Spectrum of mitochondrial DNA rearrangements in the Pearson marrow-pancreas syndrome

Hum Mol Genet. 1995 Aug;4(8):1327-30. doi: 10.1093/hmg/4.8.1327.

Abstract

The Pearson marrow-pancreas syndrome (MIM 557000) is a disorder involving the hematopoietic system and the exocrine pancreas in early infancy. We have previously shown that this disease results from a defect of oxidative phosphorylation associated with deletions of the mitochondrial DNA. We present here a series of 21 cases (including 15 unreported patients) with Pearson syndrome and describe mitochondrial DNA deletions as consistent features in this syndrome. Nine patients presented the same 4.9 kb deletion, while other patients presented different deletions ranging in size from 9 to 14 kb between tRNACyst and the D-loop. Direct repeats (4-13 bp) were consistently present in the wild-type mtDNA at the boundaries of the deletions. Deletion-dimers, deletion-multimers or duplications were observed in association with deletions. Duplications were identified both in patients who died of their Pearson syndrome and in the ones who survived and developed Kearns-Sayre syndrome, suggesting that no correlation could be made between the clinical severity and the type, size or location of the rearrangements.

MeSH terms

  • Base Sequence
  • Bone Marrow Diseases / genetics*
  • Child, Preschool
  • DNA, Mitochondrial / genetics*
  • Female
  • Gene Rearrangement*
  • Humans
  • Infant
  • Kearns-Sayre Syndrome / genetics
  • Male
  • Microsatellite Repeats
  • Molecular Sequence Data
  • Pancreatic Diseases / genetics*
  • Phenotype
  • Sequence Deletion
  • Syndrome

Substances

  • DNA, Mitochondrial