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基因近端调控元件的突变会破坏酵母人工染色体转基因小鼠中人类ε-、γ-和β-珠蛋白的表达。

Mutation of gene-proximal regulatory elements disrupts human epsilon-, gamma-, and beta-globin expression in yeast artificial chromosome transgenic mice.

作者信息

Liu Q, Bungert J, Engel J D

机构信息

Department of Biochemistry, Molecular Biology and Cell Biology, Northwestern University, Evanston, IL 60208-3500, USA.

出版信息

Proc Natl Acad Sci U S A. 1997 Jan 7;94(1):169-74. doi: 10.1073/pnas.94.1.169.

Abstract

Previous studies have defined transcriptional control elements, in addition to the promoters, that both lie near individual human beta-globin locus genes and have been implicated in their differential stage-specific regulation during development (i.e., are believed to directly participate in hemoglobin switching). We have reinvestigated the activities during erythropoiesis that might be conferred by two of the more intensively analyzed of these elements, the epsilon-globin gene 5' silencer and the beta-globin gene 3' enhancer, by deleting them from a yeast artificial chromosome that spans the human beta-globin locus, and then analyzing transgenic mice for expression of all of the human genes. These studies show that sequences within the epsilon-globin "silencer" are not only required for silencing but are also required for activation of epsilon-globin transcription; furthermore, deletion of the silencer simultaneously reduced gamma-globin transcription during the yolk sac stage of erythroid development. Analysis of the adult beta-globin gene 3' enhancer deletion showed that its deletion affects only that gene.

摘要

以往的研究已经确定了除启动子之外的转录控制元件,这些元件既位于人类β-珠蛋白基因座的各个基因附近,又被认为在发育过程中参与了它们不同阶段特异性的调控(即被认为直接参与血红蛋白转换)。我们重新研究了在红细胞生成过程中,这些元件中经过更深入分析的两个元件——ε-珠蛋白基因5'沉默子和β-珠蛋白基因3'增强子——可能赋予的活性。我们从跨越人类β-珠蛋白基因座的酵母人工染色体中删除了这两个元件,然后分析转基因小鼠中所有人类基因的表达情况。这些研究表明,ε-珠蛋白“沉默子”中的序列不仅是沉默所必需的,也是激活ε-珠蛋白转录所必需的;此外,在红细胞发育的卵黄囊阶段,删除沉默子同时降低了γ-珠蛋白的转录。对成人β-珠蛋白基因3'增强子缺失的分析表明,其缺失仅影响该基因。

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