Faculty Research 1980 - 1989

Title

Genetic and environmental control of diabetes induction by multi-dose streptozotocin in two BALB/c substrains.

Document Type

Article

Publication Date

1988

Keywords

Animal, Diabetes-Mellitus-Experimental: ge, pp, pa, Disease-Susceptibility, Drug-Administration-Schedule, Environment, Injections-Intraperitoneal, Linkage-(Genetics), Male, Mice, Mice-Inbred-BALB-C, Mutation, Phenotype, Species-Specificity, Streptozotocin, SUPPORT-NON-U-S-GOVT, SUPPORT-U-S-GOVT-P-H-S

JAX Location

1738

JAX Source

Diabetes Res 1988 Sep; 9(1):5-10.

Grant

DK17631, DK27722

Abstract

BALB/cJ male mice were resistant and BALB/cByJ males were susceptible to induction of diabetes by multi-dose streptozotocin (MSz). Although both closely-related BALB/c substrains expressed H-2d haplotype, they could be differentiated by allelic differences at three genetic loci [Qa-2 (Chr 17), Bcd-1 (Chr 5), and Afr-1]. (BALB/cJ X BALB/cByJ)F1 males inherited the BALB/cJ resistance phenotype in a dominant fashion, thereby eliminating the BALB/cJ-expressed Afr-1b (recessive) allele as the susceptibility locus. Backcross of F1 mice to the susceptible BALB/cByJ strain produced a 1:1 segregation of susceptible and resistant (F1-like) phenotypes, suggesting that susceptibility was controlled by a single recessive gene. No linkage was found between the putative susceptibility gene and the mutant BALB/cByJ Qa-2,3 gene linked to the H-2 complex or with the mutant Bcd-1c allele. Since the resistant F1 males expressed low levels of androgen-dependent mouse urinary protein characteristic of the resistant BALB/cJ parental strain, the possibility was discussed that the alleles controlling sensitivity to MSz also controlled tissue sensitivity to endogenous androgens. An environmental effect on phenotype expression was indicated when BALB/cByJ males obtained from a colony free of pneumonia virus of mice (PVM) showed an attenuated rate of response to hyperglycemia induction in comparison to males obtained previously from an enzootically infected colony.

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