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小鼠β-珠蛋白基因座控制区5' HS-3的结构与功能

Structure and function of the murine beta-globin locus control region 5' HS-3.

作者信息

Hug B A, Moon A M, Ley T J

机构信息

Department of Medicine, Jewish Hospital, Washington University Medical Center, St Louis, MO 63110.

出版信息

Nucleic Acids Res. 1992 Nov 11;20(21):5771-8. doi: 10.1093/nar/20.21.5771.

Abstract

We previously identified the murine homologue of the human beta-globin Locus Control Region (LCR) 5' HS-2. The lambda clone containing murine 5' HS-2 extends approximately 12 kb upstream from this site; here, we report the sequence of this entire upstream region. The murine homologue of 5' HS-3 is located approximately 16.0 kb upstream from the mouse epsilon y-globin gene, but no region homologous to human 5' HS-4 was present in our clone. Using a reporter system consisting of a human gamma-globin promoter driving the neomycin phosphotransferase gene (gamma-neo), we tested murine LCR fragments extending from -21 to -9 kb (with respect to the epsilon y-globin gene cap site) for activity in classical enhancer and integration site assays in K562 and MEL cells. 5' HS-2 behaved as a powerful enhancer and increased the number of productive integration events (as measured by a colony assay) in both K562 and MEL cells. 5' HS-3 had no activity in K562 cells or in transiently transfected MEL cells, but was nearly as active as 5' HS-2 in the MEL cell colony assay. Two additional tests confirmed the identification of murine 5' HS-3: first, a DNA fragment containing 5' HS-3 confers copy number-dependent, integration-site independent inducibility on a linked beta-globin gene in the MEL cell environment. Secondly, a strong DNAseI hypersensitive site maps to the location of the 5' HS-3 functional core in chromatin derived from MEL cells. Collectively, these data suggest that we have identified the murine homologue of human 5' HS-3, and that this site is functional when integrated into the chromatin of MEL cells but not K562 cells. 5' HS-3 may therefore contain information that contributes to the development-specific expression of the beta-like globin genes.

摘要

我们之前鉴定出了人类β-珠蛋白基因座控制区(LCR)5' HS-2的小鼠同源物。包含小鼠5' HS-2的λ克隆从该位点向上游延伸约12 kb;在此,我们报告整个上游区域的序列。5' HS-3的小鼠同源物位于小鼠εγ-珠蛋白基因上游约16.0 kb处,但我们的克隆中不存在与人类5' HS-4同源的区域。使用由驱动新霉素磷酸转移酶基因(γ-新霉素)的人类γ-珠蛋白启动子组成的报告系统,我们在K562和MEL细胞的经典增强子和整合位点分析中测试了从小鼠εγ-珠蛋白基因帽位点-21至-9 kb延伸的小鼠LCR片段的活性。5' HS-2表现为强大的增强子,并增加了K562和MEL细胞中有效整合事件的数量(通过集落测定法测量)。5' HS-3在K562细胞或瞬时转染的MEL细胞中无活性,但在MEL细胞集落测定中几乎与5' HS-2一样活跃。另外两项测试证实了小鼠5' HS-3的鉴定:首先,包含5' HS-3的DNA片段在MEL细胞环境中赋予与β-珠蛋白基因相连的拷贝数依赖性、整合位点独立性诱导性。其次,一个强烈的DNA酶I超敏感位点定位于源自MEL细胞的染色质中5' HS-3功能核心的位置。总体而言,这些数据表明我们已经鉴定出了人类5' HS-3的小鼠同源物,并且该位点在整合到MEL细胞而非K562细胞的染色质中时具有功能。因此,5' HS-3可能包含有助于β样珠蛋白基因发育特异性表达的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0ed/334415/09077d9b988d/nar00232-0256-a.jpg

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