Werner M H, Huth J R, Gronenborn A M, Clore G M
Laboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-0520, USA.
Cell. 1995 Jun 2;81(5):705-14. doi: 10.1016/0092-8674(95)90532-4.
The solution structure of the specific complex between the high mobility group (HMG) domain of SRY (hSRY-HMG), the protein encoded by the human testis-determining gene, and its DNA target site in the promoter of the müllerian inhibitory substance gene has been determined by multidimensional NMR spectroscopy. hSRY-HMG has a twisted L shape that presents a concave surface (made up of three helices and the N- and C-terminal strands) to the DNA for sequence-specific recognition. Binding of hSRY-HMG to its specific target site occurs exclusively in the minor groove and induces a large conformational change in the DNA. The DNA in the complex has an overall 70 degrees-80 degrees bend and is helically unwound relative to classical A- and B-DNA. The structure of the complex reveals the origin of sequence-specific binding within the HMG-1/HMG-2 family and provides a framework for understanding the effects of point mutations that cause 46X,Y sex reversal at the atomic level.
人类睾丸决定基因所编码的蛋白质——SRY的高迁移率族(HMG)结构域(hSRY-HMG)与其在苗勒管抑制物质基因启动子中的DNA靶位点之间特异性复合物的溶液结构,已通过多维核磁共振光谱法测定。hSRY-HMG呈扭曲的L形,其凹面(由三条螺旋以及N端和C端链组成)朝向DNA用于序列特异性识别。hSRY-HMG与其特异性靶位点的结合仅发生在小沟中,并诱导DNA发生大的构象变化。复合物中的DNA整体弯曲70度至80度,相对于经典的A-DNA和B-DNA呈螺旋解旋状态。该复合物的结构揭示了HMG-1/HMG-2家族内序列特异性结合的起源,并为在原子水平上理解导致46,X,Y性反转的点突变的影响提供了一个框架。