Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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MES-4, an autosome-associated HMT that participates in silencing the X chromosomes in the C. elegans germ line


ABSTRACT: Microarray-based expression profiling of dissected gonads from mes-4 mutants reveals that MES-4 is required to repress expression of a set of X-linked genes. We isolated dissected gonads from mes-4(bn85) mutant adults and compared to dissected gonads from wild type (N2 animals. RNA was linearly amplified prior to labeling for all genotypes. Comparison was done in quadruplicate on independently grown and isolated animals.

ORGANISM(S): Caenorhabditis elegans

SUBMITTER: Valerie Reinke 

PROVIDER: E-GEOD-5454 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

MES-4: an autosome-associated histone methyltransferase that participates in silencing the X chromosomes in the C. elegans germ line.

Bender Laurel B LB   Suh Jinkyo J   Carroll Coleen R CR   Fong Youyi Y   Fingerman Ian M IM   Briggs Scott D SD   Cao Ru R   Zhang Yi Y   Reinke Valerie V   Strome Susan S  

Development (Cambridge, England) 20061001 19


Germ cell development in C. elegans requires that the X chromosomes be globally silenced during mitosis and early meiosis. We previously found that the nuclear proteins MES-2, MES-3, MES-4 and MES-6 regulate the different chromatin states of autosomes versus X chromosomes and are required for germline viability. Strikingly, the SET-domain protein MES-4 is concentrated on autosomes and excluded from the X chromosomes. Here, we show that MES-4 has histone H3 methyltransferase (HMT) activity in vit  ...[more]

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