Oligomerization of the extracellular domain of Boss enhances its binding to the Sevenless receptor and its antagonistic effect on R7 induction

Evgueni A. Sevrioukov, Jason H. Walenta, Arisa Sunio, Meridee Phistry, Helmut Krämer

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

In the developing compound eye of Drosophila, neuronal differentiation of the R7 photoreceptor cell is induced by the interaction of the receptor tyrosine kinase Sevenless with its ligand Bride of sevenless (Boss), which is expressed on the neighboring R8 cell. Boss is an unusual ligand of a receptor tyrosine kinase: it is composed of a large extracellular domain, a transmembrane domain with seven membrane-spanning segments and a cytoplasmic tail. Expression of a monomeric, secreted form of the extracellular domain of Boss is not sufficient for Sevenless activation, and instead acts as a weak antagonist. Because oligomerization appears to be a critical step in the activation of receptor tyrosine kinases, we used oligomerized forms of the Boss extracellular domain to test their ability to bind to Sevenless in vivo and restore R7 induction in vivo. Oligomerization was achieved by fusion to the leucine zipper of the yeast transcription factor GCN4 or to the tetramerization helix of Lac repressor. Binding of these multivalent proteins to Sevenless could be detected in vitro by immunoprecipitation of cross-linked ligand/receptor complexes and in vivo by receptor dependent ligand localization. However, neither R8-specific or ubiquitous expression of multivalent Exboss ligands rescued the boss phenotype. Instead, these ligands acted as competitive inhibitors for wild-type Boss protein and thereby suppressed R7 induction. Therefore the role of the transmembrane or cytoplasmic domains of Boss in the activation of the Sev receptor cannot be replaced by oligomerization.

Original languageEnglish (US)
Pages (from-to)737-747
Number of pages11
JournalJournal of Cell Science
Volume111
Issue number6
StatePublished - 1998

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Ligands
Receptor Protein-Tyrosine Kinases
Lac Repressors
Leucine Zippers
Photoreceptor Cells
Immunoprecipitation
Drosophila
Tail
Carrier Proteins
Transcription Factors
Yeasts
Phenotype
Membranes
Proteins

Keywords

  • Bride of sevenless
  • Drosophila
  • Ligand
  • Oligomerization
  • Receptor tyrosine kinase signaling

ASJC Scopus subject areas

  • Cell Biology

Cite this

Oligomerization of the extracellular domain of Boss enhances its binding to the Sevenless receptor and its antagonistic effect on R7 induction. / Sevrioukov, Evgueni A.; Walenta, Jason H.; Sunio, Arisa; Phistry, Meridee; Krämer, Helmut.

In: Journal of Cell Science, Vol. 111, No. 6, 1998, p. 737-747.

Research output: Contribution to journalArticle

Sevrioukov, Evgueni A. ; Walenta, Jason H. ; Sunio, Arisa ; Phistry, Meridee ; Krämer, Helmut. / Oligomerization of the extracellular domain of Boss enhances its binding to the Sevenless receptor and its antagonistic effect on R7 induction. In: Journal of Cell Science. 1998 ; Vol. 111, No. 6. pp. 737-747.
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