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微阵列分析鉴定出由16型人乳头瘤病毒E6调控的分化相关基因。

Microarray analysis identifies differentiation-associated genes regulated by human papillomavirus type 16 E6.

作者信息

Duffy Carol L, Phillips Stacia L, Klingelhutz Aloysius J

机构信息

Department of Microbiology and Holden Cancer Center, University of Iowa, 2202 MEBRF, 375 Newton Road, Iowa City, IA 52242, USA.

出版信息

Virology. 2003 Sep 15;314(1):196-205. doi: 10.1016/s0042-6822(03)00390-8.

Abstract

In this study, we used oligonucleotide microarray analysis to determine which cellular genes are regulated by the human papillomavirus type 16 (HPV-16) E6 oncoprotein. We found that E6 causes the downregulation of a large number of cellular genes involved in keratinocyte differentiation, including genes such as small proline-rich proteins, transglutaminase, involucrin, elafin, and cytokeratins, which are normally involved in the production of the cornified cell envelope. In contrast, E6 upregulates several genes, such as vimentin, that are usually expressed in mesenchymal lineages. E6 also modulates levels of genes involved in inflammation, including Cox-1 and Nag-1. By using E6 mutants that differentially target p53 for degradation, we determined that E6 regulates cellular genes by both p53-dependent and independent mechanisms. The microarray data also indicate that HPV-16 E6 modulates certain effects of HPV-16 E7 on cellular gene expression. The identification of E6-regulated genes in this analysis provides a basis for further studies on their role in HPV infection and cellular transformation.

摘要

在本研究中,我们使用寡核苷酸微阵列分析来确定哪些细胞基因受16型人乳头瘤病毒(HPV-16)E6癌蛋白调控。我们发现,E6导致大量参与角质形成细胞分化的细胞基因下调,包括富含脯氨酸的小蛋白、转谷氨酰胺酶、内披蛋白、弹性蛋白酶和细胞角蛋白等基因,这些基因通常参与角质化细胞包膜的产生。相比之下,E6上调了一些通常在间充质谱系中表达的基因,如波形蛋白。E6还调节参与炎症的基因水平,包括Cox-1和Nag-1。通过使用差异靶向p53进行降解的E6突变体,我们确定E6通过p53依赖和独立机制调节细胞基因。微阵列数据还表明,HPV-16 E6调节HPV-16 E7对细胞基因表达的某些影响。本分析中E6调控基因的鉴定为进一步研究它们在HPV感染和细胞转化中的作用提供了基础。

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