From owner-chromosomes@net.bio.net Wed Mar 04 22:00:00 1998
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From: "Vladimir I. Stobetsky" <sto@aha.ru>
Newsgroups: bionet.genome.chromosomes
Subject: induced telomeric fusion
Date: 5 Mar 1998 19:53:23 GMT
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Dear colleagues,

The attached file saved in MS Word'97 format  has a brief information on
the phenomenon that I have discovered several years ago and the list of
publications in the area of functioning of telomeres. Please forward this
e-mail to those who work in the same field or recommend
me on who might be interested in this problem.  I would like to share my
experience and my ideas as well as to listen to your comments on this
issue.

*******************************************************
l
Key  words : CHROMOSOMA,INDUCED  TELOMERIC FUSION

The phenomenon of delayed disruption of telomeric links between
chromosomes

The history of phenomena  of mitotic chromosome transformation (MCT)
began in 1964 when the chromosome morphology  of Chinese hamster cell
line Don was described under prolonged colcemid treatment that induced
the cells with micronuclei. At the first mitotic division of these
polykaryocytes the chromosomes  with  portions of delayed spiralization
(PDS) were discovered (Stubblefield,1964).

The simultaneous treatment with colcemid and 5-bromodeoxyuridine
(5-BrdU)  of Chinese hamster cells led to appearance of dicentric
chromosomes at the first mitotic division of cells with micronuclei. The
absence of double fragments in such metaphases and the fact that they
could not be lost brought us  to the conclusion that dicentrics were
formed by  "end-to-end fusions  " (Stobetsky,1976). As the 5-BrdU was
incorporated into DNA for two  S-periods it was shown that chromosomes
in dicentrics were in the condition of telomeric fusion till the second
S-period. Therefore the discovered dicentrics were the result of delayed
disruption of telomeric links between chromosomes (Stobetsky,1978b). 

The phenomenon of delayed disruption of telomeric links between
chromosomes is the first  experimental model of the purposeful
influence on the function of telomeres in mammalian cells through MCT.
We used in our experiments the heteroploid Chinese hamster cell line
B11d-ii-FAF28 (clone237S) as a rule, but the phenomenon was   reproduced
in heteroploid Chinese hamster cell line CHO-6 also (Stobetsky,1990).
Another halogenated analogs of thymidine (HAT),except
5-fluorodeoxyuridine (5-FdU)  were applyed.

The chemicals, such as colcemid (0,1 microg/ml ), 5-BrdU (20 -50 microg/ml)
were
administrated in  actively growing cell culture, usually day after
seeding. Temperature of cell cultivation was 37_C  excepting  some
cases. The   cells   fixed  after   42   hours cultivation  with drugs.
About  30% metaphases of polykaryocytes contained dicentric chromosomes 
   
Some metaphases  contained besides  the normal chromosomes  also
chromosomes with PDS and  "chromosome pulverization".  The last
abnormalities were present in cell line B11d-ii-FAF28 (clone 237S)
after prolonged colcemid treatment alone (Stobetsky,1978a). Our
experiments  showed that chromosomes with PDS did not correspond  to
prematurely condensed chromosomes. Having analyzed  three cytogenetic
phenomena - delayed spiralization of metaphase chromosome portions,
delayed  disruption of telomeric links between chromosomes and premature
centromere division of  the X-chromosome - we concluded that in this
case the routine scheme (gene - protein - chromatin) could not work.
These phenomena are presumably associated with the existence of  a
system of MCT independent of the cytoplasm  (Stobetsky,1988c) .
	
It was shown in series of the experiments the following:

1.	The phenomenon of delayed disruption  of telomeric links between
chromosomes was reproduced in human-Chinese hamster cell hybrids
(Stobetsky et al.,1984).

2.	It was discovered that this phenomenon appeared when the 5-BrdU
was incorporated for two S-periods or during the first S-period , so the
differential incorporation of analog into sister chromatids was
necessary(Stobetsky, Mironova,1987).

3.	Another HAT such as 5-iododeoxyuridine (5-IdU) and
5-chlorodeoxyuridine (5-ChldU) also  induced telomeric chromosome fusion
in cells  with micronuclei derived from cell line B11d-ii-FAF28 (clone
237S) (Stobetsky et al.,1987;Stobetsky,Mironova,1988d).The intensity of
dicentric formation depends on molecular  weight of HAT. So the 5-BrdU
was more effective than 5-IdU,and 5-ChldU was more effective than
5-BrdU.Under subsequent incorporation of  5-IdU and 5-ChldU and vice
versa we found that strong or weak reaction in respect to dicentric
formation depends on which analog was administered in the first S-period
(Stobetsky, Mironova,1989).

4.	It was shown that certain factors exist which change the
intensity of dicentric formation. 5-azacytidine and hyperthermia  (40_
C)  enhanced the frequency of dicentric chromosomes when using 5-BrdU,
so that  sometimes tricentric  were formed (Stobetsky,Mironova,1988a;
Stobetsky,Mironova,1988b). In  the following experiments it was shown
that intensity of dicentric formation was directly connected  with the
temperature of cultivation when using 5-BrdU.The action of hyperthermia
(40_C)  during the whole  period (42 hrs) of colcemid and  5-BrdU
treatment or that  of  the hyperthermia (40_ C ) only for the first 17
hours ( the first interphase and the first mitosis) led to the increased
frequency of  dicentrics. Under condition of hypothermia (34_ C) the
frequency of dicentric formation decreases. Changes in cultivation
temperature during the last 25 hours of colcemid and 5-BrdU action (the
second interphase and the second mitosis)  exerted no influence on
dicentric formation frequency  (Stobetsky,1991a).

5.	The most significant data were obtained when Chinese hamster
cells B11d-ii-FAF28 (clone 237S) when exposed to colcemid,various HAT
and hyper-,normo and hypothermia. The minimum frequency of dicentrics
was found in the case of using  5-IdU and hypothermia (34_C) .Under
these conditions we observed the depression of mitotic activity and also
we often witnessed the chromosomes with PDS of good quality.The maximum
level of dicentrics was discovered under action of 5-ChldU and
hyperthermia  (40_ C).Chromosomes with PDS were not found  in the latter
case, but unusually  great frequency tri- and quadriradials was
registered  (Stobetsky,1991b). 

6.	Chinese hamster heteroploid  cell culture  was treated by
colcemid for 42 h ,of which within the first 17 h by 5-BrdU. Dicentric
chromosomes, that were formed at the 2nd  mitosis  after  colcemid
administration , were analysed using G-banding. Of 211 only 40 were
made  by  heterological   chromosomes.   Other 171 dicentrics fere
formed by telomeric fusion of autological  chromosomes. No correlation
was found between the length, centromeric index and frequency of
dicentric formation. (Stobetsky et al., 1994).   


References

1.	Stubblefield  E. (1964). DNA synthesis and chromosomal
morphology of Chinese hamster cells cultured in media containing
n-deacethyl-n-methylcolchicine (colcemid). In: Cytogenetics of cells in
culture. N.-Y. 223-248.

2.	Stobetsky V.I. (1976). Chromosome fusion by telomeres in cells
treated  with colcemid and 5-bromodeoxyuridine. (Russ).
Bull.Exptl.Biol.Med. No 9. 1142-1144.	

3.	Stobetsky V.I.  (1978a). Mammalian polykaryocytes in vitro. I. A
comparison of mitotic chromosome condensation in fused human
heterophasic cells and Chinese hamster cells with micronuclei .
Biologisches Zentralblatt .97: 587-594.

4.	Stobetsky V.I.  (1978b). Mammalian polykaryocytes in vitro. II.
The phenomenon of delayed disruption of telomeric links between
chromosomes.Biologisches  Zentralblatt . 97: 595-604.

5.	Stobetsky V.I., Grachev V.P., Mironova  L.L. (1984). The
phenomenon of  delayed disruption of telomeric links betveen chromosomes
in polykaryocytes from human-Chinese hamster cell hybrids. (Russ). No 7.
87-88.

6.	Stobetsky  V.I., Mironova  L.L. (1987).  A delayed disruption of
telomeric links between chromosomes in the experimentally induced cells
with micronuclei under treatment with 5-bromodeoxyuridine at the first
S-period after colcemid administration. (Russ). Tsitologia..
29:724-727.

7.	Stobetsky  V.I., Khapchaev Yu. Kh. ,Mironova  L.L. (1987). The
induction of delayed disruption of telomeric links between chromosomes
in cells with micronuclei by 5-iododeoxyuridine and 5-bromodeoxyuridine.
(Russ). Bull. Exptl. Biol. Med. No 7. 83-85.

8. 	Stobetsky V.I., Mironova L.L. (1988a). Effect of 5-azacytidine
on the number of polycentric chromosomes      in cells    with
micronuclei   during   exposure   to 5-bromodeoxyuridine. (Russ). Bull.
Exptl. Biol. Med. No4 479-480.
	
9.	Stobetsky V.I. ,Mironova  L.L.  (1988b). The enhanced intensity
of polycentric chromosome formation in cells with micronuclei after
5-bromodeoxyuridine treatment under prolonged hyperthermia at 40_C. 
(Russ). Tsitologia. 30:358-360.
	
10.	Stobetsky  V.I. (1988c).  On the nature of three cytogenetic
phenomena - delayed spiralization of metaphase chromosome portions ,
delayed disruption of telomeric links between chromosomes  and premature
centromere division of the X-chromosome . (Russ). Tsitologia .
30:1270-1272 .
	
11.	Stobetsky V.I., Mironova  L.L. (1988d). 5-Chlorodeoxyuridine
induces the formation of specific  dicentric chromosomes in cells with
micronuclei more effectively than does 
5-bromodeoxyuridine. (Russ). Tsitologia. . 30:1498-1500.
	
12.	Stobetsky  V.I. , Mironova  L.L. (1989). Telomeric fusion of
chromosomes in cells with micronuclei under  subsequent  incorporation
of halogenated analogs of thymidine into DNA.  (Russ). Tsitologia .
31:1242-1244.
	
13.	Stobetsky  V.I.  (1990).  Induction  of  specific  dicentric
chromosomes in Chinese hamster ovary cells  CHO-6 . (Russ).
Tsitologia.32:92-94.
	
14.	Stobetsky  V.I. (1991a). The induced telomeric chromosome fusion
under conditions of pulse action of hyper- or hypothermia. (Russ).
Tsitologia .33:116-118.
	
15.	Stobetsky V.I.  (1991b). Telomeric chromosome fusion in cells
with micronuclei in the conditions of combined action of hyper- or
hypothermia and halogenated analogs of thymidine . (Russ).  Bull. Exptl.
Biol. Med. No7. 72-73.
	
16.	Stobetsky  V.I., Chebotarev  A.N., Mironova  L.L. (1994).
Analysis of  chromosome combinations in dicentric at the induced
telomeric fusion. (Russ). Tsitologia. 36:60-63.

****************************************************************************
******
Vladimir I. Stobetsky
Senior Scientist
Research Institute of Pediatric Hematology
Laboratory of Cytogenetics and Molecular Biology
App. 116, 6 Novoorlovskaya St. Moscow, 119633, Russia
tel: +7 095 731 8932   
e-mail address: sto@aha.ru  



From owner-chromosomes@net.bio.net Sun Mar 08 22:00:00 1998
Path: biosci!agate!logbridge.uoregon.edu!feed2.news.erols.com!erols!Gamma.RU!srcc!news2.aha.ru!aha!not-for-mail
From: "Vladimir I. Stobetsky" <sto@aha.ru>
Newsgroups: bionet.genome.chromosomes
Subject: The phenomenon  of delayed disruption of telomeric links between chromosomes
Date: 9 Mar 1998 09:05:03 GMT
Organization: Mr. Postman
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NNTP-Posting-Host: p38.n77.dip.aha.ru
X-Newsreader: Microsoft Internet News 4.70.1161


Key  words : CHROMOSOMA,INDUCED  TELOMERIC FUSION

The phenomenon of delayed disruption of telomeric links between
chromosomes

The history of phenomena  of mitotic chromosome transformation (MCT)
began in 1964 when the chromosome morphology  of Chinese hamster cell
line Don was described under prolonged colcemid treatment that induced
the cells with micronuclei. At the first mitotic division of these
polykaryocytes the chromosomes  with  portions of delayed spiralization
(PDS) were discovered (Stubblefield,1964).

