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10.1080/19491034.2016.1276144

http://scihub22266oqcxt.onion/10.1080/19491034.2016.1276144
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C5403135!5403135!28045584
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suck abstract from ncbi


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pmid28045584      Nucleus 2017 ; 8 (2): 144-9
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  • Epigenetic countermarks in mitotic chromosome condensation #MMPMID28045584
  • van Wely KHM; Mora Gallardo C; Vann KR; Kutateladze TG
  • Nucleus 2017[]; 8 (2): 144-9 PMID28045584show ga
  • Mitosis in metazoans is characterized by abundant phosphorylation of histone H3 and involves the recruitment of condensin complexes to chromatin. The relationship between the 2 phenomena and their respective contributions to chromosome condensation in vivo remain poorly understood. Recent studies have shown that H3T3 phosphorylation decreases binding of histone readers to methylated H3K4 in vitro and is essential to displace the corresponding proteins from mitotic chromatin in vivo. Together with previous observations, these data provide further evidence for a role of mitotic histone H3 phosphorylation in blocking transcriptional programs or preserving the ?memory? PTMs. Mitotic protein exclusion can also have a role in depopulating the chromatin template for subsequent condensin loading. H3 phosphorylation thus serves as an integral step in the condensation of chromosome arms.
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