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Genome-wide identification of allele-specific expression (ASE) in response to Marek’s disease virus infection using next generation sequencing

BACKGROUND: Marek’s disease (MD), a T cell lymphoma induced by the highly oncogenic α-herpesvirus Marek’s disease virus (MDV), is the main chronic infectious disease concern threatening the poultry industry. Enhancing genetic resistance to MD in commercial poultry is an attractive method to augment...

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Autores principales: MacEachern, Sean, Muir, William M, Crosby, Seth, Cheng, Hans H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108208/
https://www.ncbi.nlm.nih.gov/pubmed/21645293
http://dx.doi.org/10.1186/1753-6561-5-S4-S14
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author MacEachern, Sean
Muir, William M
Crosby, Seth
Cheng, Hans H
author_facet MacEachern, Sean
Muir, William M
Crosby, Seth
Cheng, Hans H
author_sort MacEachern, Sean
collection PubMed
description BACKGROUND: Marek’s disease (MD), a T cell lymphoma induced by the highly oncogenic α-herpesvirus Marek’s disease virus (MDV), is the main chronic infectious disease concern threatening the poultry industry. Enhancing genetic resistance to MD in commercial poultry is an attractive method to augment MD vaccines, which is currently the control method of choice. In order to optimally implement this control strategy through marker-assisted selection (MAS) and to gain biological information, it is necessary to identify specific genes that influence MD incidence. METHODS: A genome-wide screen for allele-specific expression (ASE) in response to MDV infection was conducted. The highly inbred ADOL chicken lines 6 (MD resistant) and 7 (MD susceptible) were inter-mated in reciprocal crosses and half of the progeny challenged with MDV. Splenic RNA pools at a single time after infection for each treatment group point were generated, sequenced using a next generation sequencer, then analyzed for allele-specific expression (ASE). To validate and extend the results, Illumina GoldenGate assays for selected cSNPs were developed and used on all RNA samples from all 6 time points following MDV challenge. RESULTS: RNA sequencing resulted in 11-13+ million mappable reads per treatment group, 1.7+ Gb total sequence, and 22,655 high-confidence cSNPs. Analysis of these cSNPs revealed that 5360 cSNPs in 3773 genes exhibited statistically significant allelic imbalance. Of the 1536 GoldenGate assays, 1465 were successfully scored with all but 19 exhibiting evidence for allelic imbalance. CONCLUSIONS: ASE is an efficient method to identify potentially all or most of the genes influencing this complex trait. The identified cSNPs can be further evaluated in resource populations to determine their allelic direction and size of effect on genetic resistance to MD as well as being directly implemented in genomic selection programs. The described method, although demonstrated in inbred chicken lines, is applicable to all traits in any diploid species, and should prove to be a simple method to identify the majority of genes controlling any complex trait.
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spelling pubmed-31082082011-06-07 Genome-wide identification of allele-specific expression (ASE) in response to Marek’s disease virus infection using next generation sequencing MacEachern, Sean Muir, William M Crosby, Seth Cheng, Hans H BMC Proc Proceedings BACKGROUND: Marek’s disease (MD), a T cell lymphoma induced by the highly oncogenic α-herpesvirus Marek’s disease virus (MDV), is the main chronic infectious disease concern threatening the poultry industry. Enhancing genetic resistance to MD in commercial poultry is an attractive method to augment MD vaccines, which is currently the control method of choice. In order to optimally implement this control strategy through marker-assisted selection (MAS) and to gain biological information, it is necessary to identify specific genes that influence MD incidence. METHODS: A genome-wide screen for allele-specific expression (ASE) in response to MDV infection was conducted. The highly inbred ADOL chicken lines 6 (MD resistant) and 7 (MD susceptible) were inter-mated in reciprocal crosses and half of the progeny challenged with MDV. Splenic RNA pools at a single time after infection for each treatment group point were generated, sequenced using a next generation sequencer, then analyzed for allele-specific expression (ASE). To validate and extend the results, Illumina GoldenGate assays for selected cSNPs were developed and used on all RNA samples from all 6 time points following MDV challenge. RESULTS: RNA sequencing resulted in 11-13+ million mappable reads per treatment group, 1.7+ Gb total sequence, and 22,655 high-confidence cSNPs. Analysis of these cSNPs revealed that 5360 cSNPs in 3773 genes exhibited statistically significant allelic imbalance. Of the 1536 GoldenGate assays, 1465 were successfully scored with all but 19 exhibiting evidence for allelic imbalance. CONCLUSIONS: ASE is an efficient method to identify potentially all or most of the genes influencing this complex trait. The identified cSNPs can be further evaluated in resource populations to determine their allelic direction and size of effect on genetic resistance to MD as well as being directly implemented in genomic selection programs. The described method, although demonstrated in inbred chicken lines, is applicable to all traits in any diploid species, and should prove to be a simple method to identify the majority of genes controlling any complex trait. BioMed Central 2011-06-03 /pmc/articles/PMC3108208/ /pubmed/21645293 http://dx.doi.org/10.1186/1753-6561-5-S4-S14 Text en Copyright ©2011 MacEachern et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Proceedings
MacEachern, Sean
Muir, William M
Crosby, Seth
Cheng, Hans H
Genome-wide identification of allele-specific expression (ASE) in response to Marek’s disease virus infection using next generation sequencing
title Genome-wide identification of allele-specific expression (ASE) in response to Marek’s disease virus infection using next generation sequencing
title_full Genome-wide identification of allele-specific expression (ASE) in response to Marek’s disease virus infection using next generation sequencing
title_fullStr Genome-wide identification of allele-specific expression (ASE) in response to Marek’s disease virus infection using next generation sequencing
title_full_unstemmed Genome-wide identification of allele-specific expression (ASE) in response to Marek’s disease virus infection using next generation sequencing
title_short Genome-wide identification of allele-specific expression (ASE) in response to Marek’s disease virus infection using next generation sequencing
title_sort genome-wide identification of allele-specific expression (ase) in response to marek’s disease virus infection using next generation sequencing
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108208/
https://www.ncbi.nlm.nih.gov/pubmed/21645293
http://dx.doi.org/10.1186/1753-6561-5-S4-S14
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