Department of Plant Pathology, University of Georgia, Athens, GA 30602-7274, USA.
Mol Plant Pathol. 2005 Jan 1;6(1):23-30. doi: 10.1111/j.1364-3703.2004.00257.x.
SUMMARY Parasitism genes encoding secretory proteins expressed in the oesophageal glands of phytoparasitic nematodes play critical roles in nematode invasion of host plants, establishment of feeding sites and suppression of host defences. Two chorismate mutase (CM) genes potentially having a role in one or more of these processes were identified from a Meloidogyne incognita oesophageal gland-cell subtractive cDNA library. These M. incognita enzymes (designated as MI-CM-1 and MI-CM-2) with amino-terminal signal peptides, were significantly similar to chorismate mutases in M. javanica and bacteria. The complementation of an Escherichia coli CM-deficient mutant by the expression of Mi-cm-1 or Mi-cm-2 confirmed their CM activity. In-situ mRNA hybridization showed that the transcripts of Mi-cm-1 and Mi-cm-2 accumulated specifically in the two subventral oesophageal gland cells of M. incognita. RT-PCR analysis confirmed that their transcript abundances were high in the early parasitic juvenile stages, and low (Mi-cm-1) or undetectable (Mi-cm-2) in later parasitic stages of the nematode. Southern blot analysis revealed that these CM genes were members of a small multigene family in Meloidogyne species. The widespread presence of CMs in the specialized sedentary endoparasitic nematode species suggests that this multifunctional enzyme may be a key factor in modulating plant parasitism.
总结 寄生基因编码在植物寄生线虫食道腺中表达的分泌蛋白,在线虫入侵宿主植物、建立取食部位和抑制宿主防御方面发挥着关键作用。从南方根结线虫食道腺细胞差减 cDNA 文库中鉴定出两个可能在一个或多个这些过程中起作用的分支酸变位酶 (CM) 基因。这些 M. incognita 酶(命名为 MI-CM-1 和 MI-CM-2)具有氨基末端信号肽,与 M. javanica 和细菌中的分支酸变位酶高度相似。Mi-cm-1 或 Mi-cm-2 的表达对大肠杆菌 CM 缺陷突变体的互补证实了它们的 CM 活性。原位 mRNA 杂交显示,Mi-cm-1 和 Mi-cm-2 的转录物特异性积累在南方根结线虫的两个亚腹食道腺细胞中。RT-PCR 分析证实,它们的转录物丰度在早期寄生幼体阶段较高,而在线虫的后期寄生阶段较低(Mi-cm-1)或无法检测到(Mi-cm-2)。Southern 印迹分析表明,这些 CM 基因是 Meloidogyne 物种中小基因家族的成员。CM 在专门的定居内寄生线虫物种中的广泛存在表明,这种多功能酶可能是调节植物寄生的关键因素。