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End Rescue from YACs Using the Vectorette

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Part of the book series: Methods in Molecular Biology™ ((MIMB,volume 54))

Abstract

The vectorette unit (1) consists of a pair of annealed oligonucleotides that contain two regions of complementary nucleotide sequence flanking a 29-bp noncomplementary segment (Fig. 1). The 5′ terminus of one of these complementary regions is phosphorylated and displays a restriction enzyme-specific sticky (or blunt) end that permits ligation of vectorette units to both ends of a restriction fragment. A nested pair of polymerase chain reaction (PCR) primers, VP1 and VP2, directed toward the phosphorylated end have most of their sequence, including their 3′ termini, in the noncomplementary region of the vectorette. These oligonucleotides cannot function as PCR primers on vectorette units without synthesis of a complementary strand from a primer located in the ligated DNA. Thus, although vectorette units will ligate to themselves and to all restriction fragments with matching ends, only DNA flanked by a specific primer (from known sequence) and a vectorette will be amplified in PCR.

Oligonucleotides used in vectorette end rescue from YACs: (A) The vectorette unit and associated PCR and sequencing primers. In the blunt-ended vectorette residue X = 5′ Phospho-T; Y = A. In the GATC sticky-ended vectorette (NNNN)X = 5′ Phospho-GATCG; Y = C. (B) PCR and sequencing primers for the r(ight) and l(eft) arms of the YAC vector pYAC4 (based on sequence in ref. 3).

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References

  1. Markham, A F., Smith, J., and Anwar, R. (1990) A Method for the Amplification of Nucleotide Sequences UK patent GB-2221909 B.

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  2. Butler, R., Ogilvie, D. J., Elvin, P., Riley, J. H., Finniear, R. S., Slynn, G., et al. (1992) Walking, cloning, and mapping with yeast artificial chromosomes: a contig encompassing D21S13 and D21S16. Genomics 12, 42–51.

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  3. Riley, J. H., Butler, R., Ogilvie, D. J., Finniear, R., Jenner, D., Anand, R., et. al. (1990) A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones. Nucleic Acids Res. 18, 2887–2890.

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  4. Green, P. M. and Giannelli, F. (1991) Direct sequencing of PCR-amplified DNA, in Methods in Molecular Biology, vol. 9, Protocols in Human Molecular Genetics (Mathew, C., ed.), Humana, Clifton, NJ.

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© 1996 Humana Press Inc.

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Ogilvie, D.J., James, L.A. (1996). End Rescue from YACs Using the Vectorette. In: Markie, D. (eds) YAC Protocols. Methods in Molecular Biology™, vol 54. Humana Press. https://doi.org/10.1385/0-89603-313-9:131

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  • DOI: https://doi.org/10.1385/0-89603-313-9:131

  • Publisher Name: Humana Press

  • Print ISBN: 978-0-89603-313-9

  • Online ISBN: 978-1-59259-541-9

  • eBook Packages: Springer Protocols

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