Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2004 Jun;167(2):897-905.
doi: 10.1534/genetics.103.025049.

Paternal mitochondrial DNA transmission during nonhuman primate nuclear transfer

Affiliations

Paternal mitochondrial DNA transmission during nonhuman primate nuclear transfer

Justin C St John et al. Genetics. 2004 Jun.

Abstract

Offspring produced by nuclear transfer (NT) have identical nuclear DNA (nDNA). However, mitochondrial DNA (mtDNA) inheritance could vary considerably. In sheep, homoplasmy is maintained since mtDNA is transmitted from the oocyte (recipient) only. In contrast, cattle are heteroplasmic, harboring a predominance of recipient mtDNA along with varying levels of donor mtDNA. We show that the two nonhuman primate Macaca mulatta offspring born by NT have mtDNA from three sources: (1) maternal mtDNA from the recipient egg, (2) maternal mtDNA from the egg contributing to the donor blastomere, and (3) paternal mtDNA from the sperm that fertilized the egg from which the donor blastomere was isolated. The introduction of foreign mtDNA into reconstructed recipient eggs has also been demonstrated in mice through pronuclear injection and in humans through cytoplasmic transfer. The mitochondrial triplasmy following M. mulatta NT reported here forces concerns regarding the parental origins of mtDNA in clinically reconstructed eggs. In addition, mtDNA heteroplasmy might result in the embryonic stem cell lines generated for experimental and therapeutic purposes ("therapeutic cloning").

PubMed Disclaimer

Similar articles

Cited by

References

    1. Reprod Biomed Online. 2004 Jan;8(1):34-44 - PubMed
    1. FEBS Lett. 1998 Apr 24;426(3):357-61 - PubMed
    1. Biochem Biophys Res Commun. 1994 May 16;200(3):1374-81 - PubMed
    1. Science. 1991 Mar 22;251(5000):1488-90 - PubMed
    1. Nat Genet. 2000 Jul;25(3):255-7 - PubMed

Publication types

Substances