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Identification and characterization of the microRNA transcriptome of a moth orchid Phalaenopsis aphrodite

Orchids display unique phenotypes, functional characteristics and ecological adaptations that are not found in model plants. In this study, we aimed to characterize the microRNA (miRNA) transcriptome and identify species- and tissue-specific miRNAs in Phalaenopsis aphrodite. After data filtering and...

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Autores principales: Chao, Ya-Ting, Su, Chun-Lin, Jean, Wen-Han, Chen, Wan-Chieh, Chang, Yao-Chien Alex, Shih, Ming-Che
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920020/
https://www.ncbi.nlm.nih.gov/pubmed/24173913
http://dx.doi.org/10.1007/s11103-013-0150-0
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author Chao, Ya-Ting
Su, Chun-Lin
Jean, Wen-Han
Chen, Wan-Chieh
Chang, Yao-Chien Alex
Shih, Ming-Che
author_facet Chao, Ya-Ting
Su, Chun-Lin
Jean, Wen-Han
Chen, Wan-Chieh
Chang, Yao-Chien Alex
Shih, Ming-Che
author_sort Chao, Ya-Ting
collection PubMed
description Orchids display unique phenotypes, functional characteristics and ecological adaptations that are not found in model plants. In this study, we aimed to characterize the microRNA (miRNA) transcriptome and identify species- and tissue-specific miRNAs in Phalaenopsis aphrodite. After data filtering and cleanup, a total of 59,387,374 reads, representing 1,649,996 unique reads, were obtained from four P. aphrodite small RNA libraries. A systematic bioinformatics analysis pipeline was developed that can be used for miRNA and precursor mining, and target gene prediction in non-model plants. A total of 3,251 unique reads for 181 known plant miRNAs (belonging to 88 miRNA families), 23 new miRNAs and 91 precursors were identified. All the miRNA star sequences (miRNA*), the complementary strands of miRNA that from miRNA/miRNA* duplexes, of the predicted new miRNAs were detected in our small RNA libraries, providing additional evidence for their existence as new miRNAs in P. aphrodite. Furthermore, 240 potential miRNA-targets that appear to be involved in many different biological activities and molecular functions, especially transcription factors, were identified, suggesting that miRNAs can impact multiple processes in P. aphrodite. We also verified the cleavage sites for six targets using RNA ligase-mediated rapid amplification of 5′ ends assay. The results provide valuable information about the composition, expression and function of miRNA in P. aphrodite, and will aid functional genomics studies of orchids. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11103-013-0150-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-39200202014-02-14 Identification and characterization of the microRNA transcriptome of a moth orchid Phalaenopsis aphrodite Chao, Ya-Ting Su, Chun-Lin Jean, Wen-Han Chen, Wan-Chieh Chang, Yao-Chien Alex Shih, Ming-Che Plant Mol Biol Article Orchids display unique phenotypes, functional characteristics and ecological adaptations that are not found in model plants. In this study, we aimed to characterize the microRNA (miRNA) transcriptome and identify species- and tissue-specific miRNAs in Phalaenopsis aphrodite. After data filtering and cleanup, a total of 59,387,374 reads, representing 1,649,996 unique reads, were obtained from four P. aphrodite small RNA libraries. A systematic bioinformatics analysis pipeline was developed that can be used for miRNA and precursor mining, and target gene prediction in non-model plants. A total of 3,251 unique reads for 181 known plant miRNAs (belonging to 88 miRNA families), 23 new miRNAs and 91 precursors were identified. All the miRNA star sequences (miRNA*), the complementary strands of miRNA that from miRNA/miRNA* duplexes, of the predicted new miRNAs were detected in our small RNA libraries, providing additional evidence for their existence as new miRNAs in P. aphrodite. Furthermore, 240 potential miRNA-targets that appear to be involved in many different biological activities and molecular functions, especially transcription factors, were identified, suggesting that miRNAs can impact multiple processes in P. aphrodite. We also verified the cleavage sites for six targets using RNA ligase-mediated rapid amplification of 5′ ends assay. The results provide valuable information about the composition, expression and function of miRNA in P. aphrodite, and will aid functional genomics studies of orchids. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11103-013-0150-0) contains supplementary material, which is available to authorized users. Springer Netherlands 2013-10-31 2014 /pmc/articles/PMC3920020/ /pubmed/24173913 http://dx.doi.org/10.1007/s11103-013-0150-0 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Chao, Ya-Ting
Su, Chun-Lin
Jean, Wen-Han
Chen, Wan-Chieh
Chang, Yao-Chien Alex
Shih, Ming-Che
Identification and characterization of the microRNA transcriptome of a moth orchid Phalaenopsis aphrodite
title Identification and characterization of the microRNA transcriptome of a moth orchid Phalaenopsis aphrodite
title_full Identification and characterization of the microRNA transcriptome of a moth orchid Phalaenopsis aphrodite
title_fullStr Identification and characterization of the microRNA transcriptome of a moth orchid Phalaenopsis aphrodite
title_full_unstemmed Identification and characterization of the microRNA transcriptome of a moth orchid Phalaenopsis aphrodite
title_short Identification and characterization of the microRNA transcriptome of a moth orchid Phalaenopsis aphrodite
title_sort identification and characterization of the microrna transcriptome of a moth orchid phalaenopsis aphrodite
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920020/
https://www.ncbi.nlm.nih.gov/pubmed/24173913
http://dx.doi.org/10.1007/s11103-013-0150-0
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