先锋因素
重编程
生物
染色质
核小体
转录因子
异染色质
二价染色质
细胞生物学
组蛋白
抄写(语言学)
染色质重塑
遗传学
细胞命运测定
细胞
基因
哲学
语言学
作者
Makiko Iwafuchi,Kenneth S. Zaret
出处
期刊:Genes & Development
[Cold Spring Harbor Laboratory Press]
日期:2014-12-15
卷期号:28 (24): 2679-2692
被引量:588
标识
DOI:10.1101/gad.253443.114
摘要
A subset of eukaryotic transcription factors possesses the remarkable ability to reprogram one type of cell into another. The transcription factors that reprogram cell fate are invariably those that are crucial for the initial cell programming in embryonic development. To elicit cell programming or reprogramming, transcription factors must be able to engage genes that are developmentally silenced and inappropriate for expression in the original cell. Developmentally silenced genes are typically embedded in "closed" chromatin that is covered by nucleosomes and not hypersensitive to nuclease probes such as DNase I. Biochemical and genomic studies have shown that transcription factors with the highest reprogramming activity often have the special ability to engage their target sites on nucleosomal DNA, thus behaving as "pioneer factors" to initiate events in closed chromatin. Other reprogramming factors appear dependent on pioneer factors for engaging nucleosomes and closed chromatin. However, certain genomic domains in which nucleosomes are occluded by higher-order chromatin structures, such as in heterochromatin, are resistant to pioneer factor binding. Understanding the means by which pioneer factors can engage closed chromatin and how heterochromatin can prevent such binding promises to advance our ability to reprogram cell fates at will and is the topic of this review.
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