<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sobel J</submitter><funding>Swiss National Science Foundation</funding><pagination>8800</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8062533</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>Glucose-induced insulin secretion, a hallmark of mature β-cells, is achieved after birth and is preceded by a phase of intense proliferation. These events occurring in the neonatal period are decisive for establishing an appropriate functional β-cell mass that provides the required insulin throughout life. However, key regulators of gene expression involved in functional maturation of β-cells remain to be elucidated. Here, we addressed this issue by mapping open chromatin regions in newborn versus adult rat islets using the ATAC-seq assay. We obtained a genome-wide picture of chromatin accessible sites (~ 100,000) among which 20% were differentially accessible during maturation. An enrichment analysis of transcription factor binding sites identified a group of transcription factors that co</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Scrt1, a transcriptional regulator of β-cell proliferation identified by differential chromatin accessibility during islet maturation.</pubmed_title><pmcid>PMC8062533</pmcid><funding_grant_id>169480</funding_grant_id><funding_grant_id>188447</funding_grant_id><funding_grant_id>310030</funding_grant_id><pubmed_authors>Jacovetti C</pubmed_authors><pubmed_authors>Sobel J</pubmed_authors><pubmed_authors>Regazzi R</pubmed_authors><pubmed_authors>Menoud V</pubmed_authors><pubmed_authors>Stoll L</pubmed_authors><pubmed_authors>Elhanani O</pubmed_authors><pubmed_authors>Guay C</pubmed_authors><pubmed_authors>Rodriguez-Trejo A</pubmed_authors><pubmed_authors>Walker MD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Scrt1, a transcriptional regulator of β-cell proliferation identified by differential chromatin accessibility during islet maturation.</name><description>Glucose-induced insulin secretion, a hallmark of mature β-cells, is achieved after birth and is preceded by a phase of intense proliferation. These events occurring in the neonatal period are decisive for establishing an appropriate functional β-cell mass that provides the required insulin throughout life. However, key regulators of gene expression involved in functional maturation of β-cells remain to be elucidated. Here, we addressed this issue by mapping open chromatin regions in newborn versus adult rat islets using the ATAC-seq assay. We obtained a genome-wide picture of chromatin accessible sites (~ 100,000) among which 20% were differentially accessible during maturation. An enrichment analysis of transcription factor binding sites identified a group of transcription factors that co</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2026-05-08T06:15:52.745Z</modification><creation>2022-02-09T16:08:27.903Z</creation></dates><accession>S-EPMC8062533</accession><cross_references><pubmed>33888791</pubmed><doi>10.1038/s41598-021-88003-2</doi></cross_references></HashMap>