Auble D T, Wang D, Post K W, Hahn S
Department of Biochemistry, University of Virginia Health Science Center, Charlottesville 22908, USA.
Mol Cell Biol. 1997 Aug;17(8):4842-51. doi: 10.1128/MCB.17.8.4842.
MOT1 is an essential Saccharomyces cerevisiae protein and a member of the SNF2/SWI2 family of ATPases. MOT1 functions by removing TATA-binding protein (TBP) from DNA, and as a consequence, MOT1 can regulate transcription both in vitro and in vivo. Here we describe the in vivo and in vitro activities of MOT1 deletion and substitution mutants. The results indicate that MOT1 is targeted to TBP both in vitro and in vivo via amino acids in its nonconserved N terminus. The conserved C-terminal ATPase of MOT1 appears to contribute to TBP-DNA complex recognition in the absence of ATP, but it appears to function primarily during the actual ATP-dependent dissociation reaction. Chimeric proteins in which homologous portions of SNF2/SWI2 have been substituted for the MOT1 ATPase can bind to TBP-DNA complexes but fail to dissociate these complexes in the presence of ATP, suggesting that the specificity of action of MOT1 is also conferred by the C-terminal ATPase. ATPase assays demonstrate that the MOT1 ATPase is activated by TBP. Thus, MOT1 undergoes at least two conformational changes: (i) an allosteric effect of TBP that mediates the activation of the MOT1 ATPase and (ii) an ATP-driven "power stroke" that causes TBP-DNA complex dissociation. These results provide a general framework for understanding how members of the SNF2/SWI2 protein family use ATP to modulate protein-DNA interactions to regulate many diverse processes in cells.
MOT1是酿酒酵母中的一种必需蛋白,属于ATP酶的SNF2/SWI2家族成员。MOT1通过从DNA上去除TATA结合蛋白(TBP)发挥作用,因此,MOT1在体外和体内均可调节转录。在此,我们描述了MOT1缺失和替代突变体的体内和体外活性。结果表明,MOT1在体外和体内均通过其非保守N端的氨基酸靶向TBP。MOT1保守的C端ATP酶在无ATP时似乎有助于TBP-DNA复合物的识别,但它似乎主要在实际的ATP依赖性解离反应中发挥作用。用SNF2/SWI2的同源部分替代MOT1 ATP酶的嵌合蛋白可以结合TBP-DNA复合物,但在有ATP存在时不能解离这些复合物,这表明MOT1作用的特异性也由C端ATP酶赋予。ATP酶分析表明,MOT1 ATP酶被TBP激活。因此,MOT1经历至少两种构象变化:(i)TBP的变构效应介导MOT1 ATP酶的激活,以及(ii)ATP驱动的“动力冲程”导致TBP-DNA复合物解离。这些结果为理解SNF2/SWI2蛋白家族成员如何利用ATP调节蛋白质-DNA相互作用以调控细胞中许多不同过程提供了一个总体框架。