Skip to main content
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1999 Mar;64(3):706–711. doi: 10.1086/302296

Human molybdopterin synthase gene: genomic structure and mutations in molybdenum cofactor deficiency type B.

J Reiss 1, C Dorche 1, B Stallmeyer 1, R R Mendel 1, N Cohen 1, M T Zabot 1
PMCID: PMC1377787  PMID: 10053004

Abstract

Biosynthesis of the molybdenum cofactor (MoCo) can be divided into (1) the formation of a precursor and (2) the latter's subsequent conversion, by molybdopterin synthase, into the organic moiety of MoCo. These two steps are reflected by the complementation groups A and B and the two formally distinguished types of MoCo deficiency that have an identical phenotype. Both types of MoCo deficiency result in a pleiotropic loss of all molybdoenzyme activities and cause severe neurological damage. MOCS1 is defective in patients with group A deficiency and has been shown to encode two enzymes for early synthesis via a bicistronic transcript with two consecutive open reading frames (ORFs). MOCS2 encodes the small and large subunits of molybdopterin synthase via a single transcript with two overlapping reading frames. This gene was mapped to 5q and comprises seven exons. The coding sequence and all splice site-junction sequences were screened for mutations, in MoCo-deficient patients in whom a previous search for MOCS1 mutations had been negative. In seven of the eight patients whom we investigated, we identified MOCS2 mutations that, by their nature, are most likely responsible for the deficiency. Three different frameshift mutations were observed, with one of them found on 7 of 14 identified alleles. Furthermore, a start-codon mutation and a missense mutation of a highly conserved amino acid residue were found. The locations of the mutations confirm the functional role of both ORFs. One of the patients with identified MOCS2 mutations had been classified as type B, in complementation studies. These findings support the hypothetical mechanism, for both forms of MoCo deficiency, that formerly had been established by cell-culture experiments.

