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少棘蜈蚣毒素多肽SsmTx1全长cDNA的克隆和序列分析 被引量:1

Cloning and Characterization of a Novel Full-Length cDNA Sequence of Venom Peptide SsmTx1 from the Centipede Scolopendra subspinipes Mutilans
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摘要 构建了少棘蜈蚣毒腺组织cDNA文库.运用PCR方法从少棘蜈蚣(Scolopendra subspinipes mutilans)毒腺组织cDNA文库中筛选到一个全新的毒素多肽cDNA序列,命名为SsmTx1.SsmTx1全长为417 nt,3′和5′非编码区(UTR)分别为120 nt和54 nt,其加尾信号aataaa在距离poly(A)上游16 nt.SsmTx1序列含有一个240nt的开放阅读框(ORF),共编码80个氨基酸残基,其中包括25个氨基酸的信号肽序列和55个氨基酸的成熟毒素多肽序列,含有2对二硫键.SsmTx1毒素基因是从少棘蜈蚣毒中分离鉴定的全长毒素多肽. A cDNA library was successfully constructed from the venom gland of the centipede Scolopendra subspinipes mutilans.A novel centipede toxin gene,named SsmTx1,was isolated and characterized from the venom gland cDNA library of the centipede Scolopendra subspinipes mutilans by PCR method.The full-length cDNA sequence of SsmTx1 has 417 nt length,including 120 nt 3′ non-coding region(UTR) and 54 nt 5′ non-coding region.Its signal tail aataaa lies at the 16 nt upstream of poly(A) tail.The cDNA sequence contains a 240 nt open reading frame(ORF) with a total encode of 80 amino acid residues including 25 amino acid residues of the signal peptide and 55 amino acid residues of the mature peptide bridged by two pairs of disulfide bonds.SsmTx1 is the first full-length toxin gene from the centipede Scolopendra subspinipes mutilans.
出处 《武汉大学学报(理学版)》 CAS CSCD 北大核心 2010年第3期331-335,共5页 Journal of Wuhan University:Natural Science Edition
基金 国家自然科学基金资助项目(30800571)
关键词 少棘蜈蚣 CDNA 毒素多肽 Scolopendra subspinipes mutilans cDNA toxic peptide
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参考文献20

  • 1Stoev P. A Catalogue and Key to the Centipedes (Chilopoda) of Bulgaria[M]. Sofia-Moscow:Pensoft,2002 : 103.
  • 2Minelli A. Secretions of Centipedes. Arthropod Venoms , Handbook of Experimental Pharmacology[M]. New York: Springer-Verlag, 1978 : 74-83.
  • 3Dai C, Ma Y, Zhao Z,et al. Mucroporin, the first cationic host defense peptide from the venom of Lychas mucronatus[J]. Antimicrob Agents Chemother , 2008, 52:3967-3972.
  • 4马一保.蝎毒素基因的分离与鉴定及其分子进化研究[D].武汉:武汉大学,2009.
  • 5Melen G J, Pesce C G, Rossi M S,et al. Novel processing in a mammalian nuclear 28S pre-rRNA:Tissue- specific elimination of an 'intron ' bearing a hidden break site[J]. The EMBO Journal, 1999, 18: 3107- 3118.
  • 6Possani L D, Merino E, Corona M,etal. Peptides and genes coding for scorpion toxins that affect ion-channels[J]. Biochimie, 2000,82 : 861-868.
  • 7Cao Z J, Luo F, Wu Y L,et al. Genetic mechanisms of scorpion venom peptide diversification[J]. Toxicon, 2006,47:348-355.
  • 8Rodriguez de la, Vega R C, Possani L D. Current views on scorpion toxins specific for K^+-channels[J]. Toxicon, 2004,43 : 865-875.
  • 9Fry B G. From genome to "venome": molecular origin and evolution of the snake venom proteome inferred from phylogenetic analysis of toxin sequences and related body proteins [J]. Genome research, 2005, 15: 403-420.
  • 10He Q Y, He Q Z, Deng X C,etal. ATDB:A uni-database platform for animal toxins[J]. Nucleic Acids Research , 2008,36 : 293-297.

二级参考文献4

  • 1凌沛深,董黎辉.药用少棘蜈蚣取毒试验[J]动物学杂志,1988(04).
  • 2冉永禄,AnthonyT.Tu.巨蝮蛇(Lachesis muta)毒出血毒素的纯化和性质研究[J]动物学研究,1987(04).
  • 3汪猷,陈耀全,韩友娣,张云岩,徐寿龙,谢慧琴.蜈蚣粗毒的生物活性[J]科学通报,1985(03).
  • 4吴兴陆,陈远聪.我国十种蛇毒磷酯酶A的活力比较[J].Zoological Research,1981,2(S01):23-26. 被引量:4

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