Skip to main content
Log in

A new deletion polymorphism at D5S71 raises the linkage information on adenomatous polyposis coli: implications for presymptomatic diagnosis

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

Summary

Two independent study-groups, one in Britain and the other in the United States, were the first to report linkage between APC and a TaqI restriction fragment length polymorphism (RFLP) at D5S71 (probe C11p11) on chromosome 5q. They found no recombinants in about 50 informative meioses. The same TaqI RFLP was found to be uninformative for linkage in 15 Dutch polyposis families. The recently reported four base-pair deletion polymorphism (DEL1) at D5S71 has raised the polymorphism information content of this marker from 0.17 to 0.40 in the Dutch population. Seven of 20 polyposis families screened for the DEL1 as well as the TaqI polymorphism gave a combined peak lod score of 5.68 with no recombinants in 37 informative meioses. These data, together with those so far reported in the literature, raise the peak lod score to 17.09 at a recombination fraction of 0.05, the 95% upper confidence limit being 0.09. In combination with the use of another informative marker, D5S81 (probe YN5.48) closely mapping on the other side of APC, the presymptomatic diagnosis of the disease can be made with more than 99.9% certainty. It has to be stressed, however, that the the possible existence of more than one polyposis locus cannot, as yet, be excluded.

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

  • Aldred MA, Rees M, Tsioupra K, Leigh SEA, Neale KF, Delhanty JDA (1988) Familial polyposis coli. Lancet II:565.

  • Baker RH, Heineman MH, Miller HH, Decosse JJ (1988) Hyper-pigmented lesions of the retinal pigment epithelium in familial adenomatous polyposis. Am J Med Genet 31:427–435.

    Google Scholar 

  • Bodmer WF, Baily CJ, Bodmer J, Bussey HJR, Ellis A, Gorman P, Lucibello FC, Murday VA, Rider SH, Scambler P, Sheer D, Solomon E, Spurr NK (1987) Localization of the gene for familial adenomatous polyposis on chromosome 5. Nature 328:614–616.

    Google Scholar 

  • Breukel C, Tops CMJ, Meera Khan P (1989a) Four-base-pair deletion polymorphism at D5S71 (C11p11) linked to APC in the human chromosome 5q21–q22 region. Nucleic Acids Res 17:10512.

    Google Scholar 

  • Breukel C, Tops CMJ, Meera Khan P (1989b) A 4 base-pair deletion polymorphism in man. J Genet 68:171–183.

    Google Scholar 

  • Bülow S (1987) Familial adenomatous polyposis. Dan Med Bull 34:1–15.

    Google Scholar 

  • Bussey HJR (1975) Familial polyposis coli. Johns Hopkins University Press, Baltimore.

    Google Scholar 

  • Chapman PD, Church W, Burn J, Gunn A (1989) Congenital hypertrophy of retinal pigment epithelium: a sign of familial adenomatous polyposis. Br Med J 298:353–354.

    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 and reporting. (8th International Workshop on Human Gene Mapping) Cytogenet Cell Genet 40:356–358.

    Google Scholar 

  • Dunlop MG, Steel CM, Wyllie AH, Bird CC, Evans HJ (1989) Linkage analysis in familial adenomatous polyposis: order of C11p11 (D5S71) and Pi227 (D5S37) loci at the APC gene. Genomics 5:350–353.

    Google Scholar 

  • Lathrop GM, Lalouel (1984) Easy calculations of lodscores and genetic risks on small computers. Am J Hum Genet 36:460–465.

    Google Scholar 

  • Lau YL, Levinsky RJ, Malcolm S, Goodship J, Winter R, Pembrey M (1988) Genetic prediction in X-linked agammaglobulinaemia. Am J Med Genet 31:437–448.

    Google Scholar 

  • Leppert M, Dobbs M, Scambler P, O'Connell P, Nakamura Y, Stauffer D, Woodward S, Burt R, Hughes J, Gardner E, Lathrop M, Wasmuth J, Lalouel M, White R (1987) The gene for familial polyposis coli maps to the long arm of chromosome 5. Science 238:1411–1413.

    Google Scholar 

  • Meera Khan P, Tops CMJ, Broek M v d, Breukel C, Wijnen JT, Oldenburg M, Bos J v d, Leeuwen-Cornelisse ISJ v, Vasen HFA, Griffioen G, Verspaget HM, Hartog Jager FCA den, Lamers CBHW (1988) Close linkage of a highly polymorphic marker (D5S37) to familial adenomatous polyposis (FAP) and confirmation of FAP localization on chromosome 5q21–22. Hum Genet 79:183–185.

    Google Scholar 

  • Nakamura Y, Lathrop M, Leppert M, Dobbs M, Wasmuth J, Wolff E, Carlson M, Fujimoto E, Krapcho K, Sears T, Woodward S, Hughes J, Burt R, Gardner E, Lalouel JM, White R (1988) Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5. Am J Hum Genet 43:638–644.

    Google Scholar 

  • Tops CMJ, Griffioen G, Vasen HFA, Breukel C, Klift HMvd, Wijnen JT, Leeuwen ISJv, Hartog Jager FCA den, Nagengast FM, Lamers CBHW, Meera Khan P (1989) Presymptomatic diagnosis of familial adenomatous polyposis by bridging DNA markers. Lancet II: 1361–1363.

    Google Scholar 

  • Traboulsi EI, Maumenee IH, Krush AJ, Alcorn D, Giardiello FM, Burt RW, Hughes P, Hamilton SR (1990) Congenital hypertrophy of the retinal pigment epithelium predicts colorectal polyposis in Gardner's syndrome. Arch Ophthalmol 108:525–526.

    Google Scholar 

  • Vasen HFA, Griffioen G, Offerhaus GJA, Hartog Jager FCA den, Leeuwen-Cornelisse ISJ van, Meera Khan P, Lamers CBHW, Slooten EA van (1990) The value of screening and central registration of families with familial adenomatous polyposis. Dis Colon Rectum 33:227–230.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tops, C.M.J., Breukel, C., van der Klift, H.M. et al. A new deletion polymorphism at D5S71 raises the linkage information on adenomatous polyposis coli: implications for presymptomatic diagnosis. Hum Genet 86, 365–368 (1991). https://doi.org/10.1007/BF00201835

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00201835

Keywords

Navigation