SPL14/17 act downstream of strigolactone signalling to modulate rice root elongation in response to nitrate supply

Plant J. 2021 May;106(3):649-660. doi: 10.1111/tpj.15188. Epub 2021 Mar 17.

Abstract

Nitrogen (N) is an essential major nutrient for food crops. Although ammonium (NH4+ ) is the primary N source of rice (Oryza sativa), nitrate (NO3- ) can also be absorbed and utilized. Rice responds to NO3- application by altering its root morphology, such as root elongation. Strigolactones (SLs) are important modulators of root length. However, the roles of SLs and their downstream genes in NO3- -induced root elongation remain unclear. Here, the levels of total N and SL (4-deoxyorobanchol) and the responses of seminal root (SR) lengths to NH4+ and NO3- were investigated in rice plants. NO3- promoted SR elongation, possibly due to short-term signal perception and long-term nutrient function. Compared with NH4+ conditions, higher SL signalling/levels and less D53 protein were recorded in roots of NO3- -treated rice plants. In contrast to wild-type plants, SR lengths of d mutants were less responsive to NO3- conditions, and application of rac-GR24 (SL analogue) restored SR length in d10 (SL biosynthesis mutant) but not in d3, d14, and d53 (SL-responsive mutants), suggesting that higher SL signalling/levels participate in NO3- -induced root elongation. D53 interacted with SPL17 and inhibited SPL17-mediated transactivation from the PIN1b promoter. Mutation of SPL14/17 and PIN1b caused insensitivity of the root elongation response to NO3- and rac-GR24 applications. Therefore, we conclude that perception of SLs by D14 leads to degradation of D53 via the proteasome system, which releases the suppression of SPL14/17-modulated transcription of PIN1b, resulting in root elongation under NO3- supply.

Keywords: nitrate (NO3−); protein interaction; rice; seminal root (SR); strigolactones (SLs).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Heterocyclic Compounds, 3-Ring / metabolism*
  • Lactones / metabolism*
  • Nitrates / metabolism*
  • Nitrogen / metabolism
  • Oryza / growth & development*
  • Oryza / metabolism
  • Plant Proteins / physiology*
  • Plant Roots / growth & development*
  • Plant Roots / metabolism
  • Signal Transduction
  • Transcription Factors / physiology*

Substances

  • GR24 strigolactone
  • Heterocyclic Compounds, 3-Ring
  • Lactones
  • Nitrates
  • Plant Proteins
  • Transcription Factors
  • Nitrogen