Maekawa Takaki, Maekawa-Yoshikawa Makoto, Takeda Naoya, Imaizumi-Anraku Haruko, Murooka Yoshikatsu, Hayashi Makoto
Institut für Genetik, Ludwig-Maximilians-Universität München, Maria-Ward-Str. 1a, 80638 München, Germany.
Plant J. 2009 Apr;58(2):183-94. doi: 10.1111/j.1365-313X.2008.03774.x. Epub 2008 Dec 2.
Root nodule formation is regulated by several plant hormones, but the details of the regulation of the nodulation signaling pathway are largely unknown. In this study, the role of gibberellin (GA) in the control of root nodule symbiosis was investigated at the physiological and genetic levels in Lotus japonicus. Exogenous application of biologically active GA, GA(3), inhibited the formation of infection threads and nodules, which was counteracted by the application of a biosynthesis inhibitor of GA, Uniconazole P. Nod factor-induced root hair deformation was severely blocked in the presence of GA, which was phenocopied by nsp2 mutants. The number of spontaneous nodules triggered by the gain-of-function mutation of calcium/calmodulin-dependent kinase (CCaMK) or the lotus histidine kinase 1 (LHK1) was decreased upon the addition of GA; moreover, the overexpression of the gain-of-function mutation of L. japonicus, SLEEPY1, a positive regulator of GA signaling, resulted in a reduced nodule number, without other aspects of root development being affected. These results indicate that higher GA signaling levels specifically inhibit the nodulation signaling pathway. Nod factor-dependent induction of NSP2 and NIN was inhibited by exogenous GA. Furthermore, the cytokinin-dependent induction of NIN was suppressed by GA. From these results, we conclude that GA inhibits the nodulation signaling pathway downstream of cytokinin, possibly at NSP2, which is required for Nod factor-dependent NIN expression. These results clarify the roles of GA in the nodulation signaling pathway, and in relation to the cytokinin signaling pathway for nodulation in L. japonicus.
根瘤形成受多种植物激素调控,但结瘤信号通路调控的具体细节大多未知。在本研究中,我们在百脉根的生理和遗传水平上研究了赤霉素(GA)在控制根瘤共生中的作用。外源施加生物活性GA(GA3)会抑制侵染线和根瘤的形成,而GA生物合成抑制剂烯效唑的施加则可抵消这种抑制作用。在GA存在的情况下,结瘤因子诱导的根毛变形被严重阻断,nsp2突变体也表现出类似的表型。添加GA后,由钙/钙调蛋白依赖性激酶(CCaMK)或百脉根组氨酸激酶1(LHK1)的功能获得性突变引发的自发根瘤数量减少;此外,百脉根GA信号正调控因子SLEEPY1功能获得性突变的过表达导致根瘤数量减少,而根的其他发育方面未受影响。这些结果表明,较高的GA信号水平会特异性抑制结瘤信号通路。外源GA抑制了结瘤因子对NSP2和NIN的诱导。此外,GA还抑制了细胞分裂素对NIN的诱导。基于这些结果,我们得出结论,GA在细胞分裂素下游抑制结瘤信号通路,可能作用于NSP2,而NSP2是结瘤因子依赖性NIN表达所必需的。这些结果阐明了GA在结瘤信号通路中的作用,以及与百脉根结瘤细胞分裂素信号通路的关系。