Endogenous gibberellins affect root nodule symbiosis via transcriptional regulation of NODULE INCEPTION in Lotus japonicus

被引:18
|
作者
Akamatsu, Akira [1 ]
Nagae, Miwa [2 ]
Nishimura, Yuka [1 ]
Romero Montero, Daniela [1 ]
Ninomiya, Satsuki [1 ]
Kojima, Mikiko [3 ]
Takebayashi, Yumiko [3 ]
Sakakibara, Hitoshi [3 ,4 ]
Kawaguchi, Masayoshi [2 ]
Takeda, Naoya [1 ]
机构
[1] Kwansei Gakuin Univ, Grad Sch Sci & Technol, 2-1 Gakuen, Sanda, Hyogo 6691337, Japan
[2] Natl Inst Basic Biol, 38 Nishigonaka, Okazaki, Aichi 4448585, Japan
[3] RIKEN Ctr Sustainable Resource Sci, Tsurumi Ku, 1-7-22,Suehiro, Yokohama, Kanagawa 2300045, Japan
[4] Nagoya Univ, Grad Sch Bioagr Sci, Chikusa Ku, Nagoya, Aichi 4648601, Japan
来源
PLANT JOURNAL | 2021年 / 105卷 / 06期
基金
日本学术振兴会;
关键词
autoregulation of nodulation; cis-acting region; gibberellin; Lotus japonicus; Nodule; NODULE INCEPTION; root nodule symbiosis; RHIZOBIAL INFECTION; SYSTEMIC REGULATION; GENE-EXPRESSION; PROTEIN-KINASE; LATERAL ROOT; NODULATION; ORGANOGENESIS; CALCIUM; NIN; IDENTIFICATION;
D O I
10.1111/tpj.15128
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Legumes and nitrogen-fixing rhizobial bacteria establish root nodule symbiosis, which is orchestrated by several plant hormones. Exogenous addition of biologically active gibberellic acid (GA) is known to inhibit root nodule symbiosis. However, the precise role of GA has not been elucidated because of the trace amounts of these hormones in plants and the multiple functions of GAs. Here, we found that GA signaling acts as a key regulator in a long-distance negative-feedback system of root nodule symbiosis called autoregulation of nodulation (AON). GA biosynthesis is activated during nodule formation in and around the nodule vascular bundles, and bioactive GAs accumulate in the nodule. In addition, GA signaling induces expression of the symbiotic transcription factor NODULE INCEPTION (NIN) via a cis-acting region on the NIN promoter. Mutants with deletions of this cis-acting region have increased susceptibility to rhizobial infection and reduced GA-induced CLE-RS1 and CLE-RS2 expression, suggesting that the inhibitory effect of GAs occurs through AON. This is supported by the GA-insensitive phenotypes of an AON-defective mutant of HYPERNODULATION ABERRANT ROOT FORMATION1 (HAR1) and a reciprocal grafting experiment. Thus, endogenous GAs induce NIN expression via its GA-responsive cis-acting region, and subsequently the GA-induced NIN activates the AON system to regulate nodule formation.
引用
收藏
页码:1507 / 1520
页数:14
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