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| Subject Categories:
Cell Cycle
| Genome Stability & Dynamics
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The EMBO Journal
(2003) 22, 1688–1696, doi:10.1093/emboj/cdg154
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| Rap1p telomere association is not required for mitotic stability of a C3TA2 telomere in yeast |
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Mary Kate Alexander and Virginia A. Zakian
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Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA
To whom correspondence should be addressed
Virginia A. Zakian, vzakian@molbio.princeton.edu
Received 7 November 2002; Revised 9 January 2003; Accepted 12 February 2003.
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| Abstract |
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| Telomeric DNA usually consists of a repetitive sequence: C1–3A/TG1–3 in yeast, and C3TA2/T2AG3 in vertebrates. In yeast, the sequence-specific DNA- binding protein Rap1p is thought to be essential for telomere function. In a tlc1h mutant, the templating region of the telomerase RNA gene is altered so that telomerase adds the vertebrate telomere sequence instead of the yeast sequence to the chromosome end. A tlc1h strain has short but stable telomeres and no growth defect. We show here that Rap1p and the Rap1p-associated Rif2p did not bind to a telomere that contains purely vertebrate repeats, while the TG1–3 single-stranded DNA binding protein Cdc13p and the normally non-telomeric protein Tbf1p did bind this telomere. A chromosome with one entirely vertebrate-sequence telomere had a wild-type loss rate, and the telomere was maintained at a short but stable length. However, this telomere was unable to silence a telomere-adjacent URA3 gene, and the strain carrying this telomere had a severe defect in meiosis. We conclude that Rap1p localization to a C3TA2 telomere is not required for its essential mitotic functions. |
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| Keywords: RAP1, RIF2, telomerase, telomere, yeast |
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