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Research Article

Microdissection of and Microcloning from the Short Arm of Human Chromosome 2

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Pages 3826-3830 | Received 19 May 1986, Accepted 08 Jul 1986, Published online: 31 Mar 2023

LITERATURE CITED

  • Bootsma, D., and K. K. Kidd. 1984. Report of the committee on the genetic constitution of chromosome 2, 3, 4 and 5. Cytogenet. Cell Genet. 37:22–23.
  • Brown, S. D. M. 1985. Mapping mammalian chromosomes: new technologies for old problems. Trends Genet. 1:219–220.
  • Cavenee, W. K., T. P. Dryja, R. A. Phillips, W. F. Benedict, R. Godbout, B. L. Gallic, A. L. Murphree, L. C. Strong, and R. L. White. 1983. Expression of recessive alleles by chromosomal mechanisms in retinoblastoma. Nature (London) 305:779–784.
  • Crampton, J. M., K. E. Davies, and T. E. Knapp. 1981. The occurrence of families of repetitive sequences in a library of cloned cDNA from human lymphocytes. Nucleic Acids Res. 9:3821–3833.
  • Davies, K. E., B. D. Young, R. G. Elles, M. E. Hill, and R. Williamson. 1981. Cloning a representative library of the human X chromosome after sorting by flow cytometry. Nature (London) 293:374–376.
  • de la Chapella, A. 1985. The 1985 human gene map and human gene mapping in 1985. Cytogenet. Cell Genet. 40:1–7.
  • Feinberg, A. P., and B. Vogelstein. 1984. A technique for radiolabelling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem. 137:267–268.
  • Fisher, E. M. C., J. S. Cavanna, and S. D. M. Brown. 1985. Microdissection and microcloning of the mouse X chromosome. Proc. Natl. Acad. Sci. USA 82:5846–5849.
  • Francke, U. 1975. Regional localization of the human genes for malate dehydrogenase-1 and isocitrate dehydrogenase-1 on chromosome 2 by interspecific hybridization using human cells with the balanced reciprocal translocation t(l;2)(q32;ql3). Cytogenet. Cell Genet. 14:138–142.
  • Gilliam, T. C., P. Scambler, T. Robbins, C. Ingle, R. Williamson, and K. E. Davies. 1984. The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic lengths. Hum. Genet. 68:154–158.
  • Gusella, J. F., N. S. Wexler, M. Conneally, S. L. Naylor, M. A. Anderson, R. E. Tanzi, P. C. Watkins, K. Ottina, M. R. Wallace, A. Y. Sakaguchi, A. B. Young, I. Shoulson, E. Bonilla, and J. B. Martin. 1983. A polymorphic DNA marker genetically linked to Huntington's disease. Nature (London) 306:234–238.
  • Henning, V., P. Huijser, P. Vogt, H. Jackie, and J.-E. Edstrom. 1983. Molecular cloning of microdissected lampbrush loop DNA sequences of Drosophila hydei. EMBO J. 2:1741–1746.
  • Hoyt, M. A., D. M. Knight, A. Das, H. I. Miller, and H. Echols. 1982. Control of phage λ development by stability and synthesis of cII protein: role of the viral cIII and host hflA, himA and himD genes. Cell 31:565–573.
  • Kunkel, L. M., A. P. Monaco, W. Middlesworth, H. D. Ochs, and S. A. Latt. 1985. Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. Proc. Natl. Acad. Sci. USA 82:4778–4782.
  • Maniatis, T., R. C. Hardison, E. Lacy, J. Lauer, C. O'Connell, D. Quon, G. K. Sim, and A. Efstratiadis. 1978. The isolation of structural genes from libraries of eucaryotic DNA. Cell 15:687–701.
  • Mattei, M. G., N. Souiah, and J. F. Mattei. 1984. Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis. Hum. Genet. 66:313–334.
  • Melton, D. A., P. A. Krieg, M. R. Rebagliati, T. Maniatis, K. Zinn, and M. R. Green. 1984. Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter. Nucleic Acids Res. 12:7035–7036.
  • Moorhead, P. S., P. C. Nowell, W. J. Mellman, D. M. Battips, and D. A. Hungerford. 1960. Chromosome preparations of leukocytes cultured from human peripheral blood. Exp. Cell Res. 20:613–616.
  • Murray, J. M., K. E. Davies, P. S. Harper, L. Meredith, C. R. Mueller, and R. Williamson. 1982. Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy. Nature (London) 300:69–71.
  • Murray, N. E., W. J. Brammar, and K. Murray. 1977. Lambdoid phages that simplify the recovery of in vitro recombinants. Mol. Gen. Genet. 150:53–61.
  • McKusick, V. A. 1982. The human genome through the eyes of a clinical geneticist. Cytogenet. Cell Genet. 32:7–23.
  • Porteous, D. J., J. E. N. Morten, G. Cranston, J. Fletcher, A. Mitchell, V. van Heyningen, J. A. Fantes, P. A. Boyd, and N. D. Hastie. 1986. Molecular and physical arrangements of human DNA in HRAS1-selected, chromosome-mediated transfectants. Mol. Cell. Biol. 6:2223–2232.
  • Povey, S., N. E. Morton, and S. L. Sherman. 1985. Report of the committee on the genetic constitution of chromosomes 1 and 2. Cytogenet. Cell Genet. 40:67–106.
  • Rohme, D., H. Fox, B. Herrmann, A.-M. Frischauf, J.-E. Edstrom, P. Mains, L. M. Silver, and H. Lehrach. 1984. Molecular clones of the mouse t complex derived from microdissected metaphase chromosomes. Cell 36:783–788.
  • Scalenghe, F., E. Turco, J.-E. Edstrom, V. Pirotta, and M. L. Melli. 1981. Microdissection and cloning of DNA from a specific region of Drosophila melanogaster polytene chromosomes. Chromosoma 82:205–216.
  • Solomon, E., and W. F. Bodmer. 1979. Evolution of sickle variant gene. Lancet i:923.
  • Southern, E. M. 1975. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J. Mol. Biol. 98:503–517.
  • Tsui, L.-C., M. Buchwald, D. Barker, J. C. Braman, R. Knowlton, J. W. Schumm, H. Eiberg, J. Mohr, D. Kennedy, N. Plavsic, M. Zsiga, G. Markiewicz, G. Akots, V. Brown, C. Helms, T. Gravius, C. Parker, K. Rediker, and H. Donis-Keller. 1985. Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker. Science 230:1054–1057.
  • Wainwright, B. J., P. J. Scambler, J. Schmidtke, E. A. Watson, H.-Y. Law, M. Farrail, H. J. Cooke, H. Eiberg, and R. Williamson. 1985. Localization of cystic fibrosis locus to human chromosome 7cen-q22. Nature (London) 318:384–385.
  • White, R., S. Woodward, M. Leppert, P. O'Connell, M. Hoff, L. Herbst, J.-M. Lalouel, M. Dean, and G. Vande-Woude. 1985. A closely linked genetic marker for cystic fibrosis. Nature (London) 318:382–384.

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