Tyndall C, Watt F, Molloy P L, Vincent P C, Frommer M
Kanematsu Laboratories Royal Prince Alfred Hospital, Camperdown, NSW, Australia.
J Mol Biol. 1992 Jul 20;226(2):289-99. doi: 10.1016/0022-2836(92)90945-g.
We have analysed binding sites of nuclear protein factors to a CpG island (HTF9), which contains the promoter for a pair of overlapping, divergently-transcribed "housekeeping" genes. Using DNaseI protection assays with extracts from a range of differentiated and undifferentiated cell lines, including mouse embryonic stem (ES) and embryonal carcinoma (EC) cells, we located multiple protein binding sites on HTF9. Most of the sites were outside the defined core promoter and could bind to previously identified transcription factors. These included constitutive, inducible and apparently tissue-specific factors in an extremely asymmetric array relative to the transcription start sites of the two genes. A number of sites showed different binding specificities or affinities in different cell types, including ES cells. However, we found no factors that were specific for both ES and EC cells, and no protein-binding site protected exclusively in undifferentiated embryonic cells.
我们分析了核蛋白因子与一个CpG岛(HTF9)的结合位点,该CpG岛包含一对重叠、反向转录的“管家”基因的启动子。通过对一系列分化和未分化细胞系(包括小鼠胚胎干细胞(ES)和胚胎癌细胞(EC))提取物进行DNaseI保护分析,我们在HTF9上定位了多个蛋白质结合位点。大多数位点位于定义的核心启动子之外,并且能够与先前鉴定的转录因子结合。这些转录因子包括组成型、诱导型以及相对于两个基因转录起始位点而言极其不对称排列的明显组织特异性因子。许多位点在不同细胞类型(包括ES细胞)中表现出不同的结合特异性或亲和力。然而,我们没有发现对ES细胞和EC细胞都具有特异性的因子,也没有发现仅在未分化胚胎细胞中受到保护的蛋白质结合位点。