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两种转录因子之间的协同作用指导盘基网柄菌顶端组织者细胞中的基因表达。

Synergy between two transcription factors directs gene expression in Dictyostelium tip-organiser cells.

作者信息

Wang Hong Yu, Williams Jeffrey G

机构信息

College of Life Sciences, University of Dundee, Dow Street, Dundee, U.K.

出版信息

Int J Dev Biol. 2010;54(8-9):1301-7. doi: 10.1387/ijdb.103141hw.

Abstract

cotC requires the transcription factor CudA for its expression in the posterior, prespore cells of the slug, while the expL7 gene requires CudA for its expression in the anterior, tip-organiser region. In order to identify additional transcription factors that might mediate tip-organiser specific expression, we performed affinity chromatography on slug nuclear extracts. The affinity matrix bore cap-site distal sequences from region A of the expL7 promoter; an essential region located upstream of the CudA binding domain. One of the proteins purified was G-box binding factor (GBF), a zinc finger transcription factor which binds to G-rich elements, known as G boxes, that are present in the promoters of many developmental genes, including cotC. Previous work identified an essential sequence motif within region A and we show that this element is a G box, that binds recombinant GBF. Moreover, a G box from within the cotC promoter can substitute for region A of expL7 in directing tip-organiser specific expression of expL7. Thus the same two transcription factors, CudA and GBF, seem to co-operate to direct both tip-organiser and prespore gene expression. How then is specificity achieved? Replacing a CudA binding region in the cotC promoter with the CudA binding domain from expL7 strongly represses cotC promoter activity. Hence we suggest that differences in the topology of the multiple CudA half- sites contained within the two different CudA binding regions, coupled with differences in the signalling environment between tip-organiser cells and prespore cells, ensure correct expL7 expression.

摘要

CotC在蛞蝓后孢子前体细胞中的表达需要转录因子CudA,而expL7基因在前端顶端组织者区域的表达需要CudA。为了鉴定可能介导顶端组织者特异性表达的其他转录因子,我们对蛞蝓核提取物进行了亲和层析。亲和基质带有来自expL7启动子区域A的帽位点远端序列;这是一个位于CudA结合域上游的关键区域。纯化得到的一种蛋白质是G盒结合因子(GBF),它是一种锌指转录因子,可与富含G的元件(称为G盒)结合,这些元件存在于许多发育基因(包括cotC)的启动子中。先前的研究确定了区域A内的一个关键序列基序,我们发现该元件是一个G盒,可与重组GBF结合。此外,cotC启动子内的一个G盒可以替代expL7的区域A,以指导expL7在顶端组织者区域的特异性表达。因此,似乎是相同的两个转录因子CudA和GBF共同协作来指导顶端组织者和孢子前体基因的表达。那么特异性是如何实现的呢?用expL7的CudA结合域替换cotC启动子中的CudA结合区域会强烈抑制cotC启动子活性。因此,我们认为两个不同CudA结合区域内多个CudA半位点的拓扑结构差异,再加上顶端组织者细胞和孢子前体细胞之间信号环境的差异,确保了expL7的正确表达。

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