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Conservation of Nonsense-Mediated mRNA Decay Complex Components Throughout Eukaryotic Evolution
Nonsense-mediated mRNA decay (NMD) is an essential eukaryotic process regulating transcript quality and abundance, and is involved in diverse processes including brain development and plant defenses. Although some of the NMD machinery is conserved between kingdoms, little is known about its evolutio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709506/ https://www.ncbi.nlm.nih.gov/pubmed/29192227 http://dx.doi.org/10.1038/s41598-017-16942-w |
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author | Causier, Barry Li, Zhen De Smet, Riet Lloyd, James P. B. Van de Peer, Yves Davies, Brendan |
author_facet | Causier, Barry Li, Zhen De Smet, Riet Lloyd, James P. B. Van de Peer, Yves Davies, Brendan |
author_sort | Causier, Barry |
collection | PubMed |
description | Nonsense-mediated mRNA decay (NMD) is an essential eukaryotic process regulating transcript quality and abundance, and is involved in diverse processes including brain development and plant defenses. Although some of the NMD machinery is conserved between kingdoms, little is known about its evolution. Phosphorylation of the core NMD component UPF1 is critical for NMD and is regulated in mammals by the SURF complex (UPF1, SMG1 kinase, SMG8, SMG9 and eukaryotic release factors). However, since SMG1 is reportedly missing from the genomes of fungi and the plant Arabidopsis thaliana, it remains unclear how UPF1 is activated outside the metazoa. We used comparative genomics to determine the conservation of the NMD pathway across eukaryotic evolution. We show that SURF components are present in all major eukaryotic lineages, including fungi, suggesting that in addition to UPF1 and SMG1, SMG8 and SMG9 also existed in the last eukaryotic common ancestor, 1.8 billion years ago. However, despite the ancient origins of the SURF complex, we also found that SURF factors have been independently lost across the Eukarya, pointing to genetic buffering within the essential NMD pathway. We infer an ancient role for SURF in regulating UPF1, and the intriguing possibility of undiscovered NMD regulatory pathways. |
format | Online Article Text |
id | pubmed-5709506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57095062017-12-06 Conservation of Nonsense-Mediated mRNA Decay Complex Components Throughout Eukaryotic Evolution Causier, Barry Li, Zhen De Smet, Riet Lloyd, James P. B. Van de Peer, Yves Davies, Brendan Sci Rep Article Nonsense-mediated mRNA decay (NMD) is an essential eukaryotic process regulating transcript quality and abundance, and is involved in diverse processes including brain development and plant defenses. Although some of the NMD machinery is conserved between kingdoms, little is known about its evolution. Phosphorylation of the core NMD component UPF1 is critical for NMD and is regulated in mammals by the SURF complex (UPF1, SMG1 kinase, SMG8, SMG9 and eukaryotic release factors). However, since SMG1 is reportedly missing from the genomes of fungi and the plant Arabidopsis thaliana, it remains unclear how UPF1 is activated outside the metazoa. We used comparative genomics to determine the conservation of the NMD pathway across eukaryotic evolution. We show that SURF components are present in all major eukaryotic lineages, including fungi, suggesting that in addition to UPF1 and SMG1, SMG8 and SMG9 also existed in the last eukaryotic common ancestor, 1.8 billion years ago. However, despite the ancient origins of the SURF complex, we also found that SURF factors have been independently lost across the Eukarya, pointing to genetic buffering within the essential NMD pathway. We infer an ancient role for SURF in regulating UPF1, and the intriguing possibility of undiscovered NMD regulatory pathways. Nature Publishing Group UK 2017-11-30 /pmc/articles/PMC5709506/ /pubmed/29192227 http://dx.doi.org/10.1038/s41598-017-16942-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Causier, Barry Li, Zhen De Smet, Riet Lloyd, James P. B. Van de Peer, Yves Davies, Brendan Conservation of Nonsense-Mediated mRNA Decay Complex Components Throughout Eukaryotic Evolution |
title | Conservation of Nonsense-Mediated mRNA Decay Complex Components Throughout Eukaryotic Evolution |
title_full | Conservation of Nonsense-Mediated mRNA Decay Complex Components Throughout Eukaryotic Evolution |
title_fullStr | Conservation of Nonsense-Mediated mRNA Decay Complex Components Throughout Eukaryotic Evolution |
title_full_unstemmed | Conservation of Nonsense-Mediated mRNA Decay Complex Components Throughout Eukaryotic Evolution |
title_short | Conservation of Nonsense-Mediated mRNA Decay Complex Components Throughout Eukaryotic Evolution |
title_sort | conservation of nonsense-mediated mrna decay complex components throughout eukaryotic evolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709506/ https://www.ncbi.nlm.nih.gov/pubmed/29192227 http://dx.doi.org/10.1038/s41598-017-16942-w |
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