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与小核RNA U2互补的人类DNA序列。

Human DNA sequences complementary to the small nuclear RNA U2.

作者信息

Westin G, Monstein H J, Zabielski J, Philipson L, Pettersson U

出版信息

Nucleic Acids Res. 1981 Dec 11;9(23):6323-38. doi: 10.1093/nar/9.23.6323.

Abstract

Clones containing sequences complementary to the small nuclear RNA U2 were isolated from a human DNA library (1). Three clones, designated U2/4, U2/6 and U2/7 were purified and characterized by restriction enzyme cleavage, hybridization and heteroduplex analysis. Hybridization showed that the three clones each contained one single region which is complementary to U2 RNA. Restriction enzyme cleavage revealed furthermore that the inserted fragments in the three recombinants are different. Heteroduplex analysis identified a 240-380 bp long duplex region in each heteroduplex which includes sequences complementary to U2 RNA. Heteroduplexes between clones U2/4 and U2/7 as well as between U2/4 and U2/6 revealed two additional approximately 200 bp long homologies. The remainder of the inserts were found to lack measurable sequence homology. Two fragments from clone U2/4 were subcloned in the pBR322 vector and the subclones were used to determine the nucleotide sequence of a region in clone U2/4 which is complementary to U2 RNA. A comparison between the established sequence and the sequence for rat U2 RNA (2) reveals several discrepancies.

摘要

从人DNA文库中分离出了含有与小核RNA U2互补序列的克隆(1)。对三个命名为U2/4、U2/6和U2/7的克隆进行了纯化,并通过限制性内切酶切割、杂交和异源双链分析对其进行了表征。杂交表明,这三个克隆各自包含一个与U2 RNA互补的单一区域。限制性内切酶切割进一步显示,这三个重组体中的插入片段是不同的。异源双链分析在每个异源双链中鉴定出一个240 - 380 bp长的双链区域,其中包括与U2 RNA互补的序列。克隆U2/4和U2/7之间以及U2/4和U2/6之间的异源双链显示出另外两个约200 bp长的同源性。发现插入片段的其余部分缺乏可测量的序列同源性。将克隆U2/4的两个片段亚克隆到pBR322载体中,并使用这些亚克隆来确定克隆U2/4中与U2 RNA互补的一个区域的核苷酸序列。已确定的序列与大鼠U2 RNA的序列(2)之间的比较揭示了几个差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffe5/327606/48ef3d98bf67/nar00416-0116-a.jpg

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