<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dudka D</submitter><funding>NICHD NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>814-822</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11880906</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>638(8051)</volume><pubmed_abstract>The abundance and sequence of satellite DNA at and around centromeres is evolving rapidly despite the highly conserved and essential process through which the centromere directs chromosome inheritance&lt;sup>1-3&lt;/sup>. The impact of such rapid evolution is unclear. Here we find that sequence-dependent DNA shape dictates packaging of pericentromeric satellites in female meiosis through a conserved DNA-shape-recognizing chromatin architectural protein, high mobility group AT-hook 1 (HMGA1)&lt;sup>4,5&lt;/sup>. Pericentromeric heterochromatin in two closely related mouse species, M. musculus and M. spretus, forms on divergent satellites that differ by both density of narrow DNA minor grooves and HMGA1 recruitment. HMGA1 binds preferentially to M. musculus satellites, and depletion in M. musculus oocyt</pubmed_abstract><journal>Nature</journal><pubmed_title>Satellite DNA shapes dictate pericentromere packaging in female meiosis.</pubmed_title><pmcid>PMC11880906</pmcid><funding_grant_id>R35 GM122475</funding_grant_id><funding_grant_id>R01 HD058730</funding_grant_id><funding_grant_id>R35 GM130302</funding_grant_id><pubmed_authors>Beeravolu K</pubmed_authors><pubmed_authors>Dawicki-McKenna JM</pubmed_authors><pubmed_authors>Lampson MA</pubmed_authors><pubmed_authors>Sun X</pubmed_authors><pubmed_authors>Black BE</pubmed_authors><pubmed_authors>Akera T</pubmed_authors><pubmed_authors>Dudka D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Satellite DNA shapes dictate pericentromere packaging in female meiosis.</name><description>The abundance and sequence of satellite DNA at and around centromeres is evolving rapidly despite the highly conserved and essential process through which the centromere directs chromosome inheritance&lt;sup>1-3&lt;/sup>. The impact of such rapid evolution is unclear. Here we find that sequence-dependent DNA shape dictates packaging of pericentromeric satellites in female meiosis through a conserved DNA-shape-recognizing chromatin architectural protein, high mobility group AT-hook 1 (HMGA1)&lt;sup>4,5&lt;/sup>. Pericentromeric heterochromatin in two closely related mouse species, M. musculus and M. spretus, forms on divergent satellites that differ by both density of narrow DNA minor grooves and HMGA1 recruitment. HMGA1 binds preferentially to M. musculus satellites, and depletion in M. musculus oocyt</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2026-03-18T13:34:43.322Z</modification><creation>2025-08-18T09:54:18.133Z</creation></dates><accession>S-EPMC11880906</accession><cross_references><pubmed>39779853</pubmed><doi>10.1038/s41586-024-08374-0</doi></cross_references></HashMap>