中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Identification of probable genomic packaging signal sequence from SARS-CoV genome by bioinformatics analysis

文献类型:期刊论文

作者Qin, L; Xiong, B; Luo, C; Guo, ZM; Hao, P; Su, J; Nan, P; Feng, Y; Shi, YX; Yu, XJ
刊名ACTA PHARMACOLOGICA SINICA
出版日期2003-06
卷号24期号:6页码:489-496
关键词severe acute respiratory syndrome (SARS) packaging signal stem-loop structure N protein M protein antisense RNA interfere RNA
ISSN号1671-4083
文献子类Article
英文摘要AIM: To predict the probable genomic packaging signal of SARS-CoV by bioinformatics analysis. The derived packaging signal may be used to design antisense RNA and RNA interfere (RNAi) drugs treating SARS. METHODS: Based on the studies about the genomic packaging signals of MHV and BCoV, especially the information about primary and secondary structures, the putative genomic packaging signal of SARS-CoV were analyzed by using bioinformatic tools. Multi-alignment for the genomic sequences was performed among SARS-CoV, MHV, BCoV, PEDV and HCoV 229E. Secondary structures of RNA sequences were also predicted for the identification of the possible genomic packaging signals. Meanwhile, the N and M proteins of all five viruses were analyzed to study the evolutionary relationship with genomic packaging signals. RESULTS: The putative genomic packaging signal of SARS-CoV locates at the 3' end of ORF1b near that of MHV and BCoV, where is the most variable region of this gene. The RNA secondary structure of SARS-CoV genomic packaging signal is very similar to that of MHV and BCoV. The same result was also obtained in studying the genomic packaging signals of PEDV and HCoV 229E. Further more, the genomic sequence multi-alignment indicated that the locations of packaging signals of SARS-CoV, PEDV, and HCoV overlaped each other. It seems that the mutation rate of packaging signal sequences is much higher than the N protein, while only subtle variations for the M protein. CONCLUSIONS: The probable genomic packaging signal of SARS-CoV is analogous to that of MHV and BCoV, with the corresponding secondary RNA structure locating at the similar region of ORF1b. The positions where genomic packaging signals exist have suffered rounds of mutations, which may influence the primary structures of the N and M proteins consequently.
WOS关键词DEFECTIVE INTERFERING RNAS ; VIRAL ENVELOPE PROTEIN ; MURINE CORONAVIRUS ; VIRUS ; ENCAPSIDATION ; GENE
WOS研究方向Chemistry ; Pharmacology & Pharmacy
语种英语
CSCD记录号CSCD:1272766
WOS记录号WOS:000183575100002
出版者SHANGHAI INST MATERIA MEDICA
源URL[http://119.78.100.183/handle/2S10ELR8/274224]  
专题新药研究国家重点实验室
中科院受体结构与功能重点实验室
通讯作者Shen, X
作者单位1.Chinese Acad Sci, Shanghai Inst Biol Sci, Shanghai Inst Mat Med, State Key Lab Drug Res,Drug Discovery & Design Ct, Shanghai 201203, Peoples R China
2.Shanghai Ctr Bioinformat Technol, Shanghai 201203, Peoples R China
3.Chinese Acad Sci, Shanghai Inst Biol Sci, Shanghai 200031, Peoples R China
4.Fudan Univ, Sch Life Sci, Shanghai 200433, Peoples R China
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GB/T 7714
Qin, L,Xiong, B,Luo, C,et al. Identification of probable genomic packaging signal sequence from SARS-CoV genome by bioinformatics analysis[J]. ACTA PHARMACOLOGICA SINICA,2003,24(6):489-496.
APA Qin, L.,Xiong, B.,Luo, C.,Guo, ZM.,Hao, P.,...&Li, YX.(2003).Identification of probable genomic packaging signal sequence from SARS-CoV genome by bioinformatics analysis.ACTA PHARMACOLOGICA SINICA,24(6),489-496.
MLA Qin, L,et al."Identification of probable genomic packaging signal sequence from SARS-CoV genome by bioinformatics analysis".ACTA PHARMACOLOGICA SINICA 24.6(2003):489-496.

入库方式: OAI收割

来源:上海药物研究所

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