CALL FOR VOTES: GENSTRUCTURE/bionet.genome.gene-structure (moderated)

BIOSCI Administrator biosci-help at net.bio.net
Tue Nov 12 19:32:48 EST 1996


Voting is now open on the following proposal to create the mailing
list & newsgroup

GENSTRUCTURE/bionet.genome.gene-structure (moderated)

The charter was not modified as a result of the discussion.

*** NOTE *** We are often running several votes for other newsgroups,
so please be certain to follow the voting directions *carefully*!  If
you just send in a message saying "YES" or "NO" it will not be counted
if it is not clear which proposal you are responding to.

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Proposal for GENSTRUCTURE/bionet.genome.gene-structure (moderated)

Proposed USENET name:           bionet.genome.gene-structure

One line Description:           Genome and chromatin structure and function

Status:                         Moderated

Proposed Moderation address:    bionet-genome-gene-structure at net.bio.net
                                (genstruc-moderator at net.bio.net
                                is an alias for
                                bionet-genome-gene-structure at net.bio.net)

Moderator:			Graham Dellaire

Proposed mailing list name:     GENSTRUCTURE

Proposed e-mail addresses:      genstruc at net.bio.net
                                genstruc at daresbury.ac.uk

Charter:

The purpose of the GENSTRUCTURE newsgroup is to provide a proper forum
for the discussion of issues pertaining and involving genome and/or
chromatin structure and function (see _Topics of Discussion_).
Primarily it should enable those researchers who work in
genome/chromatin structure or related fields to communicate ideas and
information, as well as, provide a chance for collaboration among
national and international research groups.

---------------------------------------------------------------------
Topics of Discussion include:

1. Genome/chromatin accessibility and recombination
                    -recombination hotspots (mieotic and mitotic)
                    -fragile sites
                    -imprinting and recombination rates
		    -ectopic gene targeting and chromatin structure

2. 3D-organization of the nucleus
                    -chromosome territories
                    -nucleoli
                    -nuclear lamina (telomere localization)
                    -tissue or cell cycle dependent
                     positioning of chromosomes
                    -RNA tracking

3. Effect of Superhelicity and DNA topology/structure(Triple strand, Z-DNA,
   cruciform, bent etc) on biological processes such as:
                    -replication 
                     (ex. replication fork barriers, initiation sites)
                    -transcription
                     (ex. promoter function in relation to superhelicity)
                    -recombination
                     (ex. Gin and Hin invertases and superhelicity)

4. Histones and Nucleosomes and chromatin structure/function
                    -H1 repression of transcription
                    -Post translational modification of histones
                     acetylation (H4, H3), phosphorylation (H1, H3)
                     and ubiquitination (H2A, H2B)
                    -Histone variants (ex. H2A.Z in mammals, H5 of chicken)

5. Models of genome structure (Loop Domain Model, Channel Model,
   MegaBase Giant Loop Model, etc.)

6. Classical chromosome elements and their relationship to gene function
                    -centromeres (constitutive heterochromatin and 
		     gene silencing)
                    -telomeres (associated silencing and involvement
		     in position effect)

7. Evolution of the Genome
                    -isochores and base-content (GC vs. AT)
                    -formation of gene clusters and syntenic mapping
                    -repetitive elements (satellites, telomeric and
                     centromeric (alpha) repeats, lines and sines)

8. Biologically important mutants and knockouts that affect
   genome/chromatin structure
                    -ex. SNF/SWI, TOPO mutants in yeast
                    -RAD 51,52,54 knockout mice
                    -AT, BLM, FA mouse models

9. Techniques for genome/chromatin analysis
                    -cytogenetic techniques (g banding, r and q)
                    -Fluorescent In situ analysis(FISH)
                    -Confocal microscopy
                    -Electron microscopy
                    -Electron microscopy In situ analysis (EMISH)
                    -psoralen, polyamine crosslinking
                    -In vivo nucleosome foot printing
                    -Dnase I/Micrococcal Nuclease sensitivity
                    -VM26 Topoisomerase II site mapping

10. Chromatin/DNA binding proteins and their effects on chromatin structure
    and/or gene expression
                    -Polycomb proteins
                    -Rap1 (telomere silencing)
                    -alpha2-MCM1 (repression of MAT locus)
                    -CENP A/B/C (centromere structure/function)
                    -XCAP-C/E, SMC1/2 (chromatin Condensation)
                    -remodeling of chromatin by SWI/SNF proteins
                    -H-NS in bacteria (role in nucleoid topology
                     vs. gene function)

11. Nuclear Matrix (NM) and Nuclear Lamina (NL)
                    -cell cycle regulation of formation of NM and NL
                    -transcription and replications factors 
                     and the concept of a dynamic NM 
                     (ex. tissue and temporal specificity) 
                    -role of NM in signal transduction
                     (mechanistic vs. chemical signals)

12. Matrix attatchent regions (MAR's), domain boundaries and locus
    control regions (LCR's) and their relationship to gene structure
    and function.
                    -definition of transcription/replication domains
                    -model systems ex. betaglobin (LCR) SCS/SCS' of
		     the Drosophila Heat Shock Locus (HS87a7)

13. Phenomenon of Position Effect and Transvection
                    -in drosophila (HP1, polycomb, heterochromatization)
                    -in mammalian systems (silencing or variegated
                     expression of transgenes)
                    -in fungi 

14. Epigenetic effects on gene function
                    -imprinting
                    -methylation
                    -maintenance of early/late replication

15. Dosage compensation mechanisms and X chromosome inactivation
                    -MSL proteins of Drosophila
                    -XIC (Xist RNA) in mammals
                    -CpG methylation

