INHERITANCE: AdhF and AdhS codominant, both dominant to AdhN.
PHENOTYPE: The phenotype is based on electrophoresis of liver homogenate: [Electrophoretic conditions. Gel: starch, horizontal. Buffer: Continous, tris glycine, pH 8.3. Visualization. Alcohol with NAD-oxidoreductase substrate and tetrazolium stain.] Zymogram. Mobility: Cathodal. Protein structure: Dimer, intact Homozygotes appear as sinvje electromorphs in the case of AdhF and AdhS. Homozygous AdhN gives no activity. Heterozygotes AdhF/AdhS produce three electromorphs, less intense ones in the "fast" and "slow' Positions and a more intense intermediate band, as expected with a dimeric protein. Heterozygotes AdhF/AdhN and adhS/AdhN exhibit single less intense electromorphs at the "fast" or "slow" positions, respectively. AdhN homozygotes have no alcohol dehydrogenase activity by any assay, and there is no cross reactivity with purified protein from AdhF homozygotes. The null allele either produces no product or a product which is impaired to the extent that it will not cross react immunologically. Homozygous AdhN deer mice have significantly longer sleep times following ethanol induced narcosis.
![]() | Starch gel showing alcohol dehydrognase electrophoretic phenotypes in Peromyscus corresponding to genotypes: (1) AdhF/AdhF (2) AdhS/AdhS (3) AdhN/AdhN. Photograph courtesy of M.R. Felder. |
![]() | Restriction fragment length variation shown on southern blot using a Peromyscus-specific probe for the Adh-1 locus. |
This page updated 19 July 2005 by peromyscus@stkctr.biol.sc.edu
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2005, The Board of Trustees of the University of South Carolina.