@net.bio.net Sat Jul 05 23:00:00 1997
Path: biosci!LIGHT.IINET.NET.AU!bethj
From: bethj@LIGHT.IINET.NET.AU (Beth Templeton)
Newsgroups: bionet.genome.chromosomes
Subject: cloning fossil pollen
Date: 6 Jul 1997 03:43:46 -0700
Organization: iiNet Technologies (SA) Pty Ltd
Lines: 8
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Distribution: world
Message-ID: <33BF7622.F6DD4B78@light.iinet.net.au>
Reply-To: bethj@light.iinet.net.au
NNTP-Posting-Host: net.bio.net

hi ,
     just a thought knowing that pollin chromosomes  are most likely
intact ,they may be able to be isolated and cloned using a anucleated
plant cell which is then generated in a medium.
Pollin chromosomes are diploid I believe this may be a problem.
Comment?



From owner-chromosomes@net.bio.net Sat Jul 05 23:00:00 1997
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From: rcjohnsen@aol.com (Rcjohnsen)
Newsgroups: bionet.genome.chromosomes
Subject: Re: classical genetics question
Date: 6 Jul 1997 09:00:55 GMT
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References: <33BBDBC4.1133@ncgr.org>

I should think a father and son are more genetically related than two
brothers.  The son shares half his genetic material with his father.  The
same is true for the brother but brother two may share parts of the
fathers genome that brother one doesn't have.  And don't for the process
of crossing over.  That tends to make everyone genetically unique
Rcjohnsen@aol.com

From owner-chromosomes@net.bio.net Sun Jul 06 23:00:00 1997
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From: DFU <fud01@doc.mssm.edu>
Newsgroups: bionet.genome.chromosomes
Subject: Re: classical genetics question
Date: Mon, 7 Jul 1997 17:43:13 -0400
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To: "Gustavo A. Seluja" <gas@NCGR.ORG>
In-Reply-To: <33BBDBC4.1133@ncgr.org>



On 3 Jul 1997, Gustavo A. Seluja wrote:

> Perhaps I can get a definite answer to the following question.  Who is
> more genetically similar: 2 brothers or father and son?  Here, I'm
> thinking of nuclear material, and not mitochondrial genome.  Thanks to
> anyone interested in answering this question! (references will be most
> welcome)
> 
> -- 
> Gustavo A. Seluja, MSc
> Bioinformatics Associate
> National Center for Genome Resources
> 1800 Old Pecos Trail, Suite A
> Santa Fe, NM 87505
> USA
> 
> mailto:gas@ncgr.org
> http://www.ncgr.org/
> ph: 505-982-7840 - operator
> ph: 505-995-4453 - direct
> fax: 505-982-7690
> 
> 


Theoreticaly, both situations have the same amount of genetic material of
the same origin. However, brothers have more complicated (by 2X 
difference) haplotype than the father and son do. Putting them together,
the father and son are more genetically similar.


From owner-chromosomes@net.bio.net Mon Jul 07 23:00:00 1997
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From: "Dr. Thomas Heinemeyer" <thh@gbf-braunschweig.de>
Newsgroups: bionet.genome.chromosomes
Subject: TRANSFAC 3.2 database
Date: Tue, 08 Jul 1997 08:38:37 +0200
Organization: Ges. f. Biotechn. Forsch. mbH (non profit)
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TRANSFAC 3.2 is available now at:

	http://transfac.gbf.de.

On the TRANSFAC server, you will find also the sequence analysis
programs

	PatSearch
	MatInspector
	SaGa
	FastM

and Thure Etzold's SRS5 with a large collection of databases.


TRANSFAC is a database about eukaryotic transcription factors 
and their binding sites.

It consists of six cross-linked tables:

	SITE
	CELL
	FACTOR
	CLASS
	MATRIX
	GENE

It is also cross-linked with TRRD (Transcription Regulatory 
Region Database) and COMPEL from the ICG, Novosibirsk (N. A.
Kolchanov, A. E. Kel). It contains numerous cross-references
to external databases such EMBL, SWISSPROT, PIR, FLYBASE, 
EPD, and PROSITE. For further details see Wingender et al.,
Nucleic Acids Res. 25:265-268, 1997.

NEW FEATURES are:

-	Additional FACTOR and SITE entries,
-	cross-references to PDB,
-	comprehensive linkage of FACTOR entries with a proposed
	transcription factor classification sytem
	(http://transfac.gbf.de/TRANSFAC/cl/cl.html).

The TRANSFAC database comes along with several sequence analysis
tools such as 
-	PatSearch, which uses the sequence information contained
	in the SITE table for analysis of submitted sequences,
-	MatInspector, using a library of matrices selected from
	the TRANSFAC MATRIX table (see Quandt et al., Nucleic
	Acids Res. 23:4878-4884, 1995).

Moreover, the TRANSFAC server provides a new program (SaGa:
structural analysis with genetic algorithms, developed by
Stefan Meier) which can be used to identify structural
characteristics in the environment of aligned functional 
sites, e.g., transcription factor binding sites. SaGa uses a
library of structural parameters developed by H. Sklenar and
coworkers (MDC, Berlin; see Karas et al., CABIOS 12:441-446, 1996).

The SRS5 system implemented on the TRANSFAC server comprises the
following databases, in addition to the TRANSFAC  tables:

	EMBL, EMBLNEW
	SWISSPROT, SWISSNEW
	TREMBL
	REMTREMBL
	SPTREMBL
	PIR
	EPD
	PDB
	PROSITE
	ENZYME

EMBLNEW is now updated daily on the TRANSFAC SRS-Site with the
new files from European Bioinformatics Institute (EBI) in Hinxton.


