Paracrine brassinosteroid signaling at the stem cell niche controls cellular regeneration

J Cell Sci. 2018 Jan 29;131(2):jcs204065. doi: 10.1242/jcs.204065.

Abstract

Stem cell regeneration is crucial for both cell turnover and tissue healing in multicellular organisms. In Arabidopsis roots, a reduced group of cells known as the quiescent center (QC) act as a cell reservoir for surrounding stem cells during both normal growth and in response to external damage. Although cells of the QC have a very low mitotic activity, plant hormones such as brassinosteroids (BRs) can promote QC divisions. Here, we used a tissue-specific strategy to investigate the spatial signaling requirements of BR-mediated QC divisions. We generated stem cell niche-specific receptor knockout lines by placing an artificial microRNA against BRI1 (BRASSINOSTEROID INSENSITIVE 1) under the control of the QC-specific promoter WOX5. Additionally, QC-specific knock-in lines for BRI1 and its downstream transcription factor BES1 (BRI1-EMS-SUPPRESOR1) were also created using the WOX5 promoter. By analyzing the roots of these lines, we show that BES1-mediated signaling cell-autonomously promotes QC divisions, that BRI1 is essential for sensing nearby inputs and triggering QC divisions and that DNA damage promotes BR-dependent paracrine signaling in the stem cell niche as a prerequisite to stem cell replenishment.

Keywords: Brassinosteroid; Cell division; DNA damage; Paracrine; Quiescent center; Stem cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / cytology*
  • Arabidopsis / metabolism*
  • Arabidopsis Proteins / metabolism
  • Brassinosteroids / metabolism*
  • Cellular Microenvironment
  • DNA Damage
  • Down-Regulation / genetics
  • Gene Expression Regulation, Plant
  • Membrane Proteins / metabolism
  • Meristem / cytology
  • Meristem / metabolism
  • Models, Biological
  • Paracrine Communication*
  • Plant Roots / cytology
  • Plant Roots / metabolism
  • Plants, Genetically Modified
  • Regeneration*
  • Seedlings / cytology
  • Seedlings / metabolism
  • Signal Transduction*
  • Stem Cell Niche*
  • Transcription, Genetic

Substances

  • Arabidopsis Proteins
  • Brassinosteroids
  • Membrane Proteins