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Mol Cell Biol, March 1998, p. 1544-1552, Vol. 18, No. 3
Department of Biochemistry and Biophysics,
Texas A&M University, College Station, Texas 77843-2128
Received 28 August 1997/Returned for modification 8 October
1997/Accepted 17 December 1997
In addition to a reverse transcriptase activity, telomerase
is associated with a DNA endonuclease that removes nucleotides from a
primer 3' terminus prior to telomere repeat addition. Here we
examine the DNA specificity of the primer cleavage-elongation reaction
carried out by the Euplotes crassus telomerase. We
show that the primer cleavage activity copurified with the E. crassus telomerase polymerase, indicating that it either
is an intrinsic property of telomerase or is catalyzed by a
tightly associated factor. Using chimeric primers containing stretches
of telomeric DNA that could be precisely positioned on the RNA
template, we found that the cleavage site is more flexible than
originally proposed. Primers harboring mismatches in dT tracts that
aligned opposite nucleotides 37 to 40 in the RNA template were cleaved to eliminate the mismatched residues along with the adjacent 3' sequence. The cleaved product was then elongated to generate perfect telomeric repeats. Mismatches in dG tracts were not removed, implying that the nuclease does not track coordinately with the polymerase active site. Our data indicate that the telomerase-associated nuclease could provide a rudimentary proofreading function in telomere synthesis by eliminating mismatches between the DNA primer and the 5' region of the telomerase RNA template.
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Flexible Positioning of the Telomerase-Associated
Nuclease Leads to Preferential Elimination of Nontelomeric
DNA
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Corresponding author. Mailing address: Department of
Biochemistry and Biophysics, Texas A&M University, College
Station, TX 77843-2128. Phone: (409) 862-2342. Fax: (409) 845-9274. E-mail: dshippen{at}bioch.tamu.edu.
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