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ppGpp Is Present in and Functions to Regulate Sleep in Drosophila
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SUMMARYDiscovery of molecules in living systems and demonstration of their functional roles are pivotal in furthering our understanding of the molecular basis of biology. ppGpp (guanosine-5’-diphosphate, 3’-diphosphate) has been detected in prokaryotes for more than five decades. Here we report that a genetic screen followed by chemical analysis revealed the presence of ppGpp in Drosophila. It can be detected in germ-free Drosophila and its level is controlled by an enzyme encoded by themesh1gene in Drosophila. Loss of function mutations inmesh1, which encoded the ppGpp degrading enzyme led to longer sleep latency and less total sleep. These phenotypes could be rescued by wild typemesh1, but not by the enzymatically defective mutant Mesh1E66A, functionally implicating ppGpp. Ectopic expression of RelA, theE. colisynthetase for ppGpp, phenocopiedmesh1knockout mutants, whereas overexpression ofmesh1resulted in the opposite phenotypes, supporting that ppGpp is both necessary and sufficient in sleep regulation.mesh1is expressed in a specific population of neurons, and a chemoconnectomic screen followed by genetic intersection experiments implicate the pars intercerebralis (PI) as the site of ppGpp function. Our results have thus revealed that ppGpp is present in animals after long lag since its discovery in bacteria. Furthermore, we have demonstrated that ppGpp in a specific subset of neurons plays a physiological role in regulating sleep. We speculate that ppGpp may play function in mammals.
Cold Spring Harbor Laboratory
Title: ppGpp Is Present in and Functions to Regulate Sleep in Drosophila
Description:
SUMMARYDiscovery of molecules in living systems and demonstration of their functional roles are pivotal in furthering our understanding of the molecular basis of biology.
ppGpp (guanosine-5’-diphosphate, 3’-diphosphate) has been detected in prokaryotes for more than five decades.
Here we report that a genetic screen followed by chemical analysis revealed the presence of ppGpp in Drosophila.
It can be detected in germ-free Drosophila and its level is controlled by an enzyme encoded by themesh1gene in Drosophila.
Loss of function mutations inmesh1, which encoded the ppGpp degrading enzyme led to longer sleep latency and less total sleep.
These phenotypes could be rescued by wild typemesh1, but not by the enzymatically defective mutant Mesh1E66A, functionally implicating ppGpp.
Ectopic expression of RelA, theE.
colisynthetase for ppGpp, phenocopiedmesh1knockout mutants, whereas overexpression ofmesh1resulted in the opposite phenotypes, supporting that ppGpp is both necessary and sufficient in sleep regulation.
mesh1is expressed in a specific population of neurons, and a chemoconnectomic screen followed by genetic intersection experiments implicate the pars intercerebralis (PI) as the site of ppGpp function.
Our results have thus revealed that ppGpp is present in animals after long lag since its discovery in bacteria.
Furthermore, we have demonstrated that ppGpp in a specific subset of neurons plays a physiological role in regulating sleep.
We speculate that ppGpp may play function in mammals.
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