The simultaneous treatment with colcemid and 5-bromodeoxyuridine
(5-BrdU)  of Chinese hamster cells led to appearance of dicentric
chromosomes at the first mitotic division of cells with micronuclei. The
absence of double fragments in such metaphases and the fact that they
could not be lost brought us  to the conclusion that dicentrics were
formed by  "end-to-end fusions  " (Stobetsky,1976). As the 5-BrdU was
incorporated into DNA for two  S-periods it was shown that chromosomes
in dicentrics were in the condition of telomeric fusion till the second
S-period. Therefore the discovered dicentrics were the result of delayed
disruption of telomeric links between chromosomes (Stobetsky,1978b). 

The phenomenon of delayed disruption of telomeric links between
chromosomes is the first  experimental model of the purposeful
influence on the function of telomeres in mammalian cells through MCT.
We used in our experiments the heteroploid Chinese hamster cell line
B11d-ii-FAF28 (clone237S) as a rule, but the phenomenon was   reproduced
in heteroploid Chinese hamster cell line CHO-6 also (Stobetsky,1990).
Another halogenated analogs of thymidine (HAT),except
5-fluorodeoxyuridine (5-FdU)  were applyed.

The chemicals, such as colcemid (0,1 microg/ml ), 5-BrdU (20 -50 microg/ml)
were
administrated in  actively growing cell culture, usually day after
seeding. Temperature of cell cultivation was 37_C  excepting  some
cases. The   cells   fixed  after   42   hours cultivation  with drugs.
About  30% metaphases of polykaryocytes contained dicentric chromosomes 
   
Some metaphases  contained besides  the normal chromosomes  also
chromosomes with PDS and  "chromosome pulverization".  The last
abnormalities were present in cell line B11d-ii-FAF28 (clone 237S)
after prolonged colcemid treatment alone (Stobetsky,1978a). Our
experiments  showed that chromosomes with PDS did not correspond  to
prematurely condensed chromosomes. Having analyzed  three cytogenetic
phenomena - delayed spiralization of metaphase chromosome portions,
delayed  disruption of telomeric links between chromosomes and premature
centromere division of  the X-chromosome - we concluded that in this
case the routine scheme (gene - protein - chromatin) could not work.
These phenomena are presumably associated with the existence of  a
system of MCT independent of the cytoplasm  (Stobetsky,1988c) .
	
It was shown in series of the experiments the following:

1.	The phenomenon of delayed disruption  of telomeric links between
chromosomes was reproduced in human-Chinese hamster cell hybrids
(Stobetsky et al.,1984).

2.	It was discovered that this phenomenon appeared when the 5-BrdU
was incorporated for two S-periods or during the first S-period , so the
differential incorporation of analog into sister chromatids was
necessary(Stobetsky, Mironova,1987).

3.	Another HAT such as 5-iododeoxyuridine (5-IdU) and
5-chlorodeoxyuridine (5-ChldU) also  induced telomeric chromosome fusion
in cells  with micronuclei derived from cell line B11d-ii-FAF28 (clone
237S) (Stobetsky et al.,1987;Stobetsky,Mironova,1988d).The intensity of
dicentric formation depends on molecular  weight of HAT. So the 5-BrdU
was more effective than 5-IdU,and 5-ChldU was more effective than
5-BrdU.Under subsequent incorporation of  5-IdU and 5-ChldU and vice
versa we found that strong or weak reaction in respect to dicentric
formation depends on which analog was administered in the first S-period
(Stobetsky, Mironova,1989).

4.	It was shown that certain factors exist which change the
intensity of dicentric formation. 5-azacytidine and hyperthermia  (40_
C)  enhanced the frequency of dicentric chromosomes when using 5-BrdU,
so that  sometimes tricentric  were formed (Stobetsky,Mironova,1988a;
Stobetsky,Mironova,1988b). In  the following experiments it was shown
that intensity of dicentric formation was directly connected  with the
temperature of cultivation when using 5-BrdU.The action of hyperthermia
(40_C)  during the whole  period (42 hrs) of colcemid and  5-BrdU
treatment or that  of  the hyperthermia (40_ C ) only for the first 17
hours ( the first interphase and the first mitosis) led to the increased
frequency of  dicentrics. Under condition of hypothermia (34_ C) the
frequency of dicentric formation decreases. Changes in cultivation
temperature during the last 25 hours of colcemid and 5-BrdU action (the
second interphase and the second mitosis)  exerted no influence on
dicentric formation frequency  (Stobetsky,1991a).

5.	The most significant data were obtained when Chinese hamster
cells B11d-ii-FAF28 (clone 237S) when exposed to colcemid,various HAT
and hyper-,normo and hypothermia. The minimum frequency of dicentrics
was found in the case of using  5-IdU and hypothermia (34_C) .Under
these conditions we observed the depression of mitotic activity and also
we often witnessed the chromosomes with PDS of good quality.The maximum
level of dicentrics was discovered under action of 5-ChldU and
hyperthermia  (40_ C).Chromosomes with PDS were not found  in the latter
case, but unusually  great frequency tri- and quadriradials was
registered  (Stobetsky,1991b). 

6.	Chinese hamster heteroploid  cell culture  was treated by
colcemid for 42 h ,of which within the first 17 h by 5-BrdU. Dicentric
chromosomes, that were formed at the 2nd  mitosis  after  colcemid
administration , were analysed using G-banding. Of 211 only 40 were
made  by  heterological   chromosomes.   Other 171 dicentrics fere
formed by telomeric fusion of autological  chromosomes. No correlation
was found between the length, centromeric index and frequency of
dicentric formation. (Stobetsky et al., 1994).   


References

1.	Stubblefield  E. (1964). DNA synthesis and chromosomal
morphology of Chinese hamster cells cultured in media containing
n-deacethyl-n-methylcolchicine (colcemid). In: Cytogenetics of cells in
culture. N.-Y. 223-248.

2.	Stobetsky V.I. (1976). Chromosome fusion by telomeres in cells
treated  with colcemid and 5-bromodeoxyuridine. (Russ).
Bull.Exptl.Biol.Med. No 9. 1142-1144.	

3.	Stobetsky V.I.  (1978a). Mammalian polykaryocytes in vitro. I. A
comparison of mitotic chromosome condensation in fused human
heterophasic cells and Chinese hamster cells with micronuclei .
Biologisches Zentralblatt .97: 587-594.

4.	Stobetsky V.I.  (1978b). Mammalian polykaryocytes in vitro. II.
The phenomenon of delayed disruption of telomeric links between
chromosomes.Biologisches  Zentralblatt . 97: 595-604.

