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TelNet - a database for human and yeast genes involved in telomere maintenance

BACKGROUND: The ends of linear chromosomes, the telomeres, comprise repetitive DNA sequences in complex with proteins that protects them from being processed by the DNA repair machinery. Cancer cells need to counteract the shortening of telomere repeats during replication for their unlimited prolife...

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Autores principales: Braun, Delia M., Chung, Inn, Kepper, Nick, Deeg, Katharina I., Rippe, Karsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960154/
https://www.ncbi.nlm.nih.gov/pubmed/29776332
http://dx.doi.org/10.1186/s12863-018-0617-8
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author Braun, Delia M.
Chung, Inn
Kepper, Nick
Deeg, Katharina I.
Rippe, Karsten
author_facet Braun, Delia M.
Chung, Inn
Kepper, Nick
Deeg, Katharina I.
Rippe, Karsten
author_sort Braun, Delia M.
collection PubMed
description BACKGROUND: The ends of linear chromosomes, the telomeres, comprise repetitive DNA sequences in complex with proteins that protects them from being processed by the DNA repair machinery. Cancer cells need to counteract the shortening of telomere repeats during replication for their unlimited proliferation by reactivating the reverse transcriptase telomerase or by using the alternative lengthening of telomeres (ALT) pathway. The different telomere maintenance (TM) mechanisms appear to involve hundreds of proteins but their telomere repeat length related activities are only partly understood. Currently, a database that integrates information on TM relevant genes is missing. DESCRIPTION: To provide a resource for studies that dissect TM features, we here introduce the TelNet database at http://www.cancertelsys.org/telnet/. It offers a comprehensive compilation of more than 2000 human and 1100 yeast genes linked to telomere maintenance. These genes were annotated in terms of TM mechanism, associated specific functions and orthologous genes, a TM significance score and information from peer-reviewed literature. This TM information can be retrieved via different search and view modes and evaluated for a set of genes as demonstrated for an exemplary application. CONCLUSION: TelNet supports the annotation of genes identified from bioinformatics analysis pipelines to reveal possible connections with TM networks. We anticipate that TelNet will be a helpful resource for researchers that study telomeres. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12863-018-0617-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-59601542018-05-24 TelNet - a database for human and yeast genes involved in telomere maintenance Braun, Delia M. Chung, Inn Kepper, Nick Deeg, Katharina I. Rippe, Karsten BMC Genet Database BACKGROUND: The ends of linear chromosomes, the telomeres, comprise repetitive DNA sequences in complex with proteins that protects them from being processed by the DNA repair machinery. Cancer cells need to counteract the shortening of telomere repeats during replication for their unlimited proliferation by reactivating the reverse transcriptase telomerase or by using the alternative lengthening of telomeres (ALT) pathway. The different telomere maintenance (TM) mechanisms appear to involve hundreds of proteins but their telomere repeat length related activities are only partly understood. Currently, a database that integrates information on TM relevant genes is missing. DESCRIPTION: To provide a resource for studies that dissect TM features, we here introduce the TelNet database at http://www.cancertelsys.org/telnet/. It offers a comprehensive compilation of more than 2000 human and 1100 yeast genes linked to telomere maintenance. These genes were annotated in terms of TM mechanism, associated specific functions and orthologous genes, a TM significance score and information from peer-reviewed literature. This TM information can be retrieved via different search and view modes and evaluated for a set of genes as demonstrated for an exemplary application. CONCLUSION: TelNet supports the annotation of genes identified from bioinformatics analysis pipelines to reveal possible connections with TM networks. We anticipate that TelNet will be a helpful resource for researchers that study telomeres. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12863-018-0617-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-18 /pmc/articles/PMC5960154/ /pubmed/29776332 http://dx.doi.org/10.1186/s12863-018-0617-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Database
Braun, Delia M.
Chung, Inn
Kepper, Nick
Deeg, Katharina I.
Rippe, Karsten
TelNet - a database for human and yeast genes involved in telomere maintenance
title TelNet - a database for human and yeast genes involved in telomere maintenance
title_full TelNet - a database for human and yeast genes involved in telomere maintenance
title_fullStr TelNet - a database for human and yeast genes involved in telomere maintenance
title_full_unstemmed TelNet - a database for human and yeast genes involved in telomere maintenance
title_short TelNet - a database for human and yeast genes involved in telomere maintenance
title_sort telnet - a database for human and yeast genes involved in telomere maintenance
topic Database
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960154/
https://www.ncbi.nlm.nih.gov/pubmed/29776332
http://dx.doi.org/10.1186/s12863-018-0617-8
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