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
GCMO01012126GCMO01012126.1region
GCMO01012127GCMO01012127.1region
GCMO01012128GCMO01012128.1region
GCMO01012129GCMO01012129.1region
GCMO01012130GCMO01012130.1region
GCMO01012131GCMO01012131.1region
GCMO01012132GCMO01012132.1region
GCMO01012133GCMO01012133.1region
GCMO01012134GCMO01012134.1region
GCMO01012135GCMO01012135.1region
GCMO01012136GCMO01012136.1region
GCMO01012137GCMO01012137.1region
GCMO01012138GCMO01012138.1region
GCMO01012139GCMO01012139.1region
GCMO01012140GCMO01012140.1region
GCMO01012141GCMO01012141.1region
GCMO01012142GCMO01012142.1region
GCMO01012143GCMO01012143.1region
GCMO01012144GCMO01012144.1region
GCMO01012145GCMO01012145.1region
GCMO01012146GCMO01012146.1region
GCMO01012147GCMO01012147.1region
GCMO01012148GCMO01012148.1region
GCMO01012149GCMO01012149.1region
GCMO01012150GCMO01012150.1region

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