Dufresne M, Bailey J A, Dron M, Langin T
Laboratoire de Phytopathologie Moléculaire, Université Paris-Sud, Orsay, France.
Mol Plant Microbe Interact. 1998 Feb;11(2):99-108. doi: 10.1094/MPMI.1998.11.2.99.
A random insertional mutagenesis in Colletotrichum lindemuthianum, the causal agent of common bean anthracnose, generated four mutants that showed altered pathogenicity when tested on intact seedlings, excised leaves, and/or excised hypocotyls. One of these mutants, H290, produced very few lesions on bean leaves and appeared affected in its ability to penetrate the leaf cuticle. Molecular analyses showed that the border sequences of the unique integration site of the disrupting pAN7-1 plasmid in the mutant exhibited homology with conserved domains of serine/threonine protein kinases. The corresponding wild-type sequences were cloned and a gene replacement vector with a mutated copy harboring a selection marker constructed. Transformation of the wild-type pathogen produced a strain with a phenotype identical to the original mutant. Genomic and cDNA sequences indicated that the disrupted gene is a member of the serine/threonine protein kinase family. The gene, called clk1 (Colletotrichum lindemuthianum kinase 1), was weakly expressed in the mycelium of the wild-type strain grown on rich and minimal synthetic media but was undetectable during the infection even when a sensitive reverse transcriptase-polymerase chain reaction methodology was used. This study represents the first characterization of altered pathogenicity mutants in C. lindemuthianum produced by random mutagenesis and demonstrates the involvement of a member of the serine/threonine kinase gene family in the early steps of the infection process.
菜豆炭疽病的病原菌林氏炭疽菌(Colletotrichum lindemuthianum)中的随机插入诱变产生了四个突变体,在完整幼苗、离体叶片和/或离体下胚轴上进行测试时,这些突变体表现出致病性改变。其中一个突变体H290在菜豆叶片上产生的病斑极少,其穿透叶片角质层的能力似乎受到了影响。分子分析表明,突变体中破坏pAN7-1质粒独特整合位点的边界序列与丝氨酸/苏氨酸蛋白激酶的保守结构域具有同源性。克隆了相应的野生型序列,并构建了一个带有选择标记的突变拷贝的基因置换载体。野生型病原菌的转化产生了一个与原始突变体表型相同的菌株。基因组和cDNA序列表明,被破坏的基因是丝氨酸/苏氨酸蛋白激酶家族的成员。该基因被称为clk1(林氏炭疽菌激酶1),在富含营养和基本合成培养基上生长的野生型菌株的菌丝体中弱表达,但即使使用灵敏的逆转录聚合酶链反应方法,在感染过程中也检测不到。这项研究首次对通过随机诱变产生的林氏炭疽菌致病性改变突变体进行了表征,并证明了丝氨酸/苏氨酸激酶基因家族的一个成员参与了感染过程的早期步骤。