Abstract
A family with a fragile site on chromosome 6 at band p23 was examined for recombination between the fragile site and HLA. Recombination was observed in four of the 20 offspring in whom it could occur. The estimate of the genetic length of chromosome between the fragile site and HLA is 20 centimorgans (cM) with a lower 95% probability limit of 8.5 cM, placing HLA proximal to the midpoint of 6p22. The most likely regional localization is at 6p21.3, which agrees closely with methods that do not involve recombination with the fragile site. This fragile site does not measurably disrupt recombination frequency, and the allele predisposing to expression of the fragile site is situated at the fragile site.
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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Berger R., Bernheim A., Sasportes M., Hauptmann G., Hors J., Legrand L., Fellous M. Regional mapping of the HLA on the short arm of chromosome 6. Clin Genet. 1979 Mar;15(3):245–251. doi: 10.1111/j.1399-0004.1979.tb00975.x. [DOI] [PubMed] [Google Scholar]
- Borgaonkar D. S., Bias W. B. Proceedings: HL-A loci and chromosome 6. Cytogenet Cell Genet. 1974;13(1):67–68. doi: 10.1159/000130235. [DOI] [PubMed] [Google Scholar]
- Breuning M. H., van den Berg-Loonen E. M., Bernini L. F., Bijlsma J. B., van Loghem E., Meera Khan P., Nijenhuis L. E. Localization of HLA on the short arm of chromosome 6. Hum Genet. 1977 Jun 30;37(2):131–139. doi: 10.1007/BF00393575. [DOI] [PubMed] [Google Scholar]
- Cook P. J., Noades J. E., Lomas C. G., Buckton K. E., Robson E. B. Exclusion mapping illustrated by the MNSs blood group. Ann Hum Genet. 1980 Jul;44(Pt 1):61–73. doi: 10.1111/j.1469-1809.1980.tb00946.x. [DOI] [PubMed] [Google Scholar]
- Cook P. J., Robson E. B., Buckton K. E., Jacobs P. A., Polani P. E. Segregation of genetic markers in families with chromosome polymorphisms and structural rearrangements involving chromosome 1. Ann Hum Genet. 1974 Jan;37(3):261–274. doi: 10.1111/j.1469-1809.1974.tb01834.x. [DOI] [PubMed] [Google Scholar]
- Ferrando P., San Román C., Rodriguez de Cordoba S., Arnaiz-Villena A. Partial trisomy 6p: 46,XX, -10, der(10),t(6;10) (p22;q26)pat and HLA localisation. J Med Genet. 1981 Jun;18(3):231–234. doi: 10.1136/jmg.18.3.231. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goodfellow P. N., Banting G., Trowsdale J., Chambers S., Solomon E. Introduction of a human X-6 translocation chromosome into a mouse teratocarcinoma: investigation of control of HLA-A, B, C expression. Proc Natl Acad Sci U S A. 1982 Feb;79(4):1190–1194. doi: 10.1073/pnas.79.4.1190. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Magenis R. E., Hecht F., Lovrien E. W. Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man. Science. 1970 Oct 2;170(3953):85–87. doi: 10.1126/science.170.3953.85. [DOI] [PubMed] [Google Scholar]
- Shows T. B., McAlpine P. J. The 1981 catalogue of assigned human genetic markers and report of the nomenclature committee. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. Cytogenet Cell Genet. 1982;32(1-4):221–245. doi: 10.1159/000131702. [DOI] [PubMed] [Google Scholar]
- Sutherland G. R., Baker E., Mulley J. C. Genetic length of a human chromosomal segment measured by recombination between two fragile sites. Science. 1982 Jul 23;217(4557):373–374. doi: 10.1126/science.7089572. [DOI] [PubMed] [Google Scholar]
- Sutherland G. R., Jacky P. B., Baker E., Manuel A. Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23, 9p21, 9q32, and 11q23. Am J Hum Genet. 1983 May;35(3):432–437. [PMC free article] [PubMed] [Google Scholar]