Shoot-to-root translocated GmNN1/FT2a triggers nodulation and regulates soybean nitrogen nutrition

• Published in: PLoS biology 2022-08, Vol.20 (8), p.e3001739-e3001739
• Main Authors: Li, Xinxin, Zhou, Huiwen, Cheng, Ling, Ma, Niannian, Cui, Baofeng, Wang, Wenfei, Zhong, Yongjia, Liao, Hong
• Format: Article
• Language: English
• Subjects: Arabidopsis - genetics; Arabidopsis - metabolism; Biology and Life Sciences; Carbohydrates; Cloning; CRISPR; Engineering and Technology; Flowering; Gene expression; Glycine max - genetics; Glycine max - metabolism; Host plants; Leaves; Legumes; Medicine and Health Sciences; Nitrogen; Nitrogen - metabolism; Nitrogen Fixation; Nitrogenation; Nodulation; Nodules; Nutrition; Phenotypes; Physiological aspects; Plant growth; Plant Roots - genetics; Plant Roots - metabolism; Plants (botany); Shoots; Signaling; Soybean; Soybeans; Symbionts; Symbiosis - genetics; Tobacco; Translocation
• ISSN: 1545-7885; 1544-9173; 1545-7885
• DOI: 10.1371/journal.pbio.3001739

Symbiotic nitrogen fixation (SNF) provides sufficient nitrogen (N) to meet most legume nutrition demands. In return, host plants feed symbionts carbohydrates produced in shoots. However, the molecular dialogue between shoots and symbionts remains largely mysterious. Here, we report the map-based cloning and characterization of a natural variation in GmNN1, the ortholog of Arabidopsis thaliana FLOWERING LOCUS T (FT2a) that simultaneously triggers nodulation in soybean and modulates leaf N nutrition. A 43-bp insertion in the promoter region of GmNN1/FT2a significantly decreased its transcription level and yielded N deficiency phenotypes. Manipulating GmNN1/GmFT2a significantly enhanced soybean nodulation, plant growth, and N nutrition. The near-isogenic lines (NILs) carrying low mRNA abundance alleles of GmNN1/FT2a, along with stable transgenic soybeans with CRISPR/Cas9 knockouts of GmNN1/FT2a, had yellower leaves, lower N concentrations, and fewer nodules than wild-type control plants. Grafting together with split-root experiments demonstrated that only shoot GmNN1/FT2a was responsible for regulating nodulation and thereby N nutrition through shoot-to-root translocation, and this process depends on rhizobial infection. After translocating into roots, shoot-derived GmNN1/FT2a was found to interact with GmNFYA-C (nuclear factor-Y subunit A-C) to activate symbiotic signaling through the previously reported GmNFYA-C-ENOD40 module. In short, the description of the critical soybean nodulation regulatory pathway outlined herein sheds novel insights into the shoot-to-root signaling required for communications between host plants and root nodulating symbionts.