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因子TUF与RPG序列之间的联系。

Contacts between the factor TUF and RPG sequences.

作者信息

Vignais M L, Huet J, Buhler J M, Sentenac A

机构信息

Département de Biologie, Centre d'Etudes Nucléaires de Saclay, Gif-sur-Yvette, France.

出版信息

J Biol Chem. 1990 Aug 25;265(24):14669-74.

PMID:2201690
Abstract

The yeast TUF factor binds specifically to RPG-like sequences involved in multiple functions at enhancers, silencers, and telomeres. We have characterized the interaction of TUF with its optimal binding sequence, rpg-1 (1-ACACCCATACATTT-14), using a gel DNA-binding assay in combination with methylation protection and mutagenesis experiments. As many as 10 base pairs appear to be engaged in factor binding. Analysis of a collection of 30 different RPG mutants demonstrated the importance of 8 base pairs at position 2, 3, 4, 5, 6, 7, 10, and 12 and the critical role of the central GC pair at position 5. Methylation protection data on four different natural sites confirmed a close contact at positions 4, 5, 6, and 10 and suggested additional contacts at base pairs 8, 12, and 13. The derived consensus sequence was RCAAYCCRYNCAYY. A quantitative band shift analysis was used to determine the equilibrium dissociation constant for the complex of TUF and its optimal binding site rpg-1. The specific dissociation constant (K8) was found to be 1.3 x 10(-11) M. The comparison of the K8 value with the dissociation constant obtained for nonspecific DNA sites (Kn8 = 8.7 x 10(-6) M) shows the high binding selectivity of TUF for its specific RPG target.

摘要

酵母TUF因子特异性结合参与增强子、沉默子和端粒多种功能的类RPG序列。我们使用凝胶DNA结合分析结合甲基化保护和诱变实验,对TUF与其最佳结合序列rpg-1(1-ACACCCATACATTT-14)的相互作用进行了表征。多达10个碱基对似乎参与了因子结合。对30个不同RPG突变体的集合分析表明,第2、3、4、5、6、7、10和12位的8个碱基对很重要,第5位的中心GC对起关键作用。四个不同天然位点的甲基化保护数据证实了在第4、5、6和10位有紧密接触,并表明在碱基对8、12和13处有额外接触。推导的共有序列为RCAAYCCRYNCAYY。使用定量带移分析来确定TUF与其最佳结合位点rpg-1复合物的平衡解离常数。发现特异性解离常数(K8)为1.3×10^(-11) M。将K8值与非特异性DNA位点获得的解离常数(Kn8 = 8.7×10^(-6) M)进行比较,显示出TUF对其特异性RPG靶标的高结合选择性。

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