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平颏海蛇CRVP基因全长cDNA片段的克隆和序列分析
引用本文:卫剑文,钟肖芬,彭立胜,吴文言,徐安龙.平颏海蛇CRVP基因全长cDNA片段的克隆和序列分析[J].中山大学学报(自然科学版),2001,40(4):5-8.
作者姓名:卫剑文  钟肖芬  彭立胜  吴文言  徐安龙
作者单位:中山大学生命科学学院
基金项目:国家高新技术海洋领域863资助项目(819-06-06)
摘    要:通过对平颏海蛇毒腺cDNA文库的随机测序和PCR筛选,克隆得到两种分别长为1309和1307bp的编码半胱氨酸丰富毒蛋白(cysteine-rich venom protein,CRVP)的全长cDNA序列。这两种crvp基因同源性为97%,分别编码238和199个氨基酸残基,其中包括一段相同的由19个氨基酸残基组成的信号肽。氨基酸序列分析表明,这两种CRVP蛋白与蜥蜴helothermine毒素蛋白以及台湾饭铲倩CRVP毒蛋白高度同源,而且具有半胱氨酸丰富分泌蛋白(cysteine-rich secretory protein,CRISP)家族的典型结构特征。

关 键 词:平颏海蛇  半胱氨酸丰富毒蛋白  全长cDNA序列  基因克隆  序列分析  序列结构
文章编号:0529-6579(2001)04-0005-04
修稿时间:2000年9月1日

Cloning and Sequence Analysis of Full - Length cDNA Encoding Cysteine - Rich Venom Protein from Lapemis hardwickii
WEI Jian-wen,ZHON Xiao-fen,PENG Li-sheng,WU Wen-yan,XU An-long.Cloning and Sequence Analysis of Full - Length cDNA Encoding Cysteine - Rich Venom Protein from Lapemis hardwickii[J].Acta Scientiarum Naturalium Universitatis Sunyatseni,2001,40(4):5-8.
Authors:WEI Jian-wen  ZHON Xiao-fen  PENG Li-sheng  WU Wen-yan  XU An-long
Abstract:Two full-length cDNA, 1 309 and 1 307 bp in length, for cysteine-rich venom protein (CRVP) were constructed by sequencing and PCR Screening of cDNA clones from a cDNA library of venom gland of Lapemis hardwickii. The sequence identity of two cDNAs was 97%. The predicted CRVP consisted of 238 and 199 amino acid residues including a putative signal peptide of 19 residue, and they were highly homologous to a lizard helother- mine and a Taiwan Habu CRVP. Amino acid sequence analysis suggested that the CRVP had the specific sequence structure, which was conserved in cysteine - rich secretory protein (CRISP) family.
Keywords:Lapemis hardwickii  cysteine-rich venom protein
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