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A new human brain cDNA molecule: assignment to chromosome 11q21-q23.1 and description of two polymorphisms studied by the polymerase chain reaction

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Abstract

A new human brain cDNA molecule was mapped by in situ hybridization to the 11q21-q23.1 region of the human genome, probably to the 11q22 band. An EcoRI restriction site and a (GT) n repeat element within the gene were shown to be polymorphic. Both polymorphisms were readily studied by the polymerase chain reaction. A two-allele polymorphism was described for the EcoRI restriction site, whereas four different alleles were detected for the second genetic marker. The observed heterozygosities were 37% and 42% for the former and the latter polymorphism, respectively. The combined heterozygosity index was estimated to be 0.56. These new genetic markers will be useful for linkage analysis of neurogenetic diseases that have been mapped to this chromosomal region.

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References

  • Aurias A, Rimbaut C, Buffe D, Dubousset D, Mazabraud A (1983) Chromosomal translocations in Ewing's sarcoma. N Engl J Med 309:496–497

    Google Scholar 

  • Concannon P, Malhotra U, Charmley P, Reynolds J, Lange K, Gatt RA (1990) The ataxia-telangectasia gene (ATA) on chromosome 11 is distinct from ETS-1 gene. Am J Hum Genet 46:789–794

    Google Scholar 

  • Grandy DK, Litt M, Allen L, Bunzow J, Marchionni M, Makam H, Reed L, Magen RE, Civelli O (1989) The human dopamine D2 receptor gene is localized on chromosome 11q22-q23 and identifies a TaqI RFLP. Am J Hum Genet 45:778–785

    Google Scholar 

  • Heyningen V van, Porteous D (1991) Technique for region specific marker isolation to identify and clone breakpoint of interest. Second International Chromosome 11 Workshop, France. Abstract

  • Junien C, Heyningen V van, Evans G, Little P, Mannens M (1992) Report of the second chromosome 11 workshop. Genomics 12:620–625

    Google Scholar 

  • Lefebvre S, Bureau JF, Chirinian S, Brahic M (1989) Multiple sclerosis and retrovirus: screening with retroviral probes of a cDNA library constructed with poly A+RNA from active plaques (abstract). In: Head IE (ed) Fifth International Conference on AIDS. Canada, p 83. International Development Research Centre

    Google Scholar 

  • Mattei MG, Philip N, Passage E, Moisan JP, Mandel JL, Mattei JF (1985) DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome. Hum Genet 69:268–271

    Google Scholar 

  • McConville CM, Woods CG, Farrall M, Metcalfe JA, Taylor AMR (1990) Analysis of 7 polymorphic markers at chromosome 11q22–23 in 35 ataxia telangiectasia families; further evidence of linkage. Hum Genet 85:215–220

    Google Scholar 

  • Nguyen C, Mattei MG, Santoni MJ, Goridis C, Jordan BR (1986) Localization of the human NCAM gene to band q23 of chromosome 11: the third gene coding for a cell interaction molecule mapped to the distal portion of the long arm of chromosome 11. J Cell Biol 102:711–715

    Google Scholar 

  • Polymeropoulos MH, Xiao H, Glodek A, Gorski M, Adams MD, Moreno RF, Fitzgerald MG, Venter JC, Merril CR (1992) Chromosomal assignment of 46 brain cDNAs. Genomics 12:492–496

    Google Scholar 

  • Smith M, Wasmuth J, McPherson JD, Wagner C, Grandy D, Civelli O, Potkin S, Litt M (1989) Cosegregation of an 11q22.3–9p22 translocation with affective disorder: proximity of the dopamine D2 receptor gene relative to the translocation breakpoint (abstract). Am J Hum Genet 45:A220

    Google Scholar 

  • Turc-Carel C, Philip I, Berger MP, Philip T, Lenoir GM (1983) Translocation (11:22) (q24:q12) in Ewing's cell lines. N Enel J Med 309:497–498

    Google Scholar 

  • Whang-Peng J, Triche TJ, Knudsen T, Miser J, Kao-Shan S, Tsai S, Israel MA (1986) A characterization of selected small round cell tumors of childhood. Cancer Genet Cytogenet 21:185–208

    Google Scholar 

  • Ziv Y, Frydman M, Lange E, Zelnik N, Rotman G, Julier C, Jaspers NGJ, Dagan Y, Abeliovicz D, Dar H, Borochowitz Z, Lathrop M, Gatti RA, Shiloh Y (1992) Ataxia-telangectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microencephaly-cataract syndrome. Hum Genet 88:619–626

    Google Scholar 

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Lefebvre, S., Bureau, JF., Muscatelli, F. et al. A new human brain cDNA molecule: assignment to chromosome 11q21-q23.1 and description of two polymorphisms studied by the polymerase chain reaction. Hum Genet 91, 148–150 (1993). https://doi.org/10.1007/BF00222715

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  • DOI: https://doi.org/10.1007/BF00222715

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