Full Text

The Full Text of this article is available as a PDF (230.3 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Amy C. M., Williams-Ahlf B., Naggert J., Smith S. Intron-exon organization of the gene for the multifunctional animal fatty acid synthase. Proc Natl Acad Sci U S A. 1992 Feb 1;89(3):1105–1108. doi: 10.1073/pnas.89.3.1105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Boles R. G., Ment L. R., Meyn M. S., Horwich A. L., Kratz L. E., Rinaldo P. Short-term response to dietary therapy in molybdenum cofactor deficiency. Ann Neurol. 1993 Nov;34(5):742–744. doi: 10.1002/ana.410340520. [DOI] [PubMed] [Google Scholar]
  3. Bonioli E., DiStefano A., Palmieri A., Bertola A., Bellini C., Caruso U., Fantasia A. R., Minniti G., Dorche C. Combined deficiency of xanthine oxidase and sulphite oxidase due to a deficiency of molybdenum cofactor. J Inherit Metab Dis. 1996;19(5):700–701. doi: 10.1007/BF01799850. [DOI] [PubMed] [Google Scholar]
  4. Boyington J. C., Gladyshev V. N., Khangulov S. V., Stadtman T. C., Sun P. D. Crystal structure of formate dehydrogenase H: catalysis involving Mo, molybdopterin, selenocysteine, and an Fe4S4 cluster. Science. 1997 Feb 28;275(5304):1305–1308. doi: 10.1126/science.275.5304.1305. [DOI] [PubMed] [Google Scholar]
  5. Chan M. K., Mukund S., Kletzin A., Adams M. W., Rees D. C. Structure of a hyperthermophilic tungstopterin enzyme, aldehyde ferredoxin oxidoreductase. Science. 1995 Mar 10;267(5203):1463–1469. doi: 10.1126/science.7878465. [DOI] [PubMed] [Google Scholar]
  6. Davidson J. N., Chen K. C., Jamison R. S., Musmanno L. A., Kern C. B. The evolutionary history of the first three enzymes in pyrimidine biosynthesis. Bioessays. 1993 Mar;15(3):157–164. doi: 10.1002/bies.950150303. [DOI] [PubMed] [Google Scholar]
  7. Desjacques P., Mousson B., Vianey-Liaud C., Boulieu R., Bory C., Baltassat P., Divry P., Zabot M. T., Cotte J., Lagier P. Combined deficiency of xanthine oxidase and sulphite oxidase: diagnosis of a new case followed by an antenatal diagnosis. J Inherit Metab Dis. 1985;8 (Suppl 2):117–118. doi: 10.1007/BF01811486. [DOI] [PubMed] [Google Scholar]
  8. Duran M., Beemer F. A., van de Heiden C., Korteland J., de Bree P. K., Brink M., Wadman S. K., Lombeck I. Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport? J Inherit Metab Dis. 1978;1(4):175–178. doi: 10.1007/BF01805591. [DOI] [PubMed] [Google Scholar]
  9. Garrett R. M., Rajagopalan K. V. Molecular cloning of rat liver sulfite oxidase. Expression of a eukaryotic Mo-pterin-containing enzyme in Escherichia coli. J Biol Chem. 1994 Jan 7;269(1):272–276. [PubMed] [Google Scholar]
  10. Johnson J. L., Rajagopalan K. V. Structural and metabolic relationship between the molybdenum cofactor and urothione. Proc Natl Acad Sci U S A. 1982 Nov;79(22):6856–6860. doi: 10.1073/pnas.79.22.6856. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Johnson J. L., Waud W. R., Rajagopalan K. V., Duran M., Beemer F. A., Wadman S. K. Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor. Proc Natl Acad Sci U S A. 1980 Jun;77(6):3715–3719. doi: 10.1073/pnas.77.6.3715. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Johnson J. L., Wuebbens M. M., Mandell R., Shih V. E. Molybdenum cofactor biosynthesis in humans. Identification of two complementation groups of cofactor-deficient patients and preliminary characterization of a diffusible molybdopterin precursor. J Clin Invest. 1989 Mar;83(3):897–903. doi: 10.1172/JCI113974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Krawczak M., Reiss J., Cooper D. N. The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences. Hum Genet. 1992 Sep-Oct;90(1-2):41–54. doi: 10.1007/BF00210743. [DOI] [PubMed] [Google Scholar]
  14. Mendel R. R. Molybdenum cofactor of higher plants: biosynthesis and molecular biology. Planta. 1997 Dec;203(4):399–405. doi: 10.1007/s004250050206. [DOI] [PubMed] [Google Scholar]
  15. Miller S. A., Dykes D. D., Polesky H. F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988 Feb 11;16(3):1215–1215. doi: 10.1093/nar/16.3.1215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Pickart C. M., Kasperek E. M., Beal R., Kim A. Substrate properties of site-specific mutant ubiquitin protein (G76A) reveal unexpected mechanistic features of ubiquitin-activating enzyme (E1). J Biol Chem. 1994 Mar 11;269(10):7115–7123. [PubMed] [Google Scholar]
  17. Rajagopalan K. V., Johnson J. L. The pterin molybdenum cofactors. J Biol Chem. 1992 May 25;267(15):10199–10202. [PubMed] [Google Scholar]
  18. Reiss J., Christensen E., Kurlemann G., Zabot M. T., Dorche C. Genomic structure and mutational spectrum of the bicistronic MOCS1 gene defective in molybdenum cofactor deficiency type A. Hum Genet. 1998 Dec;103(6):639–644. doi: 10.1007/s004390050884. [DOI] [PubMed] [Google Scholar]
  19. Reiss J., Cohen N., Dorche C., Mandel H., Mendel R. R., Stallmeyer B., Zabot M. T., Dierks T. Mutations in a polycistronic nuclear gene associated with molybdenum cofactor deficiency. Nat Genet. 1998 Sep;20(1):51–53. doi: 10.1038/1706. [DOI] [PubMed] [Google Scholar]
  20. Stallmeyer B., Drugeon G., Reiss J., Haenni A. L., Mendel R. R. Human molybdopterin synthase gene: identification of a bicistronic transcript with overlapping reading frames. Am J Hum Genet. 1999 Mar;64(3):698–705. doi: 10.1086/302295. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Taylor S. V., Kelleher N. L., Kinsland C., Chiu H. J., Costello C. A., Backstrom A. D., McLafferty F. W., Begley T. P. Thiamin biosynthesis in Escherichia coli. Identification of ThiS thiocarboxylate as the immediate sulfur donor in the thiazole formation. J Biol Chem. 1998 Jun 26;273(26):16555–16560. doi: 10.1074/jbc.273.26.16555. [DOI] [PubMed] [Google Scholar]
  22. Wolff J. A. Naked DNA transport and expression in mammalian cells. Neuromuscul Disord. 1997 Jul;7(5):314–318. doi: 10.1016/s0960-8966(97)00055-2. [DOI] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES