4.8 Article

FRUITFULL-like genes regulate flowering time and inflorescence architecture in tomato

Journal

PLANT CELL
Volume 34, Issue 3, Pages 1002-1019

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/plcell/koab298

Keywords

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Funding

  1. Dutch Scientific Organization (NWO) [ALWOP.199]
  2. China Scholarship Council (CSC)
  3. Coordination for the Improvement of Higher Education Personnel (CAPES)
  4. CAPES/Nuffic [BEX 7686/13-7, BEX 0256/13-7]
  5. Sao Paulo Research Foundation (FAPESP) [2010/52012-4]

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Tomato FUL-like genes FUL2 and MADS-BOX PROTEIN 20 (MBP20) promote the transition from vegetative to reproductive state and repress inflorescence branching by inducing floral meristem maturation. The control of inflorescence branching may be regulated by repression of transcription factors such as TOMATO MADS-box gene 3 (TM3) and APETALA 2b (AP2b). The tomato FUL-like proteins can form heterodimers with various MADS-domain proteins, potentially forming distinct complexes to regulate flowering time and inflorescence architecture.
The timing of flowering and the inflorescence architecture are critical for the reproductive success of tomato (Solanum lycopersicum), but the gene regulatory networks underlying these traits have not been fully explored. Here, we show that the tomato FRUITFULL-like (FUL-like) genes FUL2 and MADS-BOX PROTEIN 20 (MBP20) promote the vegetative-to-reproductive transition and repress inflorescence branching by inducing floral meristem (FM) maturation. FUL1 fulfils a less prominent role and appears to depend on FUL2 and MBP20 for its upregulation in the inflorescence- and floral meristems. MBP10, the fourth tomato FUL-like gene, has probably lost its function. The tomato FUL-like proteins cannot homodimerize in in vitro assays, but heterodimerize with various other MADS-domain proteins, potentially forming distinct complexes in the transition meristem and FM. Transcriptome analysis of the primary shoot meristems revealed various interesting downstream targets, including four repressors of cytokinin signaling that are upregulated during the floral transition in ful1 ful2 mbp10 mbp20 mutants. FUL2 and MBP20 can also bind in vitro to the upstream regions of these genes, thereby probably directly stimulating cell division in the meristem upon the transition to flowering. The control of inflorescence branching does not occur via the cytokinin oxidase/dehydrogenases (CKXs) but may be regulated by repression of transcription factors such as TOMATO MADS-box gene 3 (TM3) and APETALA 2b (AP2b). The tomato MADS-domain transcription factors FUL1, FUL2, and MBP20 regulate flowering time and inflorescence architecture.

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