Skip to main content
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1999 Aug;65(2):508–518. doi: 10.1086/302507

Mitochondrial genetic analyses suggest selection against maternal lineages in bipolar affective disorder.

R Kirk 1, R A Furlong 1, W Amos 1, G Cooper 1, J S Rubinsztein 1, C Walsh 1, E S Paykel 1, D C Rubinsztein 1
PMCID: PMC1377949  PMID: 10417293

Abstract

Previous reports of preferential transmission of bipolar affective disorder (BP) from the maternal versus the paternal lines in families suggested that this disorder may be caused by mitochondrial DNA mutations. We have sequenced the mitochondrial genome in 25 BP patients with family histories of psychiatric disorder that suggest matrilineal inheritance. No polymorphism identified more than once in this sequencing showed any significant association with BP in association studies using 94 cases and 94 controls. To determine whether our BP sample showed evidence of selection against the maternal lineage, we determined genetic distances between all possible pairwise comparisons within the BP and control groups, based on multilocus mitochondrial polymorphism haplotypes. These analyses revealed fewer closely related haplotypes in the BP group than in the matched control group, suggesting selection against maternal lineages in this disease. Such selection is compatible with recurrent mitochondrial mutations, which are associated with slightly decreased fitness. Although such mismatch distribution comparisons have been used previously for analyses of population histories, this is, as far as we are aware, the first report of this method being used to study disease.

Full Text

The Full Text of this article is available as a PDF (234.3 KB).

