Abstract
The hemochromatosis (HC) gene is known to be linked to HLA-A (6p21.3); however, its precise location has been difficult to determine because of a lack of additional highly polymorphic markers for this region. The recent identification of short tandem repeat sequences (microsatellites) has now provided this area with a number of markers with similar polymorphic index to the HLA serological polymorphisms. Using four microsatellites--D6S105, D6S109, D6S89, and F13A--together with the HLA class I loci HLA-A and HLA-B in 13 large pedigrees clearly segregating for HC, we have been able to refine the location of the HC gene. We identified no recombination between HC and HLA-A or D6S105, and two-point analyses placed the HC gene within one centimorgan (cM) of HLA-A and D6S105 (HLA-A maximum of the lod score [Zmax] of 9.90 at recombination fraction [theta] of 0.0, and D6S105 Zmax of 8.26 at theta of 0.0). The markers HLA-B, D6S109, D6S89, and F13A were separated from the HC locus by recombination, defining the centromeric and telomeric limits for the HC gene as HLA-B and D6S109, respectively. A multipoint map constructed using HLA-B, HLA-A, and D6S109 indicates that the HC gene is located in a region less than 1 cM proximal to HLA-A and less than 1 cM telomeric of HLA-A. These pedigree data indicate an association between HC and specific alleles at HLA-A and D6S105 (i.e., HLA-A3 and D6S105 allele 8).(ABSTRACT TRUNCATED AT 250 WORDS)
Full text
PDF





Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bassett M. L., Halliday J. W., Powell L. W. Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis. Hepatology. 1986 Jan-Feb;6(1):24–29. doi: 10.1002/hep.1840060106. [DOI] [PubMed] [Google Scholar]
- Beckman J. S., Weber J. L. Survey of human and rat microsatellites. Genomics. 1992 Apr;12(4):627–631. doi: 10.1016/0888-7543(92)90285-z. [DOI] [PubMed] [Google Scholar]
- Edwards C. Q., Griffen L. M., Dadone M. M., Skolnick M. H., Kushner J. P. Mapping the locus for hereditary hemochromatosis: localization between HLA-B and HLA-A. Am J Hum Genet. 1986 Jun;38(6):805–811. [PMC free article] [PubMed] [Google Scholar]
- Edwards C. Q., Griffen L. M., Goldgar D., Drummond C., Skolnick M. H., Kushner J. P. Prevalence of hemochromatosis among 11,065 presumably healthy blood donors. N Engl J Med. 1988 May 26;318(21):1355–1362. doi: 10.1056/NEJM198805263182103. [DOI] [PubMed] [Google Scholar]
- Geraghty D. E., Pei J., Lipsky B., Hansen J. A., Taillon-Miller P., Bronson S. K., Chaplin D. D. Cloning and physical mapping of the HLA class I region spanning the HLA-E-to-HLA-F interval by using yeast artificial chromosomes. Proc Natl Acad Sci U S A. 1992 Apr 1;89(7):2669–2673. doi: 10.1073/pnas.89.7.2669. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hearne C. M., Ghosh S., Todd J. A. Microsatellites for linkage analysis of genetic traits. Trends Genet. 1992 Aug;8(8):288–294. doi: 10.1016/0168-9525(92)90256-4. [DOI] [PubMed] [Google Scholar]
- Jouanolle A. M., Yaouanq J., Blayau M., Périchon M., Fauchet R., Font M. P., Le Gall J. Y., David V. HLA class I gene polymorphism in genetic hemochromatosis. Hum Genet. 1990 Aug;85(3):279–282. doi: 10.1007/BF00206746. [DOI] [PubMed] [Google Scholar]
- Keats B., Ott J., Conneally M. Report of the committee on linkage and gene order. Cytogenet Cell Genet. 1989;51(1-4):459–502. doi: 10.1159/000132805. [DOI] [PubMed] [Google Scholar]
- Lathrop G. M., Lalouel J. M., Julier C., Ott J. Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci U S A. 1984 Jun;81(11):3443–3446. doi: 10.1073/pnas.81.11.3443. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Leggett B. A., Halliday J. W., Brown N. N., Bryant S., Powell L. W. Prevalence of haemochromatosis amongst asymptomatic Australians. Br J Haematol. 1990 Apr;74(4):525–530. doi: 10.1111/j.1365-2141.1990.tb06345.x. [DOI] [PubMed] [Google Scholar]
- Litt M., Jorde L. B. Linkage disequilibria between pairs of loci within a highly polymorphic region of chromosome 2Q. Am J Hum Genet. 1986 Aug;39(2):166–178. [PMC free article] [PubMed] [Google Scholar]
- Litt M., Luty J. A. Dinucleotide repeat polymorphism at the D6S89 locus. Nucleic Acids Res. 1990 Jul 25;18(14):4301–4301. doi: 10.1093/nar/18.14.4301. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Polymeropoulos M. H., Rath D. S., Xiao H., Merril C. R. Tetranucleotide repeat polymorphism at the human coagulation factor XIII A subunit gene (F13A1). Nucleic Acids Res. 1991 Aug 11;19(15):4306–4306. [PMC free article] [PubMed] [Google Scholar]
- Powell L. W., Summers K. M., Board P. G., Axelsen E., Webb S., Halliday J. W. Expression of hemochromatosis in homozygous subjects. Implications for early diagnosis and prevention. Gastroenterology. 1990 Jun;98(6):1625–1632. doi: 10.1016/0016-5085(90)91100-k. [DOI] [PubMed] [Google Scholar]
- Ranum L. P., Chung M. Y., Duvick L. A., Zoghbi H. Y., Orr H. T. Dinucleotide repeat polymorphism at the D6S109 locus. Nucleic Acids Res. 1991 Mar 11;19(5):1171–1171. doi: 10.1093/nar/19.5.1171-a. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Simon M., Le Mignon L., Fauchet R., Yaouanq J., David V., Edan G., Bourel M. A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA association. Am J Hum Genet. 1987 Aug;41(2):89–105. [PMC free article] [PubMed] [Google Scholar]
- Summers K. M., Halliday J. W., Powell L. W. Identification of homozygous hemochromatosis subjects by measurement of hepatic iron index. Hepatology. 1990 Jul;12(1):20–25. doi: 10.1002/hep.1840120105. [DOI] [PubMed] [Google Scholar]
- Summers K. M., Tam K. S., Halliday J. W., Powell L. W. HLA determinants in an Australian population of hemochromatosis patients and their families. Am J Hum Genet. 1989 Jul;45(1):41–48. [PMC free article] [PubMed] [Google Scholar]
- Trowsdale J., Ragoussis J., Campbell R. D. Map of the human MHC. Immunol Today. 1991 Dec;12(12):443–446. doi: 10.1016/0167-5699(91)90017-n. [DOI] [PubMed] [Google Scholar]
- Walter M. A., Cox D. W. Nonuniform linkage disequilibrium within a 1,500-kb region of the human immunoglobulin heavy-chain complex. Am J Hum Genet. 1991 Nov;49(5):917–931. [PMC free article] [PubMed] [Google Scholar]
- Weber J. L., Kwitek A. E., May P. E., Zoghbi H. Y. Dinucleotide repeat polymorphism at the D6S105 locus. Nucleic Acids Res. 1991 Feb 25;19(4):968–968. doi: 10.1093/nar/19.4.968. [DOI] [PMC free article] [PubMed] [Google Scholar]