Central pattern generators (CPGs) are rhythmically active neural networks that underlie many stereotyped and repetitive voluntary muscle movements such as whisking or fluid licking. Fluid licking in rodents is an example of a promising, simple model of a CPG: It is a highly stereotyped behavior characterized by rhythmic tongue and jaw movements, and it is thought to be controlled by a neural substrate distributed in the medullary reticular formation in the brainstem. In preliminary observations, we have demonstrated that mice are a superb species choice for investigating the genetic basis of the licking CPG- the common inbred strains C57BL/6J (B6) and DBA/2J (D2) have a robust, non-overlapping phenotypic difference in lick rate. The identification of genes underlying differences in lick rate should have a huge payout for the study of CPGs. Mice can then created with gene-targeted deletions or insertions, allowing for specific physiological or anatomical investigation. We propose to take advantage of a newly augmented resource for our genetic dissection of licking: The BXD advanced recombinant inbred (Rl) strain set. These mice will allow for precision genetic mapping of quantitative trait loci (QTL) that underlie behavioral traits. We propose to use a novel high-throughput assay for lick rate to test a set of -80 BXD Rl strains, and map quantitative trait loci (QTLs) with high precision that underlie strain variation in lick rate. Relevance: Complex animals such as humans possess a number of motor responses that are stereotypic and/or repetitive in nature. Comparison of the genes and mechanisms underlying stereotyped repetitive movements vs. plastic behaviors will be a source of information relevant for a number of human CMS disorders involving abnormal repetitive movements.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21NS052366-02
Application #
7340123
Study Section
Biobehavioral Regulation, Learning and Ethology Study Section (BRLE)
Program Officer
Babcock, Debra J
Project Start
2007-01-15
Project End
2010-12-31
Budget Start
2008-01-01
Budget End
2010-12-31
Support Year
2
Fiscal Year
2008
Total Cost
$191,625
Indirect Cost
Name
University of Tennessee Health Science Center
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
941884009
City
Memphis
State
TN
Country
United States
Zip Code
38163
St John, Steven J; Lu, Lu; Williams, Robert W et al. (2017) Genetic control of oromotor phenotypes: A survey of licking and ingestive behaviors in highly diverse strains of mice. Physiol Behav 177:34-43
Boughter Jr, John D; Mulligan, Megan K; St John, Steven J et al. (2012) Genetic control of a central pattern generator: rhythmic oromotor movement in mice is controlled by a major locus near Atp1a2. PLoS One 7:e38169
Shires, Courtney B; Saputra, Jennifer M; Stocks, Rose Mary S et al. (2011) Effects of sensory or motor nerve deafferentation on oromotor function in mice. Otolaryngol Head Neck Surg 144:915-20
Glatt, A Rebecca; Denton, Kelley; Boughter Jr, John D (2009) Variation in nicotine consumption in inbred mice is not linked to orosensory ability. Chem Senses 34:27-35
St John, Steven J; Boughter Jr, John D (2009) Orosensory responsiveness to and preference for hydroxide-containing salts in mice. Chem Senses 34:487-98
Reiner, David J; Jan, Taha A; Boughter Jr, John D et al. (2008) Genetic analysis of tongue size and taste papillae number and size in recombinant inbred strains of mice. Chem Senses 33:693-707
Boughter Jr, John D; Bachmanov, Alexander A (2007) Behavioral genetics and taste. BMC Neurosci 8 Suppl 3:S3