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肿瘤抑制因子 Rb 及其相关的 Rbl2 基因受 Utx 组蛋白去甲基化酶的调节。

The tumor suppressor Rb and its related Rbl2 genes are regulated by Utx histone demethylase.

机构信息

Division of Functional Genomics, Cancer Research Institute, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Ishikawa, Japan.

出版信息

Biochem Biophys Res Commun. 2010 Aug 20;399(2):238-44. doi: 10.1016/j.bbrc.2010.07.061. Epub 2010 Jul 30.

Abstract

Utx is a candidate tumor suppressor gene that encodes histone H3 lysine 27 (H3K27) demethylase. In this study, we found that ectopic expression of Utx enhanced the expression of retinoblastoma tumor suppressor gene Rb and its related gene Rbl2. This activation was dependent on the demethylase activity of Utx, and was suggested to contribute to the decreased cell proliferation induced by Utx. A chromatin immunoprecipitation assay showed that over-expressed Utx was associated with the promoter regions of Rb and Rbl2 resulting in the removal of repressive H3K27 tri-methylation and the increase in active H3K4 tri-methylation. Furthermore, siRNA-mediated knockdown of Utx revealed the recruitment of endogenous Utx protein on the promoters of Rb and Rbl2 genes. These results indicate that Rb and Rbl2 are downstream target genes of Utx and may play important roles in Utx-mediated cell growth control.

摘要

UTX 是候选肿瘤抑制基因,编码组蛋白 H3 赖氨酸 27(H3K27)去甲基酶。在这项研究中,我们发现异位表达 UTX 增强了视网膜母细胞瘤肿瘤抑制基因 Rb 及其相关基因 Rbl2 的表达。这种激活依赖于 UTX 的去甲基酶活性,并有助于降低 UTX 诱导的细胞增殖。染色质免疫沉淀分析表明,过表达的 UTX 与 Rb 和 Rbl2 的启动子区域相关联,导致抑制性 H3K27 三甲基化的去除和活性 H3K4 三甲基化的增加。此外,siRNA 介导的 UTX 敲低揭示了内源性 UTX 蛋白在 Rb 和 Rbl2 基因启动子上的募集。这些结果表明,Rb 和 Rbl2 是 UTX 的下游靶基因,可能在 UTX 介导的细胞生长控制中发挥重要作用。

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