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American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1995 Aug;57(2):224–226.

Transmission of mtDNA: cracks in the bottleneck.

J Poulton
PMCID: PMC1801550  PMID: 7668245

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bendall K. E., Sykes B. C. Length heteroplasmy in the first hypervariable segment of the human mtDNA control region. Am J Hum Genet. 1995 Aug;57(2):248–256. [PMC free article] [PubMed] [Google Scholar]
  2. Brockington M., Sweeney M. G., Hammans S. R., Morgan-Hughes J. A., Harding A. E. A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies. Nat Genet. 1993 May;4(1):67–71. doi: 10.1038/ng0593-67. [DOI] [PubMed] [Google Scholar]
  3. Chen X., Prosser R., Simonetti S., Sadlock J., Jagiello G., Schon E. A. Rearranged mitochondrial genomes are present in human oocytes. Am J Hum Genet. 1995 Aug;57(2):239–247. [PMC free article] [PubMed] [Google Scholar]
  4. Cortopassi G. A., Shibata D., Soong N. W., Arnheim N. A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues. Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7370–7374. doi: 10.1073/pnas.89.16.7370. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hauswirth W. W., Clayton D. A. Length heterogeneity of a conserved displacement-loop sequence in human mitochondrial DNA. Nucleic Acids Res. 1985 Nov 25;13(22):8093–8104. doi: 10.1093/nar/13.22.8093. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Howell N., Halvorson S., Kubacka I., McCullough D. A., Bindoff L. A., Turnbull D. M. Mitochondrial gene segregation in mammals: is the bottleneck always narrow? Hum Genet. 1992 Sep-Oct;90(1-2):117–120. doi: 10.1007/BF00210753. [DOI] [PubMed] [Google Scholar]
  7. Laipis P. J., Van de Walle M. J., Hauswirth W. W. Unequal partitioning of bovine mitochondrial genotypes among siblings. Proc Natl Acad Sci U S A. 1988 Nov;85(21):8107–8110. doi: 10.1073/pnas.85.21.8107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Larsson N. G., Tulinius M. H., Holme E., Oldfors A., Andersen O., Wahlström J., Aasly J. Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome. Am J Hum Genet. 1992 Dec;51(6):1201–1212. [PMC free article] [PubMed] [Google Scholar]
  9. Monnat R. J., Jr, Loeb L. A. Nucleotide sequence preservation of human mitochondrial DNA. Proc Natl Acad Sci U S A. 1985 May;82(9):2895–2899. doi: 10.1073/pnas.82.9.2895. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Poulton J., Holt I. J. Mitochondrial DNA: does more lead to less? Nat Genet. 1994 Dec;8(4):313–315. doi: 10.1038/ng1294-313. [DOI] [PubMed] [Google Scholar]
  11. Torroni A., Lott M. T., Cabell M. F., Chen Y. S., Lavergne L., Wallace D. C. mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region. Am J Hum Genet. 1994 Oct;55(4):760–776. [PMC free article] [PubMed] [Google Scholar]
  12. Willems P. J. Dynamic mutations hit double figures. Nat Genet. 1994 Nov;8(3):213–215. doi: 10.1038/ng1194-213. [DOI] [PubMed] [Google Scholar]

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