Nakanishi-Matsui M, Kubo T, Natori S
Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.
Eur J Biochem. 1995 Jun 1;230(2):396-400.
Previously, we purified a DNA-binding protein, named ATBP, from cultured Sarcophaga cells. This protein was found to bind specifically to (A+T) stretches that locate in the 5'-upstream region and the intron of the Sarcophaga lectin gene [Matsui, M., Kobayashi, A., Kubo, T. & Natori, S. (1994) Eur. J. Biochem. 219, 449-454]. Here, we report molecular cloning of a cDNA for ATBP. The cDNA encoded a protein with two zinc-finger motifs, an acidic domain, two glutamine-rich domains and a glutamine run. Immunofluorescence study revealed that ATBP was localized in the nuclei. Thus, ATBP is possibly a transcription factor for genes having (A+T) stretches in their promoter and/or enhancer regions.
此前,我们从培养的肉蝇细胞中纯化出一种名为ATBP的DNA结合蛋白。该蛋白被发现能特异性结合位于肉蝇凝集素基因5'-上游区域和内含子中的(A+T)序列[松井,M.,小林,A.,久保,T. & 名取,S.(1994)欧洲生物化学杂志219,449 - 454]。在此,我们报告ATBP的cDNA的分子克隆。该cDNA编码一种具有两个锌指基序、一个酸性结构域、两个富含谷氨酰胺的结构域和一个谷氨酰胺链的蛋白。免疫荧光研究表明ATBP定位于细胞核中。因此,ATBP可能是在其启动子和/或增强子区域具有(A+T)序列的基因的转录因子。