Characterisation of Upd2, a Drosophila JAK/STAT pathway ligand

Dev Biol. 2005 Dec 15;288(2):420-33. doi: 10.1016/j.ydbio.2005.09.040. Epub 2005 Nov 7.

Abstract

The characterisation of ligands that activate the JAK/STAT pathway has the potential to throw light onto a comparatively poorly understood aspect of this important signal transduction cascade. Here, we describe our analysis of the only invertebrate JAK/STAT pathway ligands identified to date, the Drosophila unpaired-like family. We show that upd2 is expressed in a pattern essentially identical to that of upd and demonstrate that the proteins encoded by this region activate JAK/STAT pathway signalling. Mutational analysis demonstrates a mutual semi-redundancy that can be visualised in multiple tissues known to require JAK/STAT signalling. In order to better characterise the in vivo function of these ligands, we developed a reporter based on a natural JAK/STAT pathway responsive enhancer and show that ectopic upd2 expression can effectively activate the JAK/STAT pathway. While both Upd and Upd2 are secreted JAK/STAT pathway agonists, tissue culture assays show that the signal-sequences of Upd and Upd2 confer distinct properties, with Upd associated primarily with the extracellular matrix and Upd2 secreted into the media. The differing biophysical characteristics identified for Upd-like molecules have implications for their function in vivo and adds another aspect to our understanding of cytokine signalling in Drosophila.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Drosophila / metabolism*
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Drosophila Proteins / physiology*
  • Enhancer Elements, Genetic
  • Extracellular Matrix / metabolism
  • Janus Kinases
  • Ligands
  • Molecular Sequence Data
  • Mutation
  • Phylogeny
  • Protein-Tyrosine Kinases / metabolism
  • Protein-Tyrosine Kinases / physiology*
  • STAT Transcription Factors / metabolism
  • STAT Transcription Factors / physiology*
  • Signal Transduction
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription Factors / physiology*
  • X Chromosome / genetics

Substances

  • Drosophila Proteins
  • Ligands
  • STAT Transcription Factors
  • Transcription Factors
  • Upd2 protein, Drosophila
  • upd1 protein, Drosophila
  • Protein-Tyrosine Kinases
  • Janus Kinases
  • hop protein, Drosophila