在未成熟的小鼠视网膜细胞中,被不规则距离的核细胞驱动的具有短DNA链接器的不规则距离的核细胞驱动的受损的双开端齐克扎克色素折叠
Brianna Kable1, Stephanie Portillo-Ledesma2, Evgenya Y Popova3
1Department Biochemistry & Molecular Biology, Penn State University College of Medicine, 500 University Drive, Hershey, PA 17033, United States.
Nucleic acids research
|June 4, 2025
概括
在视网膜发育过程中,染色体结构从开放过渡到凝结. 在不成熟细胞中,短的核细胞连接器可以防止折叠,而在成熟细胞中,较长的连接器可以为表观基因可塑性形成紧密的齐克扎克.
科学领域:
- 分子生物学分子生物学
- 结构生物学 结构生物学
- 发展生物学 发展生物学
背景情况:
- 凝聚的异染色素对于细胞特异性基因表达是必不可少的.
- 了解细胞成熟期间的染色质结构变化是表观基因组调节的关键.
研究的目的:
- 为了研究在老鼠杆光感受器成熟过程中染色质的结构转变.
- 阐明核体链条长度在异色染色体形成中的作用.
主要方法:
- 低温电子显微镜 (cryo-EM) 断层扫描
- 人工智能辅助的拒绝行为.
- 分子建模和计算机模拟.
- 结冷-EM辅助核细胞相互作用捕获
主要成果:
- 不成熟的视网膜染色体显示密切包装的核细胞与短链接器,抑制典型的两个开始的齐克扎克折叠.
- 成熟的视网膜染色体具有较少的短链核体,允许更强的紧缩.
- 未成熟的染色体表现出1 ± 1个核细胞相互作用,而成熟的染色体表现出1 ± 2个齐克扎克折叠的特征相互作用.
结论:
- 在未成熟的视网膜中,短核链阻碍了染色体的紧缩.
- 在成熟过程中增加链接DNA长度,通过齐克扎克折叠促进了全球色素凝聚.
- 这种机制可以通过染色质折叠来调节表观基因可塑性.
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