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The telomerase reverse transcriptase elongates reversed replication forks at telomeric repeats
The telomerase reverse transcriptase elongates telomeres to prevent replicative senescence. This process requires exposure of the 3′-end, which is thought to occur when two sister telomeres are generated at replication completion. Using two-dimensional agarose gel electrophoresis (2D-gels) and elect...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032592/ https://www.ncbi.nlm.nih.gov/pubmed/36947627 http://dx.doi.org/10.1126/sciadv.adf2011 |
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author | Huda, Armela Arakawa, Hiroshi Mazzucco, Giulia Galli, Martina Petrocelli, Valentina Casola, Stefano Chen, Lu Doksani, Ylli |
author_facet | Huda, Armela Arakawa, Hiroshi Mazzucco, Giulia Galli, Martina Petrocelli, Valentina Casola, Stefano Chen, Lu Doksani, Ylli |
author_sort | Huda, Armela |
collection | PubMed |
description | The telomerase reverse transcriptase elongates telomeres to prevent replicative senescence. This process requires exposure of the 3′-end, which is thought to occur when two sister telomeres are generated at replication completion. Using two-dimensional agarose gel electrophoresis (2D-gels) and electron microscopy, we found that telomeric repeats are hotspots for replication fork reversal. Fork reversal generates 3′ telomeric ends before replication completion. To verify whether these ends are elongated by telomerase, we probed de novo telomeric synthesis in situ and at replication intermediates by reconstituting mutant telomerase that adds a variant telomere sequence. We found variant telomeric repeats overlapping with telomeric reversed forks in 2D-gels, but not with normal forks, nontelomeric reversed forks, or telomeric reversed forks with a C-rich 3′-end. Our results define reversed telomeric forks as a substrate of telomerase during replication. |
format | Online Article Text |
id | pubmed-10032592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-100325922023-03-23 The telomerase reverse transcriptase elongates reversed replication forks at telomeric repeats Huda, Armela Arakawa, Hiroshi Mazzucco, Giulia Galli, Martina Petrocelli, Valentina Casola, Stefano Chen, Lu Doksani, Ylli Sci Adv Biomedicine and Life Sciences The telomerase reverse transcriptase elongates telomeres to prevent replicative senescence. This process requires exposure of the 3′-end, which is thought to occur when two sister telomeres are generated at replication completion. Using two-dimensional agarose gel electrophoresis (2D-gels) and electron microscopy, we found that telomeric repeats are hotspots for replication fork reversal. Fork reversal generates 3′ telomeric ends before replication completion. To verify whether these ends are elongated by telomerase, we probed de novo telomeric synthesis in situ and at replication intermediates by reconstituting mutant telomerase that adds a variant telomere sequence. We found variant telomeric repeats overlapping with telomeric reversed forks in 2D-gels, but not with normal forks, nontelomeric reversed forks, or telomeric reversed forks with a C-rich 3′-end. Our results define reversed telomeric forks as a substrate of telomerase during replication. American Association for the Advancement of Science 2023-03-22 /pmc/articles/PMC10032592/ /pubmed/36947627 http://dx.doi.org/10.1126/sciadv.adf2011 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Huda, Armela Arakawa, Hiroshi Mazzucco, Giulia Galli, Martina Petrocelli, Valentina Casola, Stefano Chen, Lu Doksani, Ylli The telomerase reverse transcriptase elongates reversed replication forks at telomeric repeats |
title | The telomerase reverse transcriptase elongates reversed replication forks at telomeric repeats |
title_full | The telomerase reverse transcriptase elongates reversed replication forks at telomeric repeats |
title_fullStr | The telomerase reverse transcriptase elongates reversed replication forks at telomeric repeats |
title_full_unstemmed | The telomerase reverse transcriptase elongates reversed replication forks at telomeric repeats |
title_short | The telomerase reverse transcriptase elongates reversed replication forks at telomeric repeats |
title_sort | telomerase reverse transcriptase elongates reversed replication forks at telomeric repeats |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032592/ https://www.ncbi.nlm.nih.gov/pubmed/36947627 http://dx.doi.org/10.1126/sciadv.adf2011 |
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