Edgar Wingender
Thomas Heinemeyer


-- 
Dr. Thomas Heinemeyer		Tel.:	++49(0)531 6181 295 
Ges. f. Biotechn. Forsch. mbH	Fax:	++49(0)531 6181 266 
Abt. Genomanalyse		E-Mail:	thh@gbf.de
Mascheroder Weg 1		http://transfac.gbf.de/Staff/thh.html
D-38124 Braunschweig

From owner-chromosomes@net.bio.net Tue Jul 08 23:00:00 1997
From: Damn Yankee<damnyankee@yankee.inc>
Newsgroups: bionet.genome.chromosomes
Organization: Yankee Inc.
Subject: !!!Hello!!!
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From owner-chromosomes@net.bio.net Tue Jul 08 23:00:00 1997
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From: huntpharm@aol.com (Huntpharm)
Newsgroups: bionet.genome.chromosomes
Subject: job opportunity for protein chemist
Date: 9 Jul 1997 11:35:07 GMT
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From owner-chromosomes@net.bio.net Tue Jul 08 23:00:00 1997
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From: Savita Visal <aai140@agora.ulaval.ca>
Newsgroups: bionet.genome.chromosomes
Subject: Looking for a Post-Doctoral position
Date: Wed, 09 Jul 1997 11:21:05 +0000
Organization: Dept.Biochem, Natl Chem Lab. Pune, India
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Dear Friends,
I am advertising the Resume of my friend Dr. W Ramakrishna. He is
looking for a Post-doctorate position. 
Savita
======--------=========------========--------=======--------=========

						      Resume

Name       W.RAMA KRISHNA

Address    Plant Molecular Biology Unit, 
	       Division of Biochemistry
	       National  Chemical  Laboratory, 
	       Pune  411 008   INDIA

Research Experience:      
Presently working as a postdoctoral fellow at NCL, Pune, India 

Projects: 
1) Microsatellite markers and homeobox genes and their use in
phylogenetic analysis in cereals. 
2)Sex determination in papaya.


Educational Qualification
    
    Ph.D    -  DNA fingerprinting and molecular characterization of
    (1995)     microsatellites and minisatellites in rice 
		
	       
Laboratory Training in Molecular Biology
		
	DNA, RNA isolation, Southern and Northern hybridizations, 
	DNA sequencing, genomic library construction, polysome 
	isolation, preparation of wheat germ lysate, in vitro 
	translation, RAPD & locus specific PCR, RT-PCR, DDRT-PCR, 
	Phylogenetic analysis.

References

Dr. P.K. Ranjekar,                      Dr. Vidya S. Gupta
Deputy Director & Head,                 Scientist,
Plant Molecular Biology Unit,           Plant Molecular Biology Unit,
Div Biochem Sci.,       				Div Biochem Sci.,                   
Natl  Chem Lab.,         				Nat Cheml Lab., 
Pune - 411 008  INDIA                   Pune - 411 008  INDIA
email - bio@ems.ncl.res.in              email - bio@ems.ncl.res.in
Fax 91-0212-338234                      Fax 0212-338234,
Tel 91-0212-338234                      Tel 0212-342779 

Manuscripts

1. DNA fingerprinting in rice with oligonucleotides specific for simple
repetitive DNA sequences. 
     W. Ramakrishna, M.D. Lagu, V.S. Gupta & P.K.Ranjekar.
     Theoretical & Applied Genetics (1994) 88 : 402-406.

2. DNA fingerprinting detects genetic variation in rice using
hypervariable DNA sequences.
     W. Ramakrishna, K.V.Chowdari, M.D. Lagu, V.S. Gupta & 
  	 P.K.Ranjekar. 
     Theoretical & Applied Genetics (1995) 90 : 1000-1006.

3. (CAC)5 detects DNA fingerprints and sequences homologous to gene 
   transcripts in rice. 
   V.S.Gupta, W.Ramakrishna, S.R.Rawat & P.K.Ranjekar. 
   Biochemical Genetics (1994) 32 : 1/2 : 1-8.

4. DNA fingerprinting detects genetic variability in the pearl millet
downy mildew pathogen (Sclerospora graminicola) using simple sequence
repeats. 
   J.G.Sastry, W.Ramakrishna, S.Sivaramakrishnan, R.P.Thakur, V.S.  
   Gupta & P.K. Ranjekar. 
   Theoretical & Applied Genetics (1995) 91 : 856-861.

5. DNA fingerprinting of Indian isolates of Xanthomonous oryzae pv
oryzae. 
   M.D.Rajebhonsle, K.V.Chowdari, W.Ramakrishna, S.Tamhankar, 
   V.S.Gupta, S.S.Gnanamanickam & P.K.Ranjekar.
   Theoretical & Applied Genetics (In Press).

Manuscripts communicated \ Underpreparation

1. Evolutionary changes associated with domestication at a (GA)n 
   microsatellite locus in rice.
   W.Ramakrishna, A.M.Wadia, V.S.Gupta & P.K.Ranjekar.

2. Phylogenetic conservation and evolution of human sex determining
region (SRY) gene in papaya - a dioecious plant.
   W.Ramakrishna, A.S.Parasnis, B.B.Dholakia, V.S.Gupta & P.K.Ranjekar
  (communicated to Nature Genetics)

3. Knotted1 homeobox - evolutionary significance in cereals.  
   A.Deshpande, W.Ramakrishna, G.Mulay, V.S.Gupta & P.K.Ranjekar 
  (to be communicated to Nature)
    

4. Amplification and sequencing of homeobox and microsatellites from
fossils of cereals. 
   W.Ramakrishna, A.Deshpande, A.M.Wadia, V.S.Gupta & P.K.Ranjekar 
   (to be communicated to Nature) 

5. Sex specific organization of a microsatellite in papaya. 
   A.S.Parasnis, W.Ramakrishna, V.S.Gupta & P.K.Ranjekar 
   (communicated to Proc.Natl.Acad.Sci.USA) 
   

6. mRNA differential display identifies sex specific transcripts in
papaya.
   W.Ramakrishna, A.S.Parasnis, V.S.Gupta & P.K.Ranjekar.

7. Sequence variations of rice (GATA)n microsatellite during cloning.
   A.M.Wadia, W.Ramakrishna, V.S.Gupta & P.K.Ranjekar.
 
8. Polymorphic organisation of knotted1 homeobox in cereals.
   A.Deshpande, W.Ramakrishna, G.Mulay, V.S.Gupta & P.K.Ranjekar  

9. Microsatellite polymorphisms in somaclonal variants in rice.
K.V.Choudari, 
   W.Ramakrishna, S.Tamhankar, V.S.Gupta, &  P.K.Ranjekar.

10.Molecular cloning and analysis of one member of a polymorphic family
of 
   GATA hybridizing DNA repeats in rice. A.M.Wadia, W.Ramakrishna, 
   K.V.Chowdari, V.S.Gupta & P.K.Ranjekar.


Patents Filed

1. A process for preparation of duplex polynucleotide useful for sex 
   determination of papaya plant. 
	A.S.Parasnis, W.Ramakrishna,V.S.Gupta & P.K.Ranjekar (Indian    
    patent).

