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转录因子c-Ets1与人类免疫缺陷病毒I型长末端重复序列的序列特异性结合。

Sequence specific binding of the transcription factor c-Ets1 to the human immunodeficiency virus type I long terminal repeat.

作者信息

Holzmeister J, Ludewig B, Pauli G, Simon D

机构信息

Abteilung Biochemie, Robert Koch-Institut, Berlin, Germany.

出版信息

Biochem Biophys Res Commun. 1993 Dec 30;197(3):1229-33. doi: 10.1006/bbrc.1993.2608.

Abstract

Human immunodeficiency virus type I (HIV-1) long terminal repeat (LTR) driven transcription is regulated by a variety of cellular transcription factors. Most work has focused on the two nuclear factor kappa B (NF-kB) elements indispensable for HIV-1 LTR enhancer function. We demonstrate here the specific binding of the transcription factor c-Ets1 to an U3 region of the HIV-1 LTR (nt -141 to -149) using electrophoretic mobility shift analysis with T-cell nuclear extract and in vitro translated protein. This previously not identified Ets binding site is highly conserved among different HIV-1 isolates and maps to an U3 region recently shown to be necessary for viral growth in vitro. The c-Ets proto-oncogene family of transcription factors has yet been associated with HTLV-I and HIV-2 transcription. Our present analysis suggests an important role of c-Ets proteins in HIV-1 transcription.

摘要

I型人类免疫缺陷病毒(HIV-1)的长末端重复序列(LTR)驱动的转录受多种细胞转录因子调控。大多数研究工作聚焦于HIV-1 LTR增强子功能所必需的两个核因子κB(NF-κB)元件。我们在此利用T细胞核提取物和体外翻译蛋白进行电泳迁移率变动分析,证明转录因子c-Ets1与HIV-1 LTR的U3区域(核苷酸-141至-149)存在特异性结合。这个先前未被识别的Ets结合位点在不同的HIV-1分离株中高度保守,并且定位到最近显示对体外病毒生长必需的一个U3区域。转录因子的c-Ets原癌基因家族尚未与HTLV-I和HIV-2转录相关联。我们目前的分析表明c-Ets蛋白在HIV-1转录中起重要作用。

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