Skip to main content
Log in

Genetic linkage between Huntington disease and the D4S10 locus in South African families: further evidence against non-allelic heterogeneity

  • Original Investigations
  • Published:
Human Genetics Aims and scope Submit manuscript

Summary

A study of genetic linkage between Huntington disease (HD) and the D4S10 locus (G8) has been undertaken in 10 South African (SA) families originating from the black, white and mixed acestry population groups. Allele frequencies at the D4S10 locus have been established in the non-Caucasoid population groups. There are significant differences in the allele frequencies at the D4S10 locus between the various SA populations. Clearly, information about population-specific frequencies for all polymorphisms is essential prior to the implementation of predictive testing in different population groups. Linkage has been demonstrated within this mixed group of HD families in SA using the HindIII, EcoRI and MspI polymorphisms, detected by G8. A maximum lod score of 8.14 at a recombination fraction of 0.00 (confidence limit 0–0.058) has been calculated using a combined haplotype of the HindIII and MspI polymorphisms. Taking into account the diverse ethnic backgrounds of the different SA population groups in this investigation, the data obtained from the study provide further evidence that there is probably only a single HD locus.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Bird TD, Hewitt J, Conneally PM, Hayden MR (1986) Linkage of the G8 marker on chromosome 4 to HD in a large American black family. N Engl J Med 18:1165–1166

    Google Scholar 

  • Botstein D, White RL, Skolnick M, Davis RW (1980) Construction of a genetic linkage map using restriction fragment length polymorphisms. Am J Hum Genet 32:314–331

    CAS  PubMed  Google Scholar 

  • Conneally PM, Edwards JH, Kidd KK, Lalouel JM, Morton NE, Ott J, White R (1985) Report of the committee on methods of linkage analysis and reporting. Cytogenet Cell Genet 40:356–359

    Google Scholar 

  • Conneally PM, Haines JL, Tanzi RE, Wexler NS, Penchaszadeh GK, Harper PS, Folstein SE, Cassiman JJ, Myers RH, Young AB, Hayden MR, Falek A, Tolosa ES, Crespi ES, Di Maio L, Holmgren G, Anvret M, Kanazawa I, Gusella JF (1989) Huntington disease: no evidence for locus heterogeneity. Genomics 5:304–308

    Google Scholar 

  • Farrer LA, Conneally PM (1985) A genetic model for age at onset in Huntington disease. Am J Hum Genet 37:350–357

    Google Scholar 

  • Farrer LA, Myers RH, Cupples LA, Conneally PM (1988) Considerations in using linkage analysis as a presymptomatic test for Huntington's disease. J Med Genet 25:577–588

    Google Scholar 

  • Folstein SE, Phillips III JA, Meyers DA, Chase GA, Abbott MH, Franz ML, Waber PG, Kazazian HH Jr, Conneally PM, Hobbs W, Tanzi R, Faryniarz A, Gibbons K, Gusella J (1985) Huntington's disease: two families with differing clinical features show linkage to the G8 probe. Science 229:776–779

    Google Scholar 

  • Folstein SE, Chase GA, Wahl WE, McDonnell AM, Folstein ME (1987) Huntington disease in Maryland: clinical aspects of racial variation. Am J Hum Genet 41:168–179

    Google Scholar 

  • Frontali M, Malaspina P, Rossi C, Jacopini AG, Vivona G, Pergola MS, Palena A, Novelletto A (1990) Epidemiological and linkage studies on Huntington's disease in Italy. Hum Genet 85:165–170

    Google Scholar 

  • Greenberg J (1989) A molecular service for Huntington disease in Southern Africa. S Afr Med J 76:135–137

    Google Scholar 

  • Gusella JF, Wexler NS, Conneally PM, Naylor SL, Anderson MA, Tanzi RE, Watkins TC, Ottina K, Wallace MR, Sakaguchi AY, Young AB, Shoulson I, Bonilla E, Martin JB (1983) A polymorphic DNA marker genetically linked to Huntington's disease. Nature 306:234–238

