Literature DB >> 23103171

Antagonism between MES-4 and Polycomb repressive complex 2 promotes appropriate gene expression in C. elegans germ cells.

Laura J Gaydos1, Andreas Rechtsteiner, Thea A Egelhofer, Coleen R Carroll, Susan Strome.   

Abstract

The Caenorhabditis elegans MES proteins are key chromatin regulators of the germline. MES-2, MES-3, and MES-6 form the C. elegans Polycomb repressive complex 2 and generate repressive H3K27me3. MES-4 generates H3K36me3 on germline-expressed genes. Transcript profiling of dissected mutant germlines revealed that MES-2/3/6 and MES-4 cooperate to promote the expression of germline genes and repress the X chromosomes and somatic genes. Results from genome-wide chromatin immunoprecipitation showed that H3K27me3 and H3K36me3 occupy mutually exclusive domains on the autosomes and that H3K27me3 is enriched on the X. Loss of MES-4 from germline genes causes H3K27me3 to spread to germline genes, resulting in reduced H3K27me3 elsewhere on the autosomes and especially on the X. Our findings support a model in which H3K36me3 repels H3K27me3 from germline genes and concentrates it on other regions of the genome. This antagonism ensures proper patterns of gene expression for germ cells, which includes repression of somatic genes and the X chromosomes.
Copyright © 2012 The Authors. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 23103171      PMCID: PMC3513488          DOI: 10.1016/j.celrep.2012.09.019

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  35 in total

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Journal:  Genome Res       Date:  2010-12-22       Impact factor: 9.043

2.  Subunit contributions to histone methyltransferase activities of fly and worm polycomb group complexes.

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3.  H3K36 methylation antagonizes PRC2-mediated H3K27 methylation.

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Journal:  J Biol Chem       Date:  2011-01-14       Impact factor: 5.157

4.  Genome-wide germline-enriched and sex-biased expression profiles in Caenorhabditis elegans.

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Journal:  Epigenetics Chromatin       Date:  2010-08-12       Impact factor: 4.954

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Journal:  PLoS Genet       Date:  2009-06-26       Impact factor: 5.917

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  77 in total

1.  PHF1 Tudor and N-terminal domains synergistically target partially unwrapped nucleosomes to increase DNA accessibility.

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Journal:  Nucleic Acids Res       Date:  2017-04-20       Impact factor: 16.971

2.  Phosphorylation of RNA polymerase II is independent of P-TEFb in the C. elegans germline.

Authors:  Elizabeth Anne Bowman; Christopher Ray Bowman; Jeong H Ahn; William G Kelly
Journal:  Development       Date:  2013-07-31       Impact factor: 6.868

Review 3.  Repression of somatic cell fate in the germline.

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Journal:  Cell Mol Life Sci       Date:  2015-06-05       Impact factor: 9.261

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Journal:  Development       Date:  2015-05-15       Impact factor: 6.868

Review 5.  Dynamic chromatin technologies: from individual molecules to epigenomic regulation in cells.

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6.  Pluripotent cells will not dosage compensate.

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7.  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

Review 8.  H3K27 methylation: a promiscuous repressive chromatin mark.

Authors:  Elizabeth T Wiles; Eric U Selker
Journal:  Curr Opin Genet Dev       Date:  2016-12-08       Impact factor: 5.578

9.  Genome-wide redistribution of H3K27me3 is linked to genotoxic stress and defective growth.

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10.  Reevaluation of whether a soma-to-germ-line transformation extends lifespan in Caenorhabditis elegans.

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