首页> 外文期刊>Molecular and Cellular Biology >The KRAB Zinc Finger Protein RSL1 Regulates Sex- and Tissue-Specific Promoter Methylation and Dynamic Hormone-Responsive Chromatin Configuration
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The KRAB Zinc Finger Protein RSL1 Regulates Sex- and Tissue-Specific Promoter Methylation and Dynamic Hormone-Responsive Chromatin Configuration

机译:KRAB锌指蛋白RSL1调节性别和组织特异性启动子甲基化和动态激素响应染色质的配置。

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Over 400 Krüppel-associated box zinc finger proteins (KRAB-ZFPs) are encoded in mammalian genomes. While KRAB-ZFPs strongly repress transcription in vitro, little is known about their biological function or gene targets in vivo. Regulator of sex limitation 1 (Rsl1), one of the first KRAB-Zfp genes assigned a physiological role, accentuates sex-biased liver gene expression, most dramatically for mouse sex-limited protein (Slp), which provides an in vivo reporter of KRAB-ZFP function. Slp is induced in males in the liver and kidney by growth hormone (GH) and androgen, respectively. In the liver but not kidney, the Rsl1 genotype correlates with methylation of a CpG dinucleotide in the Slp promoter that is demethylated at puberty. RSL1 binds 2 kb upstream of the Slp promoter, both in vitro and in vivo, within an enhancer containing response elements for STAT5b. Chromatin immunoprecipitation (ChIP) assays demonstrate that RSL1 recruits KAP1/TRIM28, the corepressor for KRAB action in vitro, to this enhancer. Slp induction requires rapid cycling of STAT5b in chromatin. Remarkably, RSL1 simultaneously binds adjacent to STAT5b with a reciprocal binding pattern that limits hormonal response. These experiments demonstrate a surprisingly dynamic interplay between a hormonal activator, STAT5b, and a KRAB-ZFP repressor and provide unique insights into KRAB-ZFP epigenetic mechanisms.
机译:哺乳动物基因组中编码了超过400种与Krüppel相关的框锌指蛋白(KRAB-ZFP)。尽管KRAB-ZFPs强烈抑制体外转录,但对其生物学功能或体内基因靶点知之甚少。性别限制调节因子1( Rsl1 )是最早的具有生理功能的 KRAB-Zfp 基因之一,可增强性别偏向的肝基因表达,其中小鼠-有限的蛋白( Slp ),它提供了KRAB-ZFP功能的体内报告基因。生长激素(GH)和雄激素分别在肝脏和肾脏的雄性中诱导 Slp 。在肝脏而非肾脏中, Rsl1 基因型与 Slp 启动子中CpG二核苷酸的甲基化相关,后者在青春期脱甲基。 RSL1在包含STAT5b响应元件的增强子中,在 Slp 启动子上游2 kb上游(体外 in vivo )结合。染色质免疫沉淀(ChIP)分析表明,RSL1将KAP1 / TRIM28(该蛋白在体外发挥KRAB作用的核心抑制剂)募集到该增强子。 Slp 的诱导需要染色质中STAT5b的快速循环。值得注意的是,RSL1同时以限制激素反应的双向结合模式与STAT5b相邻结合。这些实验证明了激素激活剂STAT5b和KRAB-ZFP阻遏物之间惊人的动态相互作用,并提供了对KRAB-ZFP表观遗传机制的独特见解。

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