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Identifying N(6)-methyladenosine sites using multi-interval nucleotide pair position specificity and support vector machine
N6-methyladenosine (m(6)A) refers to methylation of the adenosine nucleotide acid at the nitrogen-6 position. It plays an important role in a series of biological processes, such as splicing events, mRNA exporting, nascent mRNA synthesis, nuclear translocation and translation process. Numerous exper...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404266/ https://www.ncbi.nlm.nih.gov/pubmed/28440291 http://dx.doi.org/10.1038/srep46757 |
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author | Xing, Pengwei Su, Ran Guo, Fei Wei, Leyi |
author_facet | Xing, Pengwei Su, Ran Guo, Fei Wei, Leyi |
author_sort | Xing, Pengwei |
collection | PubMed |
description | N6-methyladenosine (m(6)A) refers to methylation of the adenosine nucleotide acid at the nitrogen-6 position. It plays an important role in a series of biological processes, such as splicing events, mRNA exporting, nascent mRNA synthesis, nuclear translocation and translation process. Numerous experiments have been done to successfully characterize m(6)A sites within sequences since high-resolution mapping of m(6)A sites was established. However, as the explosive growth of genomic sequences, using experimental methods to identify m(6)A sites are time-consuming and expensive. Thus, it is highly desirable to develop fast and accurate computational identification methods. In this study, we propose a sequence-based predictor called RAM-NPPS for identifying m(6)A sites within RNA sequences, in which we present a novel feature representation algorithm based on multi-interval nucleotide pair position specificity, and use support vector machine classifier to construct the prediction model. Comparison results show that our proposed method outperforms the state-of-the-art predictors on three benchmark datasets across the three species, indicating the effectiveness and robustness of our method. Moreover, an online webserver implementing the proposed predictor has been established at http://server.malab.cn/RAM-NPPS/. It is anticipated to be a useful prediction tool to assist biologists to reveal the mechanisms of m(6)A site functions. |
format | Online Article Text |
id | pubmed-5404266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54042662017-04-27 Identifying N(6)-methyladenosine sites using multi-interval nucleotide pair position specificity and support vector machine Xing, Pengwei Su, Ran Guo, Fei Wei, Leyi Sci Rep Article N6-methyladenosine (m(6)A) refers to methylation of the adenosine nucleotide acid at the nitrogen-6 position. It plays an important role in a series of biological processes, such as splicing events, mRNA exporting, nascent mRNA synthesis, nuclear translocation and translation process. Numerous experiments have been done to successfully characterize m(6)A sites within sequences since high-resolution mapping of m(6)A sites was established. However, as the explosive growth of genomic sequences, using experimental methods to identify m(6)A sites are time-consuming and expensive. Thus, it is highly desirable to develop fast and accurate computational identification methods. In this study, we propose a sequence-based predictor called RAM-NPPS for identifying m(6)A sites within RNA sequences, in which we present a novel feature representation algorithm based on multi-interval nucleotide pair position specificity, and use support vector machine classifier to construct the prediction model. Comparison results show that our proposed method outperforms the state-of-the-art predictors on three benchmark datasets across the three species, indicating the effectiveness and robustness of our method. Moreover, an online webserver implementing the proposed predictor has been established at http://server.malab.cn/RAM-NPPS/. It is anticipated to be a useful prediction tool to assist biologists to reveal the mechanisms of m(6)A site functions. Nature Publishing Group 2017-04-25 /pmc/articles/PMC5404266/ /pubmed/28440291 http://dx.doi.org/10.1038/srep46757 Text en Copyright © 2017, The Author(s) 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 Xing, Pengwei Su, Ran Guo, Fei Wei, Leyi Identifying N(6)-methyladenosine sites using multi-interval nucleotide pair position specificity and support vector machine |
title | Identifying N(6)-methyladenosine sites using multi-interval nucleotide pair position specificity and support vector machine |
title_full | Identifying N(6)-methyladenosine sites using multi-interval nucleotide pair position specificity and support vector machine |
title_fullStr | Identifying N(6)-methyladenosine sites using multi-interval nucleotide pair position specificity and support vector machine |
title_full_unstemmed | Identifying N(6)-methyladenosine sites using multi-interval nucleotide pair position specificity and support vector machine |
title_short | Identifying N(6)-methyladenosine sites using multi-interval nucleotide pair position specificity and support vector machine |
title_sort | identifying n(6)-methyladenosine sites using multi-interval nucleotide pair position specificity and support vector machine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404266/ https://www.ncbi.nlm.nih.gov/pubmed/28440291 http://dx.doi.org/10.1038/srep46757 |
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