| Literature DB >> 28756949 |
Aiko Iwata-Otsubo1, Jennine M Dawicki-McKenna2, Takashi Akera1, Samantha J Falk2, Lukáš Chmátal1, Karren Yang1, Beth A Sullivan3, Richard M Schultz1, Michael A Lampson4, Ben E Black5.
Abstract
Female meiosis provides an opportunity for selfish genetic elements to violate Mendel's law of segregation by increasing the chance of segregating to the egg [1]. Centromeres and other repetitive sequences can drive in meiosis by cheating the segregation process [2], but the underlying mechanisms are unknown. Here, we show that centromeres with more satellite repeats house more nucleosomes that confer centromere identity, containing the histone H3 variant CENP-A, and bias their segregation to the egg relative to centromeres with fewer repeats. CENP-A nucleosomes predominantly occupy a single site within the repeating unit that becomes limiting for centromere assembly on smaller centromeres. We propose that amplified repetitive sequences act as selfish elements by promoting expansion of CENP-A chromatin and increased transmission through the female germline.Entities:
Keywords: CENP-A; centromere; chromosome; epigenetics; histone; meiosis; meiotic drive; nucleosome; oocyte; satellite DNA
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Year: 2017 PMID: 28756949 PMCID: PMC5567862 DOI: 10.1016/j.cub.2017.06.069
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834