Comparison of Plant Telomere Locations using a PCR-generated Synthetic Probe (original) (raw)
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1Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3DS, UK
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1Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3DS, UK
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1Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3DS, UK
Search for other works by this author on:
,
1Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3DS, UK
Search for other works by this author on:
,
1Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3DS, UK
Search for other works by this author on:
1Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3DS, UK
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Published:
01 September 1993
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Antony V. Cox, Simon T. Bennett, Alexander S. Parokonny, Ann Kenton, Markella A. Callimassia, Michael D. Bennett, Comparison of Plant Telomere Locations using a PCR-generated Synthetic Probe, Annals of Botany, Volume 72, Issue 3, September 1993, Pages 239–247, https://doi.org/10.1006/anbo.1993.1104
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We have generated a telomere-specific probe by the polymerase chain reaction and used it to localize chromosome telomeres of ten unrelated angiosperm species in in situ. Concatenation of the simple monomers, 5′-(TTTAGGG)-3′, derived from the sequence of Arabidopsis thaliana telomeres, yielded a stable, versatile and reliable probe that gave a signal of high intensity following fluorescence in situ hybridization. Most species, including those with known karyotype rearrangements, showed telomere label only at chromosome termini. These findings are discussed in the context of the chromosomal events responsible for generating and stabilizing karyotype change in plants.Copyright 1993, 1999 Academic Press
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