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Molecular and Cellular Biology, September 1998, p. 4961-4970, Vol. 18, No. 9
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Identification of Kluyveromyces lactis
Telomerase: Discontinuous Synthesis along the 30-Nucleotide-Long
Templating Domain
Tracy Boswell
Fulton and
Elizabeth H.
Blackburn*
Departments of Microbiology and Immunology & Biochemistry and Biophysics, University of California, San
Francisco, San Francisco, California 94143-0414
Received 30 March 1998/Returned for modification 4 May
1998/Accepted 3 June 1998
Telomeres in the budding yeast Kluyveromyces lactis
consist of perfectly repeated 25-bp units, unlike the imprecise repeats at Saccharomyces cerevisiae telomeres and the short (6- to
8-bp) telomeric repeats found in many other eukaryotes. Telomeric DNA is synthesized by the ribonucleoprotein telomerase, which uses a
portion of its RNA moiety as a template. K. lactis
telomerase RNA, encoded by the TER1 gene, is ~1.3 kb long
and contains a 30-nucleotide templating domain, the largest ever
examined. To examine the mechanism of polymerization by this enzyme, we
identified and analyzed telomerase activity from K. lactis
whole-cell extracts. In this study, we exploited the length of the
template and the precision of copying by K. lactis
telomerase to examine primer elongation within one round of repeat
synthesis. Under all in vitro conditions tested, K. lactis
telomerase catalyzed only one round of repeat synthesis and remained
bound to reaction products. We demonstrate that K. lactis
telomerase polymerizes along the template in a discontinuous manner and
stalls at two specific regions in the template. Increasing the amount
of primer DNA-template RNA complementarity results in stalling,
suggesting that the RNA-DNA hybrid is not unpaired during elongation in
vitro and that lengthy duplexes hinder polymerization through
particular regions of the template. We suggest that these observations
provide an insight into the mechanism of telomerase and its regulation.
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, University of California San Francisco, San Francisco, CA 94143-0414. Phone: (415) 476-4912. Fax: (415) 476-8201. E-mail: porter{at}itsa.ucsf.edu.
Molecular and Cellular Biology, September 1998, p. 4961-4970, Vol. 18, No. 9
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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