A method for constructing radiation hybrid maps of whole genomes (original) (raw)

References

1. Walter, M.A. & Goodfellow, P.N. Radiation hybrids: irradiation and fusion gene transfer. Trends Genet. 9, 352–356 (1993).
   Article CAS PubMed Google Scholar
2. Goss, S.J. & Harris, H. New method for mapping genes in human chromosomes. Nature 255, 680–684 (1975).
   Article CAS PubMed Google Scholar
3. Willard, H.F., Goss, S.J., Holmes, M.T. & Munroe, D.L. Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19. Hum. Genet. 71, 138–143 (1985).
   Article CAS PubMed Google Scholar
4. Cox, D.R., Burmeister, M., Price, E.R., Kim, S. & Myers, R.M. Radiation hybrid mapping: a somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes. Science 250, 245–250 (1990).
   Article CAS PubMed Google Scholar
5. Barrett, J.H. Genetic mapping based on radiation hybrid data. Genomics 13, 95–103 (1992).
   Article CAS PubMed Google Scholar
6. Wigler, M., Pellicer, A., Silverstein, S. & Axel, R. Biochemical transfer of single-copy eucaryotic genes using total cellular DNA as donor. Cell 14, 725–731 (1978).
   Article CAS PubMed Google Scholar
7. Benham, F. et al. A method for generating hybrids containing nonselected fragments of human chromosomes. Genomics 4, 509–517 (1989).
   Article CAS PubMed Google Scholar
8. Warrington, J.A. et al. A radiation hybrid map of 18 growth-factor, growth-factor receptor, hormone receptor, or neurotransmitter receptor genes on the distal region of the long arm of chromosome-5. Genomics 13, 803–808 (1992).
   Article CAS PubMed Google Scholar
9. Siden, T.S., Kumlien, J., Schwartz, C.E. & Rohme, D. Radiation fusion hybrids for human chromosomes 3 and X generated at various irradiation doses. Somat. Cell. molec. Genet. 18, 33–44 (1992).
   Article CAS PubMed Google Scholar
10. Boehnke, M., Lange, K. & Cox, D.R. Statistical methods for multipoint radiation hybrid mapping. Am. J. hum. Genet. 49, 1174–1188 (1991).
    CAS PubMed PubMed Central Google Scholar
11. NIH/CEPH Collaborative Mapping Group. A comprehensive genetic-linkage map of the human genome. Science 258, 67–86 (1992).
12. Weissenbach, J. et al. A 2nd-generatlon linkage map of the human genome. Nature 359, 794–801 (1992).
    Article CAS PubMed Google Scholar
13. Cox, D.W. Report of the first International workshop on human chromosome 14 mapping 1993. Cytogenet. Cell Genet. 66, 2–9 (1994).
    CAS PubMed Google Scholar
14. Goodfellow, P.J., Povey, S., Nevanlinna, H.A. & Goodfellow, P.N. Generation of a panel of somatic cell hybrids containing unselected fragments of human chromosome 10 by X-ray irradiation and cell fusion: application to Isolating the MEN2A region in hybrid cells. Somat. Cell. molec. Genet. 16, 163–171 (1990).
    Article CAS PubMed Google Scholar
15. Ceccherini, I. et al. Construction of a map of chromosome 16 by using radiation hybrids. Proc. natn. Acad. Sci. U.S.A. 89, 104–108 (1992).
    Article CAS Google Scholar
16. Sefton, L., Arnaud, D., Goodfellow, P.N., Simmler, M.C. & Avner, P. Characterization of the central region containing the X-inactivation center and terminal region of the mouse X chromosome using irradiation and fusion gene transfer hybrids. Mamm. Genome 2, 21–31 (1992).
    Article CAS PubMed Google Scholar
17. Gorski, J.L., Boehnke, M., Reyner, E.L. & Burright, E.N. A radiation hybrid map of the proximal short arm of the human x-chromosome spanning incontinentia-pigmenti-1 (ip1) translocation breakpoints. Genomics 14, 657–665 (1992).