5.	Stobetsky V.I., Grachev V.P., Mironova  L.L. (1984). The
phenomenon of  delayed disruption of telomeric links betveen chromosomes
in polykaryocytes from human-Chinese hamster cell hybrids. (Russ). No 7.
87-88.

6.	Stobetsky  V.I., Mironova  L.L. (1987).  A delayed disruption of
telomeric links between chromosomes in the experimentally induced cells
with micronuclei under treatment with 5-bromodeoxyuridine at the first
S-period after colcemid administration. (Russ). Tsitologia..
29:724-727.

7.	Stobetsky  V.I., Khapchaev Yu. Kh. ,Mironova  L.L. (1987). The
induction of delayed disruption of telomeric links between chromosomes
in cells with micronuclei by 5-iododeoxyuridine and 5-bromodeoxyuridine.
(Russ). Bull. Exptl. Biol. Med. No 7. 83-85.

8. 	Stobetsky V.I., Mironova L.L. (1988a). Effect of 5-azacytidine
on the number of polycentric chromosomes      in cells    with
micronuclei   during   exposure   to 5-bromodeoxyuridine. (Russ). Bull.
Exptl. Biol. Med. No4 479-480.
	
9.	Stobetsky V.I. ,Mironova  L.L.  (1988b). The enhanced intensity
of polycentric chromosome formation in cells with micronuclei after
5-bromodeoxyuridine treatment under prolonged hyperthermia at 40_C. 
(Russ). Tsitologia. 30:358-360.
	
10.	Stobetsky  V.I. (1988c).  On the nature of three cytogenetic
phenomena - delayed spiralization of metaphase chromosome portions ,
delayed disruption of telomeric links between chromosomes  and premature
centromere division of the X-chromosome . (Russ). Tsitologia .
30:1270-1272 .
	
11.	Stobetsky V.I., Mironova  L.L. (1988d). 5-Chlorodeoxyuridine
induces the formation of specific  dicentric chromosomes in cells with
micronuclei more effectively than does 
5-bromodeoxyuridine. (Russ). Tsitologia. . 30:1498-1500.
	
12.	Stobetsky  V.I. , Mironova  L.L. (1989). Telomeric fusion of
chromosomes in cells with micronuclei under  subsequent  incorporation
of halogenated analogs of thymidine into DNA.  (Russ). Tsitologia .
31:1242-1244.
	
13.	Stobetsky  V.I.  (1990).  Induction  of  specific  dicentric
chromosomes in Chinese hamster ovary cells  CHO-6 . (Russ).
Tsitologia.32:92-94.
	
14.	Stobetsky  V.I. (1991a). The induced telomeric chromosome fusion
under conditions of pulse action of hyper- or hypothermia. (Russ).
Tsitologia .33:116-118.
	
15.	Stobetsky V.I.  (1991b). Telomeric chromosome fusion in cells
with micronuclei in the conditions of combined action of hyper- or
hypothermia and halogenated analogs of thymidine . (Russ).  Bull. Exptl.
Biol. Med. No7. 72-73.
	
16.	Stobetsky  V.I., Chebotarev  A.N., Mironova  L.L. (1994).
Analysis of  chromosome combinations in dicentric at the induced
telomeric fusion. (Russ). Tsitologia. 36:60-63.

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

******
Vladimir I. Stobetsky
Senior Scientist
Research Institute of Pediatric Hematology
Laboratory of Cytogenetics and Molecular Biology
App. 116, 6 Novoorlovskaya St. Moscow, 119633, Russia
tel: +7 095 731 8932   
e-mail address: sto@aha.ru  




From owner-chromosomes@net.bio.net Thu Mar 12 22:00:00 1998
Path: biosci!HP.FCIENCIAS.UNAM.MX!hmam
From: hmam@HP.FCIENCIAS.UNAM.MX ("Hector M. Abundis Manzano")
Newsgroups: bionet.genome.chromosomes
Subject: dromex-l
Date: 13 Mar 1998 15:48:22 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 38
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <Pine.LNX.3.95.980313171448.24852A-100000@hp.fciencias.unam.mx>
Reply-To: "Hector M. Abundis Manzano" <hmam@hp.fciencias.unam.mx>
NNTP-Posting-Host: net.bio.net

La Universidad Nacional Autonoma de Mexico, a traves del laboratorio de
Genetica de la Facultad de Ciencias, a generado una lista de discusion
sobre topicos de Drosophila en espanol, dado el creciente interes en todo
los paises en el uso de Drosophila como un sistema para realizar todo tipo
de investigaciones, se decidio crear un foro en espanol, en el cual puedan
discutirse todos aquellos puntos realacionados con Drosophila, esperamos
que esta lista sea de utilidad para toda la comunidad academica, por
lo que les hacemos una atenta invitacion a suscribirse a ella. Este foro
esta administrado por el servidor hp.fciencias. unam.mx, por lo que para
suscribirse solo tendran que enviar un mensaje a:

Majordomo@hp.fciencias.unam.mx

Con el texto subscribe dromex-l

A vuelta de correo ustedes recibiran un mensaje en el cual se les pide su
confirmacion de suscripcion, deberan de contestarlo con los datos que se
adjuntaran y asi completaran su incorparocion a la lista de suscriptores.

Para evitar la entrada de todos aquellos mensajes de publicidad que no
desean recibir, la lista de discusion es modera, razon por la cual solo
se enviaran aquellos mensajes que traten algun tema relacionado
al interes de los suscriptores.

Agradecemos de antemano, su atencion a este mensaje y los invitamos a
suscribirse y participar de manera activa enviando comoentarios, preguntas
o algun otro tema de interes comun.

Por favor hagan llegar esta invitacion a las personas interesadas en un
foro de este tipo.

Gracias
Hector Abundis
Lab. de Genetica
Fac. Ciencias, UNAM
Mexico, D.F.



