TY - JOUR
T1 - The growth regulators warts/lats and melted interact in a bistable loop to specify opposite fates in Drosophila R8 photoreceptors
AU - Mikeladze-Dvali, Tamara
AU - Wernet, Mathias F.
AU - Pistillo, Daniela
AU - Mazzoni, Esteban O.
AU - Teleman, Aurelio A.
AU - Chen, Ya Wen
AU - Cohen, Stephen
AU - Desplan, Claude
N1 - Funding Information:
This work was supported by Grant NIH R01 EY13012 to C.D., the Fleur Strand Award to T.M.-D., a fellowship from Boehringer Ingelheim to M.F.W., from EMBO to D.P., and a Dean Dissertation Fellowship from NYU to E.O.M. This investigation was conducted in a facility constructed with support from Research Facilities Improvement Grant Number C06 RR-15518-01 from the National Center for Research Resources, National Institutes of Health.
PY - 2005/9/9
Y1 - 2005/9/9
N2 - Color vision in Drosophila relies on the comparison between two color-sensitive photoreceptors, R7 and R8. Two types of ommatidia in which R7 and R8 contain different rhodopsins are distributed stochastically in the retina and appear to discriminate short (p-subset) or long wavelengths (y-subset). The choice between p and y fates is made in R7, which then instructs R8 to follow the corresponding fate, thus leading to a tight coupling between rhodopsins expressed in R7 and R8. Here, we show that warts, encoding large tumor suppressor (Lats) and melted encoding a PH-domain protein, play opposite roles in defining the yR8 or pR8 fates. By interacting antagonistically at the transcriptional level, they form a bistable loop that insures a robust commitment of R8 to a single fate, without allowing ambiguity. This represents an unexpected postmitotic role for genes controlling cell proliferation (warts and its partner hippo and salvador) and cell growth (melted).
AB - Color vision in Drosophila relies on the comparison between two color-sensitive photoreceptors, R7 and R8. Two types of ommatidia in which R7 and R8 contain different rhodopsins are distributed stochastically in the retina and appear to discriminate short (p-subset) or long wavelengths (y-subset). The choice between p and y fates is made in R7, which then instructs R8 to follow the corresponding fate, thus leading to a tight coupling between rhodopsins expressed in R7 and R8. Here, we show that warts, encoding large tumor suppressor (Lats) and melted encoding a PH-domain protein, play opposite roles in defining the yR8 or pR8 fates. By interacting antagonistically at the transcriptional level, they form a bistable loop that insures a robust commitment of R8 to a single fate, without allowing ambiguity. This represents an unexpected postmitotic role for genes controlling cell proliferation (warts and its partner hippo and salvador) and cell growth (melted).
UR - http://www.scopus.com/inward/record.url?scp=24144492150&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=24144492150&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2005.07.026
DO - 10.1016/j.cell.2005.07.026
M3 - Article
C2 - 16143107
AN - SCOPUS:24144492150
SN - 0092-8674
VL - 122
SP - 775
EP - 787
JO - Cell
JF - Cell
IS - 5
ER -