Skip to main navigation Skip to search Skip to main content

BMP and FGF signaling interact to pattern mesoderm by controlling basic helix-loop-helix transcription factor activity

  • Richard H. Row
  • , Amy Pegg
  • , Brian A. Kinney
  • , Gist H. Farr
  • , Lisa Maves
  • , Sally Lowell
  • , Valerie Wilson
  • , Benjamin L. Martin
  • Stony Brook University
  • University of Edinburgh
  • Seattle Children’s Research Institute
  • University of Washington

Research output: Contribution to journalArticlepeer-review

39 Scopus citations

Abstract

The mesodermal germ layer is patterned into mediolateral subtypes by signaling factors including BMP and FGF. How these pathways are integrated to induce specific mediolateral cell fates is not well understood. We used mesoderm derived from post-gastrulation neuromesodermal progenitors (NMPs), which undergo a binary mediolateral patterning decision, as a simplified model to understand how FGF acts together with BMP to impart mediolateral fate. Using zebrafish and mouse NMPs, we identify an evolutionarily conserved mechanism of BMP and FGF-mediated mediolateral mesodermal patterning that occurs through modulation of basic helix-loop-helix (bHLH) transcription factor activity. BMP imparts lateral fate through induction of Id helix loop helix (HLH) proteins, which antagonize bHLH transcription factors, induced by FGF signaling, that specify medial fate. We extend our analysis of zebrafish development to show that bHLH activity is responsible for the mediolateral patterning of the entire mesodermal germ layer.

Original languageEnglish
Article numbere31018
JournaleLife
Volume7
DOIs
StatePublished - Jun 7 2018

Fingerprint

Dive into the research topics of 'BMP and FGF signaling interact to pattern mesoderm by controlling basic helix-loop-helix transcription factor activity'. Together they form a unique fingerprint.

Cite this