The co-regulator dNAB interacts with Brinker to eliminate cells with reduced Dpp signaling

Oren Ziv, Yaron Suissa, Hadar Neuman, Tama Dinur, Peter Geuking, Christa Rhiner, Marta Portela, Fidel Lolo, Eduardo Moreno*, Offer Gerlitz

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

14 Scopus citations


The proper development of tissues requires morphogen activity that dictates the appropriate growth and differentiation of each cell according to its position within a developing field. Elimination of underperforming cells that are less efficient in receiving/transducing the morphogenetic signal is thought to provide a general fail-safe mechanism to avoid developmental misspecification. In the developing Drosophila wing, the morphogen Dpp provides cells with growth and survival cues. Much of the regulation of transcriptional output by Dpp is mediated through repression of the transcriptional repressor Brinker (Brk), and thus through the activation of target genes. Mutant cells impaired for Dpp reception or transduction are lost from the wing epithelium. At the molecular level, reduced Dpp signaling results in Brk upregulation that triggers apoptosis through activation of the JNK pathway. Here we show that the transcriptional co-regulator dNAB is a Dpp target in the developing wing that interacts with Brk to eliminate cells with reduced Dpp signaling through the JNK pathway. We further show that both dNAB and Brk are required for cell elimination induced by differential dMyc expression, a process that depends on reduced Dpp transduction in outcompeted cells.We propose a novel mechanism whereby the morphogen Dpp regulates the responsiveness to its own survival signal by inversely controlling the expression of a repressor, Brk, and its co-repressor, dNAB.

Original languageAmerican English
Pages (from-to)1137-1145
Number of pages9
JournalJournal of Embryology and Experimental Morphology
Issue number7
StatePublished - 1 Apr 2009


  • Brinker
  • Dpp survival signal
  • Wing development
  • dMyc (Dm)-induced cell competition
  • dNAB (Drosophila Nab)


Dive into the research topics of 'The co-regulator dNAB interacts with Brinker to eliminate cells with reduced Dpp signaling'. Together they form a unique fingerprint.

Cite this