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The long non-coding RNA expression profile of Coxsackievirus A16 infected RD cells identified by RNA-seq

Coxsackievirus A16 (CVA16) is one of major pathogens of hand, foot and mouth disease (HFMD) in children. Long non-coding RNAs (IncRNAs) have been implicated in various biological processes, but they have not been associated with CVA16 infection. In this study, we comprehensively characterized the la...

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Autores principales: Shi, Yingying, Tu, Huilin, Chen, Xiong, Zhang, Yingying, Chen, Liujun, Liu, Zhongchun, Sheng, Jiqun, Han, Song, Yin, Jun, Peng, Biwen, He, Xiaohua, Liu, Wanhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090472/
https://www.ncbi.nlm.nih.gov/pubmed/27060091
http://dx.doi.org/10.1007/s12250-015-3693-1
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author Shi, Yingying
Tu, Huilin
Chen, Xiong
Zhang, Yingying
Chen, Liujun
Liu, Zhongchun
Sheng, Jiqun
Han, Song
Yin, Jun
Peng, Biwen
He, Xiaohua
Liu, Wanhong
author_facet Shi, Yingying
Tu, Huilin
Chen, Xiong
Zhang, Yingying
Chen, Liujun
Liu, Zhongchun
Sheng, Jiqun
Han, Song
Yin, Jun
Peng, Biwen
He, Xiaohua
Liu, Wanhong
author_sort Shi, Yingying
collection PubMed
description Coxsackievirus A16 (CVA16) is one of major pathogens of hand, foot and mouth disease (HFMD) in children. Long non-coding RNAs (IncRNAs) have been implicated in various biological processes, but they have not been associated with CVA16 infection. In this study, we comprehensively characterized the landscape of IncRNAs of normal and CVA16 infected rhabdomyosarcoma (RD) cells using RNA-Seq to investigate the functional relevance of IncRNAs. We showed that a total of 760 IncRNAs were upregulated and 1210 IncRNAs were downregulated. Out of these dysregulated IncRNAs, 43.64% were intergenic, 22.31% were sense, 15.89% were intronic, 8.67% were bidirectional, 5.59% were antisense, 3.85% were sRNA host IncRNAs and 0.05% were enhancer. Six dysregulated IncRNAs were validated by quantitative PCR assays and the secondary structures of these IncRNAs were projected. Moreover, we conducted a bioinformatics analysis of an IncRNAs (ENST00000602478) to elucidate the diversity of modification and functions of IncRNAs. In summary, the current study compared the dysregulated IncRNAs profile upon CVA16 challenge and illustrated the intricate relationship between coding and IncRNAs transcripts. These results may not only provide a complete picture of transcription in CVA16 infected cells but also provide novel molecular targets for treatments of HFMD. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s12250-015-3693-1 and is accessible for authorized users.
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spelling pubmed-70904722020-03-24 The long non-coding RNA expression profile of Coxsackievirus A16 infected RD cells identified by RNA-seq Shi, Yingying Tu, Huilin Chen, Xiong Zhang, Yingying Chen, Liujun Liu, Zhongchun Sheng, Jiqun Han, Song Yin, Jun Peng, Biwen He, Xiaohua Liu, Wanhong Virol Sin Research Article Coxsackievirus A16 (CVA16) is one of major pathogens of hand, foot and mouth disease (HFMD) in children. Long non-coding RNAs (IncRNAs) have been implicated in various biological processes, but they have not been associated with CVA16 infection. In this study, we comprehensively characterized the landscape of IncRNAs of normal and CVA16 infected rhabdomyosarcoma (RD) cells using RNA-Seq to investigate the functional relevance of IncRNAs. We showed that a total of 760 IncRNAs were upregulated and 1210 IncRNAs were downregulated. Out of these dysregulated IncRNAs, 43.64% were intergenic, 22.31% were sense, 15.89% were intronic, 8.67% were bidirectional, 5.59% were antisense, 3.85% were sRNA host IncRNAs and 0.05% were enhancer. Six dysregulated IncRNAs were validated by quantitative PCR assays and the secondary structures of these IncRNAs were projected. Moreover, we conducted a bioinformatics analysis of an IncRNAs (ENST00000602478) to elucidate the diversity of modification and functions of IncRNAs. In summary, the current study compared the dysregulated IncRNAs profile upon CVA16 challenge and illustrated the intricate relationship between coding and IncRNAs transcripts. These results may not only provide a complete picture of transcription in CVA16 infected cells but also provide novel molecular targets for treatments of HFMD. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s12250-015-3693-1 and is accessible for authorized users. Springer Singapore 2016-03-31 /pmc/articles/PMC7090472/ /pubmed/27060091 http://dx.doi.org/10.1007/s12250-015-3693-1 Text en © Wuhan Institute of Virology, CAS and Springer Science+Business Media Singapore 2016
spellingShingle Research Article
Shi, Yingying
Tu, Huilin
Chen, Xiong
Zhang, Yingying
Chen, Liujun
Liu, Zhongchun
Sheng, Jiqun
Han, Song
Yin, Jun
Peng, Biwen
He, Xiaohua
Liu, Wanhong
The long non-coding RNA expression profile of Coxsackievirus A16 infected RD cells identified by RNA-seq
title The long non-coding RNA expression profile of Coxsackievirus A16 infected RD cells identified by RNA-seq
title_full The long non-coding RNA expression profile of Coxsackievirus A16 infected RD cells identified by RNA-seq
title_fullStr The long non-coding RNA expression profile of Coxsackievirus A16 infected RD cells identified by RNA-seq
title_full_unstemmed The long non-coding RNA expression profile of Coxsackievirus A16 infected RD cells identified by RNA-seq
title_short The long non-coding RNA expression profile of Coxsackievirus A16 infected RD cells identified by RNA-seq
title_sort long non-coding rna expression profile of coxsackievirus a16 infected rd cells identified by rna-seq
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090472/
https://www.ncbi.nlm.nih.gov/pubmed/27060091
http://dx.doi.org/10.1007/s12250-015-3693-1
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