Cunnac Sébastien, Boucher Christian, Genin Stéphane
Laboratoire Interactions Plantes-Microorganismes, CNRS-INRA, UMR2594, BP27, 31326 Castanet-Tolosan, France.
J Bacteriol. 2004 Apr;186(8):2309-18. doi: 10.1128/JB.186.8.2309-2318.2004.
The ability of Ralstonia solanacearum to cause disease on plants depends on its type III secretion system (TTSS) encoded by hrp genes. The expression of hrp genes and known TTSS substrates is coordinately regulated by HrpB, a member of the AraC family of transcriptional regulators. Two HrpB-regulated promoters (hrpY and popABC) were characterized by deletion analysis, and the HrpB-dependent activation of these promoters was found to be conferred by a 25-nucleotide DNA element, the hrp(II) box (TTCGn16TTCG), which is present in other hrp promoters. The hrp(II) box element is an imperfect plant inducible promoter box, an element which was originally found in hrp promoters of Xanthomonas campestris (S. Fenselau and U. Bonas, Mol. Plant-Microbe Interact. 8:845-854, 1995) but which was not characterized at the molecular level. Site-directed mutagenesis showed that the hrp(II) box is essential for hrpY promoter activation in vivo. Functional analysis of the hrp(II) box element identified critical parameters that are required for HrpB-dependent activity. Further mapping analyses of several other hrpB-dependent promoters also indicated that the position of the hrp(II) box is conserved, at -70 to -47 bp from the transcriptional start. As a first step toward identifying novel TTSS effectors, we used the hrp(II) box consensus sequence to search for potential HrpB-regulated promoters in the complete genome sequence of R. solanacearum strain GMI1000. Among the 114 genes identified, a subset of promoters was found to have a structural relationship with hrp promoters, thus providing a pool of candidate genes encoding TTSS effectors.
青枯雷尔氏菌在植物上引发疾病的能力取决于由hrp基因编码的III型分泌系统(TTSS)。hrp基因和已知的TTSS底物的表达由转录调节因子AraC家族成员HrpB协同调控。通过缺失分析对两个受HrpB调控的启动子(hrpY和popABC)进行了表征,发现这些启动子的HrpB依赖性激活是由一个25个核苷酸的DNA元件——hrp(II)框(TTCGn16TTCG)赋予的,该元件存在于其他hrp启动子中。hrp(II)框元件是一个不完美的植物诱导型启动子框,该元件最初在野油菜黄单胞菌的hrp启动子中发现(S. Fenselau和U. Bonas,《分子植物 - 微生物相互作用》8:845 - 854,1995),但未在分子水平上进行表征。定点诱变表明,hrp(II)框对于体内hrpY启动子的激活至关重要。对hrp(II)框元件的功能分析确定了HrpB依赖性活性所需的关键参数。对其他几个受HrpB调控的启动子的进一步定位分析还表明,hrp(II)框的位置是保守的,位于转录起始点上游 - 70至 - 47 bp处。作为鉴定新型TTSS效应子的第一步,我们使用hrp(II)框共有序列在青枯雷尔氏菌菌株GMI1000的全基因组序列中搜索潜在的受HrpB调控的启动子。在鉴定出的114个基因中,发现一部分启动子与hrp启动子具有结构关系,从而提供了一组编码TTSS效应子的候选基因。