Author/Authors :
Robert J. Johnston Jr.، نويسنده , , Yoshiaki Otake، نويسنده , , Pranidhi Sood، نويسنده , , Nina Vogt، نويسنده , , Rudy Behnia، نويسنده , , Daniel Vasiliauskas، نويسنده , , Elizabeth McDonald، نويسنده , , Baotong Xie، نويسنده , , Sebastian Koenig، نويسنده , , Reinhard Wolf، نويسنده , , Tiffany Cook، نويسنده , , Brian Gebelein، نويسنده , , Edo Kussell، نويسنده , , Hideki Nakagoshi، نويسنده , , Claude Desplan، نويسنده ,
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.