International Journal of Legal Medicine

, Volume 112, Issue 1, pp 27–30

Heteroplasmic substitutions in the mitochondrial DNA control region in mother and child samples

  • J. Hühne
  • H. Pfeiffer
  • B. Brinkmann
Original article

DOI: 10.1007/s004140050193

Cite this article as:
Hühne, J., Pfeiffer, H. & Brinkmann, B. Int J Leg Med (1998) 112: 27. doi:10.1007/s004140050193

Abstract

The sequences of the two hypervariable regions of the mitochondrial DNA control region (HV1 and HV2) from close maternal relatives (mother-child pairs) were compared to determine the frequency of mutations between two generations. A total of 68 blood samples were sequenced only in HV1 and 86 were analysed for HV1 and HV2. The intergenerational comparison led to the identification of six heteroplasmic point mutations affecting the children only. In one case a heteroplasmy of the maternal sequence was resolved to homoplasmy in the corresponding sequence of the child.

Key words Mitochondrial DNA Hypervariable region Heteroplasmic point mutation Length heteroplasmy 

Copyright information

© Springer-Verlag Berlin Heidelberg 1998

Authors and Affiliations

  • J. Hühne
    • 1
  • H. Pfeiffer
    • 1
  • B. Brinkmann
    • 1
  1. 1.Institute of Forensic Medicine, University of Münster, Von-Esmarch-Strasse 62, D-48149 Münster, Germany Tel + 49 0251 83 55161; Fax + 49 0251 83 55158DE

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