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PMID: 1896088 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Telomerase primer specificity and chromosome healing.

Nature ·Vol. 353 ·No. 6343 ·1991-10-03 ·Pages 451-4

Harrington LA, Greider CW

Abstract

Chromosome healing by de novo telomere addition at nontelomeric sites has been well characterized in several organisms. The Tetrahymena telomerase ribonucleoprotein uses an internal RNA template to catalyse d(TTGGGG)n telomere addition to the 3' end of telomeric sequence in vitro and in vivo. Studies of telomerase RNA indicated that hybridization of the RNA template region, 5'-CAACCCCAA-3', to the 3' end of single-stranded telomeric oligonucleotides might be important for primer recognition and utilization. The apparent requirement of telomerase for pre-existing telomeric sequence has raised questions regarding its role in chromosome healing. We report here that Tetrahymena telomerase can specifically elongate single-stranded DNA oligonucleotides whose termini are not complementary to the RNA template sequence 5'-CAACCCCAA-3'. These data suggest that telomerase may be able to heal chromosomes directly in vivo.

MeSH Terms
Animals Base Sequence Chromosomes/metabolism DNA Nucleotidylexotransferase/metabolism DNA, Protozoan/metabolism DNA, Single-Stranded/metabolism Models, Genetic Molecular Sequence Data Nucleic Acid Hybridization Oligodeoxyribonucleotides/metabolism RNA, Protozoan/metabolism Substrate Specificity Tetrahymena/enzymology,genetics
Chemicals
DNA, Protozoan DNA, Single-Stranded Oligodeoxyribonucleotides RNA, Protozoan DNA Nucleotidylexotransferase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Harrington L A
Cold Spring Harbor Laboratory, New York 11724.
Greider C W
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1991-10-03
Pages
451-4
Language
English
Region
England
NLM ID
0410462
Subset
IM
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