    Article CAS PubMed Google Scholar
18. Lawrence, S., Morton, N.E. & Cox, D.R. Radiation hybrid mapping. Proc. natn. Acad. Sci. U.S.A. 88, 7477–7480 (1991).
    Article CAS Google Scholar
19. Westerveld, A., Visser, R.P.L.S., Khan, P.M. & Bootsma, D. Loss of human genetic markers in man-Chinese hamster ovary cells. Nature New Biol. 234, 20–22 (1971).
    Article CAS PubMed Google Scholar
20. Cotter, F.C., Hampton, G.M., Nasipuri, S., Bodmer, W. & Young, B. Rapid isolation of human chromosome-specific DNA probes from a somatic cell hybrid. Genomics 7, 257–263 (1990).
    Article CAS PubMed Google Scholar
21. Orita, M., Sekiya, T. & Hayashi, K. DNA sequence polymorphisms in Alu repeats. Genomics 8, 271–278 (1990).
    Article CAS PubMed Google Scholar
22. Powell, S.J., et al. Human bradykinin b2-receptor-nucleotide-sequence analysis and assignment to chromosome-14. Genomics 15, 435–438 (1993).
    Article CAS PubMed Google Scholar
23. Polymeropoulos, M.H., Xiao, H., Rath, D.S. & Merril, C.R. Dinucleotide repeat polymorphism at the human cardiac beta-myosin gene. Nucl. Acids Res. 19, 4019 (1991).
    PubMed PubMed Central Google Scholar
24. Byth, B.C., Meijers, J.C.M. & Cox, D.W. A (ca)n repeat polymorphism in the protein-c inhibitor (pci) gene. Hum. molec. Genet. 2, 1752–1752 (1993).
    PubMed Google Scholar
25. Byth, B.C. & Cox, D.W. A (ca)n repeat polymorphism at the 5′ end of the alpha-1-antitrypsin gene (pi). Hum. molec. Genet. 2, 1752–1752 (1993).
    PubMed Google Scholar
26. Yamada, Y. et al. Human somatostatin receptor genes-localization to human chromosome-14, chromosome-17, and chromosome-22 and identification of simple tandem repeat polymorphisms. Genomics 15, 449–452 (1993).
    Article CAS PubMed Google Scholar
27. Weber, J.L., Kwitek, A.E. & May, P.E. Dinucleotide repeat polymorphism at the D14S34 locus. Nucl. Acids Res. 18, 4638 (1990).
    PubMed PubMed Central Google Scholar
28. Jordan, S.A., McWilliam, P., O'Briain, D.S. & Humphries, P. Dinucleotide repeat polymorphism attheD14S42 locus. Nucl. Acids Res. 19, 1171 (1991).
    Article CAS PubMed PubMed Central Google Scholar
29. Sharma, V., Smith, L., Allen, L., Magenis, R.E. & Litt, M. Dinucleotide repeat polymorphism at the D14S43 locus. Nucl. Acids Res. 19, 1722 (1991).
    Article CAS PubMed PubMed Central Google Scholar
30. Luty, J.A. & Litt, M. Dinucleotide repeat polymorphism at the D14S45 locus. Nucl. Acids Res. 19, 4308 (1991).
    Article CAS PubMed PubMed Central Google Scholar
31. Wang, Z. & Weber, J.L. Continuous linkage map of human chromosome 14 short tandem repeat polymorphisms. Genomics 13, 532–536 (1992).
    Article CAS PubMed Google Scholar
32. Hudson, T.J. et al. Isolation and chromosomal assignment of 100 highly Informative human simple sequence repeat polymorphisms. Genomics 13, 622–629 (1992).
    Article CAS PubMed Google Scholar
33. Polymeropoulos, M.H., Ziao, H., Ide, S.E. & Merril, C.R. Dinulceotide repaet polymorphism at the D14s99E locus. Hum. molec. Genet. 2, 490 (1993).
    Article CAS PubMed Google Scholar
34. Zhao, B. et al. The human gene for apurinic/apyrimldinic endonuclease (HAP1): sequence and localization to chromosome 14 band q12. Nucl. Acids Res. 20, 4097–4098 (1992).
    Article CAS PubMed PubMed Central Google Scholar

Download references