Hippo通路基因组蛋白修饰的空间分布模式研究。

Wenxia Su, Dimeng Zhang, Qiang Zhang, Qianzhong Li
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引用次数: 2

摘要

Hippo通路可以调节细胞的分裂、分化和凋亡,控制器官的形状和大小。研究Hippo通路基因的组蛋白修饰在胚胎干细胞中的分布规律,有助于了解组蛋白修饰和Hippo通路对干细胞自我更新的分子调控机制。本研究选取Hippo通路的YAP、TAZ、LATS1/2、MST1、SAV1等19个基因,以及胚胎干细胞中的8种组蛋白修饰,研究组蛋白修饰的空间分布规律。发现组蛋白修饰分布存在明显的类型特异性和靶区位置偏好,其中H3K4me3和H3K36me3发挥了最重要的调控作用。通过组蛋白修饰相关性分析,在YAP中检测到一个由H3K4ac、H3K4me3、H3K9ac和H3K27ac组成的组蛋白修饰功能簇。此外,获得了Hippo通路基因中组蛋白修饰的空间分布规律,为阐明组蛋白修饰调控Hippo通路基因表达的机制,揭示组蛋白修饰通过调控Hippo通路影响胚胎干细胞自我更新的分子调控机制提供了新的理论参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Study on the spatial distribution patterns of histone modifications in Hippo pathway genes.

Study on the spatial distribution patterns of histone modifications in Hippo pathway genes.

Study on the spatial distribution patterns of histone modifications in Hippo pathway genes.

Study on the spatial distribution patterns of histone modifications in Hippo pathway genes.

Hippo pathway can regulate cell division, differentiation and apoptosis, and control the shape and size of organs. To study the distribution patterns of histone modifications of Hippo pathway genes in embryonic stem cells is helpful to understand the molecular regulation mechanism of histone modification and Hippo pathway on stem cell self-renewal. In this study, 19 genes of Hippo pathway including YAP, TAZ, LATS1/2, MST1 and SAV1, and eight histone modifications in embryonic stem cells were chosen to study the spatial distribution patterns of histone modifications. It was found that there were obvious type specificity and the location preference of target regions in the distributions of histone modifications, and H3K4me3 and H3K36me3 played the most important regulatory roles. Through the correlation analysis of histone modifications, a histone modification functional cluster composed of H3K4ac, H3K4me3, H3K9ac and H3K27ac was detected in YAP. In addition, the spatial distribution patterns of histone modifications in Hippo pathway genes were obtained, which provided a new theoretical reference for elucidating the mechanism of histone modifications regulating the gene expression of Hippo pathway, and for revealing the molecular regulatory mechanism of histone modifications affecting the self-renewal of embryonic stem cells by regulating the Hippo pathway.

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