16. Chromatin structure and DNA replication
                    -ORC1 protein of yeast
                    -origins of replication 
                     (association with cruciform, bent DNA and MARS)

17. Specialized methods of nuclear packaging
                    -bacterial nucleoid
                    -packaging of DNA in spermatozoa

18. DNA repair and chromatin structure
                    -TFIIH (transcription coupled repair)
                    -p53
                    -BLM and AT genes
                    -poly-ADP-polymerase (PARP)

19. Mechanisms of genomic instability
                    -during oncogenesis
                    -process of chromosomal aberration (stable and unstable)
                     (ex. role of micronuclei in the process)
                    -chromosomal aberration during aging and mechanisms
                     of instability (ex. telomeres and telomerase)
                    

In addition this newsgroup provides:

        A forum for the exchange of information about future congresses
        and meetings in areas of molecular biology relating to genome
	structure/function.

        A forum for the exchange of information about textbooks, internet
        resources, visual materials, and computer programs.

        A source of quick help for last-minute troubleshooting,
	sources of materials, and practical advice; in areas such as
                       -Specific common resources
                        (ex. primers, antibodies, vectors)
                       -Genome analysis techniques
                       -Transgenic models and mutant cell lines


Moderation Policy:
                        
Mass-posted commercial messages, chain letters, and similar postings
not associated with or pertaining to the study of genome/chromatin
structure and function will be deleted without comment. Inappropriate
messages posted in good faith will be returned to the sender.
Messages not strictly within the charter but likely to be of interest
to many subscribers (e.g., messages dealing with transcription and
replication factors) will be accepted.

Subscribers are welcome from universities or any academic
institutions, government agencies, medical institutions, and
industrial or commercial organizations. Contributions within the
functions outlined above are encouraged.
      
                 
Proposed discussion leaders:

*Note: Area of expertise is written in brackets

Graham Dellaire,  e-mail: dellaire at odyssee.net (gdella at po-box.mcgill.ca)
Institut du Cancer de Montreal
Centre de Recherche L.C. Simard
1560 Sherbrooke Street East,
Montreal, Quebec, Canada  H2L 4M1
telephone:1 (514) 876 6936; fax: (514) 876 5476
*(Expertise:chromatin structure and recombination; Recombination
Access Mapping (RAM); genome structure analysis)


Ronald Hancock,  e-mail: ronald.hancock at crhdq.ulaval.ca
Professor
Laval University Cancer Research Centre
1 rue de l'Arsenal
Quebec, Canada G1R 2J6
telephone: 1 (418) 691-5281; fax: 1 (418) 691-5439
*(Expertise:genome organisation in vivo; models of genome structure;
topoisomerases; VM26 topoisomerase II site mapping)


Eric Milot, e-mail: milot at ch1.fgg.eur.nl
Faculty of Medicine
Dept. of Cell Biology and Genetics
P.O. Box 1738
3000 DR Rotterdam
The Netherlands
telephone: 3110 4087164; fax: 3110 4360225
*(Expertise:Chromatin context and transcription; Polycomb
protein; position effect variegation; chromosome and nuclear
organisation; dosage compensation)

**Tentative Discussion leader**

Peter Cook, e-mail: peter.cook at pathology.oxford.ac.uk
Professor of Cell Biology,
The Sir William Dunn School of Pathology,
South Parks Road,
Oxford, OX1 3RE, UK.
Telephone (direct line) : +44/0 1865 275528
Telephone (switchboard) : +44/0 1865 275500
Fax : +44/0 1865 275501
http://www.molbiol.ox.ac.uk/www/users/counsell/cook.htm
(Expertise:Chromatin/Genome Structure and Function in regard to 
transcription and replication)
----------------------------------------------------------------------

Voting is now open on the proposal for
GENSTRUCTURE/bionet.genome.gene-structure and will run
through 24:00 hrs Pacific Time on 12 December 1996.  Please send your
vote to either of the following addresses:

Address                               Location        Network
-------                               --------        -------
biovote at daresbury.ac.uk               U.K.            JANET
biovote at net.bio.net                   U.S.A.          Internet/BITNET

PLEASE BE SURE TO FOLLOW THE FORMAT BELOW - WE OFTEN RUN MORE THAN ONE
VOTE AT A TIME SO A SIMPLE "YES" OR "NO" MESSAGE WITHOUT THE NEWSGROUP
NAME MAY BE AMBIGUOUS.  Your vote should contain a single line:

YES on GENES

if you favor allowing the creation of this newsgroup or

NO on GENES

if you think that this proposal will adversely affect the
BIOSCI/bionet system.  While not intended to be an exhaustive list of
possible concerns (more specific concerns may have been raised during
the discussion period on BIOFORUM/bionet.general and interested
readers are referred to these), some general reasons for voting NO
might be if you are concerned about newsgroup proliferation and/or
believe that the proposed group will not be utilized, or if you think
that the proposed newsgroup would substantially duplicate or overlap
with the function of existing newsgroups.  If you are simply not
interested in participating in the newsgroup above, please don't cast
a NO vote, but instead just don't vote at all.

The newsgroup proposal must receive at least 80 YES votes to pass and
the number of YES votes must be greater than the number of NO votes by
at least 40.  Discussion of the newsgroup proposal is now closed and
we strongly discourage posting any messages in other forums about the
fact that a CALL FOR VOTES has been issued.

				Sincerely,

				Dave Kristofferson
				BIOSCI/bionet Manager

				biosci-help at net.bio.net



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