Viral infection induces expression of novel phased microRNAs from conserved cellular microRNA precursors.

RNA silencing, mediated by small RNAs including microRNAs (miRNAs) and small interfering RNAs (siRNAs), is a potent antiviral or antibacterial mechanism, besides regulating normal cellular gene expression critical for development and physiology. To gain insights into host small RNA metabolism under...

Full description

Bibliographic Details
Main Authors: Peng Du, Jianguo Wu, Jiayao Zhang, Shuqi Zhao, Hong Zheng, Ge Gao, Liping Wei, Yi Li
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-08-01
Series:PLoS Pathogens
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21901091/?tool=EBI
_version_ 1818722544587374592
author Peng Du
Jianguo Wu
Jiayao Zhang
Shuqi Zhao
Hong Zheng
Ge Gao
Liping Wei
Yi Li
author_facet Peng Du
Jianguo Wu
Jiayao Zhang
Shuqi Zhao
Hong Zheng
Ge Gao
Liping Wei
Yi Li
author_sort Peng Du
collection DOAJ
description RNA silencing, mediated by small RNAs including microRNAs (miRNAs) and small interfering RNAs (siRNAs), is a potent antiviral or antibacterial mechanism, besides regulating normal cellular gene expression critical for development and physiology. To gain insights into host small RNA metabolism under infections by different viruses, we used Solexa/Illumina deep sequencing to characterize the small RNA profiles of rice plants infected by two distinct viruses, Rice dwarf virus (RDV, dsRNA virus) and Rice stripe virus (RSV, a negative sense and ambisense RNA virus), respectively, as compared with those from non-infected plants. Our analyses showed that RSV infection enhanced the accumulation of some rice miRNA*s, but not their corresponding miRNAs, as well as accumulation of phased siRNAs from a particular precursor. Furthermore, RSV infection also induced the expression of novel miRNAs in a phased pattern from several conserved miRNA precursors. In comparison, no such changes in host small RNA expression was observed in RDV-infected rice plants. Significantly RSV infection elevated the expression levels of selective OsDCLs and OsAGOs, whereas RDV infection only affected the expression of certain OsRDRs. Our results provide a comparative analysis, via deep sequencing, of changes in the small RNA profiles and in the genes of RNA silencing machinery induced by different viruses in a natural and economically important crop host plant. They uncover new mechanisms and complexity of virus-host interactions that may have important implications for further studies on the evolution of cellular small RNA biogenesis that impact pathogen infection, pathogenesis, as well as organismal development.
first_indexed 2024-12-17T20:56:19Z
format Article
id doaj.art-95ea7f832f664360b7d18a683b55e0e4
institution Directory Open Access Journal
issn 1553-7366
1553-7374
language English
last_indexed 2024-12-17T20:56:19Z
publishDate 2011-08-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Pathogens
spelling doaj.art-95ea7f832f664360b7d18a683b55e0e42022-12-21T21:32:51ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742011-08-0178e100217610.1371/journal.ppat.1002176Viral infection induces expression of novel phased microRNAs from conserved cellular microRNA precursors.Peng DuJianguo WuJiayao ZhangShuqi ZhaoHong ZhengGe GaoLiping WeiYi LiRNA silencing, mediated by small RNAs including microRNAs (miRNAs) and small interfering RNAs (siRNAs), is a potent antiviral or antibacterial mechanism, besides regulating normal cellular gene expression critical for development and physiology. To gain insights into host small RNA metabolism under infections by different viruses, we used Solexa/Illumina deep sequencing to characterize the small RNA profiles of rice plants infected by two distinct viruses, Rice dwarf virus (RDV, dsRNA virus) and Rice stripe virus (RSV, a negative sense and ambisense RNA virus), respectively, as compared with those from non-infected plants. Our analyses showed that RSV infection enhanced the accumulation of some rice miRNA*s, but not their corresponding miRNAs, as well as accumulation of phased siRNAs from a particular precursor. Furthermore, RSV infection also induced the expression of novel miRNAs in a phased pattern from several conserved miRNA precursors. In comparison, no such changes in host small RNA expression was observed in RDV-infected rice plants. Significantly RSV infection elevated the expression levels of selective OsDCLs and OsAGOs, whereas RDV infection only affected the expression of certain OsRDRs. Our results provide a comparative analysis, via deep sequencing, of changes in the small RNA profiles and in the genes of RNA silencing machinery induced by different viruses in a natural and economically important crop host plant. They uncover new mechanisms and complexity of virus-host interactions that may have important implications for further studies on the evolution of cellular small RNA biogenesis that impact pathogen infection, pathogenesis, as well as organismal development.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21901091/?tool=EBI
spellingShingle Peng Du
Jianguo Wu
Jiayao Zhang
Shuqi Zhao
Hong Zheng
Ge Gao
Liping Wei
Yi Li
Viral infection induces expression of novel phased microRNAs from conserved cellular microRNA precursors.
PLoS Pathogens
title Viral infection induces expression of novel phased microRNAs from conserved cellular microRNA precursors.
title_full Viral infection induces expression of novel phased microRNAs from conserved cellular microRNA precursors.
title_fullStr Viral infection induces expression of novel phased microRNAs from conserved cellular microRNA precursors.
title_full_unstemmed Viral infection induces expression of novel phased microRNAs from conserved cellular microRNA precursors.
title_short Viral infection induces expression of novel phased microRNAs from conserved cellular microRNA precursors.
title_sort viral infection induces expression of novel phased micrornas from conserved cellular microrna precursors
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21901091/?tool=EBI
work_keys_str_mv AT pengdu viralinfectioninducesexpressionofnovelphasedmicrornasfromconservedcellularmicrornaprecursors
AT jianguowu viralinfectioninducesexpressionofnovelphasedmicrornasfromconservedcellularmicrornaprecursors
AT jiayaozhang viralinfectioninducesexpressionofnovelphasedmicrornasfromconservedcellularmicrornaprecursors
AT shuqizhao viralinfectioninducesexpressionofnovelphasedmicrornasfromconservedcellularmicrornaprecursors
AT hongzheng viralinfectioninducesexpressionofnovelphasedmicrornasfromconservedcellularmicrornaprecursors
AT gegao viralinfectioninducesexpressionofnovelphasedmicrornasfromconservedcellularmicrornaprecursors
AT lipingwei viralinfectioninducesexpressionofnovelphasedmicrornasfromconservedcellularmicrornaprecursors
AT yili viralinfectioninducesexpressionofnovelphasedmicrornasfromconservedcellularmicrornaprecursors