Red-legged partridge (Alectoris rufa) de-novo transcriptome assembly and identification of gene-related markers

The red-legged partridge (Alectoris rufa) has a great socio-economic importance as a game species and is reared by millions in farms in several European countries. The ability to respond to a wide spectrum of pathogens and environmental changes is key for farm-reared animals that, as such, face even...

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Main Authors: Natalia Sevane, Javier Cañon, Paulina G. Eusebi, Ignacio Gil, Susana Dunner
Format: Article
Language:English
Published: Elsevier 2017-03-01
Series:Genomics Data
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S221359601730017X
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spelling doaj-190849676f7d4084928527d6a412764b2020-11-25T02:05:11ZengElsevierGenomics Data2213-59602017-03-0111C13213410.1016/j.gdata.2017.02.003Red-legged partridge (Alectoris rufa) de-novo transcriptome assembly and identification of gene-related markersNatalia SevaneJavier CañonPaulina G. EusebiIgnacio GilSusana DunnerThe red-legged partridge (Alectoris rufa) has a great socio-economic importance as a game species and is reared by millions in farms in several European countries. The ability to respond to a wide spectrum of pathogens and environmental changes is key for farm-reared animals that, as such, face even higher pathogen exposure and specifically for those submitted to restocking programs. In this study, RNA-sequencing and de-novo assembly of genes expressed in different immune tissues were performed. The raw FASTQ files were submitted to the NCBI SRA database with accession number PRJNA289204. A total of 94.2 million reads were obtained and assembled into 51,403 contigs using OASES software. The final annotated partridge immune transcriptome comprises almost 7000 unigenes, available as FASTA in the supplementary material. A total of 12,828 microsatellites and 33,857 Single Nucleotide Polymorphisms (SNPs) were identified. The candidate gene sequences and the large number of potential genetic markers from the red-legged partridge transcriptome reliably identified through the use for the first time of a high coverage 100-bp paired-end RNA-seq protocol, provide new tools for future studies in this and related species, thus contributing to the ongoing development of genomic resources in avian species. Further investigation into candidate genes and gene-associated markers will help to uncover individual variability in the resistance to infections and other external aggressions in partridges.http://www.sciencedirect.com/science/article/pii/S221359601730017XRNA-seqTranscriptomic signaturesImmune responseSNPsMicrosatellites
collection DOAJ
language English
format Article
sources DOAJ
author Natalia Sevane
Javier Cañon
Paulina G. Eusebi
Ignacio Gil
Susana Dunner
spellingShingle Natalia Sevane
Javier Cañon
Paulina G. Eusebi
Ignacio Gil
Susana Dunner
Red-legged partridge (Alectoris rufa) de-novo transcriptome assembly and identification of gene-related markers
Genomics Data
RNA-seq
Transcriptomic signatures
Immune response
SNPs
Microsatellites
author_facet Natalia Sevane
Javier Cañon
Paulina G. Eusebi
Ignacio Gil
Susana Dunner
author_sort Natalia Sevane
title Red-legged partridge (Alectoris rufa) de-novo transcriptome assembly and identification of gene-related markers
title_short Red-legged partridge (Alectoris rufa) de-novo transcriptome assembly and identification of gene-related markers
title_full Red-legged partridge (Alectoris rufa) de-novo transcriptome assembly and identification of gene-related markers
title_fullStr Red-legged partridge (Alectoris rufa) de-novo transcriptome assembly and identification of gene-related markers
title_full_unstemmed Red-legged partridge (Alectoris rufa) de-novo transcriptome assembly and identification of gene-related markers
title_sort red-legged partridge (alectoris rufa) de-novo transcriptome assembly and identification of gene-related markers
publisher Elsevier
series Genomics Data
issn 2213-5960
publishDate 2017-03-01
description The red-legged partridge (Alectoris rufa) has a great socio-economic importance as a game species and is reared by millions in farms in several European countries. The ability to respond to a wide spectrum of pathogens and environmental changes is key for farm-reared animals that, as such, face even higher pathogen exposure and specifically for those submitted to restocking programs. In this study, RNA-sequencing and de-novo assembly of genes expressed in different immune tissues were performed. The raw FASTQ files were submitted to the NCBI SRA database with accession number PRJNA289204. A total of 94.2 million reads were obtained and assembled into 51,403 contigs using OASES software. The final annotated partridge immune transcriptome comprises almost 7000 unigenes, available as FASTA in the supplementary material. A total of 12,828 microsatellites and 33,857 Single Nucleotide Polymorphisms (SNPs) were identified. The candidate gene sequences and the large number of potential genetic markers from the red-legged partridge transcriptome reliably identified through the use for the first time of a high coverage 100-bp paired-end RNA-seq protocol, provide new tools for future studies in this and related species, thus contributing to the ongoing development of genomic resources in avian species. Further investigation into candidate genes and gene-associated markers will help to uncover individual variability in the resistance to infections and other external aggressions in partridges.
topic RNA-seq
Transcriptomic signatures
Immune response
SNPs
Microsatellites
url http://www.sciencedirect.com/science/article/pii/S221359601730017X
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