From owner-chromosomes@net.bio.net Fri Mar 13 22:00:00 1998
Path: biosci!agate!newsfeed.wli.net!newsfeed.direct.ca!newsfeed.sovam.com!sovam!mtu.ru!Radio-MSU.net!news2.aha.ru!aha!not-for-mail
From: "Vladimir I. Stobetsky" <sto@aha.ru>
Newsgroups: bionet.genome.chromosomes
Subject: halogenated analogs of thymidine
Date: 14 Mar 1998 06:54:19 GMT
Organization: Mr. Postman
Lines: 101
Sender: sto@p49.n77.dip.aha.ru
Message-ID: <01bd4ebb$72e36d00$LocalHost@privateu>
NNTP-Posting-Host: p49.n77.dip.aha.ru
X-Newsreader: Microsoft Internet News 4.70.1161




Key words: halogenated analogs of thymidine, human lymphocytes, allocyclic
chromosomes

Cytogenetic  abnormalities in cultured human lymphocytes under treatment
with halogenated analogs of thymidine

After prolonged co-treatment of heteroploid Chinese hamster cells with 
colcemid, that induced cells with micronuclei, and halogenated analogs of 
thymidine (HAT) such as 5-iododeoxyuridine (5-IdU),  5-bromodeoxyuridine 
(5-BrdU)  and 5-chlorodeoxyuridine (5-ChldU) were discovered  dicentric 
chromosomes formed by "end-to-end fusions" (Stobetsky,1976). Registered 
dicentrics were a result of delayed disruption  of telomeric links existed 
in interphase nucleus
(Stobetsky,1978).

In  this study we investigated the cytogenetic abnormalities in cultured 
human lymphocytes under treatment with low doses HAT.  
 In experiments we used peripheral blood  of healthy donors - man at the 
age 44 years an woman at the age 35 years. We  added to 0,5 ml heparinized 
blood 0,2 ml PHA , 6,0 ml Eagle medium and 1,5 ml calf serum. The cells 
cultured at 37o C. HAT  (20 microg/ml)  administrated at 48 h of
cultivation 
for 20 h. The cells treated with colcemid (0,1 microg/ml) during  last 1,5
h. 
Chromosome reparations made with standard method. In each case we scored 
100 metaphases.

Results

Most frequently we observed  the delay of spiralization in  the region of 
constitutive heterochromatin  in chromosome No9. 
Table No1.Frequency of chromosome abnormalities in human lymphocytes under 
  treatment with HAT.	
Type of abnormality                                                        
                                               Intact  culture      5-IdU  
 5-BrdU  5-ChldU	
                                                        Man lymphocytes	
1.Metaphases with delay spiralization or break in heterochromatin region of
chr.9.	       0	        27	         5	        1	
2.Metaphases with onechromatid break or gap (except chromosomes 1,9 and 16)
       3	         4	         5 	        9	
                                                         Woman lymphocytes	
1.	                                                                        
                                                                      0	   
     43	         12	        7	
2.	                                                                        
                                                                      2	   
       1           4 	        10	

Table 1  shows that first abnormality  have a maximum under treatment with 
5-IdU and minimum under action  of 5-ChldU for man and 
woman.Heterochromatic region of chromosome 9   look like as  prophasic  or 
as "pulverization".  Sometimes this  region appeared  as  a break  i.e.  
was  achromatic. This  table shows also that frequency of onechromatid  
breaks  increased in he  row  5-IdU  -  5-BrdU  -  5-ChldU. Locus  of delay

spiralization of the chromosome 9  we consider as allocyclic  chromosome  
as it  is or in   early prophase or  in S-phase  i.e. such chromosomes  are

allocyclic  ( The behavior of allocyclic chromosomes in Bloom's syndrome. 
Otto P.G. Otto P.A. and Eeva Therman.  Cromosoma,1981,84:337-344). So HAT  

(particularly 5-IdU)  induces  the shift some phases of mitotic cycle.  In 

favour of this  hypothesis we have found some cases of  "pulverization" of 
whole  chromosome. Intensity of this process  depends  directly  from 
molecular weight  of  HAT. We  consider that the delay disruption of 
telomeric links in cells with micronuclei  in heteroploid Chinese cell 
lines  that  induced  with  colcemid and HAT which  appeared as dicentrics 

are also allocyclic chromosomes so  the disruption of telomeric links  
occur  at the early stages of mitosis  as telomeric fusion exists  at the 
interphase. Thus  we conclude   from our experiments  that cell response 
depends  on type of   HAT  , specific  properties of cells and  mode of 
treatment.

References
1.Stobetsky  V.I. (1976). Chromosome fusion by telomeres in cells treated 
with colcemid and  5-bromodeoxyuridine. (Russ). Bull.Exptl.Biol.Med. No9. 
1142-1144.
2.Stobetsky  V.I. (1978). Mammalian polykaryocytes  in vitro.II.The 
phenomenon of delayed disruption of telomeric links between  chromosomes. 
Biologisches Zentralblatt. 97:595-604.
3.Stobetsky  V.I.  (1995). Cytogenetic   abnormalities in cultured  human 
lymphocytes undertreatment  with  halogenated analogs of thymidine.(Russ). 
Bull.Exptl.Biol.Med.  No9. 326-328.

*******************************************************
Vladimir I. Stobetsky
Senior Scientist
Research Institute of Pediatric Hematology
Laboratory of Cytogenetics and Molecular Biology
App. 116, 6 Novoorlovskaya St. Moscow, 119633, Russia
tel: +7 095 731 8932   
e-mail address: sto@aha.ru  




From owner-chromosomes@net.bio.net Fri Mar 13 22:00:00 1998
From: "Keith Broadhead" <keith@blackpool.net>
Newsgroups: bionet.genome.chromosomes
Subject: Chromosome 10
Date: Sat, 14 Mar 1998 18:40:43 -0000
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I wish to find out more about chromosome 10 deficiency. Can anyone help.
Please reply in plain english



From owner-chromosomes@net.bio.net Fri Mar 13 22:00:00 1998
Path: biosci!agate!howland.erols.net!cpk-news-hub1.bbnplanet.com!cam-news-hub1.bbnplanet.com!news.bbnplanet.com!newsfeed.sovam.com!sovam!mtu.ru!Radio-MSU.net!news2.aha.ru!aha!not-for-mail
From: "Vladimir I. Stobetsky" <sto@aha.ru>
Newsgroups: bionet.genome.chromosomes
Subject: halogenated analogs of thymidine
Date: 14 Mar 1998 16:03:58 GMT
Organization: Mr. Postman
Lines: 104
Sender: sto@p33-n67.dip.aha.ru
Message-ID: <01bd4f62$6cfc3820$214302c3@privateu>
NNTP-Posting-Host: p33-n67.dip.aha.ru
X-Newsreader: Microsoft Internet News 4.70.1161







Key words: halogenated analogs of thymidin, human lymphocytes, allocyclic
chromosomes

Cytogenetic  abnormalities in cultured human lymphocytes under treatment
with halogenated analogs of thymidine

After prolonged co-treatment of heteroploid Chinese hamster cells with 
colcemid, that induced cells with micronuclei, and halogenated analogs of 
thymidine (HAT) such as 5-iododeoxyuridine (5-IdU),  5-bromodeoxyuridine 
(5-BrdU)  and 5-chlorodeoxyuridine (5-ChldU) were discovered  dicentric 
chromosomes formed by "end-to-end fusions" (Stobetsky,1976). Registered 
dicentrics were a result of delayed disruption  of telomeric links existed 
in interphase nucleus
(Stobetsky,1978).

