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PMID: 3753840 Published · ppublish English Journal Article

Female-predominant expression of testosterone 16 alpha-hydroxylase ("I"-P-450(16)alpha) and its repression in strain 129/J.

Archives of biochemistry and biophysics ·Vol. 244 ·No. 2 ·1986-02-01 ·Pages 857-64

Noshiro M, Serabjit-Singh CJ, Bend JR, Negishi M

Abstract

Using specific testosterone 16 alpha-hydroxylase activity as the basis for selection of fractions during purification, the cytochrome P-450 ("I"-P-450(16)alpha) has been isolated from livers of phenobarbital-treated 129/J female mice [K. Devore, N. Harada, and M. Negishi (1985) Biochemistry, 24, 5632-5637]. An antibody elicited in rabbits to "I"-P-450(16)alpha was used to determine the amount of hepatic microsomal 16 alpha-hydroxylase activity due to "I"-P-450(16)alpha in untreated females and males of the two mouse strains, 129/J and BALB/cJ. The activities inhibited were 0.03 and 0.3 nmol/min/mg protein in the 129/J and BALB/cJ females, respectively. No significant level of "I"-P-450(16)alpha-dependent activity was detected in the microsomes from males of either mouse strain. Immunoblotting of microsomal proteins with the antibody to "I"-P-450(16)alpha revealed approximately a 10-fold greater amount of a 54-kDa protein in the microsomes from BALB/cJ than from 129/J females (0.03 and 0.26 pmol/micrograms protein, respectively). A cDNA clone (R17) for phenobarbital-inducible rat cytochrome P-450 selected "I"-P-450(16)alpha mRNA of mice, indicating a high degree of homology between the mRNAs of mouse "I"-P-450(16)alpha and phenobarbital-inducible rat cytochrome P-450s. Northern and dot hybridization of total mouse liver poly(A)+ RNA with the R17 cDNA probe indicated that the specific content of the hybridizable mRNA was more than 10 times higher in BALB/cJ females than in males, and that the mRNA level in female 129/J mice was very similar to that of 129/J and BALB/cJ males. The repression of "I"-P-450(16)alpha in 129/J females was inherited as an autosomal recessive trait in 129/J and BALB/cJ pairs as indicated by the levels of mRNA in female F1 offspring and the "I"-P-450(16)alpha-dependent hydroxylase activity. Female and male mice of eight more inbred strains (AKR/J, DBA/2J, C57BL/6J, C3H/HeJ, NZB/J, A/J, CBA/CaJ, and P/J) were tested for levels of mRNA. The results showed that the levels of mRNA were always 5- to 10-fold greater in the females than in the corresponding males, although there was some variation in the mRNA content in the males from the different strains. 129/J females appear to be a genetic variant where the female-predominant expression of the mRNA is repressed.

MeSH Terms
Animals Aryl Hydrocarbon Hydroxylases Cytochrome P-450 Enzyme System/analysis,biosynthesis,immunology DNA/analysis Enzyme Repression Female Male Mice Mice, Inbred Strains Microsomes, Liver/enzymology Nucleic Acid Hybridization RNA, Messenger/analysis Rabbits Sex Factors Species Specificity Steroid 16-alpha-Hydroxylase Steroid Hydroxylases/analysis,biosynthesis,immunology
Chemicals
RNA, Messenger DNA Cytochrome P-450 Enzyme System Steroid Hydroxylases Aryl Hydrocarbon Hydroxylases Steroid 16-alpha-Hydroxylase testosterone 7-alpha-hydroxylase, hamster
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Noshiro M
Serabjit-Singh C J
Bend J R
Negishi M
Article Info
Journal
Archives of biochemistry and biophysics
Abbr.
Arch Biochem Biophys
ISSN
0003-9861
Published
1986-02-01
Pages
857-64
Language
English
Region
United States
NLM ID
0372430
Subset
IM
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