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首页> 外文期刊>Biochemistry >Ga14-VP16 Ga14-AH Increase the Orientational and Axial Specificity of TATA Box Recognition by TATA Box Binding Protein
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Ga14-VP16 Ga14-AH Increase the Orientational and Axial Specificity of TATA Box Recognition by TATA Box Binding Protein

机译:Ga14-VP16 Ga14-AH增加TATA盒结合蛋白对TATA盒识别的定向和轴向特异性

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Previous work has shown that binding of the TATA box binding protein (TBP) to the TATA box is a rate-limiting step during preinitiation complex (PIC) formation. Although the transcription of eukaryotic genes normally proceeds in one direction, studies in solution have shown that TBP lacks the information necessary to orient itself on the TATA box. Instead, yeast TBP binds TATA-containing promoters in two orientations that are related by a 180 deg rotation about TBP's pseudo-2-fold symmetry axis. Recruitment of PIC components by gene-specific activators is considered a primary mechanism of transcriptional enhancement. Here we ask whether activators might function, at least in part, by increasing the fraction of PICs assembled with TBP bound in the orientation necessary for transcription. We use DNA affinity cleavage and a TBP-phenanthroline-copper conjugate to monitor the orientation of TBP in the presence of the well-studied activators Ga14-VP16 and Ga14-AH. In the absence of a transcriptional activator, only 51% of the TBP TATA box complexes were bound in the orientation necessary for the initiation of transcription. However, in the presence of saturating Ga14-VP16, 87% of the TBP bound to the TATA box was oriented correctly at equilibrium. This increase in orientational specificity corresponds to a free energy difference (#DELTA##DETA#G_(obs)) of 1.1 kcal mol~(-1) and was accompanied by a dramatic increase in axial specificity, reminiscent of the effects of transcription factors TFIIB and TFIIA reported previously. Ga14-AH also enhanced the orientational and axial specificity of the TBP TATA complex, although to a lesser extent. We suggest that these effects on specificity represent a variation of recruitment, since they require direct interactions between the activator and a PIC component but only increase the effective concentration of the correctly PIC component. These findings add to increasing evidence that recruitment may encompass a broad range of mechanisms.
机译:先前的工作表明,在预起始复合物(PIC)形成过程中,TATA盒结合蛋白(TBP)与TATA盒的结合是一个限速步骤。尽管真核基因的转录通常在一个方向上进行,但是在溶液中的研究表明,TBP缺乏将自身定位在TATA盒上所必需的信息。取而代之的是,酵母TBP在两个方向上都与包含TATA的启动子结合,这两个方向通过围绕TBP的伪2倍对称轴旋转180度而相关。通过基因特异性激活剂招募PIC组分被认为是转录增强的主要机制。在这里,我们问激活剂是否可能至少部分地通过增加结合有转录必需方向上的TBP的PIC的比例来起作用。我们使用DNA亲和力裂解和TBP-菲咯啉-铜共轭物来监测TBP在研究充分的活化剂Ga14-VP16和Ga14-AH的存在下的方向。在没有转录激活因子的情况下,只有51%的TBP TATA盒复合物以转录起始所必需的方向结合。但是,在存在饱和的Ga14-VP16的情况下,结合到TATA盒上的TBP的87%正确地处于平衡状态。定向特异性的这种增加对应于1.1 kcal mol〜(-1)的自由能差(#DELTA ## DETA#G_(obs)),并且伴随着轴向特异性的急剧增加,让人联想到转录因子的作用。 TFIIB和TFIIA先前已有报道。 Ga14-AH也增强了TBP TATA复合物的定向和轴向特异性,尽管程度较小。我们建议这些对特异性的影响代表了募集的变化,因为它们需要激活剂和PIC成分之间的直接相互作用,但只会增加正确PIC成分的有效浓度。这些发现增加了越来越多的证据表明,招聘可能包含广泛的机制。

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