From owner-recombination@net.bio.net Mon Apr 01 23:00:00 1996
Path: biosci!ns1.faseb.org!lamarck.sura.net!newsfeed.internetmci.com!uwm.edu!lll-winken.llnl.gov!nntp.coast.net!swidir.switch.ch!scsing.switch.ch!rzunews.unizh.ch!NewsWatcher!user
From: hubscher@vetbio.unizh.ch (Ulrich Hubscher)
Newsgroups: bionet.molbio.methds-reagnts,bionet.general,bionet.genome.chromosomes,bionet.molbio.proteins,bionet.molbio.yeast,bionet.virology,bionet.molbio.recombination
Subject: ANNOUNCE: EMBO Workshop on Molecular Biology of DNA Replication
Date: Tue, 02 Apr 1996 16:39:07 +0100
Organization: Universitat Zurich-Irchel
Lines: 46
Message-ID: <hubscher-0204961639070001@130.60.120.18>
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Xref: biosci bionet.molbio.methds-reagnts:42570 bionet.general:20910 bionet.genome.chromosomes:1104 bionet.molbio.proteins:7493 bionet.molbio.yeast:5039 bionet.virology:6861 bionet.molbio.recombination:153

EMBO WORKSHOP:

MOLECULAR BIOLOGY OF DNA REPLICATION

September 8 - 13, 1996 Weggis (Luzern), Switzerland


                      Organizers:
                      U. Hubscher, Zurich
                      P. Plevani, Milano
                      S. Spadari, Pavia

The main topics which will be covered are:

Regulatory mechanisms controlling entry into S-phase; replisome assembly
and its functional organization within the nucleus; protein-protein
interactions among replication proteins; structural organization of the
replisome; connection between DNA replication and other DNA transactions
(e.g. repair, transcription).

Keynote address:
Bruce Stillman
Cold Spring Harbor Laboratory
New York, USA

The registration fee of CHF 850.
includes all meals, lodging and
social events.
A certain amount of the budget will
be reserved to partially refund the
registration fee to young applicants.

Appllcations contalnlng one page abstract shoud be sent as soon as
possible but not later than May 31st, 1996 to:

EMBO WORKSHOP 96: Universitat Zurich-lrchel, Institut fur
Veterlnarbiochemie Winterthurerstrasse 190 CH-8057 Zurich, Switzerland

_____________________________________________________________________
Ulrich Hubscher
Institut fur Veterinarbiochemie               Tel: (41-1)-257-54-72
Universitat Zurich-Irchel                     Fax: (41-1)-257 59 04
Winterthurerstrasse 190
CH-8057 Zurich
Switzerland
_____________________________________________________________________

From owner-recombination@net.bio.net Wed Apr 03 23:00:00 1996
Path: biosci!rutgers!csn!news-1.csn.net!imci3!imci4!newsfeed.internetmci.com!info.ucla.edu!library.ucla.edu!news.ucdavis.edu!boris.ucdavis.edu!not-for-mail
From: ez014377@boris.ucdavis.edu (Daniel Anderson)
Newsgroups: bionet.molbio.recombination
Subject: Re: Info On Homologous recombination
Date: 3 Apr 1996 19:50:25 GMT
Organization: University of California, Davis
Lines: 12
Distribution: world
Message-ID: <4jukq1$h03@mark.ucdavis.edu>
References: <3159C961.1060@odyssee.net>
NNTP-Posting-Host: boris.ucdavis.edu
X-Newsreader: TIN [UNIX 1.3 950824BETA PL0]

Graham Dellaire (dellaire@ODYSSEE.NET) wrote:
: For a good overview of recombination of all kinds try to find this book:

Dont forget S Kowaczykowski et al review on the Biochemistry of H R.

Biochemistry of Homologous Recombination in Escherichia coli

Microbiological Reviews, Sept. 1994, p.401-465
Vol. 58, No. 3

-Dan


From owner-recombination@net.bio.net Sun Apr 07 23:00:00 1996
Path: biosci!PO-BOX.MCGILL.CA!popa0206
From: popa0206@PO-BOX.MCGILL.CA
Newsgroups: bionet.molbio.recombination
Subject: Replication EMBO workshop!!! (repost;.... server troubles)
Date: 8 Apr 1996 13:53:01 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 49
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199604082051.QAA02634@sirocco.CC.McGill.CA>
NNTP-Posting-Host: net.bio.net

THis is a repost for Ulrich

EMBO WORKSHOP:

MOLECULAR BIOLOGY OF DNA REPLICATION

September 8 - 13, 1996 Weggis (Luzern), Switzerland


                      Organizers:
                      U. Hubscher, Zurich
                      P. Plevani, Milano
                      S. Spadari, Pavia

The main topics which will be covered are:

Regulatory mechanisms controlling entry into S-phase; replisome assembly
and its functional organization within the nucleus; protein-protein
interactions among replication proteins; structural organization of the
replisome; connection between DNA replication and other DNA transactions
(e.g. repair, transcription).

