Cargando…

Verification of miRNAs in ginseng decoction by high-throughput sequencing and quantitative real-time PCR

Panax ginseng C. A. Meyer is a precious traditional Chinese medicine that has been clinically used for over thousands of years. In general, ginseng needs to be prepared to ginseng decoction before taking it. MicroRNAs are a class of small (18–24 nt), single-stranded molecules that regulate gene expr...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Yingfang, Peng, Mengyuan, Wang, Wenjuan, Chen, Yanlin, He, Zhihua, Cao, Jingjing, Lin, Zhiyun, Yang, Zemin, Gong, Mengjuan, Yin, Yongqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446053/
https://www.ncbi.nlm.nih.gov/pubmed/30984884
http://dx.doi.org/10.1016/j.heliyon.2019.e01418
_version_ 1783408289027981312
author Wang, Yingfang
Peng, Mengyuan
Wang, Wenjuan
Chen, Yanlin
He, Zhihua
Cao, Jingjing
Lin, Zhiyun
Yang, Zemin
Gong, Mengjuan
Yin, Yongqin
author_facet Wang, Yingfang
Peng, Mengyuan
Wang, Wenjuan
Chen, Yanlin
He, Zhihua
Cao, Jingjing
Lin, Zhiyun
Yang, Zemin
Gong, Mengjuan
Yin, Yongqin
author_sort Wang, Yingfang
collection PubMed
description Panax ginseng C. A. Meyer is a precious traditional Chinese medicine that has been clinically used for over thousands of years. In general, ginseng needs to be prepared to ginseng decoction before taking it. MicroRNAs are a class of small (18–24 nt), single-stranded molecules that regulate gene expression at the post-transcriptional level. Considering that ginseng miRNAs may be bioactive compounds, we used Illumina high-throughput sequencing and quantitative real-time PCR (qRT-PCR) to validate the existence of miRNAs in fresh ginseng decoction which have been boiled at high temperature. Our previous studies have demonstrated that there are several miRNAs in fresh ginseng. The roots of fresh Panax ginseng were prepared according to routine methods, from which miRNAs were extracted and sequenced. A total of 43 miRNAs were identified from water decoction by Illumina high-throughput sequencing, belonging to 71 miRNA families. The target genes of these miRNAs were predicted by sequencing, and were annotated by GO, KEGG and Nr databases. The functions of these target genes mainly included plant hormone signal transduction, transcription regulation, macromolecular metabolism and auxin signaling. Nine highly expressed miRNAs (miR159, miR167, miR396, miR166, miR168, miR156, miR165, miR162 and miR394) were verified by qRT-PCR, and the results of Illumina high-throughput sequencing and qRT-PCR were consistent. Results from this study indicate that miRNAs remained stable in P. ginseng after high-temperature boiling. Additionally, Illumina high-throughput sequencing was superior in the acquisition of higher amount of small RNAs.
format Online
Article
Text
id pubmed-6446053
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-64460532019-04-12 Verification of miRNAs in ginseng decoction by high-throughput sequencing and quantitative real-time PCR Wang, Yingfang Peng, Mengyuan Wang, Wenjuan Chen, Yanlin He, Zhihua Cao, Jingjing Lin, Zhiyun Yang, Zemin Gong, Mengjuan Yin, Yongqin Heliyon Article Panax ginseng C. A. Meyer is a precious traditional Chinese medicine that has been clinically used for over thousands of years. In general, ginseng needs to be prepared to ginseng decoction before taking it. MicroRNAs are a class of small (18–24 nt), single-stranded molecules that regulate gene expression at the post-transcriptional level. Considering that ginseng miRNAs may be bioactive compounds, we used Illumina high-throughput sequencing and quantitative real-time PCR (qRT-PCR) to validate the existence of miRNAs in fresh ginseng decoction which have been boiled at high temperature. Our previous studies have demonstrated that there are several miRNAs in fresh ginseng. The roots of fresh Panax ginseng were prepared according to routine methods, from which miRNAs were extracted and sequenced. A total of 43 miRNAs were identified from water decoction by Illumina high-throughput sequencing, belonging to 71 miRNA families. The target genes of these miRNAs were predicted by sequencing, and were annotated by GO, KEGG and Nr databases. The functions of these target genes mainly included plant hormone signal transduction, transcription regulation, macromolecular metabolism and auxin signaling. Nine highly expressed miRNAs (miR159, miR167, miR396, miR166, miR168, miR156, miR165, miR162 and miR394) were verified by qRT-PCR, and the results of Illumina high-throughput sequencing and qRT-PCR were consistent. Results from this study indicate that miRNAs remained stable in P. ginseng after high-temperature boiling. Additionally, Illumina high-throughput sequencing was superior in the acquisition of higher amount of small RNAs. Elsevier 2019-04-02 /pmc/articles/PMC6446053/ /pubmed/30984884 http://dx.doi.org/10.1016/j.heliyon.2019.e01418 Text en © 2019 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Wang, Yingfang
Peng, Mengyuan
Wang, Wenjuan
Chen, Yanlin
He, Zhihua
Cao, Jingjing
Lin, Zhiyun
Yang, Zemin
Gong, Mengjuan
Yin, Yongqin
Verification of miRNAs in ginseng decoction by high-throughput sequencing and quantitative real-time PCR
title Verification of miRNAs in ginseng decoction by high-throughput sequencing and quantitative real-time PCR
title_full Verification of miRNAs in ginseng decoction by high-throughput sequencing and quantitative real-time PCR
title_fullStr Verification of miRNAs in ginseng decoction by high-throughput sequencing and quantitative real-time PCR
title_full_unstemmed Verification of miRNAs in ginseng decoction by high-throughput sequencing and quantitative real-time PCR
title_short Verification of miRNAs in ginseng decoction by high-throughput sequencing and quantitative real-time PCR
title_sort verification of mirnas in ginseng decoction by high-throughput sequencing and quantitative real-time pcr
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446053/
https://www.ncbi.nlm.nih.gov/pubmed/30984884
http://dx.doi.org/10.1016/j.heliyon.2019.e01418
work_keys_str_mv AT wangyingfang verificationofmirnasinginsengdecoctionbyhighthroughputsequencingandquantitativerealtimepcr
AT pengmengyuan verificationofmirnasinginsengdecoctionbyhighthroughputsequencingandquantitativerealtimepcr
AT wangwenjuan verificationofmirnasinginsengdecoctionbyhighthroughputsequencingandquantitativerealtimepcr
AT chenyanlin verificationofmirnasinginsengdecoctionbyhighthroughputsequencingandquantitativerealtimepcr
AT hezhihua verificationofmirnasinginsengdecoctionbyhighthroughputsequencingandquantitativerealtimepcr
AT caojingjing verificationofmirnasinginsengdecoctionbyhighthroughputsequencingandquantitativerealtimepcr
AT linzhiyun verificationofmirnasinginsengdecoctionbyhighthroughputsequencingandquantitativerealtimepcr
AT yangzemin verificationofmirnasinginsengdecoctionbyhighthroughputsequencingandquantitativerealtimepcr
AT gongmengjuan verificationofmirnasinginsengdecoctionbyhighthroughputsequencingandquantitativerealtimepcr
AT yinyongqin verificationofmirnasinginsengdecoctionbyhighthroughputsequencingandquantitativerealtimepcr