| Literature DB >> 35483360 |
Rajesh Ranjan1, Jonathan Snedeker2, Matthew Wooten2, Carolina Chu2, Sabrina Bracero2, Taylar Mouton2, Xin Chen3.
Abstract
During Drosophila melanogaster male germline stem cell (GSC) asymmetric division, preexisting old versus newly synthesized histones H3 and H4 are asymmetrically inherited. However, the biological outcomes of this phenomenon have remained unclear. Here, we tracked old and new histones throughout the GSC cell cycle through the use of high spatial and temporal resolution microscopy. We found unique features that differ between old and new histone-enriched sister chromatids, including differences in nucleosome density, chromosomal condensation, and H3 Ser10 phosphorylation. These distinct chromosomal features lead to their differential association with Cdc6, a pre-replication complex component, and subsequent asynchronous DNA replication initiation in the resulting daughter cells. Disruption of asymmetric histone inheritance abolishes differential Cdc6 association and asynchronous S-phase entry, demonstrating that histone asymmetry acts upstream of these critical cell-cycle progression events. Furthermore, disruption of these GSC-specific chromatin features leads to GSC defects, indicating a connection between histone inheritance, cell-cycle progression, and cell fate determination.Entities:
Keywords: Cdc6; Drosophila; S phase; asymmetric cell division; cell cycle; chromatin state; chromosome condensation; germline stem cell; histones; nucleosome
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Year: 2022 PMID: 35483360 PMCID: PMC9134767 DOI: 10.1016/j.devcel.2022.04.007
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 13.417