Analysis of Litopenaeus vannamei transcriptome using the next-generation DNA sequencing technique.

BACKGROUND: Pacific white shrimp (Litopenaeus vannamei), the major species of farmed shrimps in the world, has been attracting extensive studies, which require more and more genome background knowledge. The now available transcriptome data of L. vannamei are insufficient for research requirements, a...

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Main Authors: Chaozheng Li, Shaoping Weng, Yonggui Chen, Xiaoqiang Yu, Ling Lü, Haiqing Zhang, Jianguo He, Xiaopeng Xu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3469548?pdf=render
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author Chaozheng Li
Shaoping Weng
Yonggui Chen
Xiaoqiang Yu
Ling Lü
Haiqing Zhang
Jianguo He
Xiaopeng Xu
author_facet Chaozheng Li
Shaoping Weng
Yonggui Chen
Xiaoqiang Yu
Ling Lü
Haiqing Zhang
Jianguo He
Xiaopeng Xu
author_sort Chaozheng Li
collection DOAJ
description BACKGROUND: Pacific white shrimp (Litopenaeus vannamei), the major species of farmed shrimps in the world, has been attracting extensive studies, which require more and more genome background knowledge. The now available transcriptome data of L. vannamei are insufficient for research requirements, and have not been adequately assembled and annotated. METHODOLOGY/PRINCIPAL FINDINGS: This is the first study that used a next-generation high-throughput DNA sequencing technique, the Solexa/Illumina GA II method, to analyze the transcriptome from whole bodies of L. vannamei larvae. More than 2.4 Gb of raw data were generated, and 109,169 unigenes with a mean length of 396 bp were assembled using the SOAP denovo software. 73,505 unigenes (>200 bp) with good quality sequences were selected and subjected to annotation analysis, among which 37.80% can be matched in NCBI Nr database, 37.3% matched in Swissprot, and 44.1% matched in TrEMBL. Using BLAST and BLAST2Go softwares, 11,153 unigenes were classified into 25 Clusters of Orthologous Groups of proteins (COG) categories, 8171 unigenes were assigned into 51 Gene ontology (GO) functional groups, and 18,154 unigenes were divided into 220 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. To primarily verify part of the results of assembly and annotations, 12 assembled unigenes that are homologous to many embryo development-related genes were chosen and subjected to RT-PCR for electrophoresis and Sanger sequencing analyses, and to real-time PCR for expression profile analyses during embryo development. CONCLUSIONS/SIGNIFICANCE: The L. vannamei transcriptome analyzed using the next-generation sequencing technique enriches the information of L. vannamei genes, which will facilitate our understanding of the genome background of crustaceans, and promote the studies on L. vannamei.
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spelling doaj.art-612896c248ba4b06a7de936a155d4fbe2022-12-22T02:40:29ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01710e4744210.1371/journal.pone.0047442Analysis of Litopenaeus vannamei transcriptome using the next-generation DNA sequencing technique.Chaozheng LiShaoping WengYonggui ChenXiaoqiang YuLing LüHaiqing ZhangJianguo HeXiaopeng XuBACKGROUND: Pacific white shrimp (Litopenaeus vannamei), the major species of farmed shrimps in the world, has been attracting extensive studies, which require more and more genome background knowledge. The now available transcriptome data of L. vannamei are insufficient for research requirements, and have not been adequately assembled and annotated. METHODOLOGY/PRINCIPAL FINDINGS: This is the first study that used a next-generation high-throughput DNA sequencing technique, the Solexa/Illumina GA II method, to analyze the transcriptome from whole bodies of L. vannamei larvae. More than 2.4 Gb of raw data were generated, and 109,169 unigenes with a mean length of 396 bp were assembled using the SOAP denovo software. 73,505 unigenes (>200 bp) with good quality sequences were selected and subjected to annotation analysis, among which 37.80% can be matched in NCBI Nr database, 37.3% matched in Swissprot, and 44.1% matched in TrEMBL. Using BLAST and BLAST2Go softwares, 11,153 unigenes were classified into 25 Clusters of Orthologous Groups of proteins (COG) categories, 8171 unigenes were assigned into 51 Gene ontology (GO) functional groups, and 18,154 unigenes were divided into 220 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. To primarily verify part of the results of assembly and annotations, 12 assembled unigenes that are homologous to many embryo development-related genes were chosen and subjected to RT-PCR for electrophoresis and Sanger sequencing analyses, and to real-time PCR for expression profile analyses during embryo development. CONCLUSIONS/SIGNIFICANCE: The L. vannamei transcriptome analyzed using the next-generation sequencing technique enriches the information of L. vannamei genes, which will facilitate our understanding of the genome background of crustaceans, and promote the studies on L. vannamei.http://europepmc.org/articles/PMC3469548?pdf=render
spellingShingle Chaozheng Li
Shaoping Weng
Yonggui Chen
Xiaoqiang Yu
Ling Lü
Haiqing Zhang
Jianguo He
Xiaopeng Xu
Analysis of Litopenaeus vannamei transcriptome using the next-generation DNA sequencing technique.
PLoS ONE
title Analysis of Litopenaeus vannamei transcriptome using the next-generation DNA sequencing technique.
title_full Analysis of Litopenaeus vannamei transcriptome using the next-generation DNA sequencing technique.
title_fullStr Analysis of Litopenaeus vannamei transcriptome using the next-generation DNA sequencing technique.
title_full_unstemmed Analysis of Litopenaeus vannamei transcriptome using the next-generation DNA sequencing technique.
title_short Analysis of Litopenaeus vannamei transcriptome using the next-generation DNA sequencing technique.
title_sort analysis of litopenaeus vannamei transcriptome using the next generation dna sequencing technique
url http://europepmc.org/articles/PMC3469548?pdf=render
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