华北农学报 ›› 2011, Vol. 26 ›› Issue (2): 39-42. doi: 10.7668/hbnxb.2011.02.009

所属专题: 杂粮作物 植物保护 生物技术

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谷子弯孢病菌Clga-1基因克隆及特征分析

李志勇1, 谢夏青2, 董金皋3, 董志平1   

  1. 1. 河北省农林科学院谷子研究所, 河北石家庄, 050031;
    2. 南京农业大学生命学院, 江苏南京, 210095;
    3. 河北农业大学生命科学学院, 河北保定, 071001
  • 收稿日期:2011-01-29 出版日期:2011-04-28
  • 作者简介:李志勇(1976-),男,河北邯郸人,助理研究员,主要从事谷子病害研究.
  • 基金资助:
    国家自然科学基金项目(30771354);河北省自然科学基金项目(C2004000699)

Molecular Cloning and Characterization of Clga-1 in Cochliobolus lunatus

LI Zhi-yong1, XIE Xia-qing2, DONG Jin-gao3, DONG Zhi-ping1   

  1. 1. Millet Institute of Hebei Academy of Agriculture and Forestry Sciences, Shijiazhuang 050031, China;
    2. College of Life Science, Nanjing Agricultural University, Nanjing 210095, China;
    3. College of Life Science, Agricultural University of Hebei, Baoding 071001, China
  • Received:2011-01-29 Published:2011-04-28

摘要: 谷子弯孢病菌(Cochliobolus lunatus)引起的谷子叶斑病是谷子生产上的重要病害之一,常造成严重经济损失.本研究利用候选基因法和RACE技术克隆了谷子弯孢病菌中的1个Ga基因,命名为Clga-1,在GeneBank登陆号为HQ699081.Clga-1基因开放阅读框为l 062 bp,编码353个氨基酸多肽,该开放阅读框被3个大小分别为57,9,59 bp的内含子隔开.聚类分析结果表明,谷子弯孢病菌Clga-1基因与其他植物病原真菌Ga基因的同源性很高,Southern杂交结果表明该基因以单拷贝形式存在.Clga-1基因具有其他病原真菌Ga基因具有的保守结构,如在氮端有豆蔻酰化位点,碳端具有ADP核糖基化位点.谷子弯孢病菌Clga-1基因的克隆,为进一步研究Clga-1基因在该菌致病过程中的功能奠定基础.

关键词: 谷子弯孢病菌, 异三聚体G蛋白, RACE, 序列分析

Abstract: Cochliobolus lunatus is a destructive pathogen of foxtail millet and causes significant yield losses.A G protein alpha protein genes named cfga-J(Genbank accession number:HQ69908 1)was cloned using degenerate PCR and RACE method from Cochliobolus lunatus.The predicated C/as-J gene contains a 1062 bp ORF and it was interrupted by three small introns of 57,49,59 bp.The Ctga-J gene encodes a polypeptide of 353 amino acids and phylogenetic analysis showed CtgoL-1 gene was similarity to the Ga subunit of other fungi.The analysis of Southern bloting indicated that there was a single copy of Clgct-j gene in the genome.Clga-Z gene also contained conservative motifs among the Got protein family,such as sites for myristoylation at the N-terminus,ADP-ribosylation by pertussis toxin at the C-terminus.The cloning of the gene will lay afoundation for further functional analysis of heterotrimericG protein signal transduction pathway in Cochliobolus lunatus.

Key words: Cochliobolus lunatus, Heterotrimeric G protein, RACE, Equence analysis

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引用本文

李志勇, 谢夏青, 董金皋, 董志平. 谷子弯孢病菌Clga-1基因克隆及特征分析[J]. 华北农学报, 2011, 26(2): 39-42. doi: 10.7668/hbnxb.2011.02.009.

LI Zhi-yong, XIE Xia-qing, DONG Jin-gao, DONG Zhi-ping. Molecular Cloning and Characterization of Clga-1 in Cochliobolus lunatus[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2011, 26(2): 39-42. doi: 10.7668/hbnxb.2011.02.009.

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