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人Ski原癌基因产物DNA结合功能对蛋白质辅因子的需求。

Requirement of protein co-factor for the DNA-binding function of the human ski proto-oncogene product.

作者信息

Nagase T, Mizuguchi G, Nomura N, Ishizaki R, Ueno Y, Ishii S

机构信息

Tsukuba life Science Center, Institute of Physical and Chemical Research (RIKEN), Ibaraki, Japan.

出版信息

Nucleic Acids Res. 1990 Jan 25;18(2):337-43. doi: 10.1093/nar/18.2.337.

Abstract

We identified the human c-ski gene product (c-Ski) as a protein with the apparent molecular weight of 100,000, p100c-ski, by using a c-Ski-specific polyclonal antibody. p100c-ski was a nuclear protein and p100c-ski in nuclear extracts of Molt4 cells bound to calf thymus DNA cellulose, but the bacterially synthesized c-Ski did not, suggesting that Ski was associated with another protein(s) and that the Ski complex had DNA-binding activity. This hypothesis was supported by the finding that the bacterially synthesized Ski bounds to DNA cellulose after being mixed with a nuclear extract of Molt4 cells. By use of a series of deletion mutants of Ski synthesized in an in vitro translation system, two portions in Ski were found to be necessary for the DNA binding of the Ski complex: the N-proximal portion containing a cystein/histidine-rich domain and the C-terminal portion including a region rich in basic amino acids.

摘要

我们通过使用一种c-Ski特异性多克隆抗体,将人类c-ski基因产物(c-Ski)鉴定为一种表观分子量为100,000的蛋白质,即p100c-ski。p100c-ski是一种核蛋白,Molt4细胞核提取物中的p100c-ski与小牛胸腺DNA纤维素结合,但细菌合成的c-Ski则不然,这表明Ski与其他一种或多种蛋白质相关联,并且Ski复合物具有DNA结合活性。这一假设得到了以下发现的支持:细菌合成的Ski与Molt4细胞核提取物混合后可与DNA纤维素结合。通过使用在体外翻译系统中合成的一系列Ski缺失突变体,发现Ski中的两个部分对于Ski复合物的DNA结合是必需的:包含富含半胱氨酸/组氨酸结构域的N近端部分和包含富含碱性氨基酸区域的C末端部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acc0/330272/fd827faf539b/nar00186-0116-a.jpg

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