Structural organization of the human dihydropyrimidine dehydrogenase gene

Cancer Res. 1997 May 1;57(9):1660-3.

Abstract

Deficiency of the pyrimidine catabolic enzyme, dihydropyrimidine dehydrogenase (DPD), has been shown to be responsible for a pharmacogenetic syndrome in which administration of 5-fluorouracil is associated with severe and potentially life-threatening toxicity. Following the recent availability of the cDNA for DPD, there were initial reports of several molecular defects (point mutations, deletions due to exon skipping) that were suggested as a potential molecular basis for DPD deficiency, even before the complete physical structure of the DPD gene was known. To understand the mechanism responsible for DPD deficiency, we have determined the genomic structure and organization of the human DPD gene. The gene is approximately 150 kb in length, and it consists of 23 exons, ranging in size from 69 to 1404 bp. The sequences of intronic regions flanking the exon boundaries have been determined. The physical map of the DPD gene should permit development of rapid assays to detect point mutations or small deletions in the DPD gene associated with 5-fluorouracil toxicity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Dihydrouracil Dehydrogenase (NADP)
  • Exons
  • Genes
  • Humans
  • Introns
  • Oxidoreductases / genetics*
  • RNA, Messenger / genetics

Substances

  • RNA, Messenger
  • Oxidoreductases
  • Dihydrouracil Dehydrogenase (NADP)