Keynote address:
Bruce Stillman
Cold Spring Harbor Laboratory
New York, USA

The registration fee of CHF 850.
includes all meals, lodging and
social events.
A certain amount of the budget will
be reserved to partially refund the
registration fee to young applicants.

Appllcations contalnlng one page abstract shoud be sent as soon as
possible but not later than May 31st, 1996 to:

EMBO WORKSHOP 96: Universitat Zurich-lrchel, Institut fur
Veterlnarbiochemie Winterthurerstrasse 190 CH-8057 Zurich, Switzerland

_____________________________________________________________________
Ulrich Hubscher
Institut fur Veterinarbiochemie               Tel: (41-1)-257-54-72
Universitat Zurich-Irchel                     Fax: (41-1)-257 59 04
Winterthurerstrasse 190
CH-8057 Zurich
Switzerland
_____________________________________________________________________


From owner-recombination@net.bio.net Mon Apr 08 23:00:00 1996
Path: biosci!ODYSSEE.NET!dellaire
From: dellaire@ODYSSEE.NET (Graham Dellaire)
Newsgroups: bionet.molbio.recombination
Subject: JOB LISTINGS NEW FOR APRIL!!! (McGill University!)
Date: 9 Apr 1996 16:40:43 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 189
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <01BB264B.44D78BC0@pool10_13.odyssee.net>
NNTP-Posting-Host: net.bio.net

Here are a few of the job listings this month at=20

ExpMed Job Listings=20

http://www.medcor.mcgill.ca/EXPMED/DOCS/jobs.html
****************************************************************
Job Listing #3=20

Ph.D. Project Involving Role of Nitric Oxide (NO) in Cellular Iron =
Metabolism

Prem Ponka, M.D., Ph.D=20

Lady Davis Institute For Medical Research=20

Sir Mortimer B. Davis-Jewish General Hospital

Montreal, Quebec, Canada=20

Project description:=20

Dr. Ponka has one MRC studentship voucher for which he can guaranteed a =
5-year MRC studentship to a qualified student
of his choice.=20

Areas of research=20

   1.Cellular iron metabolism=20
          role of iron in cell proliferation=20
          role of iron in free radical formation=20
          role of nitric oxide (NO) in cellular iron metabolism=20

   2.Development of new iron chelators of significance to:=20
          iron overload=20
          inhibition of free radical reactions=20
          neoplastic cell replication

   3.Erythroid differentiation=20

   4.Heme sythesis regulation

Recent publications:=20

     Richard, D.R., Neumannova, V., and Ponka, P.: Nitrogen monoxide =
decrease iron uptake from transferrin but
     does not mobilise iron from prelabelled neoplastic cells.=20
     Biochim. Biophys. Acta 1266:250-260 (1995)

     Richard, D.R., Neumannova, V., Nagy, E., and Ponka, P.: The effect =
of redox-related species of nitrogen
     monoxide on transferrin and iron uptake and cellular proliferation =
of erythroleukemia (K562) cells.=20
     Blood 86: 3211-3219 (1995)=20

     Loyevksy, M., Tsafack, A., Ponka, P., and Cabantchik, Z.I.: Mode of =
action of iron (III) chelators as
     antimalarials. IV. Potentiation of Desferal action by benzoyl- and =
isonicotinoyl-hydrazone derivative. J. Lab.
     Clin. Med. (in press)

Positions:

     Ph.D. Postion=20

          Qualifications: B.Sc. with solid background in molecular and =
cellular biology. B.Sc. in Biochemistry is an
          advantage, but high achievment in any allied field will also =
be considered favorable. g.p.a.: 3.5 of
          higher.=20


To Apply:

For further information please contact:=20

Prem Ponka, M.D., Ph.D.=20

Lady Davis Institute For Medical Research=20

Sir Mortimer B. Davis-Jewish General Hospital
3755 Cote St. Catherine Road
Montreal, Quebec, Canada
H3T 1E2=20

Tel: (514) 340 8260=20

Fax: (514) 340 7502=20
********************************************************************



Post-Doctoral Projects involving Cell and Molecular Biology of =
Neurodegenerative Disease

Dr. Andr=E9a LeBlanc, Ph.D=20

Lady Davis Institute for Medical Research=20

Montreal, Quebec, Canada=20

Project description:=20

2 POST-DOCTORAL POSITIONS IN CELL AND MOLECULAR BIOLOGY OF =
NEURODEGENERATIVE
DISEASES=20

Projects

     Amyloid =DF peptide toxicity of human neurons.=20

     Regulation of amyloid precursor protein metabolism in human =
neurons, and astrocytes.

     Molecular mechanisms of prion protein.=20

Positions:

     Two Post Doctoral Positions.=20

          Requirements for the Candidate:

          Must have a Ph.D. in either biochemistry, molecular biology, =
cell biology, or neuroscience with technical
          experience in at least two of the four categories.=20


     To Apply:

     Send Curriculum Vitae and 2-3 letters of recommendation to:=20

     Dr. Andr=E9a LeBlanc,
     Lady Davis Institute for Medical Research,=20
     Sir Mortimer B. Davis Jewish General Hospital,
     3755 Ch. Cote Ste-Catherine, Montreal, Quebec, Canada.=20
     H3T 1E2.

     *Include your telephone, Fax and e-mail numbers.=20


***************************************************************


Job Listing #5:=20

Molecular Biology of Parathyroid Gland Activity

 Dr. Geoffrey N. Hendy=20

Calcium Research Lab

Royal Victoria Hospital=20

Montreal, Quebec, Canada=20


Project description:

A studentship is available in the laboratory of Dr. Geoffry Hendy as a =
part his operating grant entitled=20
"Investigation of the Molecular Biology of Parathryoid Gland Activity"


Positions:

     1 Ph.D. position

     TO START SUMMER 1996=20

Prospective graduate students interested in recieving an MRC Studentship =
should send a curriculum vitae together with a
transcript of their academic records. This studenship is for a student =
preferably to undertake a Ph.D. under Dr. Hendy's
supervision although candidates for M.Sc. will also be considered. The =
studentship is available to start graduate studies
preferably for the summer of 1996.=20


To Apply:

Please send your curriculum vitae and a copy of your transcript to:=20

Dr. Geoffrey N. Hendy=20

Calcium Research Lab., Rm. H4.67
Royal Victoria Hospital
Montreal, Quebec
Canada H3A 1A1



From owner-recombination@net.bio.net Mon Apr 08 23:00:00 1996
Path: biosci!daresbury!imbb1.imbb.forth.gr!nefeli.imbb.forth.gr!ANASTASO
From: anastaso@nefeli.imbb.forth.gr
Newsgroups: bionet.plants,bionet.molbio.recombination
Subject: tobacco mutant seeds
Date: Tue, 09 Apr 1996 18:36:11 GMT
Organization: Imbb-forth,CREtE, creece
Lines: 25
Message-ID: <009A0999.9929E85D@nefeli.imbb.forth.gr>
Reply-To: anastaso@nefeli.imbb.forth.gr
NNTP-Posting-Host: nefeli.imbb.forth.gr
Xref: biosci bionet.plants:10866 bionet.molbio.recombination:156

Dear Netters,
  we are to mutagenise TOBACCO seeds and then select for the mutants

In order to map the position of the mutation we would need to tobacco

plants that carry known markers; ones that are known to reside at 

particular chromosomes would be very usefull to our mapping effort.

Therefore may we ask anyone who has seeds from such plants to send

us some to the address mentioned below. Thank you for your help.


Elias Anastassopoulos,

Foundation of Research and Technology-Hellas

Institute of Molecular Biology and Biotechnology

P.O.Box 1527, Heraklion, 711 10, Crete, HELLAS.

Fax # (081) 230469

email:anastaso@nefeli.imbb.froth.gr 

From owner-recombination@net.bio.net Mon Apr 08 23:00:00 1996
Path: biosci!daresbury!imbb1.imbb.forth.gr!nefeli.imbb.forth.gr!ANASTASO
From: anastaso@nefeli.imbb.forth.gr
Newsgroups: bionet.molbio.recombination
Subject: tobacco mutant seeds (email correction)
Date: Tue, 09 Apr 1996 22:26:00 GMT
Organization: Imbb-forth,CREtE, creece
Lines: 25
Message-ID: <009A09B9.B4296334@nefeli.imbb.forth.gr>
Reply-To: anastaso@nefeli.imbb.forth.gr
NNTP-Posting-Host: nefeli.imbb.forth.gr

Dear Netters,
  we are to mutagenise TOBACCO seeds and then select for the mutants

In order to map the position of the mutation we would need tobacco

plants that carry known markers; ones that are known to reside at 

particular chromosomes would be very usefull to our mapping effort.

Therefore may we ask anyone who has seeds from such plants to send

us some to the address mentioned below. Thank you for your help.


Elias Anastassopoulos,

Foundation of Research and Technology-Hellas

Institute of Molecular Biology and Biotechnology

P.O.Box 1527, Heraklion, 711 10, Crete, HELLAS.

Fax # (081) 230469

email:anastaso@nefeli.imbb.forth.gr 

From owner-recombination@net.bio.net Sat Apr 13 23:00:00 1996
Path: biosci!rutgers!gatech!newsfeed.internetmci.com!news.compuserve.com!news.production.compuserve.com!news
From: Phaedrus <75017.1050@CompuServe.COM>
Newsgroups: bionet.general,bionet.molbio.recombination
Subject: Networking transgene injectionists
Date: 14 Apr 1996 03:00:32 GMT
Organization: CompuServe, Inc. (1-800-689-0736)
Lines: 24
Message-ID: <4kppoh$dap$1@mhadg.production.compuserve.com>
Xref: biosci bionet.general:21113 bionet.molbio.recombination:159

Hi

My name is Gary Brown, working at present out of Wash. U at St 
Louis in a lab heavily involved in the generation of transgenic 
animals by both pronuclear microinjection and ES cell injection 
into blastocysts. So, what's this all about? Well, I'm 
contemplating writing a WWW Homepage resource directed at all 
those individuals out there with a technical interest in 
microinjection, with possibly a technique of the month feature, 
jobs offered, jobs wanted etc. I need to get an idea of what 
people might be interested in seeing on such a page. That's where 
maybe you, the reader of my wee scribble, might wish to 
contribute.
Also, the thought did enter my head that should people actually 
respond here that there might exist the possibility of connecting 
each other via an E-newsletter of sorts. Your thoughts please.
I believe that persons who do microinjection might be well served 
by their own organizational body. Yet again, thoughts are 
appreciated.
Nearly done. One more thing. I'm not affiliated with any 
sleazebag headhunter types IN ANY WAY, and of course would not 
use any responses to generate a list for anyone other than me.

Thanx, Gary  (75017.1050@compuserve.com)

From owner-recombination@net.bio.net Tue Apr 16 23:00:00 1996
Path: biosci!daresbury!bioftp.unibas.ch!news.vub.ac.be!news.belnet.be!swsbe6.switch.ch!scsing.switch.ch!news.belwue.de!news.uni-stuttgart.de!news
From: "Igor M. Kulic" <kulicir@cip.mathematik.uni-stuttgart.de>
Newsgroups: bionet.molbio.recombination
Subject: Invertase activity and supercoiling
Date: Wed, 17 Apr 1996 13:48:48 +0200
Organization: UNI-Stuttgart
Lines: 20
Message-ID: <3174DAA0.41C6@cip.mathematik.uni-stuttgart.de>
NNTP-Posting-Host: cip14.mathematik.uni-stuttgart.de
Mime-Version: 1.0
Content-Type: text/plain; charset=us-ascii
Content-Transfer-Encoding: 7bit
X-Mailer: Mozilla 2.0 (X11; I; AIX 2)

Does anybody know any refereces or is possibly able to help me with
following question :
  Which Inv sites on a supercoiled plasmid are more likely to be
recombined by invertase .
  I guess that sites that are closer to each other (and have the right
orietation ) are more likely to react than those that are far apart .
  For example we have the following (lineary written ) plasmid with 3
Inv sites (where "X" denotes the Inv-site and "Y" his inverted )

 
   ..X...Y.....Y.............. 

(start and end-positions should be identified )

  Is "X" generaly more likely to react with the first "Y"-site than with
the second ?  
  How strong does this probablity dependent on supercoilng of the
plasmid ?
  I would be very thankful for any hint or relevant reference if any are
known .

From owner-recombination@net.bio.net Tue Apr 16 23:00:00 1996
Path: biosci!daresbury!not-for-mail
From: Johnjoe McFadden <j.mcfadden@surrey.ac.uk>
Newsgroups: bionet.molbio.recombination
Subject: transposable elements and speciation
Date: 17 Apr 1996 10:00:47 +0100
Lines: 26
Sender: lpddist@mserv1.dl.ac.uk
Distribution: bionet
Message-ID: <4l2bvv$6dk@mserv1.dl.ac.uk>
X-Sender: bss1jm@central.surrey.ac.uk
Original-To: recom@dl.ac.uk

I am interested in the possibility of transposable elements being involved
in speciation events.

Does anybody know of examples of species or genera-specific insertion
sequences or transposable elements from prokaryotes or eukaryotes?

A few examples that I am aware of are IS200 in Salmonella species, IS6110 in
Mycobacterium tuberclulosis complex and IS900 in Mycobacterium paratuberculosis.


Any others?


Johnjoe McFadden

Johnjoe McFadden, PhD
Molecular Microbiology Group
School of Biological Sceinces
University of Surrey,
Guildford, Surrey GU2 5XH, UK.

tel: 44-(0)1483 300800 extn.2671
fax: 44-(0)1483 300374

e-mail: j.mcfadden@surrey.ac.uk


From owner-recombination@net.bio.net Tue Apr 16 23:00:00 1996
Path: biosci!MAIL.UMU.SE!hong
From: hong@MAIL.UMU.SE (Hong Qian)
Newsgroups: bionet.molbio.recombination
Subject: Looking for protein
Date: 17 Apr 1996 02:47:54 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 33
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199604170944.AA07557@mail.umu.se>
NNTP-Posting-Host: net.bio.net

Hello everyone out there:

I am a Ph D. student working for protein structure determination
by NMR method. I had finished calculating one protein structure
which contains 90 amino acids. Now I am looking for a new protein.
If someone has an over-expressed protein which is suitable for
NMR study, I would be very happy working for it.

The protein used for NMR structure calculation must fufill the 
following conditions:
1. Solvable at mili-molar range in water.
2. Stable at room temperature.
3. Molecular weight below 30 kD
4. If it contains more than 70 amino acids, it should be isotopic
labelled by nitrogen 15 or both nitrogen-15 and carbon-13.

Generally, we need around 10 mg protein for NMR study. Of course,
it depends on molecular weight of protein.

If anyone interest in this, please contact with me by email.

Hong Qian
NMR Research Group
Department of Organic Chemistry
Umea University
S- 901 87, Umea
Sweden

email: hong@indro.chem.umu.se
tel: 46-90-166936
fax: 46-90-138885



From owner-recombination@net.bio.net Tue Apr 16 23:00:00 1996
Path: biosci!ODYSSEE.NET!dellaire
From: dellaire@ODYSSEE.NET (Graham Dellaire)
Newsgroups: bionet.molbio.recombination
Subject: RE: transposable elements and speciation
Date: 17 Apr 1996 09:00:11 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 53
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <01BB2C53.C1D6AD00@pool3_1.odyssee.net>
NNTP-Posting-Host: net.bio.net



----------
From: 	Johnjoe McFadden[SMTP:j.mcfadden@surrey.ac.uk]
Sent: 	Wednesday, April 17, 1996 5:00 AM
To: 	recom@net.bio.net
Subject: 	transposable elements and speciation

>I am interested in the possibility of transposable elements being =
involved
>in speciation events.

>Does anybody know of examples of species or genera-specific insertion
>sequences or transposable elements from prokaryotes or eukaryotes?

Johnjoe McFadden, PhD
Molecular Microbiology Group
School of Biological Sceinces
University of Surrey,
Guildford, Surrey GU2 5XH, UK.
-------------------------------------------------------------------------=
----------------------------------------
Johnjoe,

Retroposons are very similar to transposons but move via an RNA =
intermediate (i.e. are reverse trascribed first as suggested by poly aaa =
tail)

Line-1 retroposons are only in mammals ((Lmd in mice and Line-1 in =
primates so far) and I think Alu's have a similar occurance (B-1 in mice =
and Alu in man). =20

Just another little note:
Another interesting thing about Lines and Alu elements is that they are =
segregated into late (heterochromatin) and early (euchromatin) =
replicating Dna bands in mitotic chromosomes, respectively. =20

To me this indicates perhaps a role in genome evolution and or =
structure.


Hope this helps,


G. Dellaire
dellaire@odyssee.net

Dept. of Medicine
Div. of Exp. Medicine
McGill University




From owner-recombination@net.bio.net Wed Apr 17 23:00:00 1996
Path: biosci!internet!biosci!not-for-mail
From: biohelp (BIOSCI Administrator)
Newsgroups: bionet.molbio.recombination
Subject: IMPORTANT - BIOSCI Fundraising Update!
Date: 18 Apr 1996 02:00:26 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 154
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199604180900.CAA27292@net.bio.net>
NNTP-Posting-Host: net.bio.net

	    BIOSCI is about halfway to its funding goal!!

I'm interrupting the usual monthly posting of the BIOSCI miniFAQ to
bring you up to date on BIOSCI fundraising progress, a topic of
concern to your future use of this resource.  Thank you in advance for
taking the time to read this message carefully.

Last year we announced that BIOSCI was going to adopt the U.S. Public
Broadcasting System model to fund its operations after our DOE/NSF
grant runs out later this year.  Unlike PBS, we are not soliciting
contributions from users; we are only selling ads on our Web pages
solely to cover our operating costs.  Our goal is to seek sponsorships
until we build up an operating reserve of about $100,000 and then
cease further promotions until we need to build the reserve back up.
(The accountants among our readership will be familiar with the
problem of deferred revenue which we can not safely utilize until ads
have been displayed for a period of time.)  We are only about halfway
to our funding goal and need to raise further funds to avoid having to
curtail services at net.bio.net.  Fundraising is time-consuming,
however, and we need your help as explained further below.

Our operating costs consist of our network connection, phone lines,
hardware maintenance (we will be getting newer and faster hardware
soon!), plus 0.7 FTE of salaries covering UNIX systems admin,
technical support, quality assurance, i.e., testing, of our system,
and administrative costs (such as the time it takes to actually
find/write/call potential sponsors and raise money!).  Although the
BIOSCI staff does get compensated for a portion of the work that they
do, this project has always received a lot of free after-hours and
"vacation" time labor, so we hope that no one will begrudge the time
that we do charge to the project to serve you.  All of the three
part-time staff members, Dave Mack, Julie Lawrence, and myself, have
full time day jobs and families in addition to working hard to keep
this service running for all of you.  Julie and Dave Mack are
subcontractors for BIOSCI; my time that is charged to the project
defrays a portion of my regular salary instead of adding to my income.

