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Transcriptome Analysis of the Brown Planthopper Nilaparvata lugens

Authors :
Hai-Jun Xu
Zeng-Rong Zhu
Yonggen Lou
Jia-An Cheng
Jian Xue
Chuan-Xi Zhang
Hang Liu
Yanbing Cheng
Yan-Yuan Bao
Bao-Ling Li
Zhiyu Peng
Source :
PLoS ONE, PLoS ONE, Vol 5, Iss 12, p e14233 (2010)
Publication Year :
2010
Publisher :
Public Library of Science, 2010.

Abstract

Background The brown planthopper (BPH) Nilaparvata lugens (Stal) is one of the most serious insect pests of rice in Asia. However, little is known about the mechanisms responsible for the development, wing dimorphism and sex difference in this species. Genomic information for BPH is currently unavailable, and, therefore, transcriptome and expression profiling data for this species are needed as an important resource to better understand the biological mechanisms of BPH. Methodology/Principal Findings In this study, we performed de novo transcriptome assembly and gene expression analysis using short-read sequencing technology (Illumina) combined with a tag-based digital gene expression (DGE) system. The transcriptome analysis assembles the gene information for different developmental stages, sexes and wing forms of BPH. In addition, we constructed six DGE libraries: eggs, second instar nymphs, fifth instar nymphs, brachypterous female adults, macropterous female adults and macropterous male adults. Illumina sequencing revealed 85,526 unigenes, including 13,102 clusters and 72,424 singletons. Transcriptome sequences larger than 350 bp were subjected to Gene Orthology (GO) and KEGG Orthology (KO) annotations. To analyze the DGE profiling, we mainly compared the gene expression variations between eggs and second instar nymphs; second and fifth instar nymphs; fifth instar nymphs and three types of adults; brachypterous and macropterous female adults as well as macropterous female and male adults. Thousands of genes showed significantly different expression levels based on the various comparisons. And we randomly selected some genes to confirm their altered expression levels by quantitative real-time PCR (qRT-PCR). Conclusions/Significance The obtained BPH transcriptome and DGE profiling data provide comprehensive gene expression information at the transcriptional level that could facilitate our understanding of the molecular mechanisms from various physiological aspects including development, wing dimorphism and sex difference in BPH.

Details

Language :
English
ISSN :
19326203
Volume :
5
Issue :
12
Database :
OpenAIRE
Journal :
PLoS ONE
Accession number :
edsair.doi.dedup.....d042ab2a9bc5fecddd0999436933e07c