TY - JOUR
T1 - Insomniac and cullin-3 regulate sleep and wakefulness in drosophila
AU - Stavropoulos, Nicholas
AU - Young, Michael W.
N1 - Funding Information:
We thank Lino Saez for his advice and guidance throughout the course of these experiments, and Dragana Rogulja for communicating her independent isolation of Nedd8 from a sleep screen. We also thank J. Stieglitz and A. Sarma for technical assistance; F. Lam and S. Syed for advice on MATLAB coding; P. Kidd for assistance with circadian analysis; D. Seay for primers; M. Crickmore, R. Galindo, R. Jackson, W. Joiner, K. Koh, H. Kramer, A. Sehgal, J. Simpson, G. Tononi, L. Vosshall, and the Bloomington, NIG-Fly, and VDRC stock centers for stocks; A. Sehgal and DSHB for antibodies; and the RU Bio-Imaging Resource Center for use of microscopes. We thank C. Bargmann, L.Vosshall, and members of the Young Lab for critical comments on the manuscript and discussions. This research was supported by NIH grants NS053087, GM054339, and MH015125 to M.W.Y., and by NIH Ruth L. Kirchstein postdoctoral fellowship GM080934 to N.S.
PY - 2011/12/22
Y1 - 2011/12/22
N2 - In a forward genetic screen in Drosophila, we have isolated insomniac, a mutant that severely reduces the duration and consolidation of sleep. Anatomically restricted genetic manipulations indicate that insomniac functions within neurons to regulate sleep. insomniac expression does not oscillate in a circadian manner, and conversely, the circadian clock is intact in insomniac mutants, suggesting that insomniac regulates sleep by pathways distinct from the circadian clock. The protein encoded by insomniac is a member of the BTB/POZ superfamily, which includes many proteins that function as adaptors for the Cullin-3 (Cul3) ubiquitin ligase complex. We show that Insomniac can physically associate with Cul3, and that reduction of Cul3 activity in neurons recapitulates the insomniac phenotype. The extensive evolutionary conservation of insomniac and Cul3 suggests that protein degradation pathways may have a general role in governing the sleep and wakefulness of animals.
AB - In a forward genetic screen in Drosophila, we have isolated insomniac, a mutant that severely reduces the duration and consolidation of sleep. Anatomically restricted genetic manipulations indicate that insomniac functions within neurons to regulate sleep. insomniac expression does not oscillate in a circadian manner, and conversely, the circadian clock is intact in insomniac mutants, suggesting that insomniac regulates sleep by pathways distinct from the circadian clock. The protein encoded by insomniac is a member of the BTB/POZ superfamily, which includes many proteins that function as adaptors for the Cullin-3 (Cul3) ubiquitin ligase complex. We show that Insomniac can physically associate with Cul3, and that reduction of Cul3 activity in neurons recapitulates the insomniac phenotype. The extensive evolutionary conservation of insomniac and Cul3 suggests that protein degradation pathways may have a general role in governing the sleep and wakefulness of animals.
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U2 - 10.1016/j.neuron.2011.12.003
DO - 10.1016/j.neuron.2011.12.003
M3 - Article
C2 - 22196332
AN - SCOPUS:84155177082
SN - 0896-6273
VL - 72
SP - 964
EP - 976
JO - Neuron
JF - Neuron
IS - 6
ER -