Structural perspective of cooperative transcription factor binding

被引:143
作者
Morgunova, Ekaterina [1 ]
Taipale, Jussi [1 ,2 ]
机构
[1] Karolinska Inst, Dept Med Biochem & Biophys, SE-17177 Stockholm, Sweden
[2] Univ Helsinki, Genome Scale Biol Res Program, POB 63, FI-00014 Helsinki, Finland
基金
瑞典研究理事会;
关键词
DNA RECOGNITION; CRYSTAL-STRUCTURE; GENE-REGULATION; ZINC FINGERS; RUNT DOMAIN; POU DOMAIN; CBF-BETA; IN-VIVO; COMPLEX; PROTEINS;
D O I
10.1016/j.sbi.2017.03.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In prokaryotes, individual transcription factors (TFs) can recognize long DNA motifs that are alone sufficient to define the genes that they induce or repress. In contrast, in higher organisms that have larger genomes, TFs recognize sequences that are too short to define unique genomic positions. In addition, development of multicellular organisms requires molecular systems that are capable of executing combinatorial logical operations. Co-operative recognition of DNA by multiple TFs allows both definition of unique genomic positions in large genomes, and complex information processing at the level of individual regulatory elements. The TFs can co-operate in multiple different ways, and the precise mechanism used for co-operation determines important features of the regulatory interactions. Here, we present an overview of the structural basis of the different mechanisms by which TFs can cooperate, focusing on insight from recent functional studies and structural analyses of specific TF-TF-DNA complexes.
引用
收藏
页码:1 / 8
页数:8
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