The negative regulation of Mesp2 by mouse Ripply2 is required to establish the rostro-caudal patterning within a somite

Development. 2007 Apr;134(8):1561-9. doi: 10.1242/dev.000836. Epub 2007 Mar 14.

Abstract

The Mesp2 transcription factor plays essential roles in segmental border formation and in the establishment of rostro-caudal patterning within a somite. A possible Mesp2 target gene, Ripply2, was identified by microarray as being downregulated in the Mesp2-null mouse. Ripply2 encodes a putative transcriptional co-repressor containing a WRPW motif. We find that Mesp2 binds to the Ripply2 gene enhancer, indicating that Ripply2 is a direct target of Mesp2. We then examined whether Ripply2 is responsible for the repression of genes under the control of Mesp2 by generating a Ripply2-knockout mouse. Unexpectedly, Ripply2-null embryos show a rostralized phenotype, in contrast to Mesp2-null mice. Gene expression studies together with genetic analyses further revealed that Ripply2 is a negative regulator of Mesp2 and that the loss of the Ripply2 gene results in the prolonged expression of Mesp2, leading to a rostralized phenotype via the suppression of Notch signaling. Our study demonstrates that a Ripply2-Mesp2 negative-feedback loop is essential for the periodic generation of the rostro-caudal polarity within a somite.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Basic Helix-Loop-Helix Transcription Factors / biosynthesis*
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Body Patterning*
  • Gene Expression Regulation, Developmental
  • Glycosyltransferases / metabolism
  • Mice
  • Mice, Knockout
  • Molecular Sequence Data
  • Repressor Proteins / genetics
  • Repressor Proteins / physiology*
  • Somites / physiology*

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Mesp2 protein, mouse
  • Repressor Proteins
  • Ripply2 protein, mouse
  • Glycosyltransferases
  • Lfng protein, mouse