2. A method for early detection of sex of papaya plant using a
microsatellite. 
   A.S.Parasnis, W.Ramakrishna, V.S.Gupta & P.K.Ranjekar. (US patent- 
   in preparation)

From owner-chromosomes@net.bio.net Wed Jul 09 23:00:00 1997
From: Damn Yankee<damnyankee@yankee.inc>
Newsgroups: bionet.genome.chromosomes
Organization: Yankee Inc.
Subject: I Am Very Sorry!!!
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Newsgroups: bionet.genome.chromosomes
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From owner-chromosomes@net.bio.net Thu Jul 10 23:00:00 1997
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From: mchowdhu@hgmp.mrc.ac.uk (Dr MZ Chowdhury)
Newsgroups: bionet.genome.chromosomes
Subject: trypsinogen
Date: 11 Jul 1997 16:42:52 +0100
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Hereditary Pancreatitis is cause by mutation in the third exon of the cationic 
trypsinogen gene. Ehrich and group have found another mutation in the second
exon.(Personal communications). They proposed that aetiology chronic pancreatitis
may be due to trysinogen mutation. Fibrocalculus pancreatic diabetes
(FCPD) where chronic pancreatitis and diabetes both occur. Aetiology of this disease not
known. We are trying to exclude trypsinogen gene mutation in FCPD families.
If any one get any new mutatin please let me know.
 
 

From owner-chromosomes@net.bio.net Sat Jul 12 23:00:00 1997
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From: jacob<jacob@friesl.net>
Newsgroups: bionet.genome.chromosomes
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From owner-chromosomes@net.bio.net Fri Jul 18 23:00:00 1997
Path: biosci!veg-physiol.med.uni-goettingen.de!HKP
From: HKP@veg-physiol.med.uni-goettingen.de (Herz-Kreislauf-Physiologie)
Newsgroups: bionet.genome.chromosomes
Subject: reply "classical genetics question"
Date: 19 Jul 1997 11:31:37 -0700
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I suppose, that this question is to be individually answered because the
two genetical similarities are quite similar (sorry for my english, two
beers....not american ones). Statistically two brothers should be more
similar than father and son:

Every brother has statistically 50% same autosomal sequences (sequences
from the same chromosome) from father and mother. That equals the 100%
of the paternal part of DNA for each of the brothers.
The difference should come from the X/Y-chromosomes. The male members of
our hypothetical family share their Y -no "plus-similarity" between
father and son... The X-chromosome of our brothers is, again
statistically, 50% identical (no cross over effects considered). So,
brothers are more similar to each other then to their parants (both of
them).

From owner-chromosomes@net.bio.net Fri Jul 18 23:00:00 1997
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From: "alan" <akon5@student.monash.edu.au>
Newsgroups: bionet.genome.chromosomes
Subject: test
Date: 19 Jul 1997 15:58:02 GMT
Organization: Monash Uni
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testing
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From owner-chromosomes@net.bio.net Sat Jul 19 23:00:00 1997
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From: "Smiffy" <smiffy@mail.anglianet.co.uk>
Newsgroups: bionet.genome.chromosomes
Subject: Re: Herpies simplex
Date: 20 Jul 97 09:48:02 GMT
Organization: Wisper
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Does any have or know where I can find information/papers on the Herpes
simplex virus and method of its insertion of gentic material within a cell
any vectors would be an added bonus.

Many thanks

From owner-chromosomes@net.bio.net Sat Jul 19 23:00:00 1997
Path: biosci!agate!ihnp4.ucsd.edu!munnari.OZ.AU!bunyip.cc.uq.edu.au!not-for-mail
From: BJ@mailbox.uq.edu.au (Bill and Jennie)
Newsgroups: bionet.genome.chromosomes
Subject: X chromosome crossover, meiosis
Date: Sun, 20 Jul 1997 00:21:07 GMT
Organization: University of Queensland
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Could anyone tell me whether, during meiosis to form human ova,
crossover of genetic material occurs on the arms of the X chromosomes?
I`m assuming that in meiosis in the human male, this does not occur,
and gametes are formed with sex chromosomes unaltered?


From owner-chromosomes@net.bio.net Sun Jul 20 23:00:00 1997
Path: biosci!bcm.tmc.edu!news.tamu.edu!sorghum.tamu.edu!user
From: ahp2343@bioch.tamu.edu (Andrew H Paterson)
Newsgroups: bionet.genome.chromosomes
Subject: Two postdoctoral positions in genome analysis
Date: Mon, 21 Jul 1997 18:31:08 -0500
Organization: TAMU
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NNTP-Posting-Date: 21 Jul 1997 23:28:13 GMT

TWO POSTDOCTORAL POSITIONS: GENOME ANALYSIS

Postdoctoral position, Unified molecular mapping of higher plant genomes.
A postdoctoral position is available (1 Sept) to develop and apply new
molecular methods for the comparative molecular analysis of diverse plant
taxa based on expressed genes, building upon extensive databases of prior
information (cf. GENETICS 138:499, 138:829, 141:391; PNAS-USA 92:6127;
SCIENCE, 269:1714-1718; NATURE GENETICS 14:380-382) and existing YAC/BAC
libraries.  The successful candidate will have a Ph.D. and strong
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commensurate with experience, competitive benefits.  To apply, mail full
CV, reprints of 2-3 first-authored publications, addresses and phones of
at least three professional references to Dr. Andrew Paterson, Plant
Genome Mapping Laboratory, Texas A&M University, College Station, TX
77843.  EMAIL ahp2343@bioch.tamu.edu.  Affirmative Action/EOE.

Postdoctoral position, Positional gene cloning in higher plants. A
postdoctoral position is available (1 Sept, possibly earlier) to isolate
well-mapped genes and QTLs that have played key roles in domestication of
grasses, especially the Sh-1 gene of sorghum, using extensive databases of
prior information (cf. GENETICS 138:499, 138:829, 141:391; PNAS-USA
92:6127; SCIENCE, 269:1714-1718; NATURE GENETICS 14:380-382), and existing
YAC/BAC libraries.  The successful candidate will have a Ph.D. and strong
publication record in genetics, molecular biology, microbiology, or allied
field, proven skills in cloning and analysis of large genomic DNAs, a high
level of professional motivation, strong communication in English, and
strong interpersonal skills.  Salary commensurate with experience,
competitive benefits. To apply, mail full CV, reprints of 2-3
first-authored publications, addresses and phones of at least three
professional references to Dr. Andrew Paterson, Plant Genome Mapping
Laboratory, Texas A&M University, College Station, TX 77843.  EMAIL
ahp2343@bioch.tamu.edu.  Affirmative Action/EOE.

