The Structural Basis of Pathogenic Subgenomic Flavivirus RNA (sfRNA) Production

被引:217
作者
Chapman, Erich G. [1 ,2 ]
Costantino, David A. [1 ,2 ]
Rabe, Jennifer L. [1 ]
Moon, Stephanie L. [3 ]
Wilusz, Jeffrey [3 ]
Nix, Jay C. [4 ]
Kieft, Jeffrey S. [1 ,2 ]
机构
[1] Univ Colorado Denver, Sch Med, Dept Biochem & Mol Genet, Aurora, CO 80045 USA
[2] Univ Colorado Denver, Sch Med, Howard Hughes Med Inst, Aurora, CO 80045 USA
[3] Colorado State Univ, Dept Microbiol Immunol & Pathol, Ft Collins, CO 80523 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Adv Light Source, Mol Biol Consortium, Berkeley, CA 94720 USA
关键词
JAPANESE ENCEPHALITIS-VIRUS; MESSENGER-RNA; WEST-NILE; MOSQUITO CELLS; DENGUE; RESISTANT; XRN1;
D O I
10.1126/science.1250897
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Flaviviruses are emerging human pathogens and worldwide health threats. During infection, pathogenic subgenomic flaviviral RNAs (sfRNAs) are produced by resisting degradation by the 5'-> 3' host cell exonuclease Xrn1 through an unknown RNA structure-based mechanism. Here, we present the crystal structure of a complete Xrn1-resistant flaviviral RNA, which contains interwoven pseudoknots within a compact structure that depends on highly conserved nucleotides. The RNA's three-dimensional topology creates a ringlike conformation, with the 5' end of the resistant structure passing through the ring from one side of the fold to the other. Disruption of this structure prevents formation of sfRNA during flaviviral infection. Thus, sfRNA formation results from an RNA fold that interacts directly with Xrn1, presenting the enzyme with a structure that confounds its helicase activity.
引用
收藏
页码:307 / 310
页数:4
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