异染色质
常染色质
生物
异染色质蛋白1
细胞生物学
组蛋白H3
染色质
组蛋白
染色质重塑
遗传学
DNA
作者
Naoki Gotō,Kazuma Suke,Nao Yonezawa,Hidenori Nishihara,Tetsuya Handa,Yuko Sato,Tomoya Kujirai,Hitoshi Kurumizaka,Kazuo Yamagata,Hiroshi Kimurâ
标识
DOI:10.1083/jcb.202310084
摘要
Histone H3 lysine36 dimethylation (H3K36me2) is generally distributed in the gene body and euchromatic intergenic regions. However, we found that H3K36me2 is enriched in pericentromeric heterochromatin in some mouse cell lines. We here revealed the mechanism of heterochromatin targeting of H3K36me2. Among several H3K36 methyltransferases, NSD2 was responsible for inducing heterochromatic H3K36me2. Depletion and overexpression analyses of NSD2-associating proteins revealed that NSD2 recruitment to heterochromatin was mediated through the imitation switch (ISWI) chromatin remodeling complexes, such as BAZ1B-SMARCA5 (WICH), which directly binds to AT-rich DNA via a BAZ1B domain-containing AT-hook-like motifs. The abundance and stoichiometry of NSD2, SMARCA5, and BAZ1B could determine the localization of H3K36me2 in different cell types. In mouse embryos, H3K36me2 heterochromatin localization was observed at the two- to four-cell stages, suggesting its physiological relevance.
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