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爱泼斯坦-巴尔病毒转录因子EBNA-2的细胞靶基因:PI3激酶p55α调节亚基的诱导及其在EREB2.5细胞存活中的作用

Cell target genes of Epstein-Barr virus transcription factor EBNA-2: induction of the p55alpha regulatory subunit of PI3-kinase and its role in survival of EREB2.5 cells.

作者信息

Spender Lindsay C, Lucchesi Walter, Bodelon Gustavo, Bilancio Antonio, Karstegl Claudio Elgueta, Asano Tomoichiro, Dittrich-Breiholz Oliver, Kracht Michael, Vanhaesebroeck Bart, Farrell Paul J

机构信息

Ludwig Institute for Cancer Research, University of Tokyo, Tokyo 113-8655, Japan.

Department of Virology, Imperial College Faculty of Medicine, Norfolk Place, London W2 1PG, UK.

出版信息

J Gen Virol. 2006 Oct;87(Pt 10):2859-2867. doi: 10.1099/vir.0.82128-0.

Abstract

Microarray analysis covering most of the annotated RNAs in the human genome identified a panel of genes induced by the Epstein-Barr virus (EBV) EBNA-2 transcription factor in the EREB2.5 human B-lymphoblastoid cell line without the need for any intermediate protein synthesis. Previous data indicating that PIK3R1 RNA (the alpha regulatory subunit of PI3-kinase) was induced were confirmed, but it is now shown that it is the p55alpha regulatory subunit that is induced. Several EBV-immortalized lymphoblastoid cell lines were shown to express p55alpha. Expression of PI3-kinase p85 regulatory and p110 catalytic subunits was not regulated by EBNA-2. Proliferation of EREB2.5 lymphoblastoid cells was inhibited by RNAi knock-down of p55alpha protein expression, loss of p55alpha being accompanied by an increase in apoptosis. p55alpha is thus a functional target of EBNA2 in EREB2.5 cells and the specific regulation of p55alpha by EBV will provide an opportunity to investigate the physiological function of p55alpha in this human cell line.

摘要

覆盖人类基因组中大部分注释RNA的微阵列分析,在EREB2.5人B淋巴母细胞系中鉴定出一组由爱泼斯坦-巴尔病毒(EBV)EBNA-2转录因子诱导的基因,无需任何中间蛋白质合成。先前表明PIK3R1 RNA(PI3激酶的α调节亚基)被诱导的数据得到了证实,但现在表明被诱导的是p55α调节亚基。几个EBV永生化的淋巴母细胞系被证明表达p55α。PI3激酶p85调节亚基和p110催化亚基的表达不受EBNA-2的调控。通过RNAi敲低p55α蛋白表达可抑制EREB2.5淋巴母细胞的增殖,p55α的缺失伴随着细胞凋亡的增加。因此,p55α是EREB2.5细胞中EBNA2的功能靶点,EBV对p55α的特异性调控将为研究p55α在该人类细胞系中的生理功能提供机会。

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