Chloroplast retrograde signal regulates flowering

Proc Natl Acad Sci U S A. 2016 Sep 20;113(38):10708-13. doi: 10.1073/pnas.1521599113. Epub 2016 Sep 6.

Abstract

Light is a major environmental factor regulating flowering time, thus ensuring reproductive success of higher plants. In contrast to our detailed understanding of light quality and photoperiod mechanisms involved, the molecular basis underlying high light-promoted flowering remains elusive. Here we show that, in Arabidopsis, a chloroplast-derived signal is critical for high light-regulated flowering mediated by the FLOWERING LOCUS C (FLC). We also demonstrate that PTM, a PHD transcription factor involved in chloroplast retrograde signaling, perceives such a signal and mediates transcriptional repression of FLC through recruitment of FVE, a component of the histone deacetylase complex. Thus, our data suggest that chloroplasts function as essential sensors of high light to regulate flowering and adaptive responses by triggering nuclear transcriptional changes at the chromatin level.

Keywords: FLC; chloroplast retrograde signals; chromatin remodeling; flowering regulation; high light.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / genetics
  • Arabidopsis / growth & development
  • Arabidopsis Proteins / genetics*
  • Carrier Proteins / genetics*
  • Cell Nucleus / genetics
  • Cell Nucleus / radiation effects
  • Chloroplasts / genetics
  • Chloroplasts / metabolism
  • Chromatin / genetics
  • Chromatin / radiation effects
  • Flowers / genetics*
  • Flowers / growth & development
  • Flowers / radiation effects
  • Gene Expression Regulation, Plant / radiation effects
  • Histone Deacetylases / genetics
  • Light
  • MADS Domain Proteins / genetics*
  • PHD Zinc Fingers / genetics*
  • Signal Transduction / genetics
  • Transcription Factors

Substances

  • Arabidopsis Proteins
  • Carrier Proteins
  • Chromatin
  • FLF protein, Arabidopsis
  • MADS Domain Proteins
  • MSI4 protein, Arabidopsis
  • Transcription Factors
  • Histone Deacetylases