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A more recent version of this article appeared on December 1, 2003
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Submitted on July 4, 2003
Revised on August 22, 2003
Accepted on August 26, 2003
1 Children's Medical Research Institute, Westmead, NSW, Australia
2 Howard Hughes Medical Institute and Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO, U.S.A.
* Corresponding author. E-mail address: TBryan{at}cmri.usyd.edu.au.
Telomerase is an enzyme that utilizes an internal RNA molecule as a template for the extension of chromosomal DNA ends. The catalytic core of telomerase consists of the RNA subunit and a protein reverse transcriptase subunit, known as TERT. It has previously been shown that both yeast and human telomerase can form dimers or multimers in which one RNA in the complex can influence the activity of another. To test the proposal that dimerization might be essential for telomerase activity, we sought to determine whether Tetrahymena thermophila telomerase is active as a dimer or a monomer. Recombinant Tetrahymena telomerase eluted from a gel filtration column at the size of a monomeric complex (one RNA plus one TERT), and those fractions showed processive telomerase activity. We were unable to detect dimerization of Tetrahymena telomerase by coprecipitation experiments, using tags on either the TERT protein or telomerase RNA. Therefore a majority, if not all, of the recombinant Tetrahymena telomerase in our reconstitution system is present as a monomeric complex. We were also unable to detect dimerization of native telomerase from mating and vegetative Tetrahymena cell extracts. These results demonstrate that Tetrahymena telomerase does not need to dimerize to be active and processive.
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