4.7 Article

BRASSINAZOLE RESISTANT 1 Mediates Brassinosteroid-Induced Calvin Cycle to Promote Photosynthesis in Tomato

期刊

FRONTIERS IN PLANT SCIENCE
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fpls.2021.811948

关键词

brassinosteroids; BRASSINAZOLE RESISTANT 1 (BZR1); Calvin cycle; Calvin cycle genes; photosynthesis; Solanum lycopersicum (tomato)

资金

  1. National Key Research and Development Program [2019YFD1001900]
  2. National Natural Science Foundation of China [31872153]
  3. Fundamental Research Funds for the Central Universities [2021FZZX001-30]

向作者/读者索取更多资源

In this study, the researchers investigated the role of brassinosteroids (BRs), a type of plant hormone, in regulating the Calvin cycle genes in tomatoes. They found that BRs can enhance the activity of the Calvin cycle and improve photosynthetic ability. This regulation is mediated by the signal effector BRASSINAZOLE RESISTANT 1 (BZR1), which directly binds to the promoters of key Calvin cycle genes. These findings suggest that BRs regulate the Calvin cycle in a BZR1-dependent manner in tomatoes, highlighting the potential of targeting BRs to increase crop yields.
Calvin cycle is a sequence of enzymatic reactions that assimilate atmospheric CO2 in photosynthesis. Multiple components are known to participate in the induction or suppression of the Calvin cycle but the mechanism of its regulation by phytohormones is still unclear. Brassinosteroids (BRs) are steroid phytohormones that promote photosynthesis and crop yields. In this study, we study the role of BRs in regulating Calvin cycle genes to further understand the regulation of the Calvin cycle by phytohormones in tomatoes. BRs and their signal effector BRASSINAZOLE RESISTANT 1 (BZR1) can enhance the Calvin cycle activity and improve the photosynthetic ability. BRs increased the accumulation of dephosphorylated form of BZR1 by 94% and induced an 88-126% increase in the transcription of key genes in Calvin cycle FBA1, RCA1, FBP5, and PGK1. BZR1 activated the transcription of these Calvin cycle genes by directly binding to their promoters. Moreover, silencing these Calvin cycle genes impaired 24-epibrassinolide (EBR)-induced enhancement of photosynthetic rate, the quantum efficiency of PSII, and V-c,V-max and J(max). Taken together, these results strongly suggest that BRs regulate the Calvin cycle in a BZR1-dependent manner in tomatoes. BRs that mediate coordinated regulation of photosynthetic genes are potential targets for increasing crop yields.

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