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组蛋白去甲基化酶 Jarid1b(Kdm5b)是 Rb 通路的一个新组成部分,在衰老过程中与 MEFs 中的 E2f 靶基因相关联。

The histone demethylase Jarid1b (Kdm5b) is a novel component of the Rb pathway and associates with E2f-target genes in MEFs during senescence.

机构信息

Division of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

出版信息

PLoS One. 2011;6(9):e25235. doi: 10.1371/journal.pone.0025235. Epub 2011 Sep 27.

Abstract

Senescence is a robust cell cycle arrest controlled by the p53 and Rb pathways that acts as an important barrier to tumorigenesis. Senescence is associated with profound alterations in gene expression, including stable suppression of E2f-target genes by heterochromatin formation. Some of these changes in chromatin composition are orchestrated by Rb. In complex with E2f, Rb recruits chromatin modifying enzymes to E2f target genes, leading to their transcriptional repression. To identify novel chromatin remodeling enzymes that specifically function in the Rb pathway, we used a functional genetic screening model for bypass of senescence in murine cells. We identified the H3K4-demethylase Jarid1b as novel component of the Rb pathway in this screening model. We find that depletion of Jarid1b phenocopies knockdown of Rb1 and that Jarid1b associates with E2f-target genes during cellular senescence. These results suggest a role for Jarid1b in Rb-mediated repression of cell cycle genes during senescence.

摘要

衰老是一种由 p53 和 Rb 通路控制的强大细胞周期停滞,它是肿瘤发生的重要障碍。衰老与基因表达的深刻改变有关,包括异染色质形成对 E2f 靶基因的稳定抑制。这些染色质组成的一些变化是由 Rb 协调的。Rb 与 E2f 结合,招募染色质修饰酶到 E2f 靶基因上,导致它们的转录抑制。为了鉴定专门在 Rb 通路中起作用的新的染色质重塑酶,我们使用了一种功能遗传筛选模型,用于绕过小鼠细胞中的衰老。我们在这个筛选模型中发现了 H3K4 去甲基酶 Jarid1b 是 Rb 通路的新组成部分。我们发现,Jarid1b 的耗竭类似于 Rb1 的敲低,并且在细胞衰老期间,Jarid1b 与 E2f 靶基因相关联。这些结果表明,Jarid1b 在 Rb 介导的衰老过程中对细胞周期基因的抑制中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff8/3181323/ce8bda0955f3/pone.0025235.g001.jpg

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