Polar body mutation load analysis in a patient with A3243G tRNALeu(UUR) point mutation

Mitochondrion. 2011 Jul;11(4):626-9. doi: 10.1016/j.mito.2011.03.123. Epub 2011 Apr 6.

Abstract

Diseases associated with point mutations in the mitochondrial DNA (mtDNA) are maternally inherited. We evaluated whether pre-implantation genetic diagnosis, based on polar body mutation load detection could be used to distinguish healthy from affected oocytes. Restriction Fragment Length Polymorphism (RFLP) analysis was used and validated, to determine A3243G tRNA(Leu(UUR)) mutation load in metaphase II oocytes and their respective first polar bodies. The results of this study show for the first time that the mutation load measured in the polar bodies correlates well with the mutation load in the respective oocytes. Therefore, human polar body analysis can be used as diagnostic tool to prevent transmission of mitochondrial disorders.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Mutational Analysis / methods*
  • Female
  • Humans
  • Leukocytes, Mononuclear / cytology
  • Metaphase
  • Mitochondrial Diseases / genetics*
  • Oocytes / cytology
  • Point Mutation*
  • Polymorphism, Restriction Fragment Length
  • RNA
  • RNA, Mitochondrial
  • RNA, Transfer, Leu / genetics*

Substances

  • RNA, Mitochondrial
  • RNA, Transfer, Leu
  • RNA