Hodel A E, Gershon P D, Quiocho F A
Howard Hughes Medical Institute, Department of Biochemistry, Baylor College of Medicine, Houston, Texas 77030, USA.
Mol Cell. 1998 Feb;1(3):443-7. doi: 10.1016/s1097-2765(00)80044-1.
Sequence-nonspecific binding of RNA, recognition of a 7-methylguanosine 5' mRNA cap, and methylation of a nucleic acid backbone are three crucial and ubiquitous events in eukaryotic nucleic acid processing and function. These three events occur concurrently in the modification of vaccinia transcripts by the methyltransferase VP39. We report the crystal structure of a ternary complex comprising VP39, coenzyme product S-adenosylhomocysteine, and a 5' m7 G-capped, single-stranded RNA hexamer. This structure reveals a novel and general mechanism for sequence-non-specific recognition of the mRNA transcript in which the protein interacts solely with the sugar-phosphate backbone of a short, single-stranded RNA helix. This report represents the first direct and detailed view of a protein complexed with single-stranded RNA or 5'-capped mRNA.
RNA的序列非特异性结合、对7-甲基鸟苷5' mRNA帽的识别以及核酸主链的甲基化是真核生物核酸加工和功能中三个关键且普遍存在的事件。这三个事件在痘苗病毒转录本由甲基转移酶VP39进行修饰的过程中同时发生。我们报道了一个三元复合物的晶体结构,该复合物由VP39、辅酶产物S-腺苷同型半胱氨酸以及一个5' m7G加帽的单链RNA六聚体组成。此结构揭示了一种对mRNA转录本进行序列非特异性识别的新颖且通用的机制,其中蛋白质仅与短单链RNA螺旋的糖磷酸主链相互作用。本报告首次直接且详细地展示了与单链RNA或5'-加帽mRNA复合的蛋白质。