组蛋白
后转座子
磷酸化
异染色质蛋白1
化学
组蛋白H3
基因沉默
异染色质
细胞生物学
EZH2型
机制(生物学)
赖氨酸
分子生物学
组蛋白H2A
端粒酶
核小体
组蛋白甲基转移酶
遗传学
生物
RNA干扰
血浆蛋白结合
表观遗传学
基因表达调控
组蛋白甲基化
HEK 293细胞
锡尔图因
作者
Jun Chen,Jiyu Chen,Zhouliang Yu,Liwei Zhang,Yanchao Liu,Xuan Ouyang,Juan Yu,Menghan Wang,Shangqiang Xie,Ming Wang,Tiantian Zhang,Zhaohui Jin,Bin Wu,Li Huang,Zijuan Gu,Lin Liu,Bing Zhu,Ping Chen,Haiyan Lin,Jicheng Zhao
标识
DOI:10.1016/j.scib.2026.01.039
摘要
The conserved histone variant H3.3 plays pivotal roles in heterochromatin formation and retrotransposon silencing. However, the molecular mechanism underlying H3.3-primed heterochromatin regulation remains elusive. Here, we demonstrate that H3.3-specific Ser31 phosphorylation and Lys27 trimethylation synergistically promote H3K9me3-heterochromatin formation. Mechanistically, polycomb protein chromobox homolog 7 (CBX7) preferentially binds Ser31-phosphorylated H3.3K27me3 nucleosomes and then recruits KRAB-associated protein 1 (KAP1), which may further engage the histone lysine 9 methyltransferase to establish H3K9me3-associated heterochromatin. Remarkably, H3K9me3 is significantly impaired when the H3.3-CBX7 interaction is disrupted, accompanied by the activation of retrotransposons. Moreover, during X-chromosome inactivation (XCI), H3K9me2/3 fails to accumulate at the inactive X (Xi) when blocking the H3.3-CBX7-KAP1 axis. Taken together, our results reveal a novel molecular mechanism by which H3.3 Ser31 phosphorylation (H3.3Ser31p) facilitates H3K9me3-heterochromatin formation during retrotransposon silencing and XCI via the H3.3K27me3-CBX7-KAP1 axis.
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