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枇杷胚性培养物ACC氧化酶基因的克隆及序列分析
引用本文:音建华,赖钟雄,林玉玲,李惠华,李丽秀.枇杷胚性培养物ACC氧化酶基因的克隆及序列分析[J].热带作物学报,2012,33(3):433-438.
作者姓名:音建华  赖钟雄  林玉玲  李惠华  李丽秀
作者单位:福建农林大学园艺植物生物工程研究所,福建福州,350002
基金项目:福建省亚热带果树及特种经济作物种质资源共享平台(No.2008N2001);国家科技支撑计划(No.2007BAD07B01)资助项目的部分内容。
摘    要:以枇杷胚性培养物(Eriobotrya japonica embryonic cultures)为材料,采用同源克隆方法,从其mRNA中分离得到ACC氧化酶(ACO)基因EjACO-1,在GenBank中登录号为GQ377219。结果表明:EjACO-1大小为 1 160 bp,编码322个氨基酸。枇杷EjACO-1与苹果、桃和梨等蔷薇科植物同源性较高,而与水稻、石斛兰等单子叶植物距离较远。此外,从枇杷基因组DNA中分离了转录为EjACO-1 mRNA的基因gACO,大小为1 517 bp,在GenBank中的登录号为GU233743。生物信息学分析显示,gACO基因中含有3个内含子,大小分别为114、240、194 bp,均符合真核生物内含子通用的GT-AG法则。EjACO基因的克隆为以后研究乙烯在枇杷中的功能奠定基础。

关 键 词:枇杷胚性培养物  ACC氧化酶  基因克隆  基因组DNA  序列分析

Cloning and Sequence Analysis of ACC Oxidase Gene from Eriobotrya japonica Embryonic Cultures
YIN Jianhu,LAI Zhongxiong,LIN Yuling,LI Huihua and LI Lixiu.Cloning and Sequence Analysis of ACC Oxidase Gene from Eriobotrya japonica Embryonic Cultures[J].Chinese Journal of Tropical Crops,2012,33(3):433-438.
Authors:YIN Jianhu  LAI Zhongxiong  LIN Yuling  LI Huihua and LI Lixiu
Institution:Institute of Horticultural Biotechnology, Fujian Agriculture and Forestry University,;Institute of Horticultural Biotechnology, Fujian Agriculture and Forestry University,;Institute of Horticultural Biotechnology, Fujian Agriculture and Forestry University,;Institute of Horticultural Biotechnology, Fujian Agriculture and Forestry University,;Institute of Horticultural Biotechnology, Fujian Agriculture and Forestry University,
Abstract:Homologous cloning method was used to clone the 1-aminocyclopropane-1-carboxylic acid oxidase(ACO)gene,EjACO-1,Eriobotrya japonica embryonic cultures.The gene,GenBank accession number GQ377219,was of 1 160 bp,encoding 322 amino acids,and highly homologous to other rosaceous plants origins(Malus x domestica,Prunus persica,Pyrus pyrifolia and so on),and was distant from that of monocotyledons(Oryza sativa,Dendrobium and so on).Moreover,gACO,which encoding EjACO-1 mRNA,was obtained from the genomic DNA.The length of gACO was 1 517 bp,and the accession number was GU180353 in GenBank.The gACO gene contained 3 introns consistent with the GT-AG dogma for eukaryotic introns,with lengths 114,240 and 194 bp,respectively.The cloning of EjACO provides a foundation for further study of ethylene function in Eriobotrya japonica.
Keywords:Eriobotrya japonica embryonic cultures  ACC oxidase  Gene cloning  Genomic DNA  Sequence analysis
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