CYP3A4 mutation causes vitamin D–dependent rickets type 3
Jeffrey D. Roizen, … , Hakon Hakonarson, Michael A. Levine
Jeffrey D. Roizen, … , Hakon Hakonarson, Michael A. Levine
Published February 20, 2018
Citation Information: J Clin Invest. 2018;128(5):1913-1918. https://doi.org/10.1172/JCI98680.
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Concise Communication Bone biology Genetics

CYP3A4 mutation causes vitamin D–dependent rickets type 3

Abstract

Genetic forms of vitamin D–dependent rickets (VDDRs) are due to mutations impairing activation of vitamin D or decreasing vitamin D receptor responsiveness. Here we describe two unrelated patients with early-onset rickets, reduced serum levels of the vitamin D metabolites 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D, and deficient responsiveness to parent and activated forms of vitamin D. Neither patient had a mutation in any genes known to cause VDDR; however, using whole exome sequencing analysis, we identified a recurrent de novo missense mutation, c.902T>C (p.I301T), in CYP3A4 in both subjects that alters the conformation of substrate recognition site 4 (SRS-4). In vitro, the mutant CYP3A4 oxidized 1,25-dihydroxyvitamin D with 10-fold greater activity than WT CYP3A4 and 2-fold greater activity than CYP24A1, the principal inactivator of vitamin D metabolites. As CYP3A4 mutations have not previously been linked to rickets, these findings provide insight into vitamin D metabolism and demonstrate that accelerated inactivation of vitamin D metabolites represents a mechanism for vitamin D deficiency.

Authors

Jeffrey D. Roizen, Dong Li, Lauren O’Lear, Muhammad K. Javaid, Nicholas J. Shaw, Peter R. Ebeling, Hanh H. Nguyen, Christine P. Rodda, Kenneth E. Thummel, Tom D. Thacher, Hakon Hakonarson, Michael A. Levine

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Figure 2

CYP3A4 (p.I301T) mutant has increased vitamin D degradative activity but decreased activity for other substrates.

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CYP3A4 (p.I301T) mutant has increased vitamin D degradative activity but...
(A) CYP3A4 (p.I301T) has increased vitamin D degradative activity. CYP3A4 p.I301T had increased inactivation of calcitriol relative to WT (**P < 0.01 by 2-way ANOVA for curve), and post hoc multiple comparison–adjusted analyses confirmed significant differences at 0.03, 0.1, and 0.3 ng/ml (**P < 0.01), and relative to CYP24A1 at 0.3 ng/ml (*P < 0.05) (n = 3 for each). (B and C) There is no difference in the relative abundance of the WT and p.I301T CYP3A4 (n = 3 for each treatment). (B) Immunoblot of cell lysates for CYP3A4 and GAPDH. (C) Quantification of the relative abundance of CYP3A4 and GAPDH. No significant differences were observed between the abundance of the WT and the p.I301T mutant. (D) CYP3A4 (p.I301T) does not have increased catalytic activity for non–vitamin D substrates. The p.I301T mutant had significantly decreased activity for luciferin IPA relative to the WT enzyme (30.0 ± 1.6 vs. 50.1 ± 1.6, n = 4 for each, ***P < 0.001). **P < 0.05. Data are presented as mean ± SEM.