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Insilico profiling of microRNAs in Korean ginseng (Panax ginseng Meyer)

MicroRNAs (miRNAs) are a class of recently discovered non-coding small RNA molecules, on average approximately 21 nucleotides in length, which underlie numerous important biological roles in gene regulation in various organisms. The miRNA database (release 18) has 18,226 miRNAs, which have been depo...

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Autores principales: Mathiyalagan, Ramya, Subramaniyam, Sathiyamoorthy, Natarajan, Sathishkumar, Kim, Yeon Ju, Sun, Myung Suk, Kim, Se Young, Kim, Yu-Jin, Yang, Deok Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Ginseng 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659641/
https://www.ncbi.nlm.nih.gov/pubmed/23717176
http://dx.doi.org/10.5142/jgr.2013.37.227
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author Mathiyalagan, Ramya
Subramaniyam, Sathiyamoorthy
Natarajan, Sathishkumar
Kim, Yeon Ju
Sun, Myung Suk
Kim, Se Young
Kim, Yu-Jin
Yang, Deok Chun
author_facet Mathiyalagan, Ramya
Subramaniyam, Sathiyamoorthy
Natarajan, Sathishkumar
Kim, Yeon Ju
Sun, Myung Suk
Kim, Se Young
Kim, Yu-Jin
Yang, Deok Chun
author_sort Mathiyalagan, Ramya
collection PubMed
description MicroRNAs (miRNAs) are a class of recently discovered non-coding small RNA molecules, on average approximately 21 nucleotides in length, which underlie numerous important biological roles in gene regulation in various organisms. The miRNA database (release 18) has 18,226 miRNAs, which have been deposited from different species. Although miRNAs have been identified and validated in many plant species, no studies have been reported on discovering miRNAs in Panax ginseng Meyer, which is a traditionally known medicinal plant in oriental medicine, also known as Korean ginseng. It has triterpene ginseng saponins called ginsenosides, which are responsible for its various pharmacological activities. Predicting conserved miRNAs by homology-based analysis with available expressed sequence tag (EST) sequences can be powerful, if the species lacks whole genome sequence information. In this study by using the EST based computational approach, 69 conserved miRNAs belonging to 44 miRNA families were identified in Korean ginseng. The digital gene expression patterns of predicted conserved miRNAs were analyzed by deep sequencing using small RNA sequences of flower buds, leaves, and lateral roots. We have found that many of the identified miRNAs showed tissue specific expressions. Using the insilico method, 346 potential targets were identified for the predicted 69 conserved miRNAs by searching the ginseng EST database, and the predicted targets were mainly involved in secondary metabolic processes, responses to biotic and abiotic stress, and transcription regulator activities, as well as a variety of other metabolic processes.
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spelling pubmed-36596412013-05-28 Insilico profiling of microRNAs in Korean ginseng (Panax ginseng Meyer) Mathiyalagan, Ramya Subramaniyam, Sathiyamoorthy Natarajan, Sathishkumar Kim, Yeon Ju Sun, Myung Suk Kim, Se Young Kim, Yu-Jin Yang, Deok Chun J Ginseng Res Articles MicroRNAs (miRNAs) are a class of recently discovered non-coding small RNA molecules, on average approximately 21 nucleotides in length, which underlie numerous important biological roles in gene regulation in various organisms. The miRNA database (release 18) has 18,226 miRNAs, which have been deposited from different species. Although miRNAs have been identified and validated in many plant species, no studies have been reported on discovering miRNAs in Panax ginseng Meyer, which is a traditionally known medicinal plant in oriental medicine, also known as Korean ginseng. It has triterpene ginseng saponins called ginsenosides, which are responsible for its various pharmacological activities. Predicting conserved miRNAs by homology-based analysis with available expressed sequence tag (EST) sequences can be powerful, if the species lacks whole genome sequence information. In this study by using the EST based computational approach, 69 conserved miRNAs belonging to 44 miRNA families were identified in Korean ginseng. The digital gene expression patterns of predicted conserved miRNAs were analyzed by deep sequencing using small RNA sequences of flower buds, leaves, and lateral roots. We have found that many of the identified miRNAs showed tissue specific expressions. Using the insilico method, 346 potential targets were identified for the predicted 69 conserved miRNAs by searching the ginseng EST database, and the predicted targets were mainly involved in secondary metabolic processes, responses to biotic and abiotic stress, and transcription regulator activities, as well as a variety of other metabolic processes. The Korean Society of Ginseng 2013-04 /pmc/articles/PMC3659641/ /pubmed/23717176 http://dx.doi.org/10.5142/jgr.2013.37.227 Text en Copyright ©2013, The Korean Society of Ginseng http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Mathiyalagan, Ramya
Subramaniyam, Sathiyamoorthy
Natarajan, Sathishkumar
Kim, Yeon Ju
Sun, Myung Suk
Kim, Se Young
Kim, Yu-Jin
Yang, Deok Chun
Insilico profiling of microRNAs in Korean ginseng (Panax ginseng Meyer)
title Insilico profiling of microRNAs in Korean ginseng (Panax ginseng Meyer)
title_full Insilico profiling of microRNAs in Korean ginseng (Panax ginseng Meyer)
title_fullStr Insilico profiling of microRNAs in Korean ginseng (Panax ginseng Meyer)
title_full_unstemmed Insilico profiling of microRNAs in Korean ginseng (Panax ginseng Meyer)
title_short Insilico profiling of microRNAs in Korean ginseng (Panax ginseng Meyer)
title_sort insilico profiling of micrornas in korean ginseng (panax ginseng meyer)
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659641/
https://www.ncbi.nlm.nih.gov/pubmed/23717176
http://dx.doi.org/10.5142/jgr.2013.37.227
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