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Fine mapping of the Huntington disease linked D4S10 locus by non-radioactive in situ hybridization

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Summary

The chromosomal localization of a unique DNA fragment, closely linked to Hintington disease (HD), was assessed in situ by hybridization with 2-acetylaminofluorene (AAF) modified probes. In these experiments, a cosmid cloned genomic fragment (c5.5) was used for hybridization. Here we present evidence that confirms the mapping of the D4S10 locus to the p16 region of chromosome 4 and assigns it to the telomere of the short arm.

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References

  • Gusella JF, Wexler NS, Conneally PM, Naylor SL, Anderson MA, Tanzi RE, Watkins PC, 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

    Google Scholar 

  • Gusella JF, Tanzi RE, Bader PI, Phelan MC, Stevenson R, Hayden MR, Hofman KJ, Faryniarz AG, Gibbons K (1985) Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome. Nature 318:75–78

    Google Scholar 

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

    Google Scholar 

  • Hopman AHN, Wiegant J, Van Duijn P (1986) A new hybridocytochemical method based on mercurated nucleic acid probes and sulfhydryl-hapten ligands. I. Stability of the mercury-sulfhydryl bond and influence of the ligand structure on immunochemical detection of the hapten. Histochemistry 84:169–178

    Google Scholar 

  • Landegent JE, Jansen in de Wal N, Baan RA, Hoeijmakers JHJ, Van der Ploeg M (1984) 2-Acetylaminofluorene-modified probes for the indirect hybridocytochemical detection of specific nucleic acid sequences. Exp Cell Res 153:61–72

    Google Scholar 

  • Landegent JE, Jansen in de Wal N, Ploem JS, Van der Ploeg M (1985a) Sensitive detection of hybridocytochemical results by means of reflection-contrast microscopy. J Histochem Cytochem 33:1241–1246

    Google Scholar 

  • Landegent JE, Jansen in de Wal N, Van Ommen G-J.B, Baas F, De Vijlder JJM, Van Duijn P, Van der Ploeg M (1985b) Chromosomal localization of a unique gene by non-autoradiographic in situ hybridization. Nature 317:175–177

    Google Scholar 

  • Laurie DA, Hulten MA (1985) Further studies on chiasma distribution and interference in the human male. Ann Hum Genet 49: 203–214

    Google Scholar 

  • Magenis E, Gusella J, Weliky K, Haight G, Sheehy B (1985) Huntington disease-linked (HD) restriction fragment polymorphism localized to band p16 of chromosome 4 by in situ hybridization. (8th Human Gene Mapping Workshop, Helsinki, Finland, 1985.) Cytogenet Cell Genet 40:685

    Google Scholar 

  • Pearson PL, Bobrow M, Vosa CG, Barlow PW (1971) Quinacrine fluorescence in mammalian chromosomes. Nature 231:326–329

    Google Scholar 

  • Ploem JS (1975) Reflection-contrast microscopy as a tool for the investigation of the attachment of living cells to glass surface. In: Van Furth R (ed) Mononuclear phagocytes in immunity, infection and pathology. Blackwell, Oxford, pp 405–421

    Google Scholar 

  • Schwartz DC, Cantor CR (1984) Separation of Yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresis. Cell 37: 67–75

    Google Scholar 

  • Sealey PG, Whittaker PA, Southern EM (1985) Removal of repeated sequences from hybridization probes. Nucleic Acids Res 13:1905–1922

    Google Scholar 

  • Tchen P, Fuchs RPP, Sage E, Leng M (1984) Chemically modified nucleic acids as immunodetectable probes in hybridization experiments. Proc Natl Acad Sci USA 81:3466–3470

    Google Scholar 

  • Van der Ploeg M, Van Duijn P (1979) Reflection versus fluorescence. Histochemistry 62:227–232

    Google Scholar 

  • Wang HS, Greenberg CR, Kalousek D, Gusella JF, Horsman D, Hayden MR (1985) Subregional assignment of the linked marker D4S10 (G8) for Huntington disease by in situ hybridization. (8th Human Gene Mapping Workshop, Helsinki, Finland, 1985.) Cytogenet Cell Genet 40:772

    Google Scholar 

  • Zabel BU, Naylor SL, Sakaguchi AY, Gusella JF (1985) Regional localization of a DNA polymorphism (D4S10) linked to Huntington's disease at 4p16–p15. (8th Human Gene Mapping Workshop, Helsinki, Finland, 1985.) Cytogenet Cell Genet 40:787

    Google Scholar 

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Landegent, J.E., Jansen in de Wal, N., Fisser-Groen, Y.M. et al. Fine mapping of the Huntington disease linked D4S10 locus by non-radioactive in situ hybridization. Hum Genet 73, 354–357 (1986). https://doi.org/10.1007/BF00279100

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  • DOI: https://doi.org/10.1007/BF00279100

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