<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Senmatsu S</submitter><funding>MEXT | Japan Society for the Promotion of Science</funding><funding>Takeda Science Foundation</funding><funding>Yamada Science Foundation</funding><pagination>295</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7935937</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4(1)</volume><pubmed_abstract>Noncoding RNAs (ncRNAs) are involved in various biological processes, including gene expression, development, and disease. Here, we identify a novel consensus sequence of a cis-element involved in long ncRNA (lncRNA) transcription and demonstrate that lncRNA transcription from this cis-element activates meiotic recombination via chromatin remodeling. In the fission yeast fbp1 gene, glucose starvation induces a series of promoter-associated lncRNAs, referred to as ﻿metabolic-stress-induced lncRNAs (mlonRNAs), which contribute to chromatin remodeling and fbp1 activation. Translocation of the cis-element required for mlonRNA into a well-characterized meiotic recombination hotspot, ade6-M26, further stimulates transcription and meiotic recombination via local chromatin remodeling. The consensus sequence of this cis-element (mlon-box) overlaps with meiotic recombination sites in the fission yeast genome. At one such site, the SPBC24C6.09c upstream region, meiotic double-strand break (DSB) formation is induced in an mlon-box-dependent manner. Therefore, mlonRNA transcription plays a universal role in chromatin remodeling and the regulation of transcription and recombination.</pubmed_abstract><journal>Communications biology</journal><pubmed_title>lncRNA transcription induces meiotic recombination through chromatin remodelling in fission yeast.</pubmed_title><pmcid>PMC7935937</pmcid><funding_grant_id>KAKENHIJP16H01314</funding_grant_id><funding_grant_id>KAKENHIJP19J20773</funding_grant_id><pubmed_authors>Oda A</pubmed_authors><pubmed_authors>Asada R</pubmed_authors><pubmed_authors>Hirota K</pubmed_authors><pubmed_authors>Hoffman CS</pubmed_authors><pubmed_authors>Senmatsu S</pubmed_authors><pubmed_authors>Ohta K</pubmed_authors></additional><is_claimable>false</is_claimable><name>lncRNA transcription induces meiotic recombination through chromatin remodelling in fission yeast.</name><description>Noncoding RNAs (ncRNAs) are involved in various biological processes, including gene expression, development, and disease. Here, we identify a novel consensus sequence of a cis-element involved in long ncRNA (lncRNA) transcription and demonstrate that lncRNA transcription from this cis-element activates meiotic recombination via chromatin remodeling. In the fission yeast fbp1 gene, glucose starvation induces a series of promoter-associated lncRNAs, referred to as ﻿metabolic-stress-induced lncRNAs (mlonRNAs), which contribute to chromatin remodeling and fbp1 activation. Translocation of the cis-element required for mlonRNA into a well-characterized meiotic recombination hotspot, ade6-M26, further stimulates transcription and meiotic recombination via local chromatin remodeling. The consensus sequence of this cis-element (mlon-box) overlaps with meiotic recombination sites in the fission yeast genome. At one such site, the SPBC24C6.09c upstream region, meiotic double-strand break (DSB) formation is induced in an mlon-box-dependent manner. Therefore, mlonRNA transcription plays a universal role in chromatin remodeling and the regulation of transcription and recombination.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-18T13:29:00.4Z</modification><creation>2025-04-06T23:16:04.855Z</creation></dates><accession>S-EPMC7935937</accession><cross_references><pubmed>33674718</pubmed><doi>10.1038/s42003-021-01798-8</doi></cross_references></HashMap>