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纯化转录因子的相互作用:酵母MATα1和PRTF与细胞类型特异性上游激活序列的结合

Interactions of purified transcription factors: binding of yeast MAT alpha 1 and PRTF to cell type-specific, upstream activating sequences.

作者信息

Tan S, Ammerer G, Richmond T J

机构信息

MRC Laboratory of Molecular Biology, Cambridge UK.

出版信息

EMBO J. 1988 Dec 20;7(13):4255-64. doi: 10.1002/j.1460-2075.1988.tb03323.x.

Abstract

Pheromone receptor transcription factor (PRTF) and MAT alpha 1 are protein transcription factors that are involved in the regulation of the alpha-specific genes in Saccharomyces cerevisiae. We have expressed MAT alpha 1 as a fusion protein in Escherichia coli and purified it from inclusion bodies in milligram quantities. The MAT alpha 1 protein was obtained after specific cleavage of the fusion protein. Quantitative band shift electrophoresis was used to determine the equilibrium dissociation constants that describe the multicomponent binding equilibrium between the PRTF and MAT alpha 1 proteins, and alpha-specific STE3 upstream activating sequence (UAS) DNA. The dissociation constant for the complex of PRTF and the a-specific UAS of STE2 was also measured and found to be 5.9 X 10(-11) M, only three times less than that for the PRTF-STE3 UAS complex. Analyses of these complexes by DNase I footprinting demonstrate that the PRTF binding site is confined to the palindromic P-box sequence in the case of the STE3 UAS, but extends symmetrically from this central region to cover 28 bp for the STE2 UAS. When MAT alpha 1 is bound to the PRTF-STE3 complex, the region of DNA protected is enlarged to that seen for the PRTF-STE2 complex. Our results using these two purified factors in vitro suggest that PRTF has nearly the same affinity for a- and alpha-specific UAS elements and that transcriptional activation requires a particular conformational state for the PRTF-DNA complex which occurs in the PRTF-STE2 and MAT alpha 1-PRTF-STE3 complexes, but not in the PRTF-STE3 complex.

摘要

信息素受体转录因子(PRTF)和MATα1是参与酿酒酵母α特异性基因调控的蛋白质转录因子。我们已将MATα1作为融合蛋白在大肠杆菌中表达,并从包涵体中以毫克量进行纯化。融合蛋白经特异性切割后获得了MATα1蛋白。采用定量凝胶迁移电泳来确定平衡解离常数,该常数描述了PRTF与MATα1蛋白以及α特异性STE3上游激活序列(UAS)DNA之间的多组分结合平衡。还测定了PRTF与STE2的a特异性UAS复合物的解离常数,发现为5.9×10⁻¹¹ M,仅比PRTF-STE3 UAS复合物的解离常数小三倍。通过DNase I足迹法对这些复合物进行分析表明,对于STE3 UAS,PRTF结合位点局限于回文P盒序列,但对于STE2 UAS,它从这个中心区域对称延伸以覆盖28 bp。当MATα1与PRTF-STE3复合物结合时,受保护的DNA区域扩大到PRTF-STE2复合物所见的区域。我们在体外使用这两种纯化因子的结果表明,PRTF对a特异性和α特异性UAS元件具有几乎相同的亲和力,并且转录激活需要PRTF-DNA复合物处于特定的构象状态,这种状态出现在PRTF-STE2和MATα1-PRTF-STE3复合物中,而不是PRTF-STE3复合物中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3618/455139/992e01c1061a/emboj00150-0230-a.jpg

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