西斯特
X-失活
染色质
X染色体
生物
长非编码RNA
遗传学
核糖核酸
基因组
染色体
抄写(语言学)
剂量补偿
基因
计算生物学
语言学
哲学
作者
J Engreitz,Amy Pandya‐Jones,Patrick McDonel,A.A. Shishkin,Klara Sirokman,Christine Surka,Sabah Kadri,Jeffrey C. Xing,Alon Goren,Eric S. Lander,Kathrin Plath,Mitchell Guttman
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2013-07-05
卷期号:341 (6147)
被引量:937
标识
DOI:10.1126/science.1237973
摘要
Understanding Xist-ance Large noncoding RNAs (lncRNAs) are increasingly appreciated to play important roles in the cell. A number of lncRNAs act to target chromatin regulatory complexes to their sites of action. Engreitz et al. (p. 10.1126/science.1237973 , published online 4 July; see the Perspective by Dimond and Fraser ) found that the mouse Xist lncRNA, which initiates X-chromosome inactivation, was transferred from its site of transcription to distant sites on the X chromosome purely through their close three-dimensional proximity to the Xist gene. Xist initially localized to the periphery of active genes on the X chromosome but gradually spread across them using its A-repeat domain, until the Xist RNA bound broadly across the inactive X chromosome in differentiated female cells.
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