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
GCMO01009751GCMO01009751.1region
GCMO01009752GCMO01009752.1region
GCMO01009753GCMO01009753.1region
GCMO01009754GCMO01009754.1region
GCMO01009755GCMO01009755.1region
GCMO01009756GCMO01009756.1region
GCMO01009757GCMO01009757.1region
GCMO01009758GCMO01009758.1region
GCMO01009759GCMO01009759.1region
GCMO01009760GCMO01009760.1region
GCMO01009761GCMO01009761.1region
GCMO01009762GCMO01009762.1region
GCMO01009763GCMO01009763.1region
GCMO01009764GCMO01009764.1region
GCMO01009765GCMO01009765.1region
GCMO01009766GCMO01009766.1region
GCMO01009767GCMO01009767.1region
GCMO01009768GCMO01009768.1region
GCMO01009769GCMO01009769.1region
GCMO01009770GCMO01009770.1region
GCMO01009771GCMO01009771.1region
GCMO01009772GCMO01009772.1region
GCMO01009773GCMO01009773.1region
GCMO01009774GCMO01009774.1region
GCMO01009775GCMO01009775.1region

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