From owner-chromosomes@net.bio.net Tue Jul 22 23:00:00 1997
Path: biosci!agate!howland.erols.net!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!mindspring!hydrant.mindspring.com!cssun.mathcs.emory.edu!cronkite.cc.uga.edu!UGA.CC.UGA.EDU!JHTSAO
From: JHTSAO@UGA.CC.UGA.EDU (jhtsao)
Newsgroups: bionet.genome.chromosomes
Subject: MAD COW DISEASE TRANSMISSIBLE TO HUMANS VIA MEAT
Date: Wed, 23 Jul 97 08:19:49 EDT
Organization: University of Georgia
Lines: 81
Message-ID: <17BB47529S86.JHTSAO@UGA.CC.UGA.EDU>
NNTP-Posting-Host: uga.cc.uga.edu

From: JHTSAO@UGA.CC.UGA.EDU (jhtsao)
Path: UGA.CC.UGA.EDU!JHTSAO
Newsgroups: rec.food.veg
Subject: MAD COW DISEASE TRANSMISSIBLE TO HUMANS VIA MEAT
Message-ID: <17BAEF23DS86.JHTSAO@UGA.CC.UGA.EDU>
Date: Thu, 17 Jul 97 17:13:33 EDT
Organization: University of Georgia
Keywords: BSE, TSE, CREUTZFELDT-JAKOB, KURU, MADCOW
 
  The following article appeared in Flagpole Magazine, Athens, GA, on July 2,
  1997, and is used by permission.  Flagpole Magazine's Website is: www.flagpole.
  com  --E-mail: flagpole@negia.net  Used by permission of the editor.
 
   "Modern Cannibalism"    by Maureen McGinley               Forget Clive Barker, Dean Koontz and Stephen King.  The most horrifying book
  of the year is a non-fiction account of the uncovering of a new form of disease
  about which you need to learn.
    Part of my motivation in writing this column is to get you readers to think
  more critically about the stuff that you eat.  There are certain basic ques-
  tions that are worth asking about food.  Who raised this?  What part of the
  world did it come from?  How was it grown?  What was it fed?  There are some
  new possible answers about meat in general and beef in particular in the book
  I just read that are deeply disturbing.
    The name of the book is _Deadly Feasts: Tracking the Secrets of a Terrifying
  New Plague._ Its author, Richard Rhodes, won a Pulitzer Prize for his last book
  on the making of the atomic bomb.  In this one, he tracks the development of a
  new class of diseases called transmissible spongiform encephalopathy (TSE), which
  includes  kuru  in New Guinea, Creutzfeldt-Jakob disease, scrapie in sheep,
  transmissible mink encephalopathy (TME), and bovine spongiform encephalopathy
  (BSE), a.k.a. mad cow disease.
    All of the TSE types share some interesting features.  They are one hundred
  percent fatal.  They share many of the same traits as Alzheimer's and A.L.S.,
  except that they are transmitted through food rather than genetically.  Their
  distinguishing characteristic is the formation of amyloid plaques in the brain.
  These plaques, which show up on tissue samples when stained with Congo red dye,
  visually remind me of bad spots on peaches.  There is no "Patient Zero," or
  single case to which all other cases may be traced back, as is the case with
  Ebola and other diseases.  The incubation period, if it may be called that,
  can be up to 40 years in humans.
    Transmissible spongiform encephalopathies are not spread by germs or viruses
  like normal diseases. Instead, the agents of transmission are crystalline in
  nature.  Some scientists refer to these things as prions.  Prions are unique
  cellular disease units because there is no known way of destroying them.
  Tissue samples which were preserved in formaldehyde have been liquefied and
  and injected into animals, which then came down with the disease.  Samples
  have also been baked in an oven at 350 degrees until they were reduced to ash
  and injected with the same results.
    Scariest of all, TSE has no inter-species transmission barrier.  This means
  that if a cow is fed on bone and blood meal, which contains ground up mink,
  monkeys, cats, dogs, sheep or other cows that have died from TSE, then that
  cow could come down with the disease as well. If that cow is then turned into
  hamburger and eaten by humans, sometime in the next 40 years, the human brains
  may turn into sponges from TSE. Also, if the humans fertilize their roses with
  bone meal and happen to inhale while doing so, or put manure from infected
  animals on their vegetables, the same thing could happen.
    Richard Rhodes does a masterful job of outlining the developments in the
  research done in this area.  He starts out describing the culture of the Fore,
  a tribe of Papua New Guinea, whose women and children (and sometimes men) ate
  their dead.  Some villages ended up consisting entirely of men.  From there, he
  traces the line through efforts to find a cure for scrapie, a lethal sheep
  disease, in Britain, TME in mink in Colorado, BSE in cattle in Britain and the
  U.S., and finally Creutzfeldt-Jakob Disease, which killed 12 young people in
  Britain.  His description of the political battles over CJD are almost comic.
  In France, many cows came down with "tractor disease," where farmers would bury
  cows who had died of BSE, so that they would not have to destroy their herds.
  Blood and bone meal was hurriedly exported both legally and illegally from
  Britain to feed European livestock in a dizzying dance of bureaucratic illogi-
  cality.
    Since I read this book, I have heard about a woman who died of
  Creutzfeldt-Jakob Disease in California, and a ban on feeding imported bone
  and blood meal to U.S. cattle.  Government officials are, of course, saying
  that it can't happen here.  In his final book of the  _2001: A Space Odyssey_
  series, Arthur Clarke kills off most of the earth's population with CJD.
    Humans are the most idiotic of creatures at times.  Like the Fore, who took
  to eating human remains because they asked the question, "Why should we waste
  this good meat?," we force livestock and other animals to become cannibals
  by feeding the ground-up remains of their own kind.  It should come as little
  surprise that disastrous consequences are now occurring.  Once again, Nature
  is trying to teach us the same old lesson: You cross the line, you pay the
  price.
 
