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Insights into Cdc13 dependent telomere length regulation

Cdc13 is a single stranded telomere binding protein that specifically localizes to the telomere ends of budding yeasts and is essential for cell viability. It caps the ends of chromosomes thus preventing chromosome end-to-end fusions and exonucleolytic degradation, events that could lead to genomic...

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Autores principales: Mason, Mark, Skordalakes, Emmanuel
Formato: Texto
Lenguaje:English
Publicado: Impact Journals LLC 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993802/
https://www.ncbi.nlm.nih.gov/pubmed/20975208
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author Mason, Mark
Skordalakes, Emmanuel
author_facet Mason, Mark
Skordalakes, Emmanuel
author_sort Mason, Mark
collection PubMed
description Cdc13 is a single stranded telomere binding protein that specifically localizes to the telomere ends of budding yeasts and is essential for cell viability. It caps the ends of chromosomes thus preventing chromosome end-to-end fusions and exonucleolytic degradation, events that could lead to genomic instability and senescence, the hallmark of aging. Cdc13 is also involved in telomere length regulation by recruiting or preventing access of telomerase to the telomeric overhang. Recruitment of telomerase to the telomeres for G-strand extension is required for continuous cell division, while preventing its access to the telomeres through capping the chromosome ends prevents mitotic events that could lead to cell immortality, the hall mark of carcinogenesis. Cdc13 and its putative homologues human CTC1 and POT1 are therefore key to many biological processes directly associated with life extension and cancer prevention and can be viewed as an ideal target for cancer and age related therapies.
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spelling pubmed-29938022010-11-30 Insights into Cdc13 dependent telomere length regulation Mason, Mark Skordalakes, Emmanuel Aging (Albany NY) Research Perspective Cdc13 is a single stranded telomere binding protein that specifically localizes to the telomere ends of budding yeasts and is essential for cell viability. It caps the ends of chromosomes thus preventing chromosome end-to-end fusions and exonucleolytic degradation, events that could lead to genomic instability and senescence, the hallmark of aging. Cdc13 is also involved in telomere length regulation by recruiting or preventing access of telomerase to the telomeric overhang. Recruitment of telomerase to the telomeres for G-strand extension is required for continuous cell division, while preventing its access to the telomeres through capping the chromosome ends prevents mitotic events that could lead to cell immortality, the hall mark of carcinogenesis. Cdc13 and its putative homologues human CTC1 and POT1 are therefore key to many biological processes directly associated with life extension and cancer prevention and can be viewed as an ideal target for cancer and age related therapies. Impact Journals LLC 2010-10-23 /pmc/articles/PMC2993802/ /pubmed/20975208 Text en Copyright: © 2010 Mason and Skordalakes http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Research Perspective
Mason, Mark
Skordalakes, Emmanuel
Insights into Cdc13 dependent telomere length regulation
title Insights into Cdc13 dependent telomere length regulation
title_full Insights into Cdc13 dependent telomere length regulation
title_fullStr Insights into Cdc13 dependent telomere length regulation
title_full_unstemmed Insights into Cdc13 dependent telomere length regulation
title_short Insights into Cdc13 dependent telomere length regulation
title_sort insights into cdc13 dependent telomere length regulation
topic Research Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993802/
https://www.ncbi.nlm.nih.gov/pubmed/20975208
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