In animals the timekeeping necessary for sleep/activity rhythms takes place within neurons located in discrete regions of the central nervous system (CNS). Remarkably, individual neuronal circadian clocks can maintain molecular and physiological rhythms in the absence of time-cues from the environment or other cells. Despite such cell-autonomous timekeeping, the orchestration of daily behavioral rhytiims depends on networks of clock neurons. I seek to understand the circuit properties of these networks and to examine the roles that identified neurons play in the control of circadian rhythms. During the ROO phase of my research! will use the anatomical, genetic, and live-imaging techniques 1 developed during the K99 phase of my grant to discover how time is kept within the brain and how it is used to orchestrate daily and seasonal changes in behavior in the fly Drosophila melanogaster. Furthermore, newly developed technologies in live imaging, fly genetics, and light-control of neuronal signaling will be developed to investigate the circuit properties of the circadian clock network in the fly brain. To understand the organization of the neuronal clock network, and fundamental questions of neuromodulatory signaling in the nervous system, I propose the following speciflc aims: 1) The development of live Imaging methods for the simultaneous manipulation and observation of neuronal signaling using optogenetic control of cell excitability in conjunction with genetically encoded sensors for cAMP and Ca2-f, H) The identiflcation of peptide/amine modulators of the neuronal clock network. Ill) The identiflcation and characterization of non-clock targets of clock neuron output using live imaging and targeted genetic manipulation approaches, IV) The genetic dissection of GPCR/cAMP/Ca2-t- signaling within these neurons. The work supported by my K99 grant supports the feasibility of all aspects of the proposed research and the resources made possible by the ROO will allow me to employ advanced imaging technologies in my study of the neuronal clock network. Furthermore, the work proposed here will address fundamental aspects of neurobiology and create new methodologies for the investigation of neuronal circuitry and the control of animal behavior.

Public Health Relevance

Circadian clocks drive daily changes in behavior and physiology and the loss of circadian function results in metat>olic derangement and decreased longevity. Determining the neuronal basis of circadian time-keeping is therefore important not only for human health (Drosophila's clock has consistently revealed principles relevant to the human clock) but also for our understanding of the neural basis of behavior.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Transition Award (R00)
Project #
5R00NS062953-05
Application #
8197941
Study Section
Special Emphasis Panel (NSS)
Program Officer
Mitler, Merrill
Project Start
2008-07-16
Project End
2012-11-30
Budget Start
2011-12-01
Budget End
2012-11-30
Support Year
5
Fiscal Year
2012
Total Cost
$241,677
Indirect Cost
$85,252
Name
University of Michigan Ann Arbor
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Schlichting, Matthias; Menegazzi, Pamela; Lelito, Katharine R et al. (2016) A Neural Network Underlying Circadian Entrainment and Photoperiodic Adjustment of Sleep and Activity in Drosophila. J Neurosci 36:9084-96
Shafer, Orie T; Yao, Zepeng (2014) Pigment-Dispersing Factor Signaling and Circadian Rhythms in Insect Locomotor Activity. Curr Opin Insect Sci 1:73-80
Yao, Z; Shafer, O T (2014) The Drosophila circadian clock is a variably coupled network of multiple peptidergic units. Science 343:1516-20
Collins, Ben; Kaplan, Harris S; Cavey, Matthieu et al. (2014) Differentially timed extracellular signals synchronize pacemaker neuron clocks. PLoS Biol 12:e1001959
Yao, Zepeng; Macara, Ann Marie; Lelito, Katherine R et al. (2012) Analysis of functional neuronal connectivity in the Drosophila brain. J Neurophysiol 108:684-96
Lelito, Katherine R; Shafer, Orie T (2012) Reciprocal cholinergic and GABAergic modulation of the small ventrolateral pacemaker neurons of Drosophila's circadian clock neuron network. J Neurophysiol 107:2096-108
Talsma, Aaron D; Christov, Christo P; Terriente-Felix, Ana et al. (2012) Remote control of renal physiology by the intestinal neuropeptide pigment-dispersing factor in Drosophila. Proc Natl Acad Sci U S A 109:12177-82
Beckwith, Esteban J; Lelito, Katherine R; Hsu, Yun-Wei A et al. (2011) Functional conservation of clock output signaling between flies and intertidal crabs. J Biol Rhythms 26:518-29