中国农业科学 ›› 2013, Vol. 46 ›› Issue (8): 1603-1609.doi: 10.3864/j.issn.0578-1752.2013.08.009

• 植物保护 • 上一篇    下一篇

玉米大斑病菌转录因子StSte12的表达特性分析及其调控基因的筛选

 张长志, 李坡, 谷守芹, 巩校东, 杨阳, 范钰, 田兰, 张晓玉, 韩建民, 董金皋   

  1. 1.河北农业大学真菌毒素与植物分子病理学实验室,河北保定 071001
    2.河北省农林科学院植物保护研究所,河北保定 071000
  • 收稿日期:2012-12-24 出版日期:2013-04-15 发布日期:2013-02-04
  • 通讯作者: 通信作者董金皋,Tel:0312-7528124;E-mail:dongjingao@126.com
  • 作者简介:张长志,E-mail:zcz_1201@126.com;李坡,E-mail:lipo-0524@163.com。张长志与李坡为同等贡献作者
  • 基金资助:

    国家自然科学基金(30471126)、河北省自然科学基金(C2012204033)

StSte12 Expression Characteristics and Preliminary Screening of Its Regulatory Genes in Setosphaeria turcica

 ZHANG  Chang-Zhi, LI  Po, GU  Shou-Qin, GONG  Xiao-Dong, YANG  Yang, FAN  Yu, TIAN  Lan, ZHANG  Xiao-Yu, HAN  Jian-Min, DONG  Jin-Gao   

  1. 1.Mycotoxin and Molecular Plant Pathology Laboratory, Agricultural University of Hebei, Baoding 071000, Hebei
    2.Plant Protection Institute, Hebei Academy of Agriculture and Forestry Sciences, Baoding 071000, Hebei
  • Received:2012-12-24 Online:2013-04-15 Published:2013-02-04

摘要: 【目的】确定玉米大斑病菌转录因子StSte12在基因组中的位置,分析目的蛋白质StSte12的结构特征;明确StSTE12在病菌不同发育时期的表达情况;筛选可能受StSte12转录因子调控的基因,分析其匹配序列的结构特征,并比较它们在病菌的中表达情况。【方法】利用生物信息学方法,确定StSte12在玉米大斑病菌基因组中的位置并解析目的蛋白质StSte12的结构特征;利用Western blot技术分析StSTE12在病菌不同发育时期的表达规律;根据酿酒酵母Ste12转录因子的下游调控基因,筛选病菌中可能受StSte12调控的功能基因;并利用生物信息学方法得出下游调控基因的结合位点;利用RT-PCR技术,分析这些基因在StSTE12 RNAi转化子与野生型菌株中的表达情况。【结果】StSTE12的 ID为105656,该基因位于scaffold_13正链的1061747-1064127位置;该蛋白具有Ste12-like蛋白特有的保守结构域(STE homeodomain和ZnF_C2H2锌指结构)及空间结构;StSTE12在附着胞时期表达量最大;筛选了部分StSte12调控基因,与StSte12的匹配序列为T\C GAAAC A\G,中间部分GAAAC非常保守;StKAR5在野生型中表达量小于StSTE12 RNAi转化子,StBEM2、StBUD8、StCHS7相反;StRAX2的表达量在野生型和转化子中一致。【结论】StSte12具有Ste12-like所特有的DNA结合结构域和空间结构;该蛋白在附着胞发育中发挥重要功能;筛选了部分StSte12的调控基因,其匹配序列可概括为T\C GAAAC A\G,且证实了这些基因受StSte12调控。

关键词: 玉米大斑病菌 , 转录因子 , StSte12 , 调控基因

Abstract: 【Objective】 The objective of this study is to locate StSte12 in genome, analyze its protein structure, confirmate its expression at different developmental stages, screen its regulatory genes which expressions were compared in Setosphaeria turcica.【Method】The location of StSte12 and its protein structures were analyzed using bioinformatics method. Its expression characteristics were detected by Western blot. The regulatory genes of StSte12 were screened according to ScSte12 of Saccharomyces cerevisiae. The binding motif of these genes was analyzed by bioinformatics. The expression level of these genes was compared between wild type strain and StSTE12 RNAi transformants using RT-PCR.【Result】The identity of StSTE12 was 105656, locating 1061747 to 1064127 of positive-strand of scaffold_13. StSte12 contained conserved domains (STE homeodomain and ZnF_C2H2 domain) and spatial structure of Ste12-like. In S. turcica appressorium period, the expression amount of StSTE12 was the largest. Some regulatory genes of StSte12 were screened, in which the binding motif combined with StSte12 was T\C GAAAC A\G. The expression level of StKAR5 in wild type strains was lager than that in StSTE12 RNAi transformants, the level of StBEM2, StBUD8, and StCHS7 were opposite to StKAR5, whereas that of StRAX2 had no obvious difference. 【Conclusion】 StSte12 has DNA binding domain and spatial structure belongs to Ste12-like Transcription factors. And it plays an important role in appressorium development of S. turcica. Some regulatory genes of StSte12 were screened, in which the binding motif was T\C GAAAC A\G, and which was regulated by StSte12.

Key words: Setosphaeria turcica , transcription factor , StSte12 , regulatory gene