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甲型流感病毒H5N1的siRNA设计 被引量:2

siRNA DESIGN TO THE H5N1 SUBTYPE OF INFLUENZA A VIRUS
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摘要 选用了甲型流感病毒 10个毒株 (全序列 )和一个 2 0 0 4年越南毒株 (部分序列 ) ,采用自己编写的计算机程序sRNAFinder,对每个毒株的 6个RNA片段的 6个编码序列进行了siRNA设计 .结合系统发育重建方法 ,利用sRNAFind er的共有序列分析功能 ,对得到的 6 10 1个siRNA分子进行了计算机筛选 .结果表明 ,设计的siRNA的分子 ,针对np和pb1应该是最有效的 ,而针对ha和na的siRNA分子设计 ,需要疾病流行期毒株的最新测序数据 ;从ns1的数据不能获得很保守的、可作为预防或治疗药物的siRNA分子 .图 1表 4参 Six complete coding sequences (cds), pb2, pb1, ha, np, na, and ns1, of 10 species of influenza A virus (IAV), including 7 species of H5N1 subtype, 1 species of H1N1 subtype, 1 species of H6N1 subtype and 1 species of H9N2 subtype, and 6 partial cds of a Vietnam species (H5N1 subtype) were scanned using the program sRNAFinder. The 6101 siRNAs were screened using the consensus analysis of the program after phylogenetic analysis (6 phylogeny trees) of the 11 species. The results indicate (i) siRNAs specific for pb1 and np could be appropriate vaccine candidate, (ii) siRNAs specific for ha or na need the sequences of IAV strain isolated from pandemic, (iii) siRNAs specific for ns1 couldn′t be candidate of prophylaxis and therapy for IAV infection. Fig 1, Tab 4, Ref 16
出处 《应用与环境生物学报》 CAS CSCD 2004年第1期133-138,共6页 Chinese Journal of Applied and Environmental Biology
关键词 甲型流感病毒 SIRNA 系统发育重建 计算机筛选 禽流感 influenza A virus H5N1 subtype siRNA sRNAFinder program phylogenetic reconstruction computer screening
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  • 1..http://www. ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax. cgi id =227859.,.
  • 2Holmes KV. SARS - Associated Coronavirus. N Engl J Med, 2003,348(20) :1948 - 1951.
  • 3Ksiazek TG, et al. A Novel Coronavirus Associated with Severe Acute Respiratory Syndrome. N Engl J Med, 2003,348(20) : 1953 - 1966.
  • 4Rota PA, et al. Characterization of a novel coronavirus associated with severe acute respiratory syndrome. Science, 2003,300 : 1394 - 1399.
  • 5Marra MA, et al. The Genome Sequence of the SARS - Associated Coronavirus. Science, 2003,300 : 1399 - 1404.
  • 6Holmes KV. SARS coronavirus: a new challenge for prevention and therapy. J Clin Invest, 2003, 111 ( 11 ) : 1605 - 1609.
  • 7Check E. Gene regulation: RNA to the rescue? nature, 2003,425:10 -12.
  • 8Zhang Y, Xu JY, Deng W, Zhang N, Cai L, Zhao Y, Bu DB, Chen RS. siRNA designs to the crucial proteins of SAILS coronavims. Prog Biochem Biophys, 2003,30 (3) : 335 - 338.
  • 9Dykxhoom DM, Novina CD, Sharp PA. Killing the messenger: short mas that silence gene expression. Nat Rev Mol Cell Biol, 2003, 4(6) :457 - 467.
  • 10Tavitian B. In vivo imaging with oligonucleotides for diagnosis and drug development. Gut, 2003 ,52( Suppl IV) :iv40 iv47.

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  • 1康洁,刘福林.RNAi的抗病毒作用及其机制[J].现代免疫学,2004,24(5):439-440. 被引量:14
  • 2李阳,倪兵,石辛甫,王希良,何仰东,肖宇,姜曼,黎万玲,吴玉章.质粒表达型siRNA对SARS-CoV复制与感染干扰的初步研究[J].第三军医大学学报,2005,27(2):91-94. 被引量:5
  • 3王芳芳,马志强,王素华.基于遗传算法的序列比对方法[J].吉林大学学报(信息科学版),2006,24(4):423-429. 被引量:6
  • 4许德晖,黄辰,刘利英,宋土生.高效siRNA设计的研究进展[J].遗传,2006,28(11):1457-1461. 被引量:21
  • 5Elbashir S M, Harborth J, Weber K, et al. Analysis of gene function in somatic mammalian cells using small interfering RNAs [J]. Methods, 2002,26 ( 2 ) : 199-212.
  • 6Reynolds A, Leake D, Boese Q, et al. Rational siR- NA design for RNA interference[J].Natbiotee-hnol, 2004,22(3) : 326-330.
  • 7Amarzguioui M,Prydz H. An algorithm for selection of functional siRNA sequences [J]. Biochem Bioph Res Co,2004,316(4): 1050-1058.
  • 8Chalk A M,Wahlestedt C,Sonnhammer E L L. Improved and automated prediction of effective siRNA [J]. Biochem Bioph Res Co,2004,319(1):264-274.
  • 9Guo S,Kemphues KJ.Par-1,a gene required for establishing polarity in C.elegans embryos,encodes a putative Ser/Thr kinase that is asymmetrically distributed [J].Cell,1995,81 (4) :611-620.
  • 10Fire A,Xu S,Mello CC ,et al.Potent and specific genetic interference by double stranded RNA in Caenorhabditis elegans [J].Nature,1998,391(6669) :806-811.

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