A cis-acting bidirectional transcription switch controls sexual dimorphism in the liverwort

EMBO J. 2019 Mar 15;38(6):e100240. doi: 10.15252/embj.2018100240. Epub 2019 Jan 4.

Abstract

Plant life cycles alternate between haploid gametophytes and diploid sporophytes. While regulatory factors determining male and female sexual morphologies have been identified for sporophytic reproductive organs, such as stamens and pistils of angiosperms, those regulating sex-specific traits in the haploid gametophytes that produce male and female gametes and hence are central to plant sexual reproduction are poorly understood. Here, we identified a MYB-type transcription factor, MpFGMYB, as a key regulator of female sexual differentiation in the haploid-dominant dioicous liverwort, Marchantia polymorpha MpFGMYB is specifically expressed in females and its loss resulted in female-to-male sex conversion. Strikingly, MpFGMYB expression is suppressed in males by a cis-acting antisense gene SUF at the same locus, and loss-of-function suf mutations resulted in male-to-female sex conversion. Thus, the bidirectional transcription module at the MpFGMYB/SUF locus acts as a toggle between female and male sexual differentiation in M. polymorpha gametophytes. Arabidopsis thaliana MpFGMYB orthologs are known to be expressed in embryo sacs and promote their development. Thus, phylogenetically related MYB transcription factors regulate female gametophyte development across land plants.

Keywords: Marchantia polymorpha; R2R3 MYB‐type transcription factor; antisense transcription; lncRNA; sexual differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / genetics
  • Arabidopsis / growth & development
  • Arabidopsis / metabolism
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism
  • Gametogenesis, Plant / genetics*
  • Gene Expression Regulation, Plant*
  • Germ Cells, Plant / growth & development
  • Germ Cells, Plant / metabolism
  • Hepatophyta / genetics*
  • Hepatophyta / growth & development
  • Hepatophyta / metabolism
  • Phylogeny
  • Plant Proteins / genetics*
  • Plant Proteins / metabolism
  • Proto-Oncogene Proteins c-myb / genetics
  • Proto-Oncogene Proteins c-myb / metabolism
  • Regulatory Elements, Transcriptional*
  • Sex Characteristics*
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Transcription, Genetic

Substances

  • Arabidopsis Proteins
  • Plant Proteins
  • Proto-Oncogene Proteins c-myb
  • Transcription Factors