<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Soudet J</submitter><funding>Swiss National Science Foundation</funding><pagination>4515-4528</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9071385</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>50(8)</volume><pubmed_abstract>Eukaryotic genomes are pervasively transcribed by RNA polymerase II (RNAPII), and transcription of long non-coding RNAs often overlaps with coding gene promoters. This might lead to coding gene repression in a process named Transcription Interference (TI). In Saccharomyces cerevisiae, TI is mainly driven by antisense non-coding transcription and occurs through re-shaping of promoter Nucleosome-Depleted Regions (NDRs). In this study, we developed a genetic screen to identify new players involved in Antisense-Mediated Transcription Interference (AMTI). Among the candidates, we found the HIR histone chaperone complex known to be involved in de novo histone deposition. Using genome-wide approaches, we reveal that HIR-dependent histone deposition represses the promoters of SAGA-dependent genes </pubmed_abstract><journal>Nucleic acids research</journal><pubmed_title>Antisense-mediated repression of SAGA-dependent genes involves the HIR histone chaperone.</pubmed_title><pmcid>PMC9071385</pmcid><funding_grant_id>31003A_182344</funding_grant_id><funding_grant_id>153331</funding_grant_id><funding_grant_id>182344</funding_grant_id><funding_grant_id>31003A_153331</funding_grant_id><pubmed_authors>Pastucha AM</pubmed_authors><pubmed_authors>Maffioletti A</pubmed_authors><pubmed_authors>Soudet J</pubmed_authors><pubmed_authors>Bakir Z</pubmed_authors><pubmed_authors>Beyrouthy N</pubmed_authors><pubmed_authors>Menendez D</pubmed_authors><pubmed_authors>Stutz F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Antisense-mediated repression of SAGA-dependent genes involves the HIR histone chaperone.</name><description>Eukaryotic genomes are pervasively transcribed by RNA polymerase II (RNAPII), and transcription of long non-coding RNAs often overlaps with coding gene promoters. This might lead to coding gene repression in a process named Transcription Interference (TI). In Saccharomyces cerevisiae, TI is mainly driven by antisense non-coding transcription and occurs through re-shaping of promoter Nucleosome-Depleted Regions (NDRs). In this study, we developed a genetic screen to identify new players involved in Antisense-Mediated Transcription Interference (AMTI). Among the candidates, we found the HIR histone chaperone complex known to be involved in de novo histone deposition. Using genome-wide approaches, we reveal that HIR-dependent histone deposition represses the promoters of SAGA-dependent genes </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-05-19T03:12:47.261Z</modification><creation>2025-04-04T07:56:20.982Z</creation></dates><accession>S-EPMC9071385</accession><cross_references><pubmed>35474134</pubmed><doi>10.1093/nar/gkac264</doi></cross_references></HashMap>