  (C) Flagpole Magazine, 1997

From owner-chromosomes@net.bio.net Tue Jul 22 23:00:00 1997
Path: biosci!agate!newsfeed.kornet.nm.kr!news.maxwell.syr.edu!infeed1.internetmci.com!newsfeed.internetmci.com!mindspring!hydrant.mindspring.com!cssun.mathcs.emory.edu!cronkite.cc.uga.edu!UGA.CC.UGA.EDU!JHTSAO
From: JHTSAO@UGA.CC.UGA.EDU (jhtsao)
Newsgroups: bionet.genome.chromosomes
Subject: Re: MAD COW DISEASE TRANSMISSIBLE TO HUMANS VIA MEAT
Date: Wed, 23 Jul 97 08:21:40 EDT
Organization: University of Georgia
Lines: 199
Message-ID: <17BB47599S86.JHTSAO@UGA.CC.UGA.EDU>
NNTP-Posting-Host: uga.cc.uga.edu

From: JHTSAO@UGA.CC.UGA.EDU (jhtsao)
Path: UGA.CC.UGA.EDU!JHTSAO
Newsgroups: rec.food.veg
Subject: Re: MAD COW DISEASE TRANSMISSIBLE TO HUMANS VIA MEAT
Message-ID: <17BB29619S86.JHTSAO@UGA.CC.UGA.EDU>
Date: Mon, 21 Jul 97 10:39:42 EDT
Organization: University of Georgia
References: <17BAEF23DS86.JHTSAO@UGA.CC.UGA.EDU> <19970718174832655743@mri2.mri.montana.edu>
 
In article <19970718174832655743@mri2.mri.montana.edu>
umbjm@gemini.oscs.montana.edu (John Mercer) writes:
 
>
>jhtsao <JHTSAO@UGA.CC.UGA.EDU> wrote:
>
>>   The following article appeared in Flagpole Magazine, Athens, GA, on July
>>   2, 1997, and is used by permission.  Flagpole Magazine's Website is:
>>   www.flagpole. com  --E-mail: flagpole@negia.net  Used by permission of
>>   the editor.
>>
>>    "Modern Cannibalism"    by Maureen McGinley               Forget Clive
>>   Barker, Dean Koontz and Stephen King.  The most horrifying book of the
>>   year is a non-fiction account of the uncovering of a new form of disease
>>   about which you need to learn.
>
>Yes, you certainly do!
>
>>     Part of my motivation in writing this column is to get you readers to
>>   think more critically about the stuff that you eat.  There are certain
>>   basic ques- tions that are worth asking about food.  Who raised this?
>>   What part of the world did it come from?  How was it grown?  What was it
>>   fed?  There are some new possible answers about meat in general and beef
>>   in particular in the book I just read that are deeply disturbing. The
>>   name of the book is _Deadly Feasts: Tracking the Secrets of a Terrifying
>>   New Plague._ Its author, Richard Rhodes, won a Pulitzer Prize for his
>>   last book on the making of the atomic bomb.  In this one, he tracks the
>>   development of a new class of diseases called transmissible spongiform
>>   encephalopathy (TSE), which includes  kuru  in New Guinea,
>>   Creutzfeldt-Jakob disease, scrapie in sheep, transmissible mink
>>   encephalopathy (TME), and bovine spongiform encephalopathy (BSE), a.k.a.
>>   mad cow disease.
>
>Rhodes never claims, as does the poster, that the disease is transmitted
>by eating meat. There is no evidence to date linking vCJD to
>meat-eating. Brain-eating, yes; meat-eating, no.
>
>See the difference?
>
>---snip---
>
>
>--
>John Mercer
>Scientist
>McLaughlin Research Institute
 
Ever heard of brains for breakfast?  :-)
It's not vegetarian, but in some parts of the U.S. you find it on the
menus of small town restaurants. I was not vegetarian until after reading
Rhodes' book, but even back in those days the idea of scrambled brains as
a breakfast dish offended me.
 
Let me quote some passages from the book:
p. 208
...Dr. James Ironside is a pathologist with the British National CJD Sur-
veillance Unit in Edinburgh.  In September 1995, studying a brain cross
section from the teenage boy who had recently died of Creutzfeldt-Jakob
disease, Ironside found amyloid plaques so large that they looked under the
microscope like chrysanthemum blooms. They were not confined to the cere-
bellum, the pathologist determined, but spread throughout the brain. They
stained for PrP.  Unlike the smaller plaques of ordinary CJD, these florid
plaques were surrounded by a zone of spongiform change--a destructive
halo of holes.
   Ironside had never seen this unusual pattern of damage before, but he
knew that sporadic CJD pathology varied widely from case to case. He was
startled, then, when another teenage case turned up almost immediately with
identical pathology. He alerted the director of the Surveillance Unit, Dr.
Robert Will.  Will mobilized the Unit's staff.  Staff members quickly
turned up six more suspect cases in young people.  At first Will and Ironside
thought the youthfulness of the victims might be the reason for the similari-
ties in their pathology.  When the physicians checked the medical literature,
however, they learned that the few rare cases of CJD in people under thirty
in Britain and Europe showed no such florid plaques widespread in the brain.
Late in 1995, Surveillance Unit staff began traveling the country interviewing
the victims' families to rule out familial CJD or iatrogenic CJD from growth
hormone or surgery.
   By the end of February 1996, Will and Ironside knew they had an epidemiolo-
gical cluster: eight cases of CJD in young people that all showed a new neuro-
pathological profile of florid plaques, early loss of coordination and late
dementia.  Will arranged to report the ominous new finding to the Spongiform
Encephalopathy Advisory Committee (SEAC), a group of scientists and physicians
appointed to advise the British government on BSE. A SEAC meeting was set for
March 8.  Ironside opened the meeting with slides illustrating the unusual
pathology.  The SEAC chairman, Dr. John Pattison, remembers the moment vividly:
"Before he said anything, we could see what it was.  It was dramatically dif-
ferent."  Another SEAC member, Dr. Jeffrey Almond, recalls near panic.  "The
atmosphere became genuinely quite tense.Some of us were afrain that this really
maybe indicated a transmission (of BSE) to humans.
...Will and Ironside now had a tenth case to report.  All ten showed the same
unique pathology  All had what (Carleton) Gajdusek (Nobel Prize-winning
researcher) would later identify as kuru plaques: the florid plaques may not
have been seen in Britain and Europe, but they were diagnostic signs of kuru
in Papua New Guinea....SEAC finalized its recommendations the next morning.
They included destroying all British cattle over thirty months of age.
p. 212. Robert Will would tell a London newspaper of these ten cases that
"their brain tissue displayed a distinctive disease pattern closer to the
damage inflicted on a cow's brain by BSE than the damage normal CJD inflicts
on humans."
    At the SEAC session on March 19, senior members of the British Cabinet
tried to suppress any announcement of the new variant form of CJD, arguing
that the scientists might be wrong.  The Secretary of State for Health,
Stephen Dorrell, insisted that the public had to be told.  Wednesday, March
20, speaking in the House of Commons, Dorrell informed a stunned nation that
BSE had probably spread to humans from eating beef.
    Wouldn't you know.
p.217. French and British researchers reported in June that they had success-
fully infected rhesus monkeys with BSE and that the resulting lesions looked
like the new-variant CJD (vCJD), with florid kuru plaques haloed with holes.
"It's the first experimental argument," the French researchers told the media--
 
