Slattery Matthew, Zhou Tianyin, Yang Lin, Dantas Machado Ana Carolina, Gordân Raluca, Rohs Remo
Department of Biomedical Sciences, University of Minnesota Medical School, Duluth, MN 55812, USA; Developmental Biology Center, University of Minnesota, Minneapolis, MN 55455, USA.
Molecular and Computational Biology Program, Departments of Biological Sciences, Chemistry, Physics, and Computer Science, University of Southern California, Los Angeles, CA 90089, USA.
Trends Biochem Sci. 2014 Sep;39(9):381-99. doi: 10.1016/j.tibs.2014.07.002. Epub 2014 Aug 14.
Transcription factors (TFs) influence cell fate by interpreting the regulatory DNA within a genome. TFs recognize DNA in a specific manner; the mechanisms underlying this specificity have been identified for many TFs based on 3D structures of protein-DNA complexes. More recently, structural views have been complemented with data from high-throughput in vitro and in vivo explorations of the DNA-binding preferences of many TFs. Together, these approaches have greatly expanded our understanding of TF-DNA interactions. However, the mechanisms by which TFs select in vivo binding sites and alter gene expression remain unclear. Recent work has highlighted the many variables that influence TF-DNA binding, while demonstrating that a biophysical understanding of these many factors will be central to understanding TF function.
转录因子(TFs)通过解读基因组内的调控DNA来影响细胞命运。转录因子以特定方式识别DNA;基于蛋白质-DNA复合物的三维结构,已确定了许多转录因子这种特异性背后的机制。最近,结构观点已通过来自许多转录因子DNA结合偏好的高通量体外和体内探索数据得到补充。这些方法共同极大地扩展了我们对转录因子与DNA相互作用的理解。然而,转录因子在体内选择结合位点并改变基因表达的机制仍不清楚。最近的研究突出了影响转录因子与DNA结合的诸多变量,同时表明对这些众多因素的生物物理理解对于理解转录因子功能至关重要。