Interlocked feedforward loops control cell-type-specific Rhodopsin expression in the Drosophila eye

Cell. 2011 Jun 10;145(6):956-68. doi: 10.1016/j.cell.2011.05.003.

Abstract

How complex networks of activators and repressors lead to exquisitely specific cell-type determination during development is poorly understood. In the Drosophila eye, expression patterns of Rhodopsins define at least eight functionally distinct though related subtypes of photoreceptors. Here, we describe a role for the transcription factor gene defective proventriculus (dve) as a critical node in the network regulating Rhodopsin expression. dve is a shared component of two opposing, interlocked feedforward loops (FFLs). Orthodenticle and Dve interact in an incoherent FFL to repress Rhodopsin expression throughout the eye. In R7 and R8 photoreceptors, a coherent FFL relieves repression by Dve while activating Rhodopsin expression. Therefore, this network uses repression to restrict and combinatorial activation to induce cell-type-specific expression. Furthermore, Dve levels are finely tuned to yield cell-type- and region-specific repression or activation outcomes. This interlocked FFL motif may be a general mechanism to control terminal cell-fate specification.

Publication types

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

MeSH terms

  • Animals
  • Drosophila / cytology
  • Drosophila / embryology*
  • Drosophila / metabolism*
  • Drosophila Proteins / genetics*
  • Drosophila Proteins / metabolism
  • Eye / embryology
  • Feedback, Physiological
  • Gene Expression Regulation, Developmental*
  • Gene Regulatory Networks*
  • Homeodomain Proteins / metabolism
  • Photoreceptor Cells, Invertebrate / metabolism*
  • Rhodopsin / genetics*
  • Transcription Factors / metabolism

Substances

  • Drosophila Proteins
  • Homeodomain Proteins
  • Transcription Factors
  • dve protein, Drosophila
  • oc protein, Drosophila
  • salm protein, Drosophila
  • Rhodopsin