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J. Biol. Chem., Vol. 260, Issue 18, 9949-9952, 08, 1985
D Peffley and M Sinensky
A somatic cell mutant (Mev-1) auxotrophic for mevalonate by virtue of a
complete lack of detectable 3-hydroxy-3-methylglutaryl coenzyme A (HMG-
CoA) synthase activity has been shown to demonstrate a requirement for a
non-sterol mevalonate-derived product for regulation of synthesis of
HMG-CoA reductase. A comparison of the effects of 25-hydroxycholesterol and
the combination of 25-hydroxycholesterol and mevalonate on HMG-CoA
reductase activity, synthesis, and mRNA levels in Mev-1 is presented in
this report. The results show a close correlation between activity, rate of
synthesis, and mRNA levels for Mev-1 cells treated with 25-
hydroxycholesterol alone. Under the conditions of these experiments these
effects are relatively small (approximately a 4-fold decrease). A much
larger inhibition of HMG-CoA reductase activity and rate of synthesis
(approximately 50-fold) is observed upon treatment of Mev-1 cells with a
combination of 25-hydroxycholesterol and mevalonate. Yet, under these
conditions mRNA levels are still reduced by only a factor of 4. These
results are interpreted to suggest that the non-sterol mevalonate-derived
regulatory product of HMG-CoA reductase acts by a translational control
mechanism.
Regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase synthesis by a non-sterol mevalonate-derived product in Mev-1 cells. Apparent translational control
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