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短根同源基因通过前馈调节 D 型细胞周期蛋白促进大豆根瘤的形成。

SHORT-ROOT paralogs mediate feedforward regulation of D-type cyclin to promote nodule formation in soybean.

机构信息

College of Horticulture, Fujian Agriculture and Forestry University, Fuzhou 350002, China.

College of Life Sciences, Fujian Agriculture and Forestry University, Fuzhou 350002, China.

出版信息

Proc Natl Acad Sci U S A. 2022 Jan 18;119(3). doi: 10.1073/pnas.2108641119.

DOI:10.1073/pnas.2108641119
PMID:35022232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8784155/
Abstract

Nitrogen fixation in soybean takes place in root nodules that arise from de novo cell divisions in the root cortex. Although several early nodulin genes have been identified, the mechanism behind the stimulation of cortical cell division during nodulation has not been fully resolved. Here we provide evidence that two paralogs of soybean SHORT-ROOT (GmSHR) play vital roles in soybean nodulation. Expression of and () is induced in cortical cells at the beginning of nodulation, when the first cell divisions occur. The expression level of is positively associated with cortical cell division and nodulation. Knockdown of GmSHR5 inhibits cell division in outer cortical layers during nodulation. Knockdown of both paralogs disrupts the cell division throughout the cortex, resulting in poorly organized nodule primordia with delayed vascular tissue formation. GmSHR4/5 function by enhancing cytokinin signaling and activating early nodulin genes. Interestingly, D-type cyclins act downstream of GmSHR4/5, and GmSHR4/5 form a feedforward loop regulating D-type cyclins. Overexpression of D-type cyclins in soybean roots also enhanced nodulation. Collectively, we conclude that the GmSHR4/5-mediated pathway represents a vital module that triggers cytokinin signaling and activates D-type cyclins during nodulation in soybean.

摘要

大豆中的氮固定发生在根瘤中,根瘤是根皮层中从头开始的细胞分裂产生的。虽然已经鉴定出几个早期豆球蛋白基因,但在结瘤过程中刺激皮层细胞分裂的机制尚未完全解决。在这里,我们提供的证据表明,大豆SHORT-ROOT(GmSHR)的两个同源基因在大豆结瘤中起着至关重要的作用。在结瘤开始时,即第一次细胞分裂发生时,和()在皮层细胞中表达。的表达水平与皮层细胞分裂和结瘤呈正相关。在结瘤过程中敲低 GmSHR5 会抑制外皮层细胞的分裂。敲低两个同源基因会破坏整个皮层的细胞分裂,导致组织排列不良的根瘤原基,血管组织形成延迟。GmSHR4/5 通过增强细胞分裂素信号传导并激活早期豆球蛋白基因起作用。有趣的是,D 型细胞周期蛋白在 GmSHR4/5 的下游起作用,并且 GmSHR4/5 形成一个正反馈环来调节 D 型细胞周期蛋白。在大豆根中过表达 D 型细胞周期蛋白也增强了结瘤。总的来说,我们得出结论,GmSHR4/5 介导的途径代表了一个重要的模块,它在大豆结瘤过程中触发细胞分裂素信号传导并激活 D 型细胞周期蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/46a740e7713a/pnas.2108641119fig06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/a5ac5723263c/pnas.2108641119fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/f8625b75d2a7/pnas.2108641119fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/10af302b117b/pnas.2108641119fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/e80836f90388/pnas.2108641119fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/947eb60afa81/pnas.2108641119fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/46a740e7713a/pnas.2108641119fig06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/a5ac5723263c/pnas.2108641119fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/f8625b75d2a7/pnas.2108641119fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/10af302b117b/pnas.2108641119fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/e80836f90388/pnas.2108641119fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/947eb60afa81/pnas.2108641119fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58e6/8784155/46a740e7713a/pnas.2108641119fig06.jpg

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