Cargando…

Whole transcriptome sequencing of Pseudomonas syringae pv. actinidiae-infected kiwifruit plants reveals species-specific interaction between long non-coding RNA and coding genes

An outbreak of kiwifruit bacterial canker disease caused by Pseudomonas syringae pv. actinidiae (Psa) beginning in 2008 caused disaster to the kiwifruit industry. However the mechanisms of interaction between kiwifruit and Psa are unknown. Long noncoding RNAs (lncRNAs) are known to regulate many bio...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Zupeng, Liu, Yifei, Li, Li, Li, Dawei, Zhang, Qiong, Guo, Yangtao, Wang, Shuaibin, Zhong, Caihong, Huang, Hongwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501815/
https://www.ncbi.nlm.nih.gov/pubmed/28687784
http://dx.doi.org/10.1038/s41598-017-05377-y
_version_ 1783248856010457088
author Wang, Zupeng
Liu, Yifei
Li, Li
Li, Dawei
Zhang, Qiong
Guo, Yangtao
Wang, Shuaibin
Zhong, Caihong
Huang, Hongwen
author_facet Wang, Zupeng
Liu, Yifei
Li, Li
Li, Dawei
Zhang, Qiong
Guo, Yangtao
Wang, Shuaibin
Zhong, Caihong
Huang, Hongwen
author_sort Wang, Zupeng
collection PubMed
description An outbreak of kiwifruit bacterial canker disease caused by Pseudomonas syringae pv. actinidiae (Psa) beginning in 2008 caused disaster to the kiwifruit industry. However the mechanisms of interaction between kiwifruit and Psa are unknown. Long noncoding RNAs (lncRNAs) are known to regulate many biological processes, but comprehensive repertoires of kiwifruit lncRNAs and their effects on the interaction between kiwifruit and Psa are unknown. Here, based on in-depth transcriptomic analysis of four kiwifruit materials at three stages of infection with Psa, we identified 14,845 transcripts from 12,280 loci as putative lncRNAs. Hierarchical clustering analysis of differentially-expressed transcripts reveals that both protein-coding and lncRNA transcripts are expressed species-specifically. Comparing differentially-expressed transcripts from different species, variations in pattern-triggered immunity (PTI) were the main causes of species-specific responses to infection by Psa. Using weighted gene co-expression network analysis, we identified species-specific expressed key lncRNAs which were closely related to plant immune response and signal transduction. Our results illustrate that different kiwifruit species employ multiple different plant immunity layers to fight against Psa infection, which causes distinct responses. We also discovered that lncRNAs might affect kiwifruit responses to Psa infection, indicating that both protein-coding regions and noncoding regions can affect kiwifruit response to Psa infection.
format Online
Article
Text
id pubmed-5501815
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-55018152017-07-10 Whole transcriptome sequencing of Pseudomonas syringae pv. actinidiae-infected kiwifruit plants reveals species-specific interaction between long non-coding RNA and coding genes Wang, Zupeng Liu, Yifei Li, Li Li, Dawei Zhang, Qiong Guo, Yangtao Wang, Shuaibin Zhong, Caihong Huang, Hongwen Sci Rep Article An outbreak of kiwifruit bacterial canker disease caused by Pseudomonas syringae pv. actinidiae (Psa) beginning in 2008 caused disaster to the kiwifruit industry. However the mechanisms of interaction between kiwifruit and Psa are unknown. Long noncoding RNAs (lncRNAs) are known to regulate many biological processes, but comprehensive repertoires of kiwifruit lncRNAs and their effects on the interaction between kiwifruit and Psa are unknown. Here, based on in-depth transcriptomic analysis of four kiwifruit materials at three stages of infection with Psa, we identified 14,845 transcripts from 12,280 loci as putative lncRNAs. Hierarchical clustering analysis of differentially-expressed transcripts reveals that both protein-coding and lncRNA transcripts are expressed species-specifically. Comparing differentially-expressed transcripts from different