Cargando…
A k-mer scheme to predict piRNAs and characterize locust piRNAs
Motivation: Identifying piwi-interacting RNAs (piRNAs) of non-model organisms is a difficult and unsolved problem because piRNAs lack conservative secondary structure motifs and sequence homology in different species. Results: In this article, a k-mer scheme is proposed to identify piRNA sequences,...
Autores principales: | , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051322/ https://www.ncbi.nlm.nih.gov/pubmed/21224287 http://dx.doi.org/10.1093/bioinformatics/btr016 |
_version_ | 1782199470410170368 |
---|---|
author | Zhang, Yi Wang, Xianhui Kang, Le |
author_facet | Zhang, Yi Wang, Xianhui Kang, Le |
author_sort | Zhang, Yi |
collection | PubMed |
description | Motivation: Identifying piwi-interacting RNAs (piRNAs) of non-model organisms is a difficult and unsolved problem because piRNAs lack conservative secondary structure motifs and sequence homology in different species. Results: In this article, a k-mer scheme is proposed to identify piRNA sequences, relying on the training sets from non-piRNA and piRNA sequences of five model species sequenced: rat, mouse, human, fruit fly and nematode. Compared with the existing ‘static’ scheme based on the position-specific base usage, our novel ‘dynamic’ algorithm performs much better with a precision of over 90% and a sensitivity of over 60%, and the precision is verified by 5-fold cross-validation in these species. To test its validity, we use the algorithm to identify piRNAs of the migratory locust based on 603 607 deep-sequenced small RNA sequences. Totally, 87 536 piRNAs of the locust are predicted, and 4426 of them matched with existing locust transposons. The transcriptional difference between solitary and gregarious locusts was described. We also revisit the position-specific base usage of piRNAs and find the conservation in the end of piRNAs. Therefore, the method we developed can be used to identify piRNAs of non-model organisms without complete genome sequences. Availability: The web server for implementing the algorithm and the software code are freely available to the academic community at http://59.79.168.90/piRNA/index.php. Contact: lkang@ioz.ac.cn Supplementary information: Supplementary data are available at Bioinformatics online. |
format | Text |
id | pubmed-3051322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30513222011-03-10 A k-mer scheme to predict piRNAs and characterize locust piRNAs Zhang, Yi Wang, Xianhui Kang, Le Bioinformatics Original Papers Motivation: Identifying piwi-interacting RNAs (piRNAs) of non-model organisms is a difficult and unsolved problem because piRNAs lack conservative secondary structure motifs and sequence homology in different species. Results: In this article, a k-mer scheme is proposed to identify piRNA sequences, relying on the training sets from non-piRNA and piRNA sequences of five model species sequenced: rat, mouse, human, fruit fly and nematode. Compared with the existing ‘static’ scheme based on the position-specific base usage, our novel ‘dynamic’ algorithm performs much better with a precision of over 90% and a sensitivity of over 60%, and the precision is verified by 5-fold cross-validation in these species. To test its validity, we use the algorithm to identify piRNAs of the migratory locust based on 603 607 deep-sequenced small RNA sequences. Totally, 87 536 piRNAs of the locust are predicted, and 4426 of them matched with existing locust transposons. The transcriptional difference between solitary and gregarious locusts was described. We also revisit the position-specific base usage of piRNAs and find the conservation in the end of piRNAs. Therefore, the method we developed can be used to identify piRNAs of non-model organisms without complete genome sequences. Availability: The web server for implementing the algorithm and the software code are freely available to the academic community at http://59.79.168.90/piRNA/index.php. Contact: lkang@ioz.ac.cn Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2011-03-15 2011-01-11 /pmc/articles/PMC3051322/ /pubmed/21224287 http://dx.doi.org/10.1093/bioinformatics/btr016 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Zhang, Yi Wang, Xianhui Kang, Le A k-mer scheme to predict piRNAs and characterize locust piRNAs |
title | A k-mer scheme to predict piRNAs and characterize locust piRNAs |
title_full | A k-mer scheme to predict piRNAs and characterize locust piRNAs |
title_fullStr | A k-mer scheme to predict piRNAs and characterize locust piRNAs |
title_full_unstemmed | A k-mer scheme to predict piRNAs and characterize locust piRNAs |
title_short | A k-mer scheme to predict piRNAs and characterize locust piRNAs |
title_sort | k-mer scheme to predict pirnas and characterize locust pirnas |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051322/ https://www.ncbi.nlm.nih.gov/pubmed/21224287 http://dx.doi.org/10.1093/bioinformatics/btr016 |
work_keys_str_mv | AT zhangyi akmerschemetopredictpirnasandcharacterizelocustpirnas AT wangxianhui akmerschemetopredictpirnasandcharacterizelocustpirnas AT kangle akmerschemetopredictpirnasandcharacterizelocustpirnas AT zhangyi kmerschemetopredictpirnasandcharacterizelocustpirnas AT wangxianhui kmerschemetopredictpirnasandcharacterizelocustpirnas AT kangle kmerschemetopredictpirnasandcharacterizelocustpirnas |