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赛米利疱疹病毒小RNA与白细胞介素-4信使核糖核酸的AUUUA重复序列竞争序列特异性因子,包括一种新的70K蛋白。

Herpesvirus saimiri small RNA and interleukin-4 mRNA AUUUA repeats compete for sequence-specific factors including a novel 70K protein.

作者信息

Geck P, Medveczky M M, Chou C S, Brown A, Cus J, Medveczky P G

机构信息

Department of Medical Microbiology and Immunology, College of Medicine, University of South Florida, Tampa 33612.

出版信息

J Gen Virol. 1994 Sep;75 ( Pt 9):2293-301. doi: 10.1099/0022-1317-75-9-2293.

Abstract

A highly oncogenic strain of the lymphotropic tumour virus herpesvirus saimiri (HVS; strain 484-77) expresses four small RNAs (HSUR1 to 4) in high copy numbers in transformed T cells. In HSUR1 and HSUR2 the 5' terminal regions contain conserved AUUUA sequence repeats. The same AUUUA repeats occur in the 3' non-coding regions of growth factor, lymphokine and protooncogene mRNAs, and the sequence is involved in rapid mRNA degradation. We report here that by using a highly specific u.v. cross-linking method we identified a novel 70K binding factor with AUUUA sequence specificity. Non-radiolabelled competition and V8 protease analysis show that the protein can form a complex with the 3' non-coding region of interleukin-4 mRNA and bind the AUUUA repeats of a HVS small RNA. We also detected an AUUUA-specific minor 32K human protein with the same electrophoretic mobility as a marmoset factor implicated in growth factor mRNA destabilization. The findings are consistent with the hypothesis that the viral small RNAs can compete for factors involved in rapid degradation of growth factor mRNAs and may contribute to viral oncogenesis.

摘要

嗜淋巴细胞肿瘤病毒猴疱疹病毒(HVS;484 - 77株)的一种高度致癌毒株在转化的T细胞中高拷贝表达四种小RNA(HSUR1至4)。在HSUR1和HSUR2中,5'末端区域含有保守的AUUUA序列重复。相同的AUUUA重复序列出现在生长因子、淋巴因子和原癌基因mRNA的3'非编码区域,且该序列参与mRNA的快速降解。我们在此报告,通过使用一种高度特异性的紫外线交联方法,我们鉴定出一种具有AUUUA序列特异性的新型70K结合因子。非放射性标记竞争和V8蛋白酶分析表明,该蛋白可与白细胞介素-4 mRNA的3'非编码区域形成复合物,并结合HVS小RNA的AUUUA重复序列。我们还检测到一种AUUUA特异性的32K次要人类蛋白,其电泳迁移率与一种参与生长因子mRNA去稳定化的狨猴因子相同。这些发现与以下假设一致,即病毒小RNA可竞争参与生长因子mRNA快速降解的因子,并可能有助于病毒致癌作用。

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