In  this study we investigated the cytogenetic abnormalities in cultured 
human lymphocytes under treatment with low doses HAT. Scheme of experiments

 In experiments we used peripheral blood  of healthy donors - man at the 
age 44 years an woman at the age 35 years. We  added to 0,5 ml heparinized 
blood 0,2 ml PHA , 6,0 ml Eagle medium and 1,5 ml calf serum. The cells 
cultured at 37o C. HAT  (20 microg/ml)  administrated at 48 h of
cultivation 
for 20 h. The cells treated with colcemid (0,1 microg/ml) during  last 1,5
h. 
Chromosome reparations made with standard method. In each case we scored 
100 metaphases.

Results

Most frequently we observed  the delay of spiralization in  the region of 
constitutive heterochromatin  in chromosome No9. 

...
Table No1.Frequency of chromosome abnormalities in human lymphocytes under 
  treatment with HAT.	
Type of abnormality	Intact  culture	     5-IdU	    5-BrdU	   5-ChldU	
                                                        Man lymphocytes	
1.Metaphases with delay spiralization or break in heterochromatin region of
chr.9.	       0	        27	         5	        1	
2.Metaphases with onechromatid break or gap (except chromosomes 1,9 and 16)
       3	         4	         5 	        9	
                                                         Woman lymphocytes	
1.	        0	         43	         12	        7	
2.	        2	           1     	           4 	        10	




Table 1  shows that first abnormality  have a maximum under treatment with 
5-IdU and minimum under action  of 5-ChldU for man and 
woman.Heterochromatic region of chromosome 9   look like as  prophasic  or 
as "pulverization".  Sometimes this  region appeared  as  a break  i.e.  
was  achromatic. This  table shows also that frequency of onechromatid  
breaks  increased in he  row  5-IdU  -  5-BrdU  -  5-ChldU. Locus  of delay

spiralization of the chromosome 9  we consider as allocyclic  chromosome  
as it  is or in   early prophase or  in S-phase  i.e. such chromosomes  are

allocyclic  ( The behavior of allocyclic chromosomes in Bloom's syndrome. 
Otto P.G. Otto P.A. and Eeva Therman.  Cromosoma,1981,84:337-344). So HAT  

(particularly 5-IdU)  induces  the shift some phases of mitotic cycle.  In 

favour of this  hypothesis we have found some cases of  "pulverization" of 
whole  chromosome. Intensity of this process  depends  directly  from 
molecular weight  of  HAT. We  consider that the delay disruption of 
telomeric links in cells with micronuclei  in heteroploid Chinese cell 
lines  that  induced  with  colcemid and HAT which  appeared as dicentrics 

are also allocyclic chromosomes so  the disruption of telomeric links  
occur  at the early stages of mitosis  as telomeric fusion exists  at the 
interphase. Thus  we conclude   from our experiments  that cell response 
depends  on type of   HAT  , specific  properties of cells and  mode of 
treatment.

References
1.Stobetsky  V.I. (1976). Chromosome fusion by telomeres in cells treated 
with colcemid and  5-bromodeoxyuridine. (Russ). Bull.Exptl.Biol.Med. No9. 
1142-1144.
2.Stobetsky  V.I. (1978). Mammalian polykaryocytes  in vitro.II.The 
phenomenon of delayed disruption of telomeric links between  chromosomes. 
Biologisches Zentralblatt. 97:595-604.
3.Stobetsky  V.I.  (1995). Cytogenetic   abnormalities in cultured  human 
lymphocytes undertreatment  with  halogenated analogs of thymidine.(Russ). 
Bull.Exptl.Biol.Med.  No9. 326-328.

*******************************************************
Vladimir I. Stobetsky
Senior Scientist
Research Institute of Pediatric Hematology
Laboratory of Cytogenetics and Molecular Biology
App. 116, 6 Novoorlovskaya St. Moscow, 119633, Russia
tel: +7 095 731 8932   
e-mail address: sto@aha.ru  




From owner-chromosomes@net.bio.net Fri Mar 13 22:00:00 1998
Path: biosci!agate!howland.erols.net!feed2.news.erols.com!erols!newsfeed.xcom.net!cam-news-hub1.bbnplanet.com!news.bbnplanet.com!newsfeed.sovam.com!sovam!mtu.ru!Radio-MSU.net!news2.aha.ru!aha!not-for-mail
From: "Vladimir I. Stobetsky" <sto@aha.ru>
Newsgroups: bionet.genome.chromosomes
Subject: halogenated analogs of thymidine
Date: 14 Mar 1998 15:59:23 GMT
Organization: Mr. Postman
Lines: 104
Sender: sto@p33-n67.dip.aha.ru
Message-ID: <01bd4f58$0a6bdf80$LocalHost@privateu>
NNTP-Posting-Host: p33-n67.dip.aha.ru
X-Newsreader: Microsoft Internet News 4.70.1161







Key words: halogenated analogs of thymidin, human lymphocytes, allocyclic
chromosomes

Cytogenetic  abnormalities in cultured human lymphocytes under treatment
with halogenated analogs of thymidine

After prolonged co-treatment of heteroploid Chinese hamster cells with 
colcemid, that induced cells with micronuclei, and halogenated analogs of 
thymidine (HAT) such as 5-iododeoxyuridine (5-IdU),  5-bromodeoxyuridine 
(5-BrdU)  and 5-chlorodeoxyuridine (5-ChldU) were discovered  dicentric 
chromosomes formed by "end-to-end fusions" (Stobetsky,1976). Registered 
dicentrics were a result of delayed disruption  of telomeric links existed 
in interphase nucleus
(Stobetsky,1978).

