z-logo
open-access-imgOpen Access
INDUCIBLE MONOOXYGENASE ACTIVITIES AND 3-METHYLCHOLANTHRENE-INITIATED TUMORIGENESIS IN MOUSE RECOMBINANT INBRED SUBLINES
Author(s) -
Steven A. Atlas,
Benjamin A. Taylor,
Bhalchandra A. Diwan,
Daniel W. Nebert
Publication year - 1976
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1093/genetics/83.3.537
Subject(s) - inbred strain , biology , monooxygenase , locus (genetics) , cytochrome p450 , cytochrome , gene , genetics , recombinant dna , methylcholanthrene , carcinogenesis , enzyme , enzyme inducer , microbiology and biotechnology , carcinogen , biochemistry
The induction of a certain group of hepatic monooxygenase activities by polycyclic aromatic compounds is regulated by the same locus or gene cluster controlling the formation of cytochrome P1–450 (P–448) in mice. Certain inbred strains of mice are "responsive" (Ahb) to such induction, whereas others are "nonresponsive" (Ahd). A pair of closely related sublines that differ with respect to the Ahlocus (for aromatic hydrocarbon responsiveness) were used to identify or confirm the pleiotropic effects of this gene. The lines were derived by sibling-mating without selection from (C57L/J × AKR/J)F2 mice; the two sublines were separated at the F12 generation. Ten microsomal monooxygenase activities and one cytosol enzyme activity known to be associated with the Ah locus were similarly associated with cytochrome P1–450 formation in these recombinant inbred sublines as well. Nine additional hepatic monooxygenase activities studied were found not to be associated with the Ah locus; certain of these activities were increased slightly, following treatment of nonresponsive as well as responsive mice with polycyclic aromatic compounds. The Ahb-containing subline was highly susceptible to 3-methylcholanthrene-induced subcutaneous sarcomas, whereas the Ah-d-containing subline was relatively resistant. These results emphasize the potential importance of this particular enzyme for the study of coordinated regulation in mammals.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom