<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Chavez SR</submitter><funding>NICHD NIH HHS</funding><funding>NIA NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><pubmed_abstract>The proper coordination of transcription factors, ATP dependent chromatin remodelers and histone modifications is essential for tissue specific gene expression, but how gene expression is regulated at these different levels is not well understood. In &lt;i>C. elegans&lt;/i>, H3K4 methylation that is acquired in the germline is reprorgammed at fertilization by the H3K4me1/2 demethlyase SPR-5/LSD1/KDM1A and the H3K9 methyltransferase MET2/SETDB1/KMT2E. SPR-5/MET-2 maternal reprogramming is required to help establish the germline-soma distinction and prevent developmental delay by preventing inherited H3K4 methylation from inappropriately maintaining germline gene expression in somatic tissues. To determine if the DREAM transcriptional repressor complex and the MEC NuRD ATP dependent nucleosome rem</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2025.07.23.666413</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12330697</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The Dream and MEC NuRD Complexes reinforce SPR-5/MET-2 maternal reprogramming to maintain the germline-soma distinction.</pubmed_title><pmcid>PMC12330697</pmcid><funding_grant_id>T32 AG087922</funding_grant_id><funding_grant_id>R15 GM148887</funding_grant_id><funding_grant_id>T32 NS096050</funding_grant_id><funding_grant_id>K12 GM000680</funding_grant_id><funding_grant_id>P30 AG066511</funding_grant_id><funding_grant_id>T34 GM140948</funding_grant_id><funding_grant_id>T32 GM149422</funding_grant_id><funding_grant_id>F32 HD097920</funding_grant_id><funding_grant_id>P40 OD010440</funding_grant_id><funding_grant_id>T32 GM008490</funding_grant_id><funding_grant_id>F31 HD100145</funding_grant_id><pubmed_authors>Schmeichel KL</pubmed_authors><pubmed_authors>Blancher SD</pubmed_authors><pubmed_authors>Carpenter BS</pubmed_authors><pubmed_authors>Chavez SR</pubmed_authors><pubmed_authors>Gosrani SP</pubmed_authors><pubmed_authors>Birol O</pubmed_authors><pubmed_authors>Reeves MN</pubmed_authors><pubmed_authors>Morgan-Benitez SL</pubmed_authors><pubmed_authors>Nguyen SK</pubmed_authors><pubmed_authors>Dozier J</pubmed_authors><pubmed_authors>Brockett JS</pubmed_authors><pubmed_authors>Rodriguez JD</pubmed_authors><pubmed_authors>Katz DJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Dream and MEC NuRD Complexes reinforce SPR-5/MET-2 maternal reprogramming to maintain the germline-soma distinction.</name><description>The proper coordination of transcription factors, ATP dependent chromatin remodelers and histone modifications is essential for tissue specific gene expression, but how gene expression is regulated at these different levels is not well understood. In &lt;i>C. elegans&lt;/i>, H3K4 methylation that is acquired in the germline is reprorgammed at fertilization by the H3K4me1/2 demethlyase SPR-5/LSD1/KDM1A and the H3K9 methyltransferase MET2/SETDB1/KMT2E. SPR-5/MET-2 maternal reprogramming is required to help establish the germline-soma distinction and prevent developmental delay by preventing inherited H3K4 methylation from inappropriately maintaining germline gene expression in somatic tissues. To determine if the DREAM transcriptional repressor complex and the MEC NuRD ATP dependent nucleosome rem</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-04-08T15:43:53.325Z</modification><creation>2026-04-08T05:24:15.912Z</creation></dates><accession>S-EPMC12330697</accession><cross_references><pubmed>40777264</pubmed><doi>10.1101/2025.07.23.666413</doi></cross_references></HashMap>