Nas Transgenic Mouse Line Allows Visualization of Notch Pathway Activity in Vivo

Genesis. 2006 Jun;44(6):277-86. doi: 10.1002/dvg.20208.

Abstract

The Notch signaling pathway plays multiple and important roles in mammals. However, several aspects of its action, in particular, the precise mapping of its sites of activity, remain unclear. To address this issue, we generated a transgenic line carrying a construct consisting of a nls-lacZ reporter gene under the control of a minimal promoter and multiple RBP-Jkappa binding sites. Here we show that this transgenic line, which we termed NAS (for Notch Activity Sensor), displays an expression profile that is consistent with current knowledge on Notch activity sites in mice, even though it may not report on all these sites. Moreover, we observe that NAS transgene expression is abolished in a RBP-Jkappa-deficient background, indicating that it indeed requires Notch/RBP-Jkappa signaling pathway activity. Thus, the NAS transgenic line constitutes a valuable and versatile tool to gain further insights into the complex and various functions of the Notch signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arteries / embryology
  • Arteries / metabolism
  • Base Sequence
  • Chromosomal Proteins, Non-Histone / genetics
  • Female
  • Gene Expression
  • Genes, Reporter
  • Heart / embryology
  • Immunoglobulin J Recombination Signal Sequence-Binding Protein / genetics*
  • Immunoglobulin J Recombination Signal Sequence-Binding Protein / metabolism
  • Lac Operon
  • Male
  • Mice
  • Mice, Transgenic / embryology
  • Mice, Transgenic / physiology*
  • Models, Biological
  • Molecular Sequence Data
  • Myocardium / metabolism
  • Promoter Regions, Genetic
  • Receptors, Notch / metabolism*
  • Receptors, Notch / physiology
  • Signal Transduction*
  • Somites / metabolism
  • Transgenes

Substances

  • Chromosomal Proteins, Non-Histone
  • Immunoglobulin J Recombination Signal Sequence-Binding Protein
  • Receptors, Notch
  • spermatid transition proteins