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大鼠生长激素基因座染色质中的脱氧核糖核酸酶I超敏位点以及具有这些位点区域的增强子活性

DNase I-hypersensitive sites in the chromatin of rat growth hormone gene locus and enhancer activity of regions with these sites.

作者信息

Aizawa A, Yoneyama T, Kazahari K, Ono M

机构信息

Department of Molecular Biology, School of Medicine, Kitasato University, Kanagawa, Japan.

出版信息

Nucleic Acids Res. 1995 Jun 25;23(12):2236-44. doi: 10.1093/nar/23.12.2236.

Abstract

In this study, a determination was made of the chromatin structure of the rat growth hormone (GH) gene locus by DNase I sensitivity analysis using GC [GH+, prolactin (PRL)-], 235 (GH-, PRL+), GH3 (GH+, PRL+) and liver (GH-, PRL-) cells. From 7 kb upstream from the transcription start site to 19 kb downstream from the polyadenylation site, two major DNase I-hypersensitive sites (M-DHS; UIA, UIIA) and three M-DHS (DIA, DII, DIII) were found within 2 kb upstream and 7 kb downstream regions, respectively. Two minor DHS (m-DHS; UIB, UIIB) in the upstream region and one m-DHS (DIB) downstream were shown to be associated with M-DHS. Thus, a total of five M-DHS and three m-DHS were mapped on the rat GH gene locus. Among these, five (UIIB, UIA, UIB, DIB, DIA) including two (UIA, DIA) M-DHS were specific for GH-producing cells. UIIA and DIII were M-DHS only in PRL-producing 235 cells while the major hypersensitivity of DII was detected in GH-producing cells and liver cells. Assessment of the enhancing activity of the DHS regions indicated novel enhancers in one upstream and two downstream regions that function well with the GH promoter in GC cells. These enhancers, each appearing different, coincided with m-DHS but not M-DHS in GC cells, and were not activated by Pit-1. Based on these observations, the following functions of five M-DHS and three m-DHS regions were defined: enhancer; locus control region (LCR); switch region serving for conversion from GH/PRL-producing cells to PRL-producing cells; and a region having a structural function in chromatin.

摘要

在本研究中,通过使用GC [生长激素(GH)阳性、催乳素(PRL)阴性]、235(GH阴性、PRL阳性)、GH3(GH阳性、PRL阳性)和肝脏(GH阴性、PRL阴性)细胞进行DNase I敏感性分析,对大鼠生长激素(GH)基因座的染色质结构进行了测定。从转录起始位点上游7 kb到聚腺苷酸化位点下游19 kb,分别在2 kb上游和7 kb下游区域发现了两个主要的DNase I高敏位点(M-DHS;UIA、UIIA)和三个M-DHS(DIA、DII、DIII)。上游区域的两个次要高敏位点(m-DHS;UIB、UIIB)和下游的一个m-DHS(DIB)显示与M-DHS相关。因此,在大鼠GH基因座上共定位了五个M-DHS和三个m-DHS。其中,包括两个(UIA、DIA)M-DHS在内的五个(UIIB、UIA、UIB、DIB、DIA)对产生GH的细胞具有特异性。UIIA和DIII仅在产生PRL的235细胞中是M-DHS,而DII的主要高敏性在产生GH的细胞和肝细胞中被检测到。对DHS区域增强活性的评估表明,在一个上游区域和两个下游区域存在新的增强子,它们在GC细胞中与GH启动子协同作用良好。这些增强子在GC细胞中各自表现不同,与m-DHS而非M-DHS一致,并且不被Pit-1激活。基于这些观察结果,定义了五个M-DHS和三个m-DHS区域的以下功能:增强子;基因座控制区(LCR);用于从产生GH/PRL的细胞转变为产生PRL的细胞的转换区域;以及在染色质中具有结构功能的区域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a66f/307013/16b3b6e01038/nar00012-0168-a.jpg

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