Van Gijsegem Frédérique, Wlodarczyk Aleksandra, Cornu Amandine, Reverchon Sylvie, Hugouvieux-Cotte-Pattat Nicole
Laboratoire Interactions Plantes Pathogènes, UMR217 INRA/AgroParisTech/UPMC Univ Paris 6, 16 rue Claude Bernard, 75231 Paris, Cedex 05, France.
Mol Plant Microbe Interact. 2008 Nov;21(11):1471-81. doi: 10.1094/MPMI-21-11-1471.
Analysis of the regulators of the LacI family was performed in order to identify those potentially involved in pathogenicity of Erwinia chrysanthemi (Dickeya dadantii). Among the 18 members of the LacI family, the function of 11 members is either known or predicted and only 7 members have, as yet, no proposed function. Inactivation of these seven genes, called lfaR, lfbR, lfcR, lfdR, lfeR, lffR, and lfgR, demonstrated that four of them are important for plant infection. The lfaR and lfcR mutants showed a reduced virulence on chicory, Saintpaulia sp., and Arabidopsis. The lfeR mutant showed a reduced virulence on Arabidopsis. The lfdR mutant was more efficient than the wild-type strain in initiating maceration on Saintpaulia sp. The genetic environment of each regulator was examined to detect adjacent genes potentially involved in a common function. Construction of transcriptional fusions in these neighboring genes demonstrated that five regulators, LfaR, LfcR, LfeR, LffR, and LfgR, act as repressors of adjacent genes. Analysis of these fusions also indicated that the genes controlled by LfaR, LfcR, LfgR, and LffR are expressed during plant infection. Moreover, addition of crude plant extracts to culture medium demonstrated that the expression of the LfaR- and LfgR-controlled genes is specifically induced by plant components.
为了鉴定那些可能参与菊欧文氏菌(达旦迪基氏菌)致病性的调控因子,对LacI家族的调控因子进行了分析。在LacI家族的18个成员中,11个成员的功能已知或已被预测,只有7个成员目前尚无功能推测。对这7个基因(分别称为lfaR、lfbR、lfcR、lfdR、lfeR、lffR和lfgR)进行失活研究,结果表明其中4个基因对植物感染很重要。lfaR和lfcR突变体在菊苣、非洲紫罗兰和拟南芥上的毒力降低。lfeR突变体在拟南芥上的毒力降低。lfdR突变体在引发非洲紫罗兰组织浸解方面比野生型菌株更有效。研究了每个调控因子的基因环境,以检测可能参与共同功能的相邻基因。对这些相邻基因构建转录融合体表明,5个调控因子LfaR、LfcR、LfeR、LffR和LfgR作为相邻基因的阻遏物发挥作用。对这些融合体的分析还表明,受LfaR、LfcR、LfgR和LffR调控的基因在植物感染期间表达。此外,向培养基中添加粗植物提取物表明,受LfaR和LfgR调控的基因的表达受到植物成分的特异性诱导。