"and a very strong one--in favor of a link" between the two diseases. BSE
transmission to macaques, reported the same month in _Nature_, gave further
evidence of a link: "...The pathological 'signature' of the BSE agent in...
kuru plaques were seen in tow macaques inoculated at the same time with
sporadic CJD.  Interpreting those results, a Swiss neuropathologist found
"unsettling" the fact that the modest amounts of infected tissue inoculated
directly into the brains of the vCJD macaques were "well within the range
of brain tissue present in commercial food products for human consumption
until a few years ago."  We can hope, the neurolopathologist observed, "that
the oral route of administration will be considerably less efficient."
But the six sheep Douglass Hogg had mentioned had each been fed only five
hundred milligrams of brain extract--about one-fiftieth of an ounce--and the
fact that so small an oral dose had infected one with BSE did not encourage
optimism.
p.220. ...Just as MAFF had restricted access to its animal studies and sta-
tistics, so did Robert Will of the CJD Surveillance Unit restrict information
on his ongoing investigation of new suspect cases of vCJD.  But when French
scientists reported two additional, highly suspect French cases in spring
1996, Will refused to reciprocate wtih information on further British cases
he might be investigating.  Someone leaked the information:  the London
Sunday Times reported in June that beyond the eleven previously confirmed
in Britain and one in France, the CJD Surveillance Unit was following five
more suspect cases in the summer of 1996.
       Carleton Gajdusek called me in mid-July sounding apocalyptic.       .
"They don't have the least idea what caused the human cases," he told me.
"It's kuru and nothing but kuru, and any species could be carrying it--dairy
cows, beef cattle, pigs, chickens.  They need to assess the risk and deal
with it realistically.  All the pigs in England fed on this meat-and-bone
meal.  The disease hasn't turned up in pigs only because you don't keep pigs
alive for seven or eight years; they're killed after two or three years at
most.  When we kept pigs we'd inoculated in our laboratory for eight years,
they came down with scrapie.  Probably all the pigs in England are infected.
And that means not only pork.  It means your pigskin wallet. It means catgut
surgical suture, because that's made of pig tissue. All the chickens fed on
meat-and-bone meal; they're probably infected.  You put that stuff in a chicken
and it goes right through. A vegetarian could get it from chickenshit that
they put on vegetables.  It could be in tallow, in butter--how the hell am
I supposed to measure infectivity in butter?  No one on earth knows how to
do that.  These people who've come down with CJD have given blood.  It's
undoubtedly in the blood supply.  The answer in that case is, stop giving
anyone blood who doesn't really need it.  Bob Will and those people don't
know anything about where it came from.  But I'll tell you this.  If it
turns up in one kid under fifteen, it's kuru.  And by the way, it could
be in the milk.  That hasn't been excluded either."
P.221....Dr. John Collinge, a neurologist at St. Mary's Hospital in London,
and colleagues including James Ironside reported in _Nature_ that the
molecular signature of BSE in cattle matched the molecular signature of
variant CJD.
p.220...With BSE, (Richard) Lacey pointed out, there was no certainty that
the source of infection had been cut off; indeed, there was evidence that
animals were still becoming infected with BSE and every reason to suspect
that animals incubating BSE were still entering the human food supply.
The consequences, he feared, could be dire for the British as they had
been dire for the Fore.  "If it seems that the incubation-period average
for CJD in humans begins to be about twenty-five years, maybe thirty years,"
he told me grimly, "then the peak human epidemic will come around the year
2015.  If the current numbers of variant CJD cases increase by fifty percent
per year compound, as they well might, that wuld take it to about two hundred
thousand cases a year by then." HUMAN cases, that is: 200,000 deaths PER
YEAR.
p. 230...The British government, by making the wrong public-health choices,
has conducted a frightening natural experiment, allowing a lethal disease
agent to spread through the human food supply, exposing the entire British
population.  There is every reason to believe exposure is continuing, from
infected beef and possibly from infected lamb and mutton as well.
...The lack of vCJD deaths outside France doesn't mean that the rest of the
continent is free of human infection; the French deaths indicate merely
that exposure began there earlier.  Nor do the limited number of vCJD
deaths identified so far offer any basis for assessing the future of the
disease agent.  The ease with which BSE crosses species barriers and the fact
that it is easily transmissible orally in small doses suggest that it may
be an exceptionally virulent strain.
p.231. What about the rest of the world?  If TSEs occur sporadically in
animal species, as CJD does in humans, then no population anywhere in the
world that eats meat is entirely free of risk.
------
Excerpts from the book _Deadly Feasts: Tracking the Secrets of a Terrifying
New Plague_, by Richard Rhodes (Pulitzer Prize winning author), published
by Simon and Schuster, New York, 1997.

From owner-chromosomes@net.bio.net Thu Jul 24 23:00:00 1997
Path: biosci!daresbury!not-for-mail
From: Rifat Hamoudi <rifat@icr.ac.uk>
Newsgroups: bionet.genome.chromosomes
Subject: Type III restriction enzymes
Date: 25 Jul 1997 01:48:40 +0100
Lines: 18
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <5r8t58$h17@mserv1.dl.ac.uk>
Reply-To: rifat@icr.ac.uk
Delivery-Receipt-To: Rifat Hamoudi <rifat@icr.ac.uk>
MIME-Version: 1.0
X-Authentication: IMSP
Original-To: biochrom@dl.ac.uk


Hi,

	Does anyone know where I can obtain Type III restriction 
enzymes (e.g. 25bp cutters).

If you know of a place that make them I would be grateful if you
could let me know.

thanks.


