Unknown

Dataset Information

0

Genetic evidence that the human CYP2R1 enzyme is a key vitamin D 25-hydroxylase.


ABSTRACT: The synthesis of bioactive vitamin D requires hydroxylation at the 1 alpha and 25 positions by cytochrome P450 enzymes in the kidney and liver, respectively. The mitochondrial enzyme CYP27B1 catalyzes 1 alpha-hydroxylation in the kidney but the identity of the hepatic 25-hydroxylase has remained unclear for >30 years. We previously identified the microsomal CYP2R1 protein as a potential candidate for the liver vitamin D 25-hydroxylase based on the enzyme's biochemical properties, conservation, and expression pattern. Here, we report a molecular analysis of a patient with low circulating levels of 25-hydroxyvitamin D and classic symptoms of vitamin D deficiency. This individual was found to be homozygous for a transition mutation in exon 2 of the CYP2R1 gene on chromosome 11p15.2. The inherited mutation caused the substitution of a proline for an evolutionarily conserved leucine at amino acid 99 in the CYP2R1 protein and eliminated vitamin D 25-hydroxylase enzyme activity. These data identify CYP2R1 as a biologically relevant vitamin D 25-hydroxylase and reveal the molecular basis of a human genetic disease, selective 25-hydroxyvitamin D deficiency.

SUBMITTER: Cheng JB 

PROVIDER: S-EPMC419671 | biostudies-literature | 2004 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Genetic evidence that the human CYP2R1 enzyme is a key vitamin D 25-hydroxylase.

Cheng Jeffrey B JB   Levine Michael A MA   Bell Norman H NH   Mangelsdorf David J DJ   Russell David W DW  

Proceedings of the National Academy of Sciences of the United States of America 20040505 20


The synthesis of bioactive vitamin D requires hydroxylation at the 1 alpha and 25 positions by cytochrome P450 enzymes in the kidney and liver, respectively. The mitochondrial enzyme CYP27B1 catalyzes 1 alpha-hydroxylation in the kidney but the identity of the hepatic 25-hydroxylase has remained unclear for >30 years. We previously identified the microsomal CYP2R1 protein as a potential candidate for the liver vitamin D 25-hydroxylase based on the enzyme's biochemical properties, conservation, a  ...[more]

Similar Datasets

| S-EPMC7657391 | biostudies-literature
| S-EPMC8346186 | biostudies-literature
| S-EPMC3190681 | biostudies-literature
| S-EPMC8699237 | biostudies-literature
| S-EPMC8699237 | biostudies-literature
| S-EPMC34697 | biostudies-literature
| S-EPMC4490307 | biostudies-literature
| S-EPMC1217927 | biostudies-other
| S-EPMC3521459 | biostudies-literature
| S-EPMC4184076 | biostudies-literature