De novo assembly and characterisation of the field pea transcriptome using RNA-Seq

Publication Overview
TitleDe novo assembly and characterisation of the field pea transcriptome using RNA-Seq
AuthorsSudheesh S, Sawbridge TI, Cogan NO, Kennedy P, Forster JW, Kaur S
TypeJournal Article
Journal NameBMC genomics
Volume16
Issue1
Year2015
Page(s)611
CitationSudheesh S, Sawbridge TI, Cogan NO, Kennedy P, Forster JW, Kaur S. De novo assembly and characterisation of the field pea transcriptome using RNA-Seq. BMC genomics. 2015; 16(1):611.

Abstract

BACKGROUND
Field pea (Pisum sativum L.) is a cool-season grain legume that is cultivated world-wide for both human consumption and stock-feed purposes. Enhancement of genetic and genomic resources for field pea will permit improved understanding of the control of traits relevant to crop productivity and quality. Advances in second-generation sequencing and associated bioinformatics analysis now provide unprecedented opportunities for the development of such resources. The objective of this study was to perform transcriptome sequencing and characterisation from two genotypes of field pea that differ in terms of seed and plant morphological characteristics.

RESULTS
Transcriptome sequencing was performed with RNA templates from multiple tissues of the field pea genotypes Kaspa and Parafield. Tissue samples were collected at various growth stages, and a total of 23 cDNA libraries were sequenced using Illumina high-throughput sequencing platforms. A total of 407 and 352 million paired-end reads from the Kaspa and Parafield transcriptomes, respectively were assembled into 129,282 and 149,272 contigs, which were filtered on the basis of known gene annotations, presence of open reading frames (ORFs), reciprocal matches and degree of coverage. Totals of 126,335 contigs from Kaspa and 145,730 from Parafield were subsequently selected as the reference set. Reciprocal sequence analysis revealed that c. 87 % of contigs were expressed in both cultivars, while a small proportion were unique to each genotype. Reads from different libraries were aligned to the genotype-specific assemblies in order to identify and characterise expression of contigs on a tissue-specific basis, of which 87 % were expressed in more than one tissue, while others showed distinct expression patterns in specific tissues, providing unique transcriptome signatures.

CONCLUSION
This study provided a comprehensive assembled and annotated transcriptome set for field pea that can be used for development of genetic markers, in order to assess genetic diversity, construct linkage maps, perform trait-dissection and implement whole-genome selection strategies in varietal improvement programs, as well to identify target genes for genetic modification approaches on the basis of annotation and expression analysis. In addition, the reference field pea transcriptome will prove highly valuable for comparative genomics studies and construction of a finalised genome sequence.

Features
This publication contains information about 271,056 features:
Feature NameUniquenameType
GCMO01016001GCMO01016001.1region
GCMO01016002GCMO01016002.1region
GCMO01016003GCMO01016003.1region
GCMO01016004GCMO01016004.1region
GCMO01016005GCMO01016005.1region
GCMO01016006GCMO01016006.1region
GCMO01016007GCMO01016007.1region
GCMO01016008GCMO01016008.1region
GCMO01016009GCMO01016009.1region
GCMO01016010GCMO01016010.1region
GCMO01016011GCMO01016011.1region
GCMO01016012GCMO01016012.1region
GCMO01016013GCMO01016013.1region
GCMO01016014GCMO01016014.1region
GCMO01016015GCMO01016015.1region
GCMO01016016GCMO01016016.1region
GCMO01016017GCMO01016017.1region
GCMO01016018GCMO01016018.1region
GCMO01016019GCMO01016019.1region
GCMO01016020GCMO01016020.1region
GCMO01016021GCMO01016021.1region
GCMO01016022GCMO01016022.1region
GCMO01016023GCMO01016023.1region
GCMO01016024GCMO01016024.1region
GCMO01016025GCMO01016025.1region

Pages

Properties
Additional details for this publication include:
Property NameValue
LanguageEnglish
Language Abbreng
Publication TypeJournal Article
Journal CountryEngland
Publication ModelElectronic
ISSN1471-2164
eISSN1471-2164
Publication Date2015
Journal AbbreviationBMC Genomics
DOI10.1186/s12864-015-1815-7
Elocation10.1186/s12864-015-1815-7