Rifat.

rifat@icr.ac.uk




From owner-chromosomes@net.bio.net Thu Jul 24 23:00:00 1997
Path: biosci!GAES.GRIFFIN.PEACHNET.EDU!mhopkin
From: mhopkin@GAES.GRIFFIN.PEACHNET.EDU ("Mark Hopkins")
Newsgroups: bionet.genome.chromosomes
Subject: unsubscribe
Date: 25 Jul 1997 05:05:34 -0700
Organization: Plant Genetic Resources Conservation Unit
Lines: 5
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199707251204.IAA09824@gaes.griffin.peachnet.edu>
NNTP-Posting-Host: net.bio.net

To whom it may concern;

  Please unsubscribe.  Thank you.

Mark

From owner-chromosomes@net.bio.net Sat Jul 26 23:00:00 1997
Path: biosci!internet!biosci!not-for-mail
From: biohelp (BIOSCI Administrator)
Newsgroups: bionet.genome.chromosomes
Subject: BIOSCI/bionet miniFAQ & Fundraiser
Date: 27 Jul 1997 02:00:07 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
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Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199707270900.CAA01992@net.bio.net>
NNTP-Posting-Host: net.bio.net

(LAST REVISION: 30-JUL-95)

This BIOSCI "miniFAQ" is designed to answer the questions that come up
the *most frequently*.  The main BIOSCI FAQ (Frequently Asked
Questions) is accessible on the World Wide Web at URL
http://www.bio.net/.

If you can not find an answer to your question in this or other
documentation, the BIOSCI technical support staff answers e-mail
queries sent to

		       biosci-help@net.bio.net

We can only answer questions about the use of the newsgroups and
mailing lists.  We unfortunately do not have the staff to do Internet
information searches or answer scientific questions.  Please post
those to the appropriate BIOSCI/bionet newsgroups.


	Contents:
	--------
	0) BIOSCI NEEDS YOUR SUPPORT!!

	1) Using the WWW to access the BIOSCI/bionet newsgroups.

	2) What to do about "spams," i.e., junk mail, ads, etc.

	3) Examples of subscribing and unsubscribing to the mailing lists.

	4) The BIOSCI user address and research interest directory.


0) BIOSCI NEEDS YOUR SUPPORT!!
------------------------------
BIOSCI's government funding has been expended, and we are now
operating solely from advertising revenue that we have raised from our
Web site at http://www.bio.net/.  We need just a few minutes of your
time to help us serve you.

You can do two important things which will take very little time for
you individually and will immensely help us continue to help you.

First, please use our WWW system at http://www.bio.net/ to access the
archives.  You can post or reply to messages via your Web browser as
described in item #1 below.  Your usage helps attract sponsors. If you
contact any of our sponsors, please be sure to thank them for
supporting BIOSCI. It is critical for them to get this feedback if
they are to continue their sponsorship for the long term.

Second, if you work for a company or organization that provides
products or services of interest to the biology community, please pass
this message on to your marketing or marketing communications
department or other appropriate group.  Please ask them to help
support BIOSCI by sponsoring our Web site and explain the uses and
benefits of the system to the biology community. If they are
interested, they can then contact us for further information at our
tech support address, biosci-help@net.bio.net.


1) Using the WWW to access the BIOSCI/bionet newsgroups.
--------------------------------------------------------
As of 10 December 1995, all BIOSCI/bionet full newsgroups are
accessible through the World Wide Web (WWW) at URL http://www.bio.net.
One can read and reply publicly or privately to both recent postings
and archived messages through one's Web browser if it is configured
properly to send e-mail.  Each newsgroup is equipped with its own WAIS
index.  The main BIOSCI home page also has access to the BIO-JOURNALS
Table of Contents database WAIS index and the BIOSCI user address
database described in another item further below.


2) What to do about "spams," i.e., junk mail, ads, etc.
-------------------------------------------------------
BIOSCI is a set of parallel USENET newsgroups (the "bionet" groups),
mailing lists, and a hypermail archive at URL http://www.bio.net/.
The same postings are distributed on all media (except for a small
number of mailing-list-only groups at net.bio.net).  Unfortunately it
is becoming a despicable practice on the Internet (by a few people out
to make a fast buck) to do automated mass postings to thousands of
newsgroups and mailing lists.  These attempts to grab free advertising
are refered to as "spams" in the usual, somewhat boneheaded, net
terminology.  USENET is more susceptible to this practice, and many
spams originate on the USENET groups and then are passed on to the
mailing lists.  However, spammers also get lists of mailing addresses
and hit these too, so neither medium is immune.

What should you do personally if you get junk mail?
---------------------------------------------------
Just delete it and move on without reading it further.  Filing a
protest is becoming increasingly useless because spammers are often
disguising the addresses where the messages are sent from.  Unless you
really understand Internet mail systems, your attempt at protest by
sending replies to the message will often end up being sent to the
address of an innocent person that the spammer is victimizing.

What can BIOSCI/bionet do to protect its newsgroups?
----------------------------------------------------
The only solution currently available is to moderate the newsgroup.
If this newsgroup is already moderated, then you are in good shape.
Moderation protects the USENET distribution from about 95% of the
spams that are being sent to date and protects the mailing lists
completely.  Moderation means, however, that someone has to take the
time to review each message before it goes out.  We have set up
software here that simply allows the moderator to forward to an
address at net.bio.net messages that (s)he wishes to have distributed.
This takes no more time than that needed to read the message and pass
it on, say about 1 min. per message.

Most newsgroups currently have a discussion leader who is responsible
for their newsgroup.  The discussions leaders and their e-mail
addresses are listed in the BIOSCI Information Sheet which is
available on the Web at http://www.bio.net/.  If a newsgroup is being
hit with too many junk postings, please contact the discussion leader
for that group and see if there is interest in moderating the group.
Please do not assume that by simply posting a complaint to the
newsgroup itself, anyone on the BIOSCI staff will act on your
complaint.  With close to 100 newsgroups to run, the BIOSCI staff has
to rely on the discussion leaders of each newsgroup to report problems
directly to us at biosci-help@net.bio.net.

We will moderate any of our newsgroups if the discussion leader tells
us that the readership of the group wishes to do so and if a moderator
is willing to do the work.  For most BIOSCI/bionet groups, this
entails only a few minutes of work each day.

Moderating a newsgroup will resolve probably 95% of the junk postings
on the USENET distribution.  Unfortunately there are easy ways for
determined spammers to override the moderation mechanism on USENET,
but we can protect our e-mail subscribers from unwanted postings if
the newsgroup is moderated.  You can also access our newsgroups over
the WWW at URL http://www.bio.net.  While this Web interface will not
stop spammers from trying to post to the groups, this will give you
yet another way, besides using USENET news, to keep the junk out of
your personal mail files.  For those of you with local USENET news
systems, the Web interface will also give you faster access to new
newsgroups and recent postings.


