Fat regulates expression of four-jointed reporters in vivo through a 20 bp element independently of the Hippo pathway

Dev Biol. 2019 Jun 1;450(1):23-33. doi: 10.1016/j.ydbio.2019.03.004. Epub 2019 Mar 9.

Abstract

Development of an organism requires accurate coordination between the growth of a tissue and orientation of cells within the tissue. The large cadherin Fat has been shown to play a role in both of these processes. Fat is involved in the establishment of planar cell polarity and regulates growth through the Hippo pathway, a developmental cascade that controls proliferation and apoptosis. Both Fat and the Hippo pathway are known to regulate transcription of four-jointed, although the nature of this regulation is unknown. In this study, we test whether Fat affects four-jointed transcription via or independently of Hippo pathway. Our analysis of the four-jointed regulatory region reveals a 1.2 kb element that functions as an enhancer for graded expression of Four-jointed in the eye imaginal disc. Within this enhancer element, we identify a 20 bp fragment that is critical for regulation by Fat but not by Hippo. Our findings suggest that Fat and the Hippo pathway control four-jointed expression independently of each other and none of the transcription factors known to function downstream of the Hippo pathway are required to regulate four-jointed expression through the 1.2 kb element.

Keywords: Enhancer; Eye imaginal disc; Fat; Four-jointed; Hippo pathway; Planar cell polarity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion Molecules* / genetics
  • Cell Adhesion Molecules* / metabolism
  • Drosophila Proteins* / biosynthesis
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila melanogaster
  • Enhancer Elements, Genetic*
  • Gene Expression Regulation, Developmental*
  • Genes, Reporter
  • Intracellular Signaling Peptides and Proteins* / genetics
  • Intracellular Signaling Peptides and Proteins* / metabolism
  • Membrane Glycoproteins* / biosynthesis
  • Membrane Glycoproteins* / genetics
  • Protein Serine-Threonine Kinases* / genetics
  • Protein Serine-Threonine Kinases* / metabolism
  • Signal Transduction*
  • Transcription, Genetic*

Substances

  • Cell Adhesion Molecules
  • Drosophila Proteins
  • Intracellular Signaling Peptides and Proteins
  • Membrane Glycoproteins
  • fj protein, Drosophila
  • ft protein, Drosophila
  • Protein Serine-Threonine Kinases
  • hpo protein, Drosophila

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