species, variations in pattern-triggered immunity (PTI) were the main causes of species-specific responses to infection by Psa. Using weighted gene co-expression network analysis, we identified species-specific expressed key lncRNAs which were closely related to plant immune response and signal transduction. Our results illustrate that different kiwifruit species employ multiple different plant immunity layers to fight against Psa infection, which causes distinct responses. We also discovered that lncRNAs might affect kiwifruit responses to Psa infection, indicating that both protein-coding regions and noncoding regions can affect kiwifruit response to Psa infection. Nature Publishing Group UK 2017-07-07 /pmc/articles/PMC5501815/ /pubmed/28687784 http://dx.doi.org/10.1038/s41598-017-05377-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wang, Zupeng
Liu, Yifei
Li, Li
Li, Dawei
Zhang, Qiong
Guo, Yangtao
Wang, Shuaibin
Zhong, Caihong
Huang, Hongwen
Whole transcriptome sequencing of Pseudomonas syringae pv. actinidiae-infected kiwifruit plants reveals species-specific interaction between long non-coding RNA and coding genes
title Whole transcriptome sequencing of Pseudomonas syringae pv. actinidiae-infected kiwifruit plants reveals species-specific interaction between long non-coding RNA and coding genes
title_full Whole transcriptome sequencing of Pseudomonas syringae pv. actinidiae-infected kiwifruit plants reveals species-specific interaction between long non-coding RNA and coding genes
title_fullStr Whole transcriptome sequencing of Pseudomonas syringae pv. actinidiae-infected kiwifruit plants reveals species-specific interaction between long non-coding RNA and coding genes
title_full_unstemmed Whole transcriptome sequencing of Pseudomonas syringae pv. actinidiae-infected kiwifruit plants reveals species-specific interaction between long non-coding RNA and coding genes
title_short Whole transcriptome sequencing of Pseudomonas syringae pv. actinidiae-infected kiwifruit plants reveals species-specific interaction between long non-coding RNA and coding genes
title_sort whole transcriptome sequencing of pseudomonas syringae pv. actinidiae-infected kiwifruit plants reveals species-specific interaction between long non-coding rna and coding genes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501815/
https://www.ncbi.nlm.nih.gov/pubmed/28687784
http://dx.doi.org/10.1038/s41598-017-05377-y
work_keys_str_mv AT wangzupeng wholetranscriptomesequencingofpseudomonassyringaepvactinidiaeinfectedkiwifruitplantsrevealsspeciesspecificinteractionbetweenlongnoncodingrnaandcodinggenes
AT liuyifei wholetranscriptomesequencingofpseudomonassyringaepvactinidiaeinfectedkiwifruitplantsrevealsspeciesspecificinteractionbetweenlongnoncodingrnaandcodinggenes
AT lili wholetranscriptomesequencingofpseudomonassyringaepvactinidiaeinfectedkiwifruitplantsrevealsspeciesspecificinteractionbetweenlongnoncodingrnaandcodinggenes
AT lidawei wholetranscriptomesequencingofpseudomonassyringaepvactinidiaeinfectedkiwifruitplantsrevealsspeciesspecificinteractionbetweenlongnoncodingrnaandcodinggenes
AT zhangqiong wholetranscriptomesequencingofpseudomonassyringaepvactinidiaeinfectedkiwifruitplantsrevealsspeciesspecificinteractionbetweenlongnoncodingrnaandcodinggenes
AT guoyangtao wholetranscriptomesequencingofpseudomonassyringaepvactinidiaeinfectedkiwifruitplantsrevealsspeciesspecificinteractionbetweenlongnoncodingrnaandcodinggenes
AT wangshuaibin wholetranscriptomesequencingofpseudomonassyringaepvactinidiaeinfectedkiwifruitplantsrevealsspeciesspecificinteractionbetweenlongnoncodingrnaandcodinggenes
AT zhongcaihong wholetranscriptomesequencingofpseudomonassyringaepvactinidiaeinfectedkiwifruitplantsrevealsspeciesspecificinteractionbetweenlongnoncodingrnaandcodinggenes
AT huanghongwen wholetranscriptomesequencingofpseudomonassyringaepvactinidiaeinfectedkiwifruitplantsrevealsspeciesspecificinteractionbetweenlongnoncodingrnaandcodinggenes