Roles of CsBRC1-like in leaf and lateral branch development in cucumber

Plant Sci. 2021 Jan:302:110681. doi: 10.1016/j.plantsci.2020.110681. Epub 2020 Oct 9.

Abstract

TEOSINTE BRANCHED1/CYCLOIDEA/PCF (TCP) family genes, as plant-specific transcription factors, play vital roles in flower pattern, leaf development and plant architecture. Our recent study shows that the TCP gene BRANCHED1 (CsBRC1) specifically regulates shoot branching in cucumber. Here, we found CsBRC1 had a closely related paralogous gene CsBRC1-like. The synteny analysis revealed that these two genes originated from a segmental duplication. CsBRC1-like displayed different expression patterns in cucumber compared with CsBRC1, indicating that they may have functional differentiation. Ectopic expression of CsBRC1-like in Arabidopsis brc1-1 mutant resulted in reduced rosette branches and rosette leaves, whereas silencing CsBRC1-like in cucumber only led to a deformed true leaf of seedling rather than affecting the shoot branching. RNA-seq analysis of wild-type and CsBRC1-like-RNAi plants implicated that CsBRC1-like might regulate early leaf development through affecting the transcripts of auxin and cytokinin related genes in cucumber. Moreover, CsBRC1-like directly interacts with CsTCP10a and CsBRC1 in vivo. Our results demonstrated that CsBRC1-like has a specific role in regulating leaf development, and CsBRC1-like and CsBRC1 may have overlapping roles in shoot branching.

Keywords: CsBRC1; CsBRC1-like; Cucumber; Leaf development; Shoot branching.

MeSH terms

  • Arabidopsis
  • Cucumis sativus / genetics
  • Cucumis sativus / growth & development*
  • Cucumis sativus / ultrastructure
  • In Situ Hybridization
  • Microscopy, Electron, Scanning
  • Phylogeny
  • Plant Leaves / growth & development*
  • Plant Leaves / ultrastructure
  • Plant Proteins / physiology*
  • Plant Shoots / genetics
  • Plant Shoots / growth & development*
  • Plant Stems / growth & development*
  • Plants, Genetically Modified
  • Real-Time Polymerase Chain Reaction
  • Sequence Alignment
  • Synteny
  • Transcription Factors / genetics
  • Transcription Factors / physiology*
  • Transcriptome

Substances

  • Plant Proteins
  • Transcription Factors