ASB7是H3K9me3平衡的负调节者
Liwen Zhou1, Zhenxuan Chen1, Yezi Zou2
1Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Guangzhou, China.
概括
一项新的研究确定ASB7是基因组H3氨酸9三甲基化 (H3K9me3) 稳态的关键调节剂. 这一发现揭示了控制表观遗传的动态电路,并防止过度的异染色质形成.
科学领域:
- 表观遗传学
- 染色体生物学
- 分子生物学
背景情况:
- 维护 histone H3 lysine 9 三甲基化 (H3K9me3) 需要一个正反循环.
- 限制H3K9me3平衡的反机制尚不清楚.
研究的目的:
- 确定H3K9me3稳态的新型调节剂.
- 阐明控制H3K9me3动态的分子机制.
主要方法:
- 基因组规模的CRISPR-Cas9查.
- 鉴定CUL5ASB7E3无素结合酶.
- 蛋白与蛋白的相互作用和降解途径的分析.
主要成果:
- 通过促进SUV39H1降解,ASB7作为H3K9me3的负调节剂.
- HP1将ASB7引入异性染色体.
- 在分裂过程中,ASB7的CDK1酸化防止SUV39H1的降解,恢复H3K9me3.
结论:
- 一个涉及HP1,SUV39H1和ASB7的动态电路调节H3K9me3平衡.
- 这种循环保证了表观遗传的忠实.
- 这些发现可以防止过度的异性染色素形成.
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