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转录因子RFX1/EF-C和ATF-1与人增殖细胞核抗原启动子的腺病毒E1A反应元件相关联。

Transcription factors RFX1/EF-C and ATF-1 associate with the adenovirus E1A-responsive element of the human proliferating cell nuclear antigen promoter.

作者信息

Labrie C, Lee B H, Mathews M B

机构信息

Cold Spring Harbor Laboratory, NY 11724-2208, USA.

出版信息

Nucleic Acids Res. 1995 Sep 25;23(18):3732-41. doi: 10.1093/nar/23.18.3732.

Abstract

The proliferating cell nuclear antigen (PCNA) is an adenovirus E1A-inducible factor that is intimately linked to the processes of DNA replication and cell cycle regulation. Previously, we defined a novel cis-acting element, the PCNA E1A-responsive element (PERE), that confers induction by the E1A 243R oncoprotein upon the human PCNA promoter. To better understand the regulation of PCNA expression by E1A 243R, we have identified cellular transcription factors that associate with the PERE. In electrophoretic mobility shift assays, the PERE formed three major complexes (P1, P2 and P3) with proteins in nuclear extracts from HeLa or 293 cells. Formation of complexes P2 and P3, which correlates with PCNA promoter activity in vivo, requires the activating transcription factor (ATF) binding site found within the PERE [Labrie et al. (1993) Mol. Cell. Biol., 13, 1697-1707]. Antibody interference experiments and mobility shift assays performed with in vitro-synthesized protein indicated that the transcription factor ATF-1 is a major component of these complexes. Similar assays demonstrated that the hepatitis B virus enhancer-associated protein RFX1 constitutes a major component of the P1 complex. In addition, we examined the binding of proteins to the minimal E1A-responsive promoter to identify other factors important for transcription from the PCNA promoter. Mobility shift assays revealed that a fragment encompassing the region from -87 to +62 relative to the transcription initiation site forms at least five complexes, EH1-EH5, with HeLa cell nuclear extracts. The transcription factor YY1 associates with the initiator element of the PCNA promoter. The identification of these transcription factors will allow their roles in the activation of PCNA by E1A to be evaluated.

摘要

增殖细胞核抗原(PCNA)是一种腺病毒E1A诱导因子,与DNA复制和细胞周期调控过程密切相关。此前,我们定义了一种新型顺式作用元件,即PCNA E1A反应元件(PERE),它可使E1A 243R癌蛋白诱导人PCNA启动子。为了更好地理解E1A 243R对PCNA表达的调控,我们鉴定了与PERE相关的细胞转录因子。在电泳迁移率变动分析中,PERE与来自HeLa或293细胞核提取物中的蛋白质形成了三种主要复合物(P1、P2和P3)。复合物P2和P3的形成与体内PCNA启动子活性相关,这需要PERE内的激活转录因子(ATF)结合位点[拉布里等人(1993年)《分子与细胞生物学》,13卷,1697 - 1707页]。抗体干扰实验以及用体外合成蛋白进行的迁移率变动分析表明,转录因子ATF - 1是这些复合物的主要成分。类似实验表明,乙肝病毒增强子相关蛋白RFX1是P1复合物的主要成分。此外,我们检测了蛋白质与最小E1A反应启动子的结合,以鉴定对PCNA启动子转录重要的其他因子。迁移率变动分析显示,相对于转录起始位点,一个包含 - 87至 + 62区域的片段与HeLa细胞核提取物形成至少五种复合物,即EH1 - EH5。转录因子YY1与PCNA启动子的起始元件相关。这些转录因子的鉴定将有助于评估它们在E1A激活PCNA中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbec/307273/e47eb67c3d89/nar00018-0132-a.jpg

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