首页|绿竹光系统Ⅰ捕光叶绿素a/b结合蛋白基因的cDNA全长克隆及分析

绿竹光系统Ⅰ捕光叶绿素a/b结合蛋白基因的cDNA全长克隆及分析

扫码查看
为了从分子水平研究竹子光合作用的机理,采用RT-PCR及RACE方法从绿竹中分离了cab家族的一个基因,命名为BoLhca4-1(GenBank注册号为EF690303).BoLhca4-1的cDNA序列全长931 bp.含有一个735 bp的开放阅读框,编码了一个244 aa的蛋白,分子量大小约为26.8 ku.序列分析结果表明,BoLhcn4-1是光系统Ⅰ的一个捕光叶绿素复合蛋白基因,编码肽链与禾本科植物水稻的cab蛋白有着很高的同源性,达到86.1%.系统进化树分析表明,BoLhca4-1编码蛋白与水稻的cab蛋白亲缘关系较近.另外,对绿竹不同组织中BoLco4-1基因的表达进行RT-PCR检测发现,其在叶片中的表达量较鞘和茎中要高.
Cloning and characterization of a full cDNA of photosystem I gene encoding the light harvesting chlorophyll a/b-binding protein from Bambusa oldhamii
To study the molecular mechanism of photosynthesis, the BoLhca4-1 (GenBank accession number; EF690303) , a member of the cab gene family, was isolated from Bambusa oldhamii by RT-PCR and RACE. The cDNA of BoLhca4-1 is 931 bp in length,which contains an 735 bp open reading frame (ORF) , encoding a poly-peptide of 244 amino acids with predicted molecular mass of 26. 8 ku. The results of sequence analysis showed that the BoLhca4-1 is a cab binding protein gene of photosystem Ⅰ and its encoding protein is highly homologous to the cab protein from rice with 86.1% identity. In addition, it was found that the Lhca4-1 was more related to the rice cab protein from the Phylogenetic tree. Based on the RT-PCR method, it was identified that BoLhcaAA gene displays a higher expression level in leaf tissue than that in sheath and stem.

Bambusa oldhamiiphotosystem Ⅰlight harvesting chlorophyll a/b-binding protein (cab)gene cloningexpression analysis

李雪平、彭镇华、高志民、牟少华

展开 >

国际竹藤网络中心国家林业局竹藤科学与技术重点开放实验室,北京,100102

中国林业科学研究院林业研究所,北京,100091

绿竹 光系统1 捕光叶绿素a/b结合蛋白 基因克隆 表达分析

林业公益性行业科研专项国家自然科学基金国际竹藤网络中心基本科研业务费重点项目

200704001309723281632008002

2010

安徽农业大学学报
安徽农业大学

安徽农业大学学报

CSTPCDCSCD北大核心
影响因子:0.412
ISSN:1672-352X
年,卷(期):2010.37(4)
  • 7
  • 8