4.4 Article

Overexpression of the 3' half of the PHYB partially suppresses dwarfism in the brassinosteroid-insensitive bri1-5 mutant

Journal

JOURNAL OF PLANT BIOLOGY
Volume 59, Issue 1, Pages 83-91

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s12374-016-0513-6

Keywords

Brassinosteroid; bri1; Gateway-cDNA library; Overexpression mutagenesis; phyB

Categories

Funding

  1. Next-Generation BioGreen21 Program, Rural Development Administration, Republic of Korea [PJ01104501, PJ01104502]
  2. Cooperative Research Program for Agricultural Science and Technology Development, Rural Development Administration, Republic of Korea [PJ01168501]
  3. Basic Science Research Program through the National Research Foundation of Korea (NRF) [2013R1A1A2059445]
  4. National Research Foundation of Korea [2013R1A1A2059445] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Brassinosteroids (BRs) control virtually every aspect of plant growth and development. BRs act alone or in combination with other signals. To identify the signaling components that interact with BRs, we screened for mutants that suppress the dwarf phenotypes of brassinosteroid insensitive 1-5 (bri1-5) using an overexpression mutagenesis method. We established a mutant population by introducing a cDNA library in which cDNA was overexpressed under a constitutive promoter into Arabidopsis bri1-5 plants, which lacked a functional brassinosteroid (BR) receptor. One of the mutants, dubbed 'bri1-5 with long petioles' (blp), was selected based on its suppression phenotype. blp contained a chimeric DNA consisting of the 3' half of PHYB, a 2-bp insertion, and a part of the chloroplast ribosomal RNA gene. Re-introduction of the chimeric DNA into bri1-5 recapitulated the blp phenotype. Prompted by the phenotypic similarity between blp and phyB, we examined both the transcript and protein levels of PHYB in the mutants. The levels were lower in blp 35Spro:PHYB than in 35Spro:PHYB plants, suggesting that introduction of the chimeric gene interfered with the stability of PHYB transcripts. Genome-wide screening for a specific target phenotype resulted in the finding that overexpression of the 3' half of PHYB in the sense direction can cause a loss-of-function phenotype, and that PHYB plays an important role in BR signaling. Our results validate overexpression mutagenesis as a method to identify the function of Arabidopsis genes.

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