In  this study we investigated the cytogenetic abnormalities in cultured 
human lymphocytes under treatment with low doses HAT. Scheme of experiments

 In experiments we used peripheral blood  of healthy donors - man at the 
age 44 years an woman at the age 35 years. We  added to 0,5 ml heparinized 
blood 0,2 ml PHA , 6,0 ml Eagle medium and 1,5 ml calf serum. The cells 
cultured at 37o C. HAT  (20 microg/ml)  administrated at 48 h of
cultivation 
for 20 h. The cells treated with colcemid (0,1 microg/ml) during  last 1,5
h. 
Chromosome reparations made with standard method. In each case we scored 
100 metaphases.

Results

Most frequently we observed  the delay of spiralization in  the region of 
constitutive heterochromatin  in chromosome No9. 

..
Table No1.Frequency of chromosome abnormalities in human lymphocytes under 
  treatment with HAT.	
Type of abnormality	Intact  culture	     5-IdU	    5-BrdU	   5-ChldU	
                                                        Man lymphocytes	
1.Metaphases with delay spiralization or break in heterochromatin region of
chr.9.	       0	        27	         5	        1	
2.Metaphases with onechromatid break or gap (except chromosomes 1,9 and 16)
       3	         4	         5 	        9	
                                                         Woman lymphocytes	
1.	        0	         43	         12	        7	
2.	        2	           1     	           4 	        10	




Table 1  shows that first abnormality  have a maximum under treatment with 
5-IdU and minimum under action  of 5-ChldU for man and 
woman.Heterochromatic region of chromosome 9   look like as  prophasic  or 
as "pulverization".  Sometimes this  region appeared  as  a break  i.e.  
was  achromatic. This  table shows also that frequency of onechromatid  
breaks  increased in he  row  5-IdU  -  5-BrdU  -  5-ChldU. Locus  of delay

spiralization of the chromosome 9  we consider as allocyclic  chromosome  
as it  is or in   early prophase or  in S-phase  i.e. such chromosomes  are

allocyclic  ( The behavior of allocyclic chromosomes in Bloom's syndrome. 
Otto P.G. Otto P.A. and Eeva Therman.  Cromosoma,1981,84:337-344). So HAT  

(particularly 5-IdU)  induces  the shift some phases of mitotic cycle.  In 

favour of this  hypothesis we have found some cases of  "pulverization" of 
whole  chromosome. Intensity of this process  depends  directly  from 
molecular weight  of  HAT. We  consider that the delay disruption of 
telomeric links in cells with micronuclei  in heteroploid Chinese cell 
lines  that  induced  with  colcemid and HAT which  appeared as dicentrics 

are also allocyclic chromosomes so  the disruption of telomeric links  
occur  at the early stages of mitosis  as telomeric fusion exists  at the 
interphase. Thus  we conclude   from our experiments  that cell response 
depends  on type of   HAT  , specific  properties of cells and  mode of 
treatment.

References
1.Stobetsky  V.I. (1976). Chromosome fusion by telomeres in cells treated 
with colcemid and  5-bromodeoxyuridine. (Russ). Bull.Exptl.Biol.Med. No9. 
1142-1144.
2.Stobetsky  V.I. (1978). Mammalian polykaryocytes  in vitro.II.The 
phenomenon of delayed disruption of telomeric links between  chromosomes. 
Biologisches Zentralblatt. 97:595-604.
3.Stobetsky  V.I.  (1995). Cytogenetic   abnormalities in cultured  human 
lymphocytes undertreatment  with  halogenated analogs of thymidine.(Russ). 
Bull.Exptl.Biol.Med.  No9. 326-328.

*******************************************************
Vladimir I. Stobetsky
Senior Scientist
Research Institute of Pediatric Hematology
Laboratory of Cytogenetics and Molecular Biology
App. 116, 6 Novoorlovskaya St. Moscow, 119633, Russia
tel: +7 095 731 8932   
e-mail address: sto@aha.ru  




From owner-chromosomes@net.bio.net Wed Mar 25 22:00:00 1998
Path: biosci!rutgers!rockyd.rockefeller.edu!newsfeed.nyu.edu!newsfeed.gte.net!news.maxwell.syr.edu!Supernews60!supernews.com!Supernews69!not-for-mail
From: "Jamie Hinojosa" <locus25@HUB.ofthe.NEt>
Newsgroups: bionet.genome.chromosomes
Subject: chromosome 15 in the P region
Date: Wed, 25 Mar 1998 21:48:46 -0600
Organization: All USENET -- http://www.Supernews.com
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my wife is a physical therapist work with a baby that has a problem with
chormesome 15 in the P region.  yet, no one knows what this syndrome or
defect is called or know what it is about.  if anyone has any info on this
particular defect or has any idea where i could get more information on this
subject, please let me know.

locus25@hub.ofthe.net

thank you



From owner-chromosomes@net.bio.net Wed Mar 25 22:00:00 1998
Path: biosci!agate!news-spur1.maxwell.syr.edu!news.maxwell.syr.edu!news-peer.sprintlink.net!news-backup-east.sprintlink.net!news-in-east.sprintlink.net!news-pen-1.sprintlink.net!news.sprintlink.net!Sprint!mn6.swip.net!mn5.swip.net!not-for-mail
From: sublett@swipnet.se (SubLett)
Newsgroups: bionet.genome.chromosomes
Subject: Genetic manipulation....
Date: Thu, 26 Mar 1998 23:06:34 GMT
Organization: A customer of Tele2
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Hi, My name is Kim Sarenstam, and I'm writing a project work for
school.. it's about genetic manipulation, including hybrid-DNA,
cloning etc...

As of now, I was wondering if there was anyone out there who
has any information on this subject, website, personal experience
or such, I'm not that very used to USENET, so I would appreciate
if you could mail me at : sublett@swipnet.se

If you find this message annoying, or in the wrong place, I have to 
apologize for myself, sorry...

