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A novel motif in telomerase reverse transcriptase regulates telomere repeat addition rate and processivity
Telomerase is a specialized reverse transcriptase that adds telomeric DNA repeats onto chromosome termini. Here, we characterize a new telomerase-specific motif, called motif 3, in the catalytic domain of telomerase reverse transcriptase, that is crucial for telomerase function and evolutionally con...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847249/ https://www.ncbi.nlm.nih.gov/pubmed/20044353 http://dx.doi.org/10.1093/nar/gkp1198 |
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author | Xie, Mingyi Podlevsky, Joshua D. Qi, Xiaodong Bley, Christopher J. Chen, Julian J.-L. |
author_facet | Xie, Mingyi Podlevsky, Joshua D. Qi, Xiaodong Bley, Christopher J. Chen, Julian J.-L. |
author_sort | Xie, Mingyi |
collection | PubMed |
description | Telomerase is a specialized reverse transcriptase that adds telomeric DNA repeats onto chromosome termini. Here, we characterize a new telomerase-specific motif, called motif 3, in the catalytic domain of telomerase reverse transcriptase, that is crucial for telomerase function and evolutionally conserved between vertebrates and ciliates. Comprehensive mutagenesis of motif 3 identified mutations that remarkably increase the rate or alter the processivity of telomere repeat addition. Notably, the rate and processivity of repeat addition are affected independently by separate motif 3 mutations. The processive telomerase action relies upon a template translocation mechanism whereby the RNA template and the telomeric DNA strand separate and realign between each repeat synthesis. By analyzing the mutant telomerases reconstituted in vitro and in cells, we show that the hyperactive mutants exhibit higher repeat addition rates and faster enzyme turnovers, suggesting higher rates of strand-separation during template translocation. In addition, the strong correlation between the processivity of the motif 3 mutants and their ability to use an 8 nt DNA primer, suggests that motif 3 facilitates realignment between the telomeric DNA and the template RNA following strand-separation. These findings support motif 3 as a key determinant for telomerase activity and processivity. |
format | Text |
id | pubmed-2847249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28472492010-04-01 A novel motif in telomerase reverse transcriptase regulates telomere repeat addition rate and processivity Xie, Mingyi Podlevsky, Joshua D. Qi, Xiaodong Bley, Christopher J. Chen, Julian J.-L. Nucleic Acids Res Molecular Biology Telomerase is a specialized reverse transcriptase that adds telomeric DNA repeats onto chromosome termini. Here, we characterize a new telomerase-specific motif, called motif 3, in the catalytic domain of telomerase reverse transcriptase, that is crucial for telomerase function and evolutionally conserved between vertebrates and ciliates. Comprehensive mutagenesis of motif 3 identified mutations that remarkably increase the rate or alter the processivity of telomere repeat addition. Notably, the rate and processivity of repeat addition are affected independently by separate motif 3 mutations. The processive telomerase action relies upon a template translocation mechanism whereby the RNA template and the telomeric DNA strand separate and realign between each repeat synthesis. By analyzing the mutant telomerases reconstituted in vitro and in cells, we show that the hyperactive mutants exhibit higher repeat addition rates and faster enzyme turnovers, suggesting higher rates of strand-separation during template translocation. In addition, the strong correlation between the processivity of the motif 3 mutants and their ability to use an 8 nt DNA primer, suggests that motif 3 facilitates realignment between the telomeric DNA and the template RNA following strand-separation. These findings support motif 3 as a key determinant for telomerase activity and processivity. Oxford University Press 2010-04 2009-12-30 /pmc/articles/PMC2847249/ /pubmed/20044353 http://dx.doi.org/10.1093/nar/gkp1198 Text en © The Author(s) 2009. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Molecular Biology Xie, Mingyi Podlevsky, Joshua D. Qi, Xiaodong Bley, Christopher J. Chen, Julian J.-L. A novel motif in telomerase reverse transcriptase regulates telomere repeat addition rate and processivity |
title | A novel motif in telomerase reverse transcriptase regulates telomere repeat addition rate and processivity |
title_full | A novel motif in telomerase reverse transcriptase regulates telomere repeat addition rate and processivity |
title_fullStr | A novel motif in telomerase reverse transcriptase regulates telomere repeat addition rate and processivity |
title_full_unstemmed | A novel motif in telomerase reverse transcriptase regulates telomere repeat addition rate and processivity |
title_short | A novel motif in telomerase reverse transcriptase regulates telomere repeat addition rate and processivity |
title_sort | novel motif in telomerase reverse transcriptase regulates telomere repeat addition rate and processivity |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847249/ https://www.ncbi.nlm.nih.gov/pubmed/20044353 http://dx.doi.org/10.1093/nar/gkp1198 |
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