E(y)1/TAF9 mediates the transcriptional output of Notch signaling in Drosophila

J Cell Sci. 2014 Sep 1;127(Pt 17):3830-9. doi: 10.1242/jcs.154583. Epub 2014 Jul 11.

Abstract

Transcriptional activation of Notch signaling targets requires the formation of a ternary complex that involves the intracellular domain of the Notch receptor (NICD), DNA-binding protein Suppressor of Hairless [Su(H), RPBJ in mammals] and coactivator Mastermind (Mam). Here, we report that E(y)1/TAF9, a component of the transcription factor TFIID complex, interacts specifically with the NICD-Su(H)-Mam complex to facilitate the transcriptional output of Notch signaling. We identified E(y)1/TAF9 in a large-scale in vivo RNA interference (RNAi) screen for genes that are involved in a Notch-dependent mitotic-to-endocycle transition in Drosophila follicle cells. Knockdown of e(y)1/TAF9 displayed Notch-mutant-like phenotypes and defects in target gene and activity reporter expression in both the follicle cells and wing imaginal discs. Epistatic analyses in these two tissues indicated that E(y)1/TAF9 functions downstream of Notch cleavage. Biochemical studies in S2 cells demonstrated that E(y)1/TAF9 physically interacts with the transcriptional effectors of Notch signaling Su(H) and NICD. Taken together, our data suggest that the association of the NICD-Su(H)-Mastermind complex with E(y)1/TAF9 in response to Notch activation recruits the transcription initiation complex to induce Notch target genes, coupling Notch signaling with the transcription machinery.

Keywords: Drosophila; E(y)1; Notch pathway; TAF9; TFIID complex; Transcriptional regulation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / growth & development
  • Drosophila melanogaster / metabolism*
  • Gene Expression Regulation, Developmental / genetics*
  • Phenotype
  • Receptors, Notch / metabolism*
  • Signal Transduction / genetics*
  • TATA-Binding Protein Associated Factors / metabolism*
  • Transcription Factor TFIID / metabolism*
  • Wings, Animal / metabolism

Substances

  • Drosophila Proteins
  • N protein, Drosophila
  • Receptors, Notch
  • TATA-Binding Protein Associated Factors
  • Transcription Factor TFIID
  • e(y)1 protein, Drosophila