Abstract

It was shown previously that four immunochemically identical forms of phenobarbital-induced hepatic cytochrome P-450 exist in unique combinations which characterize different strains and colonies of rats (Vlasuk, G. P., Ghrayeb, J., Ryan, D. E., Reik, L., Thomas, P. E., Levin, W., and Walz, F. G., Jr. (1982) Biochemistry 21, 789-798). One colony of Long-Evans rats exhibited only cytochromes P-450bLE and P-450e among these immunorelated enzymes; whereas, one colony of Holtzman rats was characterized by cytochromes P-450bH and P-450e. After phenobarbital treatment, hepatic poly(A)+-mRNA was isolated from these groups of rats and translated in vitro. The 35S-labeled products were immunoisolated with antibody to cytochrome P-450bLE and analyzed by two-dimensional gel electrophoresis. The results indicated that the products synthesized in vitro correspond exactly to the two particular forms of the enzyme that characterize liver microsomes from each of these groups of rats. It is concluded that different structural genes encode these immunorelated forms of cytochrome P-450 and that significant post-translational processing of their polypeptide products does not occur in vivo.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call