NIGT1 represses plant growth and mitigates phosphate starvation signaling to balance the growth response tradeoff in rice

Yuxin Zhang(Institute of Agricultural Resources and Regional Planning), Qianqian Zhang(Institute of Agricultural Resources and Regional Planning), Meina Guo(Beijing Forestry University), Xueqing Wang(Institute of Agricultural Resources and Regional Planning), Tianjie Li(Institute of Agricultural Resources and Regional Planning), Qingyu Wu(Institute of Agricultural Resources and Regional Planning), Lihui Li(Chinese Academy of Agricultural Sciences), Keke Yi(Institute of Agricultural Resources and Regional Planning), Wenyuan Ruan(Institute of Agricultural Resources and Regional Planning)
Journal of Integrative Plant Biology
April 25, 2023
Cited by 15Open Access
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Abstract

Inorganic phosphate (Pi) availability is an important factor which affects the growth and yield of crops, thus an appropriate and effective response to Pi fluctuation is critical. However, how crops orchestrate Pi signaling and growth under Pi starvation conditions to optimize the growth defense tradeoff remains unclear. Here we show that a Pi starvation-induced transcription factor NIGT1 (NITRATE-INDUCIBLE GARP-TYPE TRANSCRIPTIONAL REPRESSOR 1) controls plant growth and prevents a hyper-response to Pi starvation by directly repressing the expression of growth-related and Pi-signaling genes to achieve a balance between growth and response under a varying Pi environment. NIGT1 directly binds to the promoters of Pi starvation signaling marker genes, like IPS1, miR827, and SPX2, under Pi-deficient conditions to mitigate the Pi-starvation responsive (PSR). It also directly represses the expression of vacuolar Pi efflux transporter genes VPE1/2 to regulate plant Pi homeostasis. We further demonstrate that NIGT1 constrains shoot growth by repressing the expression of growth-related regulatory genes, including brassinolide signal transduction master regulator BZR1, cell division regulator CYCB1;1, and DNA replication regulator PSF3. Our findings reveal the function of NIGT1 in orchestrating plant growth and Pi starvation signaling, and also provide evidence that NIGT1 acts as a safeguard to avoid hyper-response during Pi starvation stress in rice.


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