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Engineered resistance and hypersusceptibility through functional metabolic studies of 100 genes in soybean to its major pathogen the soybean cyst nematode

机译:通过对大豆中100个基因对其主要病原体大豆囊肿线虫的功能性代谢研究对工程化的抗药性和高敏感性

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摘要

During pathogen attack, the host plant induces genes to ward off the pathogen while the pathogen often produces effector proteins to increase susceptibility of the host. Gene expression studies of syncytia formed in soybean root by soybean cyst nematode (Heterodera glycines) identified many genes altered in expression in resistant and susceptible roots. However, it is difficult to assess the role and impact of these genes on resistance using gene expression patterns alone. We selected 100 soybean genes from published microarray studies and individually overexpressed them in soybean roots to determine their impact on cyst nematode development. Nine genes reduced the number of mature females by more than 50 % when overexpressed, including genes encoding ascorbate peroxidase, β-1,4-endoglucanase, short chain dehydrogenase, lipase, DREPP membrane protein, calmodulin, and three proteins of unknown function. One gene encoding a serine hydroxymethyltransferase decreased the number of mature cyst nematode females by 45 % and is located at the Rhg4 locus. Four genes increased the number of mature cyst nematode females by more than 200 %, while thirteen others increased the number of mature cyst nematode females by more than 150 %. Our data support a role for auxin and ethylene in susceptibility of soybean to cyst nematodes. These studies highlight the contrasting gene sets induced by host and nematode during infection and provide new insights into the interactions between host and pathogen at the molecular level. Overexpression of some of these genes result in a greater decrease in the number of cysts formed than recognized soybean cyst nematode resistance loci.
机译:在病原体侵袭期间,宿主植物诱导基因抵御病原体,而病原体通常产生效应蛋白以增加宿主的敏感性。大豆孢囊线虫(Heterodera甘氨酸)在大豆根中形成合胞体的基因表达研究确定了许多在抗性和易感根中表达发生改变的基因。但是,仅使用基因表达模式很难评估这些基因对抗药性的作用和影响。我们从已发表的微阵列研究中选择了100个大豆基因,并在大豆根中单独过表达它们,以确定它们对囊肿线虫发育的影响。过度表达时,有9个基因使成熟雌性的数量减少了50%以上,包括编码抗坏血酸过氧化物酶,β-1,4-内葡聚糖酶,短链脱氢酶,脂肪酶,DREPP膜蛋白,钙调蛋白和三种功能未知的蛋白的基因。一种编码丝氨酸羟甲基转移酶的基因使成熟的囊肿线虫雌性数量减少了45%,并且位于Rhg4基因座。四个基因使成熟的囊肿线虫雌性数量增加了200%以上,而另外13个基因使成熟的囊肿线虫雌性数量增加了150%以上。我们的数据支持生长素和乙烯在大豆对囊肿线虫敏感性中的作用。这些研究突出了宿主和线虫在感染过程中诱导的相反基因集,并提供了在分子水平上宿主与病原体之间相互作用的新见解。这些基因中的某些基因的过表达导致形成的囊肿数量比公认的大豆囊肿线虫抗性基因座减少更多。

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