Literature DB >> 14976312

Recruitment and spreading of the C. elegans dosage compensation complex along X chromosomes.

Györgyi Csankovszki1, Patrick McDonel, Barbara J Meyer.   

Abstract

To achieve X-chromosome dosage compensation, organisms must distinguish X chromosomes from autosomes. We identified multiple, cis-acting regions that recruit the Caenorhabditis elegans dosage compensation complex (DCC) through a search for regions of X that bind the complex when detached from X. The DCC normally assembles along the entire X chromosome, but not all detached regions recruit the complex, despite having genes known to be dosage compensated on the native X. Thus, the DCC binds first to recruitment sites, then spreads to neighboring X regions to accomplish chromosome-wide gene repression. From a large chromosomal domain, we defined a 793-base pair fragment that functions in vivo as an X-recognition element to recruit the DCC.

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Year:  2004        PMID: 14976312     DOI: 10.1126/science.1092938

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  66 in total

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Authors:  Alexander V Strunnikov
Journal:  Plasmid       Date:  2005-10-17       Impact factor: 3.466

Review 2.  The contradictory definitions of heterochromatin: transcription and silencing.

Authors:  Kathryn L Huisinga; Brent Brower-Toland; Sarah C R Elgin
Journal:  Chromosoma       Date:  2006-02-28       Impact factor: 4.316

Review 3.  Dosage compensation, the origin and the afterlife of sex chromosomes.

Authors:  Jan Larsson; Victoria H Meller
Journal:  Chromosome Res       Date:  2006       Impact factor: 5.239

4.  The enhancement of pericentromeric cohesin association by conserved kinetochore components promotes high-fidelity chromosome segregation and is sensitive to microtubule-based tension.

Authors:  Carrie A Eckert; Daniel J Gravdahl; Paul C Megee
Journal:  Genes Dev       Date:  2007-01-22       Impact factor: 11.361

5.  X chromosome repression by localization of the C. elegans dosage compensation machinery to sites of transcription initiation.

Authors:  Sevinc Ercan; Paul G Giresi; Christina M Whittle; Xinmin Zhang; Roland D Green; Jason D Lieb
Journal:  Nat Genet       Date:  2007-02-11       Impact factor: 38.330

6.  Revisiting the X:A signal that specifies Caenorhabditis elegans sexual fate.

Authors:  John M Gladden; Behnom Farboud; Barbara J Meyer
Journal:  Genetics       Date:  2007-10-18       Impact factor: 4.562

7.  A ONECUT homeodomain protein communicates X chromosome dose to specify Caenorhabditis elegans sexual fate by repressing a sex switch gene.

Authors:  John M Gladden; Barbara J Meyer
Journal:  Genetics       Date:  2007-08-24       Impact factor: 4.562

8.  Two classes of dosage compensation complex binding elements along Caenorhabditis elegans X chromosomes.

Authors:  Timothy A Blauwkamp; Gyorgyi Csankovszki
Journal:  Mol Cell Biol       Date:  2009-02-02       Impact factor: 4.272

9.  Chromosome-wide mechanisms to decouple gene expression from gene dose during sex-chromosome evolution.

Authors:  Bayly S Wheeler; Erika Anderson; Christian Frøkjær-Jensen; Qian Bian; Erik Jorgensen; Barbara J Meyer
Journal:  Elife       Date:  2016-08-30       Impact factor: 8.140

10.  xol-1, the master sex-switch gene in C. elegans, is a transcriptional target of the terminal sex-determining factor TRA-1.

Authors:  Balázs Hargitai; Vera Kutnyánszky; Timothy A Blauwkamp; Attila Steták; Györgyi Csankovszki; Krisztina Takács-Vellai; Tibor Vellai
Journal:  Development       Date:  2009-12       Impact factor: 6.868

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