Suzaki Takuya, Ito Momoyo, Yoro Emiko, Sato Shusei, Hirakawa Hideki, Takeda Naoya, Kawaguchi Masayoshi
National Institute for Basic Biology, Okazaki 444-8585, Japan School of Life Science, The Graduate University for Advanced Studies, Okazaki 444-8585, Japan
National Institute for Basic Biology, Okazaki 444-8585, Japan.
Development. 2014 Jun;141(12):2441-5. doi: 10.1242/dev.107946. Epub 2014 May 21.
Many leguminous plants have a unique ability to reset and alter the fate of differentiated root cortical cells to form new organs of nitrogen-fixing root nodules during legume-Rhizobium symbiosis. Recent genetic studies on the role of cytokinin signaling reveal that activation of cytokinin signaling is crucial to the nodule organogenesis process. However, the genetic mechanism underlying the initiation of nodule organogenesis is poorly understood due to the low number of genes that have been identified. Here, we have identified a novel nodulation-deficient mutant named vagrant infection thread 1 (vag1) after suppressor mutant screening of spontaneous nodule formation 2, a cytokinin receptor gain-of-function mutant in Lotus japonicus. The VAG1 gene encodes a protein that is putatively orthologous to Arabidopsis ROOT HAIRLESS 1/HYPOCOTYL 7, a component of the plant DNA topoisomerase VI that is involved in the control of endoreduplication. Nodule phenotype of the vag1 mutant shows that VAG1 is required for the ploidy-dependent cell growth of rhizobial-infected cells. Furthermore, VAG1 mediates the onset of endoreduplication in cortical cells during early nodule development, which may be essential for the initiation of cortical cell proliferation that leads to nodule primordium formation. In addition, cortical infection is severely impaired in the vag1 mutants, whereas the epidermal infection threads formation is normal. This suggests that the VAG1-mediated endoreduplication of cortical cells may be required for the guidance of symbiotic bacteria to host meristematic cells.
许多豆科植物具有一种独特的能力,即在豆科植物与根瘤菌共生过程中,重置并改变分化的根皮层细胞的命运,以形成固氮根瘤的新器官。最近关于细胞分裂素信号传导作用的遗传学研究表明,细胞分裂素信号传导的激活对根瘤器官发生过程至关重要。然而,由于已鉴定的基因数量较少,根瘤器官发生起始的遗传机制仍知之甚少。在此,我们在对日本百脉根中细胞分裂素受体功能获得型突变体自发根瘤形成2进行抑制突变体筛选后,鉴定出一个新的结瘤缺陷突变体,命名为流浪感染丝1(vag1)。VAG1基因编码一种蛋白质,该蛋白质被推测与拟南芥根无毛1/下胚轴7同源,后者是植物DNA拓扑异构酶VI的一个组成部分,参与内复制的控制。vag1突变体的根瘤表型表明,VAG1是根瘤菌感染细胞的倍性依赖性细胞生长所必需的。此外,VAG1在根瘤早期发育过程中介导皮层细胞内复制的起始,这可能对导致根瘤原基形成的皮层细胞增殖的起始至关重要。此外,vag1突变体中的皮层感染严重受损,而表皮感染丝的形成正常。这表明皮层细胞的VAG1介导的内复制可能是共生细菌导向宿主分生细胞所必需的。