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Genetic linkage analysis of bipolar affective disorder in an Old Order Amish pedigree

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Summary

We have used genetic linkage analysis in an effort to identify a gene responsible for bipolar affective disorder (BAD) in an Old Order Amish pedigree. The initial study of this pedigree showed strong evidence for linkage of the chromosome 11p15 markers HRAS1 and the insulin gene (INS) to BAD, whereas a second report found no evidence for linkage. We have independently determined the INS and HRAS1 genotypes from 81 individuals in this pedigree. A polymerase chain reaction (PCR) assay was used to score INS alleles that are difficult to distinguish from one another by conventional agarose gel electrophoresis. In addition, we used four separate diagnostic models to score individuals with psychiatric illness as either affected or unaffected. No evidence of significant linkage between BAD and the markers was found with either two-point or multipoint analysis regardless of which diagnostic model was used. However, exclusion of the region of chromosome 11 between INS and RAS1 as a possible location for the BAD gene in this family depended on the diagnostic model. Further genetic linkage studies with additional DNA markers that span the genome are necessary to determine the chromosomal location of the BAD gene in this family.

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References

  • Baron M, Risch N, Hamburger R, Mandel B, Kushner S, Newman M, Drumer D et al (1987) Genetic linkage between X-chromosome markers and bipolar affective illness. Nature 326:289–392

    Article  CAS  PubMed  Google Scholar 

  • Bell GI, Karam JH, Rutter WJ (1981) Polymorphic DNA region adjacent to the 5′ end of the human insulin gene. Proc Natl Acad Sci USA 78:5759–5763

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bell GI, Selby MJ, Rutter WJ (1982) The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences. Nature 295:31–35

    Article  CAS  PubMed  Google Scholar 

  • Detera-Wadleigh SD, Berrettine WH, Goldin LR, Boorman D, Anderson S, Gershon ES (1987) Close linkage of c-Harvey-ras-1 and the insulin gene to affective disorder is ruled out in three North American pedigrees. Nature 325:806–808

    Article  CAS  PubMed  Google Scholar 

  • Egeland JA, Gerhard DS, Pauls DI, Sussex JN, Kidd KK, Allen CR, Hostetter AM, Housman DE (1987) Bipolar affective disorders linked to DNA markers on chromosome 11. Nature 325:783–787

    Article  CAS  PubMed  Google Scholar 

  • Feinberg A, Vogelstein B (1982) A technique for radiolabelling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 132:6–13

    Article  Google Scholar 

  • Hodgkinson S, Sherrington R, Gurling H, Marchbanks R, Reeders S, Mallet J, McInnis M, Petursson H, Brynjolfsson J (1987) Molecular genetic evidence for heterogeneity in manic depression. Nature 325:805–806

    Article  CAS  PubMed  Google Scholar 

  • Keats B, Ott J, Conneally M (1989) Report of the committee on linkage and gene order. Cytogenet Cell Genet 51:459–502

    Article  CAS  PubMed  Google Scholar 

  • Kelsoe JR, Ginns EL, Egeland JA, Gerhard DS, Goldstein AM, Bale SJ, Pauls DL, Long RT, Kidd KK, Conte G, Houseman DE, Paul SM (1989) Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish. Nature 342:238–243

    Article  CAS  PubMed  Google Scholar 

  • Lathrop GM, Laouel JM, Julier C, Ott J (1984) Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci USA 81:3443–3446

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Mendlewicz J, Simon P, Sevy S, Charon F, Brocas H, Legros S, Vassart G (1987) Polymorphic DNA marker on X chromosome and manic depression. Lancet II:1230–1232

    Article  Google Scholar 

  • Nakamura Y, Leppert M, O'Connell P, Wolff R, Holm T, Culver M, Martin C, Fujimoto E, Hoff M, Kumlin E (1987) Variable number of tandem repeat (VNTR) markers for human gene mapping. Science 235:1616–1622

    Article  CAS  PubMed  Google Scholar 

  • NIGMS (1990) 1990/1991 Catalog of cell lines: NIGMS Human Genetic Mutant Cell Respository. (National Institutes of Health puplication no. 91–2011) National Institute of Health, Bethesda, Md, pp 362–377

    Google Scholar 

  • Pritchard CA, Casher D, Bull L, Cox DR, Myers RM (1990) A cloned DNA segment from the telomeric region of human chromosome 4p is not detectably rearranged in Huntington disease patients. Proc Natl Acad Sci USA 87:7309–7313

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Smith H, Birnstiel M (1976) A simple method for DNA restriction site mapping. Nucleic Acids Res 3:2387–2398

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Weissman MM (1988) Affective disorders in five United States communities. Psychol Med 18:141–153

    Article  CAS  PubMed  Google Scholar 

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Law, A., Richard, C.W., Cottingham, R.W. et al. Genetic linkage analysis of bipolar affective disorder in an Old Order Amish pedigree. Hum Genet 88, 562–568 (1992). https://doi.org/10.1007/BF00219345

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