Besides having to relocate the project, we were very busy this last
year building new infrastructure such as our WWW hypermail interface
to the system.  This was released last December along with scores of
WAIS indices for the newsgroups.  Virtually everything is complete,
although we do continue to find and fix bugs (many through your
helpful feedback!).  We are still having some problems with our WAIS
indexing.  The archives continue to grow rapidly.  We are running over
100 indexes now versus three previously and any systems crashes cause
greater havoc with the indexing than before!  We are still working to
fix this as fast as our resources permit and appreciate your patience,
but we have been able to automate a lot of the infrastructure to
reduce labor as compared to past requirements.

We have also implemented new software to make moderation of
BIOSCI/bionet newsgroups much easier and combat the growing problem of
Internet junk mail and USENET "spamming."  About 20% of our groups are
now moderated, many of them by the BIOSCI staff!  This, for example,
made a major difference last year in the quality of content in our
EMPLOYMENT/bionet.jobs.offered newsgroup which many commercial
concerns and recruiting firms are using **without charge** to recruit
candidates for positions in the biological sciences.

We are also now in a position to have sponsors for individual
newsgroups as you will have noticed if you have visited
http://www.bio.net/ and clicked on "Access the BIOSCI/bionet
newsgroups" recently.

So, how can you help??
----------------------

As noted above it can take a lot of time to contact potential sponsors
if I have to do it all myself.  Our request is quite simple.  You can
do two important things which will take very little time for you
individually.  

First, please use our WWW system at http://www.bio.net/ to access the
archives.  You can now post or reply to messages via your Web browser.
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.

Our hope is to quickly raise several large corporate/institutional
sponsors on our heavily-used WWW locations (some stats appended
below), and then end this sponsorship campaign so that our resources
can continue to be used for service provision, not fundraising.  Many
of our specialty newsgroup WWW archives are still used by small
communities of scientists (and they haven't been heavily promoted
yet).  While these may be valuable niche markets to some advertisers,
it will generate more labor and overhead having to find these
sponsors, fairly price the locations, and deal with lots of smaller
sponsorships than fewer mid-to large sponsors.  We are striving to
keep our operation as lean and efficient as possible since we are not
trying to make careers out of running BIOSCI.  We are trying if at all
possible to avoid the administrative overhead entailed with processing
lots of small payments to reach our fundraising goals.

I'd like to thank all of you for your help in advance. In helping us,
you are also helping yourselves, not only in keeping this resource
available for all of the both large and small research communities
that we serve, but also by alleviating the need for us to go back and
compete with researchers for tight grant dollars!  We promised NSF
when we were awarded the BIOSCI grant that we would carry out this
mission to make the service self-supporting.  With your help, we will
succeed in continuing BIOSCI's work into its second decade.  Thank you
very much!

				Sincerely,

				Dave Kristofferson
				BIOSCI/bionet Manager

				biosci-help@net.bio.net


A list of our prime WWW sponsorship locations follow.  Please contact
us for further details.
----------------------------------------------------------------------

The overall BIOSCI WWW pages are currently visited by users from close
to 5500 unique computer hosts per week.  Web servers only log the
Internet computer/host name and frequently more than one individual
can connect to us from a particular host.

Main home page, http://www.bio.net, visited recently by about 2100
unique hosts per week

Main Newsgroups archives page, http://www.bio.net/archives.html,
visited recently by about 1200 Unique hosts per week

BIO-JOURNALS archive page, http://www.bio.net/BIO-JOURNALS.html,
visited recently by about 1000 unique hosts per week.

EMPLOYMENT archive pages: http://www.bio.net:80/hypermail/EMPLOYMENT/ 
and monthly header pages, visited recently by about 800 unique hosts
per week.

Address database search page, http://www.bio.net/addrsearch.html,
visited recently by about 450 unique hosts per week.

Methods newsgroup archive pages, http://www.bio.net:80/hypermail/METHDS-
REAGNTS/ and monthly header pages, visited recently by about 350
unique hosts per week.

Ads can also be displayed on various combinations of other
BIOSCI/bionet newsgroups.  Please contact us at
biosci-help@net.bio.net for details.
----------------------------------------------------------------------

From owner-recombination@net.bio.net Thu Apr 18 23:00:00 1996
Path: biosci!ODYSSEE.NET!dellaire
From: dellaire@ODYSSEE.NET (Graham Dellaire)
Newsgroups: bionet.molbio.recombination
Subject: RE: transposable elements and speciation
Date: 19 Apr 1996 06:40:20 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 48
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <01BB2DD2.E8AAA460@pool3_6.odyssee.net>
NNTP-Posting-Host: net.bio.net



----------
From: 	Ashok Aiyar[SMTP:aiyar@ebv.oncology.wisc.edu]
Sent: 	Wednesday, April 17, 1996 5:29 PM
To: 	dellaire@ODYSSEE.NET
Subject: 	Re: transposable elements and speciation

[This message has also been posted.]
On 17 Apr 1996 09:00:11 -0700, Graham Dellaire <dellaire@ODYSSEE.NET> =
wrote:

>Retroposons are very similar to transposons but move via an RNA=20
>intermediate (i.e. are reverse trascribed first as suggested by poly =
aaa
>tail)
>
>Line-1 retroposons are only in mammals ((Lmd in mice and Line-1 in
>primates so far) and I think Alu's have a similar occurance (B-1 in =
mice
>and Alu in man).

Has anyone actually known an Alu to transpose in human cells?  I=20
know of one experiment (published in Cell, around Dec. 1987) that
purported to show Alu transposition, but this result was later shown
to be likely caused by BLUR8 contamination.

Curious,
Ashok
--
Ashok Aiyar
Department of Oncology                aiyar@ebv.oncology.wisc.edu
Univ. of Wisconsin-Madison                    tel: (608) 262-6697

I am not sure about alu's as they do not encode their own RT or =
integrase (recombinase) so it is harder to think what events might lead =
up to their activation and consequent move to a new site...=20

Line-1 's on the other hand encode 2 ORF's and one of them is a putative
RT gene.  It is believed that one or two proto lines in the mammalian =
genome are able to transpose (retrotranspose that is) during =
embryological development.  I think their was some work done in sperm of =
mice that indicated that this movement occurred quite readily.  I will =
try to get the reference soon.


G. Dellaire


From owner-recombination@net.bio.net Sun Apr 21 23:00:00 1996
Path: biosci!ODYSSEE.NET!dellaire
From: dellaire@ODYSSEE.NET (Graham Dellaire)
Newsgroups: bionet.molbio.recombination
Subject: POSTDOC AND PHD positions in MONTREAL (NEW)
Date: 22 Apr 1996 16:48:45 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 178
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <01BB3083.33323CC0@cisco2_8.odyssee.net>
NNTP-Posting-Host: net.bio.net

Job Listing 

Identification of Putative Target sites of Repressor/Activators in Yeast

 Dr. Bernard Turcotte 

Assistant Professor, 
Dept. of Medicine
McGill University 

Montreal, Quebec, Canada 


Project description:

Among the organisms that are used as models for the genome project, yeast (S. cerevisae) is the first one with its
complete sequence determined. Given the fact that yeast has a small genome size (14 Mbps), few intronic sequences
and that many processes are highly conserved from yeasst to man, it constitutes a powerful model. As a result, many
studies oare aimed at identifying the role of the various open reading frames (ORF's) revealed by the yeast sequencing
project. However, less attention has been paid to the analysis of promoter regions. Since these regions are rather short
and can be easily located, yeast offers a good model to study these sequences. 

The aim of the project is to identify putative target sites fro activators (or repressors) of gene transcription by searching
a database with DNA sequences that are recognized by zinc finger proteins. Predictions made from the search will then
be verified experimentally. These studies should allow the identification of vaarious gene networks. 


Positions:

     1 Ph.D. position and 1 Post-doctoral position

     Financial support is currently available. Funding being provided for the project by the Canadian Genome Analysis
     and Technology Program 

Prospective post-doctoral candidates or graduate students interested in the above project should send a curriculum
vitae together with a transcript of their academic records. 



To Apply:

For further information please contact: 

Dr. Bernard Turcotte

Assistant Professor,
Dept. of Medicine,
McGill University

Molecular Endocrinology Laboratory
Room H7.82 
Royal Victoria Hospital
687 Pine Ave. West
Montreal H3A 1A1 

Tel. 514-842-1231 Ext. 5046 FAX: 514-982-0893 

E-mail: turcotte@lan1.molonc.mcgill.ca 
---------------------------------------------------------------------------

Job Listing 

Cell Signalling Mechanisms with respect to Insulin and Growth Factor Action

 Dr. Barry Posner 

Polypeptide Laboratory

McGill University 

Montreal, Quebec, Canada 


Project description:

A studentship award is available for the study of cell signalling mechanisms focused particularly on insulin and growth
factor action. 


Positions:

     1 Ph.D. position 

Prospective graduate students should send a curriculum vitae together with a transcript of their academic records. 

DEADLINE MAY 15TH 1996 


To Apply:

Please send your curriculum vitae and a copy of your transcript to: 

Dr. Barry Posner 

Polypeptide Laboratory
McGill University
3640 University St. Rm W 315
Montreal, Quebec
Canada H3A 2B2 
---------------------------------------------------------------------------------------------

Job Listing 

Ph.D. Project Involving Role of Nitric Oxide (NO) in Cellular Iron Metabolism


Prem Ponka, M.D., Ph.D 

Lady Davis Institute For Medical Research 

Sir Mortimer B. Davis-Jewish General Hospital

Montreal, Quebec, Canada 

Project description: 

Dr. Ponka has one MRC studentship voucher for which he can guaranteed a 5-year MRC studentship to a qualified
student of his choice. 

