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编码人核不均一核糖核蛋白A1的活性基因的分离。选择性剪接的证据。

Isolation of an active gene encoding human hnRNP protein A1. Evidence for alternative splicing.

作者信息

Biamonti G, Buvoli M, Bassi M T, Morandi C, Cobianchi F, Riva S

机构信息

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

出版信息

J Mol Biol. 1989 Jun 5;207(3):491-503. doi: 10.1016/0022-2836(89)90459-2.

Abstract

Heterogeneous nuclear ribonucleoprotein (hnRNP) core protein A1 is a major component of mammalian hnRNP 40 S particles. We describe the structure of an active A1 gene and report on the partial characterization of the A1 gene family. About 30 A1-specific sequences are present per haploid human genome: 15 such sequences were isolated from a human genomic DNA library. Many corresponded to pseudogenes of the processed type but by applying a selection for actively transcribed regions we isolated an active A1 gene. The gene spans a region of 4.6 x 10(3) base-pairs and it is split into ten exons that encode the 320 amino acid residues of the protein. The amino acid sequence derived from the exon sequences is identical with that deduced from cDNA and reported for the protein. One intron exactly separates the two structural domains that constitute the protein. Each of the two RNA-binding domains in protein A1 is encoded by one exon. Experimental evidence indicates that the A1 gene can encode for more than one protein by alternative splicing. The gene is preceded by a strong promoter that contains at least two CCAAT boxes and two possible Sp1 binding sites, but it lacks a TATA box.

摘要

不均一核核糖核蛋白(hnRNP)核心蛋白A1是哺乳动物hnRNP 40 S颗粒的主要成分。我们描述了一个活性A1基因的结构,并报告了A1基因家族的部分特征。单倍体人类基因组中约有30个A1特异性序列:从人类基因组DNA文库中分离出15个这样的序列。许多对应于加工型假基因,但通过对活跃转录区域进行筛选,我们分离出了一个活性A1基因。该基因跨度为4.6×10³个碱基对,被分割成10个外显子,编码该蛋白的320个氨基酸残基。从外显子序列推导的氨基酸序列与从cDNA推导并报道的该蛋白的氨基酸序列相同。一个内含子恰好将构成该蛋白的两个结构域分开。蛋白A1中的两个RNA结合结构域各由一个外显子编码。实验证据表明,A1基因可通过可变剪接编码不止一种蛋白质。该基因之前有一个强启动子,其中至少包含两个CCAAT框和两个可能的Sp1结合位点,但它缺少TATA框。

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