{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T04:10:55Z","timestamp":1787026255687,"version":"build-2736575974"},"reference-count":301,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2026,4,1]],"date-time":"2026-04-01T00:00:00Z","timestamp":1775001600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Cell Dev. Biol."],"abstract":"<jats:p>\n                    The field of centromere biology was launched in 1980 with the isolation of a 120-bp centromeric DNA fragment from\n                    <jats:italic>Saccharomyces cerevisiae<\/jats:italic>\n                    . Fifteen years later, the discovery that the yeast histone H3 variant Cse4 is the conserved counterpart of human CENP-A established both proteins as the defining epigenetic marks of centromeres. Subsequent genetic screens, biochemical and molecular biology studies have elucidated how Cse4 is specifically targeted to and stably maintained at centromeres. The mislocalization of Cse4 beyond centromeres disrupts transcriptional programs and drives chromosomal instability and aneuploidy. This review traces Cse4 research from its early breakthroughs to current insights into its regulatory pathways. Although derived from yeast, these mechanistic advances provide a conceptual framework for understanding analogous, and likely conserved, processes in humans, where CENP-A biology remains less well defined but is increasingly being implicated in cancer and therapy resistance when perturbed.\n                  <\/jats:p>","DOI":"10.3389\/fcell.2026.1782273","type":"journal-article","created":{"date-parts":[[2026,4,1]],"date-time":"2026-04-01T05:42:22Z","timestamp":1775022142000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":3,"title":["Keeping it centered: decoding the activities that regulate yeast histone H3 variant Cse4 and confine it to centromeres"],"prefix":"10.3389","volume":"14","author":[{"given":"Martina","family":"Greco","sequence":"first","affiliation":[{"name":"Department of Cellular, Computational and Integrative Biology (CIBIO), University of Trento","place":["Trento, Italy"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Joanna","family":"Klim","sequence":"additional","affiliation":[{"name":"Department of Cellular, Computational and Integrative Biology (CIBIO), University of Trento","place":["Trento, Italy"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peter","family":"De Wulf","sequence":"additional","affiliation":[{"name":"Department of Cellular, Computational and Integrative Biology (CIBIO), University of Trento","place":["Trento, Italy"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1965","published-online":{"date-parts":[[2026,4,1]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","first-page":"576","DOI":"10.1038\/nature09594","article-title":"Tension directly stabilizes reconstituted kinetochore-microtubule attachments","volume":"468","author":"Akiyoshi","year":"2010","journal-title":"Nature"},{"key":"B2","doi-asserted-by":"publisher","first-page":"e1003216","DOI":"10.1371\/journal.pgen.1003216","article-title":"The Mub1\/Ubr2 ubiquitin ligase complex regulates the conserved Dsn1 kinetochore protein","volume":"9","author":"Akiyoshi","year":"2013","journal-title":"PLoS Genet."},{"key":"B3","doi-asserted-by":"publisher","first-page":"572","DOI":"10.1038\/nature05632","article-title":"Translational and rotational settings of H2A.Z nucleosomes across the Saccharomyces cerevisiae genome","volume":"446","author":"Albert","year":"2007","journal-title":"Nature"},{"key":"B4","doi-asserted-by":"publisher","first-page":"288","DOI":"10.1101\/gad.322040.118","article-title":"Sfp1 regulates transcriptional networks driving cell growth and division through multiple promoter-binding modes","volume":"33","author":"Albert","year":"2019","journal-title":"Genes Dev."},{"key":"B5","doi-asserted-by":"publisher","first-page":"e48913","DOI":"10.15252\/embr.201948913","article-title":"CENP-C unwraps the human CENP-A nucleosome through the H2A C-terminal tail","volume":"20","author":"Ali-Ahmad","year":"2019","journal-title":"EMBO Rep."},{"key":"B6","doi-asserted-by":"publisher","first-page":"119","DOI":"10.1186\/1476-4598-8-119","article-title":"CENPA overexpression promotes genome instability in pRb-depleted human cells","volume":"8","author":"Amato","year":"2009","journal-title":"Mol. 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