3) Examples of subscribing and unsubscribing to the mailing lists.
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From owner-chromosomes@net.bio.net Sat Jul 26 23:00:00 1997
Path: biosci!daresbury!uninett.no!news-feed.inet.tele.dk!europa.clark.net!4.1.16.34!cpk-news-hub1.bbnplanet.com!su-news-hub1.bbnplanet.com!news.bbnplanet.com!news.alt.net!news1.alt.net!huron.eel.ufl.edu!usenet.ece.ufl.edu!freenet2.afn.org!afn50752
From: Danny Oakes <afn50752@afn.org>
Newsgroups: bionet.cellbiol,bionet.genome.chromosomes,bionet.molbio.methd-reagnts,sci.bio.botany,sci.bio.misc,sci.agriculture,sci.environment,rec.gardens,rec.gardens.edible,rec.gardens.orchids
Subject: plant cloning wheel w/testtubes ?
Date: Sun, 27 Jul 1997 04:29:13 -0400
Lines: 60
Message-ID: <Pine.A32.3.95.970727033748.32425A-100000@freenet2.afn.org>
Reply-To: Danny Oakes <afn50752@afn.org>
NNTP-Posting-Host: freenet2.afn.org
Mime-Version: 1.0
Content-Type: TEXT/PLAIN; charset=US-ASCII
Xref: biosci bionet.cellbiol:7838 bionet.genome.chromosomes:1760

First, let me apologize for my cross-posting.  I don't usually do
this; but, I really would like info on the following:

Did anyone else see this and can any of you tell me where to get
more info on the following ?

Several years ago, I saw a TV show news or documentary that showed
some group of people creating many identical plants from one plant.
From the looks of the room, I assume that this was all taking place
in a university environment or a very small company startup operation.
They took a little tiny sliver(?) of the parent plant.  They placed
the sliver in a test tube with a fairly clear liquid that filled the
tube to around half full and I believe they placed a stopper in the
top of the tube.

The tubes were then inserted into holes in a round circular piece of 
plywood(?)  disk, about 1/2 inch thick and about 36 to 48 inches in
diameter.  This disk was rotating at a very slow speed, about one
revolution per minute.  The plane of the rotating disk was angled up
from a horizontal plane, at an angle of approximately 60 to maybe 75
degrees.

I also assume there was some grow lights involved or maybe the assembly
was placed outside for light source energy.

The plant sliver gradually developed roots in the liquid medium while
on the rotating disk.  The program implied and showed that each of
small beginning plants were about 3 inches long from root tip to plant
top.  I'm not quite sure how they maintained the point that I would
call (due to my plant ignorance) the "ground level" or maybe "trunk/root
boundary" of the plant.

I would like to find out more about the entire process.  I would especially
like to find out what the clear liquid was, in the test tube. 

Can anyone help ???  Please e-mail me directly or call me if you are local.

If you need any engineering-type questions answered, please feel free to
ask.  I am currently un-employed ad have plenty of time on my hands due
mainly to age descrimination (53yo), arthritis and diabetes.  I am trying
to find something to do with my time.

I also have another idea about how to grow minature plants of any type of
plants using a computer controlled green house using my own software.  If
anyone local to me has a desire to get involved with this idea, I think we
could make a lot of money.  This paragraph has nothing to do with the
request for information asked for above. 

Thanks in advance.

Danny Oakes
licensed professional engineer in the state of Florida
Gainesville, Florida
(352) 495-3371 day or night







From owner-chromosomes@net.bio.net Mon Jul 28 23:00:00 1997
Path: biosci!daresbury!is.bbsrc.ac.uk!news
From: David Hills <david.hills@bbsrc.ac.uk>
Newsgroups: bionet.genome.chromosomes
Subject: PROPORTION OF CHROMS. SEQUENCED
Date: 29 Jul 1997 11:12:55 GMT
Organization: Roslin Institute (Edinburgh)
Lines: 4
Message-ID: <5rkj7n$l1p@is.bbsrc.ac.uk>
NNTP-Posting-Host: pc0616.ri.bbsrc.ac.uk
Mime-Version: 1.0
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Where can I find out what and how much of the human chromosomes have been 
sequenced?
Dave


From owner-chromosomes@net.bio.net Wed Jul 30 23:00:00 1997
Path: biosci!KUCCNX.KOREA.AC.KR!skmgl
From: skmgl@KUCCNX.KOREA.AC.KR (skmgl)
Newsgroups: bionet.genome.chromosomes
Subject: one or two hybridization??
Date: 30 Jul 1997 23:02:42 -0700
Organization: KOREA UNIV. graduated school of Biotechnology
Lines: 5
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <33E02ACE.C15@kuccnx.korea.ac.kr>
Reply-To: skmgl@kuccnx.korea.ac.kr
NNTP-Posting-Host: net.bio.net

hi,
I don't know about one or two hybridization system.
(It's principles and methods et al...)
Please tell me informations.
regards

From owner-chromosomes@net.bio.net Thu Jul 31 23:00:00 1997
Newsgroups: bionet.genome.chromosomes
From: katie@ifm.mh-hannover.de (Katrin Ausmeier)
Subject: mouse genome and markers
Content-Type: text/plain; charset=ISO-8859-1
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Content-Transfer-Encoding: 8bit
Organization: Inst. Molecular Biology
X-Newsreader: Yet Another NewsWatcher 2.4.0
Mime-Version: 1.0
Date: Fri, 1 Aug 1997 16:48:37 GMT
Lines: 11
Path: biosci!news.Stanford.EDU!su-news-hub1.bbnplanet.com!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!news.apfel.de!fu-berlin.de!uniol!news.rz.uni-hildesheim.de!tyr.mhrz.mh-hannover.de!MHH!katie

Hi, 
I'm a student in a lab in germany working on a mouse mutation called Fused
toes. The mutation is characterized by a large deletion of the genomic DNA
on chromosome 8 in region D. I would like to determine the size of the
deleted region by checking some genomic markers. (The maximum size of the
deletion should be 1000 kb, because I could not observe changes in the
chromosome structure.)
Is there anyone who can explain me which markers I could use in my
experiments??? 
Regards
Katrin Ausmeier

