Stein Adam J, Fuchs Gabriele, Fu Chunmei, Wolin Sandra L, Reinisch Karin M
Department of Cell Biology, Yale University School of Medicine, New Haven, Connecticut 06510.
Department of Cell Biology, Yale University School of Medicine, New Haven, Connecticut 06510; Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut 06510.
Cell. 2005 May 20;121(4):529-539. doi: 10.1016/j.cell.2005.03.009.
The Ro 60 kDa autoantigen is a major target of the immune response in patients with systemic lupus erythematosus. In vertebrate cells, Ro binds misfolded small RNAs and likely functions in RNA quality control. In eukaryotes and bacteria, Ro also associates with small RNAs called Y RNAs. We present structures of unliganded Ro and Ro complexed with two RNAs at 1.95 and 2.2 A resolution, respectively. Ro consists of a von Willebrand factor A domain and a doughnut-shaped domain composed of HEAT repeats. In the complex, a fragment of Y RNA binds on the outer surface of the HEAT-repeat ring, and single-stranded RNA binds in the toroid hole. Mutagenesis supports a binding site for misfolded RNAs that encompasses both sites, with a single-stranded end inserted into the toroid cavity. Our experiments suggest that one role of Y RNAs may be to regulate access of other RNAs to Ro.
Ro 60 kDa自身抗原是系统性红斑狼疮患者免疫反应的主要靶点。在脊椎动物细胞中,Ro与错误折叠的小RNA结合,可能在RNA质量控制中发挥作用。在真核生物和细菌中,Ro还与称为Y RNA的小RNA相关联。我们分别以1.95 Å和2.2 Å的分辨率展示了未结合配体的Ro以及与两种RNA复合的Ro的结构。Ro由一个血管性血友病因子A结构域和一个由HEAT重复序列组成的甜甜圈形结构域组成。在复合物中,Y RNA的一个片段结合在HEAT重复序列环的外表面,单链RNA结合在环形孔中。诱变支持一个包含两个位点的错误折叠RNA结合位点,单链末端插入环形腔中。我们的实验表明,Y RNA的一个作用可能是调节其他RNA与Ro的结合。