Selected References

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

  1. Anderson S., Bankier A. T., Barrell B. G., de Bruijn M. H., Coulson A. R., Drouin J., Eperon I. C., Nierlich D. P., Roe B. A., Sanger F. Sequence and organization of the human mitochondrial genome. Nature. 1981 Apr 9;290(5806):457–465. doi: 10.1038/290457a0. [DOI] [PubMed] [Google Scholar]
  2. Angst J., Frey R., Lohmeyer B., Zerbin-Rüdin E. Bipolar manic-depressive psychoses: results of a genetic investigation. Hum Genet. 1980;55(2):237–254. doi: 10.1007/BF00291773. [DOI] [PubMed] [Google Scholar]
  3. Corpet F. Multiple sequence alignment with hierarchical clustering. Nucleic Acids Res. 1988 Nov 25;16(22):10881–10890. doi: 10.1093/nar/16.22.10881. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Dunner D. L., Fieve R. R. Psychiatric illness in fathers of men with bipolar primary affective disorder. Arch Gen Psychiatry. 1975 Sep;32(9):1134–1137. doi: 10.1001/archpsyc.1975.01760270066007. [DOI] [PubMed] [Google Scholar]
  5. Endicott J., Spitzer R. L. A diagnostic interview: the schedule for affective disorders and schizophrenia. Arch Gen Psychiatry. 1978 Jul;35(7):837–844. doi: 10.1001/archpsyc.1978.01770310043002. [DOI] [PubMed] [Google Scholar]
  6. Gershon E. S., Badner J. A., Detera-Wadleigh S. D., Ferraro T. N., Berrettini W. H. Maternal inheritance and chromosome 18 allele sharing in unilineal bipolar illness pedigrees. Am J Med Genet. 1996 Apr 9;67(2):202–207. doi: 10.1002/(SICI)1096-8628(19960409)67:2<202::AID-AJMG11>3.0.CO;2-N. [DOI] [PubMed] [Google Scholar]
  7. Gill P., Ivanov P. L., Kimpton C., Piercy R., Benson N., Tully G., Evett I., Hagelberg E., Sullivan K. Identification of the remains of the Romanov family by DNA analysis. Nat Genet. 1994 Feb;6(2):130–135. doi: 10.1038/ng0294-130. [DOI] [PubMed] [Google Scholar]
  8. Goetzl U., Green R., Whybrow P., Jackson R. X linkage revisited. A further family study of manic-depressive illness. Arch Gen Psychiatry. 1974 Nov;31(5):665–672. doi: 10.1001/archpsyc.1974.01760170059010. [DOI] [PubMed] [Google Scholar]
  9. Grigoroiu-Serbanescu M., Martinez M., Nöthen M. M., Propping P., Milea S., Mihailescu R., Marinescu E. Patterns of parental transmission and familial aggregation models in bipolar affective disorder. Am J Med Genet. 1998 Sep 7;81(5):397–404. [PubMed] [Google Scholar]
  10. Helzer J. E., Winokur G. A family interview study of male manic depressives. Arch Gen Psychiatry. 1974 Jul;31(1):73–77. doi: 10.1001/archpsyc.1974.01760130055009. [DOI] [PubMed] [Google Scholar]
  11. Kato T., Stine O. C., McMahon F. J., Crowe R. R. Increased levels of a mitochondrial DNA deletion in the brain of patients with bipolar disorder. Biol Psychiatry. 1997 Nov 15;42(10):871–875. doi: 10.1016/S0006-3223(97)00012-7. [DOI] [PubMed] [Google Scholar]
  12. Kogelnik A. M., Lott M. T., Brown M. D., Navathe S. B., Wallace D. C. MITOMAP: a human mitochondrial genome database--1998 update. Nucleic Acids Res. 1998 Jan 1;26(1):112–115. doi: 10.1093/nar/26.1.112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. McMahon F. J., Stine O. C., Meyers D. A., Simpson S. G., DePaulo J. R. Patterns of maternal transmission in bipolar affective disorder. Am J Hum Genet. 1995 Jun;56(6):1277–1286. [PMC free article] [PubMed] [Google Scholar]
  14. Miyaoka H., Suzuki Y., Taniyama M., Miyaoka Y., Shishikura K., Kamijima K., Atsumi Y., Matsuoka K. Mental disorders in diabetic patients with mitochondrial transfer RNA(Leu) (UUR) mutation at position 3243. Biol Psychiatry. 1997 Sep 15;42(6):524–526. doi: 10.1016/S0006-3223(97)00280-1. [DOI] [PubMed] [Google Scholar]
  15. Parsons T. J., Muniec D. S., Sullivan K., Woodyatt N., Alliston-Greiner R., Wilson M. R., Berry D. L., Holland K. A., Weedn V. W., Gill P. A high observed substitution rate in the human mitochondrial DNA control region. Nat Genet. 1997 Apr;15(4):363–368. doi: 10.1038/ng0497-363. [DOI] [PubMed] [Google Scholar]
  16. Reich T., Clayton P. J., Winokur G. Family history studies: V. The genetics of mania. Am J Psychiatry. 1969 Apr;125(10):1358–1369. doi: 10.1176/ajp.125.10.1358. [DOI] [PubMed] [Google Scholar]
  17. Rieder M. J., Taylor S. L., Tobe V. O., Nickerson D. A. Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome. Nucleic Acids Res. 1998 Feb 15;26(4):967–973. doi: 10.1093/nar/26.4.967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Rogers A. R., Harpending H. Population growth makes waves in the distribution of pairwise genetic differences. Mol Biol Evol. 1992 May;9(3):552–569. doi: 10.1093/oxfordjournals.molbev.a040727. [DOI] [PubMed] [Google Scholar]
  19. Rust S., Funke H., Assmann G. Mutagenically separated PCR (MS-PCR): a highly specific one step procedure for easy mutation detection. Nucleic Acids Res. 1993 Aug 11;21(16):3623–3629. doi: 10.1093/nar/21.16.3623. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Slatkin M., Hudson R. R. Pairwise comparisons of mitochondrial DNA sequences in stable and exponentially growing populations. Genetics. 1991 Oct;129(2):555–562. doi: 10.1093/genetics/129.2.555. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Smeraldi E., Negri F., Melica A. M. A genetic study of affective disorders. Acta Psychiatr Scand. 1977 Nov;56(5):382–398. doi: 10.1111/j.1600-0447.1977.tb06679.x. [DOI] [PubMed] [Google Scholar]
  22. Spitzer R. L., Endicott J., Robins E. Research diagnostic criteria: rationale and reliability. Arch Gen Psychiatry. 1978 Jun;35(6):773–782. doi: 10.1001/archpsyc.1978.01770300115013. [DOI] [PubMed] [Google Scholar]
  23. Trzebiatowska-Trzeciak O. Genetical analysis of unipolar and bipolar endogenous affective psychoses. Br J Psychiatry. 1977 Nov;131:478–485. doi: 10.1192/bjp.131.5.478. [DOI] [PubMed] [Google Scholar]
  24. Vogel H. P. Fertility and sibship size in a psychiatric patient population. A comparison with national census data. Acta Psychiatr Scand. 1979 Nov;60(5):483–503. doi: 10.1111/j.1600-0447.1979.tb00558.x. [DOI] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES