This proposal seeks to identify genes implicated in the normal expression and regulation of sleep and the sleep EEG in mice. We have identified several sleep and EEG related phenotypes that strongly vary with genotype in inbred strains of mice. In this proposal, we intend to follow these candidate phenotypes in segregating progeny derived from the inbred strains for which these phenotypes differed the most. We propose to first study the segregation of """"""""candidate"""""""" phenotypes in a set of 21 recombinant inbred (RI) strains of mice that were derived from two progenitor strains (i.e. AKR x DBA/2). Subsequent pheno- and genotyping of inter-and/or backcross progeny will yield more detailed information on genomic localizations that may be used to explain genotypic variance in the traits of interest (QTL-mapping and linkage analysis). Furthermore, we can make use of these spontaneous intra-species differences in sleep to answer basic sleep physiology issues. These issues concern the homeostatic regulation of SWS and REMS, their interaction with each other and with brain temperature, and the neurophysiological substrate of SWS intensity measured by EEG delta power. The large difference in the time constant of the wakefulness-dependent increase in SWS delta power between AKR and DBA/2 that we have found, is of special interest because it suggests that the accumulation of sleep need is under genetic control. Identifying genetic factors underlying the normal expression and regulation of sleep and the sleep EEG will further our understanding of the neurophysiological mechanisms that govern sleep and will potentially have large implications for sleep disorders in general and those with a genetic predisposition in particular.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL064148-03
Application #
6390599
Study Section
Special Emphasis Panel (ZHL1-CSR-R (S1))
Program Officer
Twery, Michael
Project Start
1999-09-30
Project End
2003-08-31
Budget Start
2001-09-01
Budget End
2002-08-31
Support Year
3
Fiscal Year
2001
Total Cost
$355,632
Indirect Cost
Name
Stanford University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
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Xie, Xinmin; Dumas, Theodore; Tang, Lamont et al. (2005) Lack of the alanine-serine-cysteine transporter 1 causes tremors, seizures, and early postnatal death in mice. Brain Res 1052:212-21
Larkin, Jennie E; Yokogawa, Tohei; Heller, H Craig et al. (2004) Homeostatic regulation of sleep in arrhythmic Siberian hamsters. Am J Physiol Regul Integr Comp Physiol 287:R104-11
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Franken, Paul; Tafti, Mehdi (2003) Genetics of sleep and sleep disorders. Front Biosci 8:e381-97
Franken, Paul; Gip, Phung; Hagiwara, Grace et al. (2003) Changes in brain glycogen after sleep deprivation vary with genotype. Am J Physiol Regul Integr Comp Physiol 285:R413-9
Shaw, Paul J; Franken, Paul (2003) Perchance to dream: solving the mystery of sleep through genetic analysis. J Neurobiol 54:179-202
Tafti, Mehdi; Franken, Paul (2002) Invited review: genetic dissection of sleep. J Appl Physiol 92:1339-47
Ruby, Norman F; Brennan, Thomas J; Xie, Xinmin et al. (2002) Role of melanopsin in circadian responses to light. Science 298:2211-3
Wisor, Jonathan P; O'Hara, Bruce F; Terao, Akira et al. (2002) A role for cryptochromes in sleep regulation. BMC Neurosci 3:20

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