Literature DB >> 3071998

Specificity of androgen resistance in Mus caroli kidney.

C M Wilson1, D F Kimberlin, J E Griffin, J D Wilson.   

Abstract

Androgen controls the expression of beta-glucuronidase and several other proteins in the kidney of the standard laboratory mouse, Mus musculus. Other species within the genus Mus exhibit a variety of response patterns for kidney beta-glucuronidase and other markers of androgen action. We have investigated the mechanism of androgen action in M. caroli, a Mus species that does not produce beta-glucuronidase in response to testosterone. The failure of testosterone to induce beta-glucuronidase in M. caroli females cannot be overcome by treatment with dihydrotestosterone, with pharmacological doses of testosterone propionate or dihydrotestosterone propionate, or with a variety of potent androgen analogues. All of these compounds induce kidney beta-glucuronidase in M. musculus females and kidney ornithine decarboxylase, submandibular gland renin, and submandibular gland epidermal growth factor in both M. caroli and M. musculus females. Furthermore, kidney androgen receptor proteins from M. caroli and M. musculus animals have the same sedimentation characteristics on sucrose density gradients. These data indicate that androgen resistance in M. caroli is not due to deficient 5 alpha-reductase or aberrant hormone metabolism producing suboptimal levels of functional androgen and is not caused by a defective androgen receptor. They suggest that the resistance of beta-glucuronidase in M. caroli kidney to induction by androgen occurs at the level of the beta-glucuronidase gene.

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Year:  1988        PMID: 3071998     DOI: 10.1007/bf02395517

Source DB:  PubMed          Journal:  Biochem Genet        ISSN: 0006-2928            Impact factor:   1.890


  21 in total

1.  Evolution of steroid-inducible RP2 mRNA expression in the mouse kidney.

Authors:  J Tseng-Crank; F G Berger
Journal:  Genetics       Date:  1987-08       Impact factor: 4.562

Review 2.  Genetic regulation of mammalian glucuronidase.

Authors:  R T Swank; K Paigen; R Davey; V Chapman; C Labarca; G Watson; R Ganschow; E J Brandt; E Novak
Journal:  Recent Prog Horm Res       Date:  1978

3.  A study of the androgen receptors in a variety of androgen-sensitive tissues.

Authors:  W I Mainwaring; F R Mangan
Journal:  J Endocrinol       Date:  1973-10       Impact factor: 4.286

4.  Genetic control of glucuronidase induction in mice.

Authors:  R T Swank; K Paigen; R E Ganschow
Journal:  J Mol Biol       Date:  1973-12-05       Impact factor: 5.469

5.  Nuclear androgen receptors in the mouse kidney: validation of a new assay.

Authors:  V Isomaa; A E Pajunen; C W Bardin; O A Jänne
Journal:  Endocrinology       Date:  1982-09       Impact factor: 4.736

Review 6.  Testosterone: a major determinant of extragenital sexual dimorphism.

Authors:  C W Bardin; J F Catterall
Journal:  Science       Date:  1981-03-20       Impact factor: 47.728

7.  Genetic control of renin activity in the submaxillary gland of the mouse.

Authors:  C M Wilson; E G Erdös; J F Dunn; J D Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

8.  Differences in the androgen response between two mouse species.

Authors:  P W Houben; L P Bullock; T O Fox
Journal:  Biochem Genet       Date:  1986-12       Impact factor: 1.890

9.  Androgen and progestin stimulation of ornithine decarboxylase activity in the mouse kidney.

Authors:  L P Bullock
Journal:  Endocrinology       Date:  1983-06       Impact factor: 4.736

10.  The interaction of androgen and thyroid hormones in the submandibular gland of the genetically hypothyroid (hyt/hyt) mouse.

Authors:  C M Wilson; J E Griffin; R C Reynolds; J D Wilson
Journal:  Endocrinology       Date:  1985-06       Impact factor: 4.736

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