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Extracting Extra-Telomeric Phenotypes from Telomerase Mouse Models
Telomerase reverse transcriptase (TERT) is the protein component of telomerase and combined with an RNA molecule, telomerase RNA component, forms the telomerase enzyme responsible for telomere elongation. Telomerase is essential for maintaining telomere length from replicative attrition and thus con...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Yonsei University College of Medicine
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874908/ https://www.ncbi.nlm.nih.gov/pubmed/24339280 http://dx.doi.org/10.3349/ymj.2014.55.1.1 |
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author | Sung, Young Hoon Ali, Muhammad Lee, Han-Woong |
author_facet | Sung, Young Hoon Ali, Muhammad Lee, Han-Woong |
author_sort | Sung, Young Hoon |
collection | PubMed |
description | Telomerase reverse transcriptase (TERT) is the protein component of telomerase and combined with an RNA molecule, telomerase RNA component, forms the telomerase enzyme responsible for telomere elongation. Telomerase is essential for maintaining telomere length from replicative attrition and thus contributes to the preservation of genome integrity. Although diverse mouse models have been developed and studied to prove the physiological roles of telomerase as a telomere-elongating enzyme, recent studies have revealed non-canonical TERT activities beyond telomeres. To gain insights into the physiological impact of extra-telomeric roles, this review revisits the strategies and phenotypes of telomerase mouse models in terms of the extra-telomeric functions of telomerase. |
format | Online Article Text |
id | pubmed-3874908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Yonsei University College of Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-38749082014-01-01 Extracting Extra-Telomeric Phenotypes from Telomerase Mouse Models Sung, Young Hoon Ali, Muhammad Lee, Han-Woong Yonsei Med J Review Article Telomerase reverse transcriptase (TERT) is the protein component of telomerase and combined with an RNA molecule, telomerase RNA component, forms the telomerase enzyme responsible for telomere elongation. Telomerase is essential for maintaining telomere length from replicative attrition and thus contributes to the preservation of genome integrity. Although diverse mouse models have been developed and studied to prove the physiological roles of telomerase as a telomere-elongating enzyme, recent studies have revealed non-canonical TERT activities beyond telomeres. To gain insights into the physiological impact of extra-telomeric roles, this review revisits the strategies and phenotypes of telomerase mouse models in terms of the extra-telomeric functions of telomerase. Yonsei University College of Medicine 2014-01-01 2013-11-29 /pmc/articles/PMC3874908/ /pubmed/24339280 http://dx.doi.org/10.3349/ymj.2014.55.1.1 Text en © Copyright: Yonsei University College of Medicine 2014 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Sung, Young Hoon Ali, Muhammad Lee, Han-Woong Extracting Extra-Telomeric Phenotypes from Telomerase Mouse Models |
title | Extracting Extra-Telomeric Phenotypes from Telomerase Mouse Models |
title_full | Extracting Extra-Telomeric Phenotypes from Telomerase Mouse Models |
title_fullStr | Extracting Extra-Telomeric Phenotypes from Telomerase Mouse Models |
title_full_unstemmed | Extracting Extra-Telomeric Phenotypes from Telomerase Mouse Models |
title_short | Extracting Extra-Telomeric Phenotypes from Telomerase Mouse Models |
title_sort | extracting extra-telomeric phenotypes from telomerase mouse models |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874908/ https://www.ncbi.nlm.nih.gov/pubmed/24339280 http://dx.doi.org/10.3349/ymj.2014.55.1.1 |
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