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一种与腺病毒早期EIIa启动子内增强子元件结合的细胞转录因子的纯化及功能鉴定。

Purification and functional characterization of a cellular transcription factor that binds to an enhancer element within the adenovirus early EIIa promoter.

作者信息

Jalinot P, Wintzerith M, Gaire M, Hauss C, Egly J M, Kédinger C

机构信息

Centre National de la Recherche Scientifique, Unité 184 de Biologie Moléculaire et de Génie, Génétique, Faculté de Médecine, Strasbourg, France.

出版信息

Proc Natl Acad Sci U S A. 1988 Apr;85(8):2484-8. doi: 10.1073/pnas.85.8.2484.

Abstract

The adenovirus EIa-inducible early EIIa (EIIaE) promoter is comprised of several sequence elements essential for constitutive and induced expression. We report here the purification of the host-cell factor that interacts with the major upstream element of this promoter, extending between positions -90 and -70 with respect to the main EIIaE cap site and exhibiting enhancer properties. The purified factor, which corresponds to a 40- to 43-kDa polypeptide, specifically binds to its recognition site and stimulates EIIaE promoter activity when added to an in vitro transcription system, reconstituted from purified factors and RNA polymerase. The implication of this factor in the control of the other adenovirus early genes is discussed.

摘要

腺病毒E1a诱导的早期EIIa(EIIaE)启动子由几个对组成型和诱导型表达至关重要的序列元件组成。我们在此报告了与该启动子主要上游元件相互作用的宿主细胞因子的纯化,该元件相对于主要EIIaE帽位点在-90至-70位之间延伸并具有增强子特性。纯化的因子对应于一种40至43 kDa的多肽,它特异性结合其识别位点,并在添加到由纯化因子和RNA聚合酶重构的体外转录系统中时刺激EIIaE启动子活性。讨论了该因子在腺病毒其他早期基因调控中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cd0/280021/7c5cf56c714e/pnas00260-0078-a.jpg

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