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一种大鼠核磷蛋白的DNA结合特性

The DNA-binding properties of a rat nuclear phosphoprotein.

作者信息

Cowan D B, Chaban G, Liew C C

机构信息

Department of Clinical Biochemistry, Banting Institute, University of Toronto, Ontario, Canada.

出版信息

Biochem J. 1991 Mar 15;274 ( Pt 3)(Pt 3):687-91. doi: 10.1042/bj2740687.

Abstract

The non-histone nuclear phosphoprotein B2 (Mr 68,000; pI 6.5-8.2) was found to bind specifically defined fragments of DNA. With the use of monoclonal IgG2A antibodies prepared against this nuclear antigen, nucleosomal DNA fragments associated with phosphoprotein B2 were isolated and cloned. Nine cloned fragments were sequenced and analysed for similarity. The clone having the most similarity to the others was chosen to serve as a model in gel shift and footprinting assays. Subsequently, the DNA binding site was found to reside within a 30 bp region. Synthetic oligonucleotides corresponding to this site confirmed the specificity of DNA binding exhibited by the nuclear antigen as demonstrated in competition assays. Moreover, a 5'-TATTAG/C-3' motif was found to exist within the binding site and in the other sequenced clones, possibly implicating the involvement of this motif in protein binding.

摘要

发现非组蛋白核磷蛋白B2(分子量68,000;等电点6.5 - 8.2)能特异性结合特定的DNA片段。利用针对这种核抗原制备的单克隆IgG2A抗体,分离并克隆了与磷蛋白B2相关的核小体DNA片段。对9个克隆片段进行了测序并分析其相似性。选择与其他片段最相似的克隆用作凝胶迁移和足迹分析的模型。随后,发现DNA结合位点位于一个30 bp的区域内。与该位点对应的合成寡核苷酸在竞争分析中证实了核抗原所表现出的DNA结合特异性。此外,在结合位点以及其他测序克隆中发现存在一个5'-TATTAG/C-3'基序,这可能意味着该基序参与了蛋白质结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e042/1149966/e9cc89dd13c8/biochemj00163-0072-a.jpg

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