野桑蚕酚氧化酶原基因PPO1的克隆及其特征(英文)  

Cloning and characterization of Bombyx mandarina prophenoloxidase gene PPO1

作　　者：张永亮[1] 盛东峰[1] 朱勇[2] 

机构地区：[1]周口师范学院生命科学系,河南周口466001 [2]西南大学生物技术学院,重庆400715

出　　处：《浙江大学学报（农业与生命科学版）》2012年第3期256-262,共7页Journal of Zhejiang University:Agriculture and Life Sciences

基　　金：Project supported by National Basic Research Program of China(040208);Special Foundation for Doctoral Discipline of Ministry of Education of China(20060635008);the Key Discipline Construction of Zhoukou Normal University

摘　　要：利用反转录-聚合酶链式反应(RT-PCR)克隆野桑蚕(Bombyx mandarina)酚氧化酶原基因PPO1,获得其cDNA序列;该序列长2 086bp,含有一个2 058bp的完整开放阅读框,编码一个由685个氨基酸残基组成的蛋白质;该基因推导的氨基酸序列与其他鳞翅目昆虫PPO1基因相应的氨基酸序列有较高的同源性,该序列具有它们的PPO基因所共有的典型特征。RT-PCR检测分析表明该基因仅在野桑蚕的头部和血液中表达,而Northern杂交检测表明该基因仅在血液中有表达。这些结果为进一步研究该基因的功能提供了分子基础。The complemental deoxyribonucleic acid（cDNA）of Bombyx rnandarina prophenoloxidase gene PP01 was cloned by reverse transcription-polymerase chain reaction （RT-PCR）. The results showed that the cDNA with 2 086 bp in length contained an open reading frame （ORF） of 2 058 bp which encoded 685 amino acid residues. The deduced amino acid sequence had a high identity to the reported sequence of PP01 from other lepidopterous insects and shared the typical structural features of PPO from other insects. The PP01 gene was only expressed in head and blood of B. mandarina by RT-PCR, and only expressed in blood by Northern blot analysis. These results provide a molecular basis for further studying the function of PP01 gene in B. mandarina.

关 键 词：野桑蚕 酚氧化酶原基因PPO1 克隆 序列分析 基因表达 

分 类 号：Q78[生物学—分子生物学] Q966