Thanks
Kim Sarenstam

From owner-chromosomes@net.bio.net Thu Mar 26 22:00:00 1998
Path: biosci!unmsm.edu.pe!1000209
From: 1000209@unmsm.edu.pe ("DANIEL ORE[1000209@UNMSM.EDU.PE]")
Newsgroups: bionet.genome.chromosomes
Subject: Consultation of RT-PCR in leuKemia
Date: 26 Mar 1998 18:06:46 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 19
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <c=US%a=_%p=UNMSM%l=SERVER_A01-980327015024Z-2747@server_a01.campus.unmsm.edu.pe>
NNTP-Posting-Host: net.bio.net

Sr :

                   A consultation because in the leukemia tests where
involved in
                   gene brc (crom 22) and the gene c-abl (crom9), there
is one formacion of a
                   chimera, for I diagnose of this is used a test of
RT-PCR, (transcriptasa
                   reversa), my question is because it is not used as it
sample the DNA of the
                   patient and because the RNA, if it is that in the
constitution of the DNA is the
                   problem. 
				Thank you

		Daniel Ore Chavez
		Universidad Nacional Mayor de San Marcos
		Facultad de Ciencias Biologicas
		E-mail: 1000209@unmsm.edu.pe

From owner-chromosomes@net.bio.net Thu Mar 26 22:00:00 1998
Path: biosci!internet!biosci!not-for-mail
From: biohelp (BIOSCI Administrator)
Newsgroups: bionet.genome.chromosomes
Subject: BIOSCI/bionet miniFAQ & Fundraiser
Date: 27 Mar 1998 02:00:17 -0800
Organization: BIOSCI International Newsgroups for Molecular Biology
Lines: 233
Sender: daemon@net.bio.net
Distribution: world
Message-ID: <199803271000.CAA23731@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.
------------------------------------------------------------------
PLEASE NOTE: The BIOSCI management does NOT act on
subscription/unsubscription requests that are posted improperly to the
newsgroups and mailing lists.  People who do this only bother everyone
on the lists to no avail.  Please be sure to follow the proper
procedures below.

Gory details are in the BIOSCI Information sheets on the Web at
http://www.bio.net.  Below we give an example utilizing the
METHODS-AND-REAGENTS list at both of our two BIOSCI sites:

Users in the Americas and Pacific Rim countries who use the BIOSCI
------------------------------------------------------------------
node at computer net.bio.net:
----------------------------

A) Determine the "listname" which is the <=8 character mail address
                                         ^^^^^^^^^^^^^
   for the group.  These can be found in the BIOSCI Info. Sheet.  For
   the METHODS-AND-REAGENTS group the mailing address is
   methods@net.bio.net.  The listname is the portion of the address to
   the left of the @ sign, i.e., "methods".  The listname is used with
   the "subscribe" and "unsubscribe" commands illustrated below.

B) Mail all commands in the body of a mail message addressed to
   biosci-server@net.bio.net.  Do NOT send commands to the newsgroup
   posting addresses!  Leave the Subject: line blank, any text on it
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From owner-chromosomes@net.bio.net Thu Mar 26 22:00:00 1998
Path: biosci!agate!newsfeed.wli.net!su-news-hub1.bbnplanet.com!news.bbnplanet.com!data.ramona.vix.com!nnrp2.crl.com!not-for-mail
From: Bryan Ness <botany.guide@miningco.com>
Newsgroups: bionet.genome.chromosomes
Subject: Polyploidy: More is Better
Date: Fri, 27 Mar 1998 15:52:50 -0800
Organization: The Mining Company
Lines: 13
Message-ID: <351C3BD2.BE2D0673@miningco.com>
NNTP-Posting-Host: 165.113.252.247
Mime-Version: 1.0
Content-Type: text/plain; charset=us-ascii
Content-Transfer-Encoding: 7bit
X-Mailer: Mozilla 4.04 [en] (Win95; I)

Learn a little about the genetics of polyploidy and how widespread it is
among plants.  Ponder some of the reasons why plants find polyploidy
advantageous.  Read the article "Polyploidy: More is Better" featured
this week at The Botany Site by going to the following URL:
http://botany.miningco.com/library/weekly/aa032598.htm

There is much more at The Botany Site as well, including past features,
a "Name That Plant Contest," featured links, a bulletin board and a chat
area.  Learn more about The Botany Site by following the link below.
--
______________________________________________________________
Bryan Ness, Botany Guide           http://botany.miningco.com/
botany.guide@miningco.com

From owner-chromosomes@net.bio.net Fri Mar 27 22:00:00 1998
Path: biosci!agate!howland.erols.net!ais.net!uunet!in4.uu.net!venus.hkstar.com!hkstar2!news@hkstar.com
From: unixon_31@hotmail.com
Newsgroups: bionet.genome.chromosomes
Subject: 17-BETA-HYDROXYSTEROID-OXIDOREDUCTASE
Date: Sat, 28 Mar 1998 15:16:25 -0800
Organization: Hong Kong Star Internet Ltd.
Lines: 12
Message-ID: <351D84C9.24FF@hotmail.com>
NNTP-Posting-Host: ip-51-19.dialup.hkstar.com
Mime-Version: 1.0
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X-Mailer: Mozilla 3.02 (Win95; I; 16bit)

17-BETA-HYDROXYSTEROID-OXIDOREDUCTASE

Does any one know of any existing vitamins , minerals etc... that can
inhibit 17-BETA-HYDROXYSTEROID-OXIDOREDUCTASE 's ability to turn
androstenedione into testosterone ?
Zinc , saw palmetto ,vitamin b 6 are known to have inhibitory effect on
testosterone's conversion to dihytestosterone by preventing 5 alpha
reductase from doing its job.
 
Thanks

ref: 17-BETA-HYDROXYSTEROID-OXIDOREDUCTASE

From owner-chromosomes@net.bio.net Tue Mar 31 23:00:00 1998
Path: biosci!news.Stanford.EDU!su-news-hub1.bbnplanet.com!cpk-news-hub1.bbnplanet.com!news.bbnplanet.com!Cabal.CESspool!bofh.vszbr.cz!feed1.news.luth.se!luth.se!news.lth.se!merkurius.lu.se!not-for-mail
From: David Hagerberg <David.Hagerberg@mbioekol.lu.se>
Newsgroups: bionet.genome.chromosomes
Subject: Definition of gene cloning
Date: Wed, 01 Apr 1998 09:25:50 +0200
Organization: Lund University
Lines: 12
Message-ID: <3521EBFE.B4E0AD2A@mbioekol.lu.se>
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Hello,

I am looking for the exact definition of "gene cloning". Does anyone
know it by heart or can you tell me where to find it?

Please respond to Jorgen.Holmen@eu.pnu.com since I am borrowing this
computer.

Thanx

/Jorgen


