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UHRF1 通过启动子相关的非编码 RNA 调控前列腺癌细胞中的 CDH1。

UHRF1 regulates CDH1 via promoter associated non-coding RNAs in prostate cancer cells.

机构信息

Department of Biotechnology and Life Sciences, University of Insubria, 21052 Busto Arsizio, VA, Italy.

Department of Biotechnology and Life Sciences, University of Insubria, 21052 Busto Arsizio, VA, Italy; IGBMC, BP10142, 1 rue Laurent Fries, 67404 Illkirch Cedex, France.

出版信息

Biochim Biophys Acta Gene Regul Mech. 2018 Mar;1861(3):258-270. doi: 10.1016/j.bbagrm.2018.02.006. Epub 2018 Feb 18.

DOI:10.1016/j.bbagrm.2018.02.006
PMID:29466696
Abstract

Non-coding RNAs (ncRNAs) transcribed from the promoter and the downstream region can affect the expression of the corresponding coding genes. It has been shown that sense-directed ncRNAs arising from the promoter region of the E-cadherin gene (CDH1) mediate its repression. Here, we show that an antisense-directed ncRNA (paRCDH1-AS) transcribed from the CDH1 promoter is necessary for its expression. paRCDH1-AS acts as a hooking scaffold by recruiting the epigenetic regulators, UHRF1, DNMT3A, SUV39H1 and SUZ12, involved in CDH1 repression. The binding of epigenetic regulators to paCRDH1-AS, indeed, prevents their localization to the chromatin on CDH1 promoter. Moreover, paRCDH1-AS silencing induces CDH1 repression and a switch of the epigenetic profile on the promoter towards a more closed chromatin. Using bioinformatic and experimental approaches we defined that the promoter of the paRCDH1-AS is shared with the E-cadherin gene, showing a bidirectional promoter activity. We found that UHRF1 controls both CDH1 and paRCDH1-AS by directly binding this bidirectional promoter region. Our study provides evidences, for the first time, that UHRF1 recruitment can be affected by promoter-associated non-coding RNAs, opening new perspective regarding the role of UHRF1 in these complex regulatory networks.

摘要

非编码 RNA(ncRNA)由启动子和下游区域转录,可以影响相应编码基因的表达。已经表明,E-钙黏蛋白(CDH1)基因启动子区域产生的有意义的 ncRNA 介导其抑制。在这里,我们表明,由 CDH1 启动子转录的反义导向 ncRNA(paRCDH1-AS)是其表达所必需的。paRCDH1-AS 作为一个挂钩支架,通过招募涉及 CDH1 抑制的表观遗传调节剂,UHRF1、DNMT3A、SUV39H1 和 SUZ12。表观遗传调节剂与 paCRDH1-AS 的结合,实际上阻止了它们在 CDH1 启动子上的染色质定位。此外,paRCDH1-AS 的沉默诱导 CDH1 抑制,并使启动子上的表观遗传特征向更封闭的染色质转变。通过生物信息学和实验方法,我们确定了 paRCDH1-AS 的启动子与 E-钙黏蛋白基因共享,表现出双向启动子活性。我们发现 UHRF1 通过直接结合这个双向启动子区域来控制 CDH1 和 paRCDH1-AS。我们的研究首次提供了证据,表明 UHRF1 的募集可以受到启动子相关非编码 RNA 的影响,为 UHRF1 在这些复杂的调控网络中的作用开辟了新的视角。

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