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角质形成细胞中 microRNA 203 的表达依赖于 E6 对 p53 水平的调节。

MicroRNA 203 expression in keratinocytes is dependent on regulation of p53 levels by E6.

机构信息

Centre for Cancer Research and Cell Biology, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, Northern Ireland, United Kingdom.

出版信息

J Virol. 2010 Oct;84(20):10644-52. doi: 10.1128/JVI.00703-10. Epub 2010 Aug 11.

Abstract

A screen of microRNA (miRNA) expression following differentiation in human foreskin keratinocytes (HFKs) identified changes in several miRNAs, including miRNA 203 (miR-203), which has previously been shown to play an important role in epithelial cell biology by regulating p63 levels. We investigated how expression of human papillomavirus type 16 (HPV16) oncoproteins E6 and E7 affected miR-203 expression during proliferation and differentiation of HFKs. We demonstrated that miR-203 expression is reduced in HFKs where p53 function is compromised, either by the viral oncoprotein E6 or by knockout of p53 using short hairpin RNAs (p53i). We show that the induction of miR-203 observed during calcium-induced differentiation of HFKs is significantly reduced in HFKs expressing E6 and in p53i HFKs. Induction of miR-203 in response to DNA damage is also reduced in the absence of p53. We report that proliferation of HFKs is dependent on the level of miR-203 expression and that overexpression of miR-203 can reduce overproliferation in E6/E7-expressing and p53i HFKs. In summary, these results indicate that expression of miR-203 is dependent on p53, which may explain how expression of HPV16 E6 can disrupt the balance between proliferation and differentiation, as well as the response to DNA damage, in keratinocytes.

摘要

在人包皮角质形成细胞(HFKs)分化后进行的 microRNA(miRNA)表达筛选,确定了几个 miRNA 的变化,包括 miRNA 203(miR-203),先前的研究表明它通过调节 p63 水平在上皮细胞生物学中发挥重要作用。我们研究了人乳头瘤病毒 16 型(HPV16)致癌蛋白 E6 和 E7 的表达如何在 HFKs 的增殖和分化过程中影响 miR-203 的表达。我们证明,在 p53 功能受到病毒致癌蛋白 E6 或短发夹 RNA(p53i)敲除损害的 HFKs 中,miR-203 的表达减少。我们表明,在 HFKs 中钙诱导分化过程中观察到的 miR-203 的诱导,在表达 E6 和 p53i HFKs 中显著降低。在没有 p53 的情况下,对 DNA 损伤的 miR-203 诱导也减少。我们报告说,HFKs 的增殖依赖于 miR-203 表达水平,并且 miR-203 的过表达可以减少 E6/E7 表达和 p53i HFKs 中的过度增殖。总之,这些结果表明 miR-203 的表达依赖于 p53,这可能解释了 HPV16 E6 的表达如何破坏角质形成细胞中增殖与分化之间的平衡,以及对 DNA 损伤的反应。

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