Areas of research 

   1.Cellular iron metabolism 
          role of iron in cell proliferation 
          role of iron in free radical formation 
          role of nitric oxide (NO) in cellular iron metabolism 

   2.Development of new iron chelators of significance to: 
          iron overload 
          inhibition of free radical reactions 
          neoplastic cell replication

   3.Erythroid differentiation 

   4.Heme sythesis regulation

Recent publications: 

     Richard, D.R., Neumannova, V., and Ponka, P.: Nitrogen monoxide decrease iron uptake from transferrin
     but does not mobilise iron from prelabelled neoplastic cells. 
     Biochim. Biophys. Acta 1266:250-260 (1995)

     Richard, D.R., Neumannova, V., Nagy, E., and Ponka, P.: The effect of redox-related species of nitrogen
     monoxide on transferrin and iron uptake and cellular proliferation of erythroleukemia (K562) cells. 
     Blood 86: 3211-3219 (1995) 

     Loyevksy, M., Tsafack, A., Ponka, P., and Cabantchik, Z.I.: Mode of action of iron (III) chelators as
     antimalarials. IV. Potentiation of Desferal action by benzoyl- and isonicotinoyl-hydrazone derivative. J.
     Lab. Clin. Med. (in press)

Positions:

     Ph.D. Postion 

          Qualifications: B.Sc. with solid background in molecular and cellular biology. B.Sc. in Biochemistry
          is an advantage, but high achievment in any allied field will also be considered favorable. g.p.a.:
          3.5 of higher. 


To Apply:

For further information please contact: 

Prem Ponka, M.D., Ph.D. 

Lady Davis Institute For Medical Research 

Sir Mortimer B. Davis-Jewish General Hospital
3755 Cote St. Catherine Road
Montreal, Quebec, Canada
H3T 1E2 

Tel: (514) 340 8260 

Fax: (514) 340 7502 

----------------------------------------------------------------------------------------------



From owner-recombination@net.bio.net Sun Apr 21 23:00:00 1996
Newsgroups: bionet.molbio.recombination
Path: biosci!daresbury!bioftp.unibas.ch!news.vub.ac.be!news.belnet.be!swsbe6.switch.ch!scsing.switch.ch!news.belwue.de!fu-berlin.de!news.dfn.de!newsjunkie.ans.net!newsfeeds.ans.net!howland.reston.ans.net!newsfeed.internetmci.com!in1.uu.net!sangam!iitb!powai!niharika.phy.iitb.ernet.in!krishnan
From: krishnan@PROBLEM_WITH_INEWS_DOMAIN_FILE (s krishnan)
Subject: Workshop on Biotechnology
Sender: news@powai.cc.iitb.ernet.in (news system user)
Message-ID: <Dq9DJy.3Ln@powai.cc.iitb.ernet.in>
Date: Mon, 22 Apr 1996 10:09:34 GMT
Organization: Computer Centre, IIT Bombay - 400 076, India
X-Newsreader: TIN [version 1.2 PL2]
Lines: 36


 International Symposium on 'Cyanobacterial Biotechnology',

                   September 18-21, 1996

       Venue:  National Facility for Marine Cyanobacteria
               Bharathidasan University
               Tiruchirapalli 620 024
               India

     Review papers covering all aspects Cyanobacterial 
Biotechnology are invited from 30 senior scientists from 
different countries.  Response so far from 150 scientists 
all over the world.  Interested persons can participate 
either observers or send abstract for poster presentation 
immediately.  Registration US $ 100 for scientists and 
US $ 50 for bonafide students.  Registration after May 31, 
1996 would involve an additional US$ 50 for both categories.  
Registration fee includes accommodation, food and conference 
materials for the symposium period.  For further details 
contact

Dr. G. Subramanian,
Director, 
National Facility Marine Cyanobacteria, 
Bharathidasan University, 
Tiruchirapalli 620 024, 
India

Telephone +91 431 660352, Fax +91 431 660245,

E.mail.   nfmc@bdu.rect.ernet.in

In case, if you have problems with the above email address,
send mail to krishnan@phy.iitb.ernet.in


From owner-recombination@net.bio.net Tue Apr 30 23:00:00 1996
Path: biosci!SPARC2.CC.NCKU.EDU.TW!s5883105
From: s5883105@SPARC2.CC.NCKU.EDU.TW (Ming-Chuan Hong)
Newsgroups: bionet.molbio.recombination
Subject: test
Date: 1 May 1996 08:38:14 -0700
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 2
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199605011538.XAA13374@mail.ncku.edu.tw>
NNTP-Posting-Host: net.bio.net

Test!


