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Diverse mechanisms for spliceosome-mediated 3′ end processing of telomerase RNA
The 3′ end of Schizosaccharomyces pombe telomerase RNA (SpTER1) is generated by spliceosomal cleavage, a reaction that corresponds to the first step of splicing. The observation that the spliceosome functions in 3′ end processing raised questions about the evolutionary origin and conservation of thi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299874/ https://www.ncbi.nlm.nih.gov/pubmed/25598145 http://dx.doi.org/10.1038/ncomms7104 |
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author | Kannan, Ram Helston, Rachel M. Dannebaum, Richard O. Baumann, Peter |
author_facet | Kannan, Ram Helston, Rachel M. Dannebaum, Richard O. Baumann, Peter |
author_sort | Kannan, Ram |
collection | PubMed |
description | The 3′ end of Schizosaccharomyces pombe telomerase RNA (SpTER1) is generated by spliceosomal cleavage, a reaction that corresponds to the first step of splicing. The observation that the spliceosome functions in 3′ end processing raised questions about the evolutionary origin and conservation of this mechanism. We now present data in support of spliceosomes generating 3′ ends of telomerase RNAs in other fungi. Strikingly, the mechanistic basis for restricting spliceosomal splicing to the first transesterification reaction differs substantially among species. Unlike S. pombe, two other fission yeasts rely on hyperstabilization of the U6 snRNA—5′ splice site interaction to impede the 2nd step of splicing. In contrast, a non-canonical 5′ splice site blocks the second transesterification reaction in Aspergillus species. These results demonstrate a conserved role for spliceosomes functioning in 3′ end processing. Divergent mechanisms of uncoupling the two steps of splicing argue for multiple origins of this pathway. |
format | Online Article Text |
id | pubmed-4299874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42998742015-02-09 Diverse mechanisms for spliceosome-mediated 3′ end processing of telomerase RNA Kannan, Ram Helston, Rachel M. Dannebaum, Richard O. Baumann, Peter Nat Commun Article The 3′ end of Schizosaccharomyces pombe telomerase RNA (SpTER1) is generated by spliceosomal cleavage, a reaction that corresponds to the first step of splicing. The observation that the spliceosome functions in 3′ end processing raised questions about the evolutionary origin and conservation of this mechanism. We now present data in support of spliceosomes generating 3′ ends of telomerase RNAs in other fungi. Strikingly, the mechanistic basis for restricting spliceosomal splicing to the first transesterification reaction differs substantially among species. Unlike S. pombe, two other fission yeasts rely on hyperstabilization of the U6 snRNA—5′ splice site interaction to impede the 2nd step of splicing. In contrast, a non-canonical 5′ splice site blocks the second transesterification reaction in Aspergillus species. These results demonstrate a conserved role for spliceosomes functioning in 3′ end processing. Divergent mechanisms of uncoupling the two steps of splicing argue for multiple origins of this pathway. Nature Pub. Group 2015-01-19 /pmc/articles/PMC4299874/ /pubmed/25598145 http://dx.doi.org/10.1038/ncomms7104 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kannan, Ram Helston, Rachel M. Dannebaum, Richard O. Baumann, Peter Diverse mechanisms for spliceosome-mediated 3′ end processing of telomerase RNA |
title | Diverse mechanisms for spliceosome-mediated 3′ end processing of telomerase RNA |
title_full | Diverse mechanisms for spliceosome-mediated 3′ end processing of telomerase RNA |
title_fullStr | Diverse mechanisms for spliceosome-mediated 3′ end processing of telomerase RNA |
title_full_unstemmed | Diverse mechanisms for spliceosome-mediated 3′ end processing of telomerase RNA |
title_short | Diverse mechanisms for spliceosome-mediated 3′ end processing of telomerase RNA |
title_sort | diverse mechanisms for spliceosome-mediated 3′ end processing of telomerase rna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299874/ https://www.ncbi.nlm.nih.gov/pubmed/25598145 http://dx.doi.org/10.1038/ncomms7104 |
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