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Beauchamp, G. K.

Publications and source records attributed to Beauchamp, G. K..

2 recordsLinked to original sources

Genetics of mouse behavioral and peripheral neural responses to sucrose

Mice of the C57BL/6ByJ (B6) strain have higher consumption of, and stronger peripheral neural responses to, sucrose solution than do mice of the 129P3/J (129) strain. To identify quantitative trait loci (QTLs) responsible for this strain difference and evaluate the contribution of peripheral taste responsiveness to individual differences in sucrose intake, we produced an intercross (F2) of 627 mice, measured their sucrose consumption in two-bottle choice tests, recorded the electrophysiological activity of the chorda tympani nerve elicited by sucrose in a subset of F2 mice, and genotyped the mice with DNA markers distributed in every mouse chromosome. We confirmed a sucrose consumption QTL (Scon2, or Sac) on mouse chromosome (Chr) 4, harboring the Tas1r3 gene, which encodes the sweet taste receptor subunit T1R3 and affects both behavioral and neural responses to sucrose. For sucrose consumption, we also detected five new main-effect QTLs Scon6 (Chr2), Scon7 (Chr5), Scon8 (Chr8), Scon3 (Chr9) and a sex-specific QTL Scon9 (Chr15), and an interacting QTL pair Scon4 (Chr1) and Scon3 (Chr9). No additional QTLs for the taste nerve responses to sucrose were detected besides the previously known one on Chr4 (Scon2). Identification of the causal genes and variants for these sucrose consumption QTLs may point to novel mechanisms beyond peripheral taste sensitivity that could be harnessed to control obesity and diabetes.

animal behavior and cognition↗

Genetics of mouse Tas1r3-independent sucrose intake

We have previously shown that variation in sucrose intake among inbred mouse strains is due in part to polymorphisms in the Tas1r3 gene, which encodes a sweet taste receptor subunit and accounts for the Sac locus on distal Chr4. To discover other quantitative trait loci (QTLs) influencing sucrose intake, voluntary daily sucrose intake was measured in an F2 intercross with the Sac locus fixed; in backcross, reciprocal consomic strains; and in single- and double-congenic strains. Chromosome mapping identified Scon3, located on Chr9, and epistasis of Scon3 with Scon4 on Chr1. Mice with different combinations of Scon3 and Scon4 genotypes differed more than threefold in sucrose intake. To understand how these two QTLs influenced sucrose intake, we measured resting metabolism, glucose and insulin tolerance, and peripheral taste responsiveness in congenic mice. We found that the combinations of Scon3 and Scon4 genotypes influenced thermogenesis and the oxidation of fat and carbohydrate. Results of glucose and insulin tolerance tests, peripheral taste tests, and gustatory nerve recordings ruled out plasma glucose homoeostasis and peripheral taste sensitivity as major contributors to the differences in voluntary sucrose consumption. Our results provide evidence that these two novel QTLs influence mouse-to-mouse variation in sucrose intake and that both likely act through a common postoral mechanism.

animal behavior and cognition↗