    CAS  PubMed  Google Scholar 

  • Harper PS, Sarfarazi M (1985) Genetic prediction and family structure in Huntington's chorea. BMJ 290:1929–1931

    Google Scholar 

  • Hayden MR (1981) Huntington's chorea. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Hayden MR, Robbins C, Allard D, Haines J, Fox S, Wasmuth J, Fahy M, Bloch M (1988) Improved predictive testing for Huntington Disease by using three linked DNA markers. Am J Hum Genet 43:689–694

    Google Scholar 

  • Holloway S, Millan FA, Curtis A, Mennie M, Brock DJH (1989) Genetic linkage between Huntington's disease and D4S10 (G8) in Scottish families. Clin Genet 35:133–138

    Google Scholar 

  • Ikonen E, Palo J, Ott J, Gusella J, Somer H, Karila L, Palotie A, Peltonen L (1990) Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus. Am J Hum Genet 46:5–11

    Google Scholar 

  • JenkinsT (1972) Genetic polymorphisms of Man in Southern Africa. PhD Thesis, University of London, pp 473–480, 463–467

  • Joubert J, Botha MC (1988) Huntington disease in South African blacks. S Afr Med 73:489–494

    Google Scholar 

  • Kanazawa I, Kondo I, Ikeda J-E, Ikeda T, Shizu Y, Yoshida M, Narabayashi H, Kuroda S, Tsunoda H, Mizuta E, Okuno Y, Sugawara K, Murata M, Takahashi M, Gusella JF (1990) Studies on DNA markers (D4S10 and D4S43/S127) genetically linked to Huntington's disease in Japanese families. Hum Genet 85:257–260

    Google Scholar 

  • Ott J (1974) Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. Am J Hum Genet 26:588–597

    Google Scholar 

  • Ott J (1985) Variability of the recombination fraction. In: Analysis of human genetic linkage. Johns Hopkins University Press, Baltimore London, pp 115–119, 200–203

    Google Scholar 

  • Skraastad MI, Bakker E, Lange LF de, Vegter-van der Vlis M, Klein-Breteler EG, Ommen GJB van, Pearson PL (1989) Mapping of recombinants near the Huntington disease locus by using G8 (D4S10) and newly isolated markers in the D4S10 region. Am J Hum Genet 44:560–566

    Google Scholar 

  • Swinscow TDV (1976) Statistics at Square One. British Medical Association, London

    Google Scholar 

  • Vandenplas S, Wiid I, Grobler-Rabie A, Brebner K, Ricketts M, Wallis G, Bester A, Boyd C, Mathew C (1984) Blot hybridisation analysis of genomic DNA. J Med Genet 21:164–172

    CAS  PubMed  Google Scholar 

  • Wasmuth JJ, Hewitt J, Smith B, Allard D, Haines JL, Skarecky D, Partlow E, Hayden MR (1988) A highly polymorphic locus very tightly linked to the Huntington's disease gene. Nature 332:734–736

    Google Scholar 

  • Wright HH, Still CN, Abramson RK (1981) Huntington's disease in black kindreds in South Carolina. Arch Neurol 38:412–414

    Google Scholar 

  • Youngman S, Sarfarazi M, Quarrell OWJ, Conneally PM, Gibbons K, Harper PS, Shaw DJ, Tanzi RE, Wallace MR, Gusella JF (1986) Studies of a DNA marker (G8) genetically linked to Huntington disease in British families. Hum Genet 73:333–339

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Greenberg, L.J., Martell, R.W., Theilman, J. et al. Genetic linkage between Huntington disease and the D4S10 locus in South African families: further evidence against non-allelic heterogeneity. Hum Genet 87, 701–708 (1991). https://doi.org/10.1007/BF00201729

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00201729

Keywords

Navigation