Abstract

Blueberry is an economically important berry crop. Both production and consumption of blueberries have increased sharply worldwide in recent years at least partly due to their known health benefits. The development of improved genomic resources for blueberry, such as a well-assembled genome and transcriptome, could accelerate breeding through genomic-assisted approaches. To enrich available transcriptome data and identify genes potentially involved in fruit quality, RNA sequencing was performed on fruit tissue from two northern-adapted hybrid blueberry breeding populations. RNA-seq was carried out using the Illumina HiSeqTM 2500 platform. Because of the absence of a reference-grade genome for blueberry, a transcriptome was de novo assembled from this RNA-seq data and other publicly available transcriptome data from blueberry downloaded from the National Center for Biotechnology Information (NCBI) Short Read Archive (SRA) using Trinity. After removing redundancy, this resulted in a dataset of 91,861 blueberry unigenes. This unigene dataset was functionally annotated using the NCBI-Nr protein database. All raw reads from the breeding populations were deposited in the NCBI SRA with accession numbers SRR6281886, SRR6281887, SRR6281888, and SRR6281889. The de novo transcriptome assembly was deposited at NCBI Transcriptome Shotgun Assembly (TSA) database with accession number GGAB00000000. These data will provide real expression evidence for the blueberry genome gene prediction and gene functional annotation and a reference transcriptome for future gene expression studies involving blueberry fruit.

Highlights

  • Trinity software was used to perform de novo assembly of clean reads from this data and other blueberry transcriptome data downloaded from National Center for Biotechnology Information (NCBI) Short Read Archive (SRA)

  • The transcriptomes of two northern-adapted rabbiteye hybrid blueberry breeding populations were generated from RNA extracts of bulked fruit tissue samples of plants with and without the epicuticular waxy coating on the fruit

  • The other publicly available RNA-seq datasets included: SRR1187632, SRR1187673, SRR1187674, SRR1187675, SRR1187676, SRR1187677, SRR1188088, SRR1188089, SRR1188090, SRR1188091, SRR1188222, SRR1188230, SRR1188236, SRR1188240, SRR1188242, SRR1188247, SRR1188258, SRR1188265, SRR1188270, SRR1188282, SRR1188283, SRR942391, and SRR950441. This assembly was functionally annotated by NCBI-Nr protein database and assigned Gene Ontology (GO) identity (Fig. 1). Both raw RNA-seq reads and the de novo transcriptome assembly can be accessed in the NCBI repository, with the SRA accession number SRR6281886 for ‘Nocturne’ x T 300 population non-waxy library, SRR6281887 for ‘Nocturne’ x T 300 population waxy library, SRR6281888 for ‘Nocturne’ x US 1212 population non-waxy library, and SRR6281889 for ‘Nocturne’ x US 1212 population waxy library, and with the Transcriptome Shotgun Assembly (TSA) accession number GGAB00000000 for the assembled unigene transcriptome dataset

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Summary

Introduction

Total RNA was extracted from bulked waxy and non-waxy fruit tissue from two blueberry breeding features populations segregating for the waxy coating on fruit. Trinity software was used to perform de novo assembly of clean reads from this data and other blueberry transcriptome data downloaded from NCBI SRA.

Results
Conclusion
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