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尾巨桉HMGR基因的克隆及表达分析

蒋春 张华玲 彭江

广西植物2012,Vol.32Issue(1):113-117,5.
广西植物2012,Vol.32Issue(1):113-117,5.DOI:10.3969/j.issn.1000-3142.2012.01.022

尾巨桉HMGR基因的克隆及表达分析

Molecular Cloning and expression analysis of 3-hydroxy-3-methylglutaryl-CoA Reductase Gene from Eucalyptus urophylla × E.grandis

蒋春 1张华玲 2彭江2

作者信息

  • 1. 四川大学生命科学学院生物资源与生态环境教育部重点实验室,四川成都610064
  • 2. 西南大学生命科学学院三峡库区生态环境教育部重点实验室,重庆400715
  • 折叠

摘要

Abstract

The gene encoding 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR)was cloned by Rapid Amplification of cDNA Ends (RACE)method, the full-length EuHMGR cDNA was 1955 bp, containing a 1 560 bp open reading frame, encoding a peptide of 519 amino acids. Bioinformatics analysis indicated EuHMGR contained two HMG-CoA binding motifs and two NADP(H)binding motifs;and it had a 3-D structure with"V"homology-based on modeling, containing N-domain,S-domain and L-domain. There was a 319 bp intron in EuHMGR gene genomic DNA sequence compared with the cDNA sequence. Tissue expression profile analysis by Real-Time quantitative PCR indicated EuHMGR expression was the highest in stem,followed by leaf and no expression in root. The paper would supply some information to the function analysis and genetic transformation of EuHMGR from Eucalyptus urophylla × E. grandis.

关键词

尾巨桉/HMGR/生物信息学/内含子/组织特异性表达

Key words

Eucalyptus urophyla×E. grandis/ HMGR/ bioinformatics/ intron/ tissue specific expression

分类

农业科技

引用本文复制引用

蒋春,张华玲,彭江..尾巨桉HMGR基因的克隆及表达分析[J].广西植物,2012,32(1):113-117,5.

基金项目

重庆市自然科学基金重点项目(2009BA1004) (2009BA1004)

三峡库区生态环境教育部重点实验室开放基金(EF200609) (EF200609)

广西植物

OA北大核心CSCDCSTPCD

1000-3142

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