Chromatin Dynamics in Lineage Commitment and Cellular Reprogramming

被引:12
作者
Shchuka, Virlana M. [1 ]
Malek-Gilani, Nakisa [1 ]
Singh, Gurdeep [1 ]
Langroudi, Lida [1 ]
Dhaliwal, Navroop K. [1 ]
Moorthy, Sakthi D. [1 ]
Davidson, Scott [1 ]
Macpherson, Neil N. [1 ]
Mitchell, Jennifer A. [1 ]
机构
[1] Univ Toronto, Dept Cell & Syst Biol, Toronto, ON M5S 3G5, Canada
基金
加拿大健康研究院; 加拿大创新基金会;
关键词
embryonic stem cell; induced pluripotent stem cell; reprogramming; chromatin; epigenetics; chromatin looping; transcription factor; gene expression; differentiation; EMBRYONIC STEM-CELLS; TRANSCRIPTION-FACTOR; HISTONE MODIFICATIONS; REGULATORY CIRCUITRY; PLURIPOTENCY FACTORS; SOX10; EXPRESSION; GENE-EXPRESSION; HUMAN GENOME; PAX6; LOCUS; ENHANCERS;
D O I
10.3390/genes6030641
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Dynamic structural properties of chromatin play an essential role in defining cell identity and function. Transcription factors and chromatin modifiers establish and maintain cell states through alteration of DNA accessibility and histone modifications. This activity is focused at both gene-proximal promoter regions and distally located regulatory elements. In the three-dimensional space of the nucleus,distal elements are localized in close physical proximity to the gene-proximal regulatory sequences through the formation of chromatin loops. These looping features in the genome are highly dynamic as embryonic stem cells differentiate and commit to specific lineages, and throughout reprogramming as differentiated cells reacquire pluripotency. Identifying these functional distal regulatory regions in the genome provides insight into the regulatory processes governing early mammalian development and guidance for improving the protocols that generate induced pluripotent cells.
引用
收藏
页码:641 / 661
页数:21
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