Wilkinson-White Lorna, Lester Krystal L, Ripin Nina, Jacques David A, Mitchell Guss J, Matthews Jacqueline M
School of Molecular Bioscience, The University of Sydney, Sydney, New South Wales, 2042, Australia.
Protein Sci. 2015 Oct;24(10):1649-59. doi: 10.1002/pro.2760. Epub 2015 Aug 20.
The transcription factor GATA1 helps regulate the expression of thousands of genes involved in blood development, by binding to single or double GATA sites on DNA. An important part of gene activation is chromatin looping, the bringing together of DNA elements that lie up to many thousands of basepairs apart in the genome. It was recently suggested, based on studies of the closely related protein GATA3, that GATA-mediated looping may involve interactions of each of two zinc fingers (ZF) with distantly spaced DNA elements. Here we present a structure of the GATA1 ZF region bound to pseudopalindromic double GATA site DNA, which is structurally equivalent to a recently-solved GATA3-DNA complex. However, extensive analysis of GATA1-DNA binding indicates that although the N-terminal ZF (NF) can modulate GATA1-DNA binding, under physiological conditions the NF binds DNA so poorly that it cannot play a direct role in DNA-looping. Rather, the ability of the NF to stabilize transcriptional complexes through protein-protein interactions, and thereby recruit looping factors such as Ldb1, provides a more compelling model for GATA-mediated looping.
转录因子GATA1通过与DNA上的单或双GATA位点结合,帮助调控数千个参与血液发育的基因的表达。基因激活的一个重要部分是染色质环化,即将基因组中相距数千个碱基对的DNA元件聚集在一起。最近,基于对密切相关蛋白GATA3的研究表明,GATA介导的环化可能涉及两个锌指(ZF)中的每一个与远距离间隔的DNA元件的相互作用。在这里,我们展示了与假回文双GATA位点DNA结合的GATA1 ZF区域的结构,其在结构上等同于最近解析的GATA3-DNA复合物。然而,对GATA1-DNA结合的广泛分析表明,尽管N端锌指(NF)可以调节GATA1-DNA结合,但在生理条件下,NF与DNA的结合非常差,以至于它不能在DNA环化中发挥直接作用。相反,NF通过蛋白质-蛋白质相互作用稳定转录复合物,从而招募诸如Ldb1等环化因子的能力,为GATA介导的环化提供了一个更有说服力的模型。