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人类不均一核糖核蛋白A1基因表达。启动子的结构与功能特征

Human hnRNP protein A1 gene expression. Structural and functional characterization of the promoter.

作者信息

Biamonti G, Bassi M T, Cartegni L, Mechta F, Buvoli M, Cobianchi F, Riva S

机构信息

Istituto di Genetica Biochimica ed Evoluzionistica del C.N.R., Pavia, Italy.

出版信息

J Mol Biol. 1993 Mar 5;230(1):77-89. doi: 10.1006/jmbi.1993.1127.

Abstract

hnRNP protein A1 (34 kDa, pl 9.5) is a prominent member of the family of proteins (hnRNP proteins) that associate with the nascent transcripts of RNA polymerase II and that accompany the hnRNA through the maturation process and the export to the cytoplasm. New evidence suggests an active and specific role for some of these proteins, including protein A1, in splicing and transport. Contrary to the other hnRNP proteins, the intracellular level of protein A1 was reported to change as a function of proliferation state and cell type. In this work we analyse the A1 gene expression in different cells under different growth and differentiation conditions. Proliferation dependent expression was observed in lymphocytes and fibroblasts while purified neurons express high A1 mRNA levels both in the proliferative (before birth) and in the quiescent (after birth) state. Transformed cell lines exhibit very high (proliferation independent) A1 mRNA levels compared to differentiated tissues. A structural and functional characterization of the A1 gene promoter was carried out by means of DNase I footprinting and CAT assays. The observed promoter features can account for both elevated and regulated mRNA transcription. At least 12 control elements are contained in the 734 nucleotides upstream of the transcription start site. Assays with the deleted and/or mutated promoter indicate a co-operation of multiple transcriptional elements, distributed over the entire promoter, in determining the overall activity and the response to proliferative stimuli (serum).

摘要

异质性核糖核蛋白A1(34千道尔顿,等电点9.5)是与RNA聚合酶II的新生转录本相关联,并伴随核内不均一RNA(hnRNA)经历成熟过程并输出至细胞质的蛋白质家族(异质性核糖核蛋白)中的重要成员。新证据表明这些蛋白质中的一些,包括蛋白质A1,在剪接和转运中发挥着积极且特定的作用。与其他异质性核糖核蛋白不同,据报道蛋白质A1的细胞内水平会随增殖状态和细胞类型而变化。在这项研究中,我们分析了不同生长和分化条件下不同细胞中A1基因的表达情况。在淋巴细胞和成纤维细胞中观察到了增殖依赖性表达,而纯化的神经元在增殖状态(出生前)和静止状态(出生后)均表达高水平的A1信使核糖核酸(mRNA)。与分化组织相比,转化细胞系呈现出非常高的(不依赖增殖的)A1 mRNA水平。通过脱氧核糖核酸酶I足迹法和氯霉素乙酰转移酶(CAT)分析对A1基因启动子进行了结构和功能表征。观察到的启动子特征可以解释mRNA转录的升高和调控。转录起始位点上游734个核苷酸中至少包含12个调控元件。对缺失和/或突变启动子的分析表明,分布在整个启动子上的多个转录元件协同作用,决定了整体活性以及对增殖刺激(血清)的反应。

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