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非洲爪蟾一个编码小核核糖核蛋白(U1 70K)的基因的结构与表达

Structure and expression of a Xenopus gene encoding an snRNP protein (U1 70K).

作者信息

Etzerodt M, Vignali R, Ciliberto G, Scherly D, Mattaj I W, Philipson L

机构信息

European Molecular Biology Laboratory, Heidelberg, FRG.

出版信息

EMBO J. 1988 Dec 20;7(13):4311-21. doi: 10.1002/j.1460-2075.1988.tb03330.x.

Abstract

A cDNA and two genes for the Xenopus laevis U snRNP 70K protein have been cloned and partially sequenced. The cDNA encodes a protein whose predicted mol. wt is 57 kd but which migrates as a 70 kd protein in SDS-PAGE when translated in vitro from a cDNA transcript. The predicted protein sequences of the human and Xenopus U1 70K are shown to be very similar. Analysis of several genomic clones suggests that there are at least two, and possibly more, different genes coding for the 70K protein in the Xenopus genome. The two genes analysed in detail cover approximately 16 kb and are divided into 10 exons of which the last exon covers more than half of the protein coding sequence. During Xenopus development several different stage-specific RNAs hybridizing to the U1 70K cDNA are detected. The promoter region of one of the cloned genes is demonstrated to be functionally active, and to show apparent differences from other pol II promoters.

摘要

非洲爪蟾U snRNP 70K蛋白的一个cDNA和两个基因已被克隆并进行了部分测序。该cDNA编码一种预测分子量为57kd的蛋白质,但当从cDNA转录本体外翻译时,它在SDS-PAGE中以70kd蛋白的形式迁移。人类和非洲爪蟾U1 70K的预测蛋白质序列显示非常相似。对几个基因组克隆的分析表明,非洲爪蟾基因组中至少有两个,也可能更多,不同的基因编码70K蛋白。详细分析的两个基因覆盖约16kb,分为10个外显子,其中最后一个外显子覆盖了一半以上的蛋白质编码序列。在非洲爪蟾发育过程中,检测到几种与U1 70K cDNA杂交的不同阶段特异性RNA。其中一个克隆基因的启动子区域被证明具有功能活性,并且与其他聚合酶II启动子存在明显差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d605/455147/2dbe05df5335/emboj00150-0284-a.jpg

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