Cargando…

Genome-Wide Association and Gene Co-expression Network Analyses Reveal Complex Genetics of Resistance to Goss’s Wilt of Maize

Goss’s bacterial wilt and leaf blight is a disease of maize caused by the gram positive bacterium Clavibacter michiganensis subsp. nebraskensis (Cmn). First discovered in Nebraska, Goss’s wilt has now spread to major maize growing states in the United States and three provinces in Canada. Previous s...

Descripción completa

Detalles Bibliográficos
Autores principales: Singh, Amritpal, Li, Guangyong, Brohammer, Alex B., Jarquin, Diego, Hirsch, Candice N., Alfano, James R., Lorenz, Aaron J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6778796/
https://www.ncbi.nlm.nih.gov/pubmed/31362973
http://dx.doi.org/10.1534/g3.119.400347
_version_ 1783456823494311936
author Singh, Amritpal
Li, Guangyong
Brohammer, Alex B.
Jarquin, Diego
Hirsch, Candice N.
Alfano, James R.
Lorenz, Aaron J.
author_facet Singh, Amritpal
Li, Guangyong
Brohammer, Alex B.
Jarquin, Diego
Hirsch, Candice N.
Alfano, James R.
Lorenz, Aaron J.
author_sort Singh, Amritpal
collection PubMed
description Goss’s bacterial wilt and leaf blight is a disease of maize caused by the gram positive bacterium Clavibacter michiganensis subsp. nebraskensis (Cmn). First discovered in Nebraska, Goss’s wilt has now spread to major maize growing states in the United States and three provinces in Canada. Previous studies conducted using elite maize inbred lines and their hybrids have shown that resistance to Goss’s wilt is a quantitative trait. The objective of this study was to further our understanding of the genetic basis of resistance to Goss’s wilt by using a combined approach of genome-wide association mapping and gene co-expression network analysis. Genome-wide association analysis was accomplished using a diversity panel consisting of 555 maize inbred lines and a set of 450 recombinant inbred lines (RILs) from three bi-parental mapping populations, providing the most comprehensive screening of Goss’s wilt resistance to date. Three SNPs in the diversity panel and 10 SNPs in the combined dataset, including the diversity panel and RILs, were found to be significantly associated with Goss’s wilt resistance. Each significant SNP explained 1–5% of the phenotypic variation for Goss’s wilt (total of 8–11%). To augment the results of genome-wide association mapping and help identify candidate genes, a time course RNA sequencing experiment was conducted using resistant (N551) and susceptible (B14A) maize inbred lines. Gene co-expression network analysis of this time course experiment identified one module of 141 correlated genes that showed differential regulation in response to Cmn inoculations in both resistant and susceptible lines. SNPs inside and flanking these genes explained 13.3% of the phenotypic variation. Among 1,000 random samples of genes, only 8% of samples explained more phenotypic variance for Goss’s wilt resistance than those implicated by the co-expression network analysis. While a statistically significant enrichment was not observed (P < 0.05), these results suggest a possible role for these genes in quantitative resistance at the field level and warrant more research on combining gene co-expression network analysis with quantitative genetic analyses to dissect complex disease resistance traits. The results of the GWAS and co-expression analysis both support the complex nature of resistance to this important disease of maize.
format Online
Article
Text
id pubmed-6778796
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Genetics Society of America
record_format MEDLINE/PubMed
spelling pubmed-67787962019-10-07 Genome-Wide Association and Gene Co-expression Network Analyses Reveal Complex Genetics of Resistance to Goss’s Wilt of Maize Singh, Amritpal Li, Guangyong Brohammer, Alex B. Jarquin, Diego Hirsch, Candice N. Alfano, James R. Lorenz, Aaron J. G3 (Bethesda) Investigations Goss’s bacterial wilt and leaf blight is a disease of maize caused by the gram positive bacterium Clavibacter michiganensis subsp. nebraskensis (Cmn). First discovered in Nebraska, Goss’s wilt has now spread to major maize growing states in the United States and three provinces in Canada. Previous studies conducted using elite maize inbred lines and their hybrids have shown that resistance to Goss’s wilt is a quantitative trait. The objective of this study was to further our understanding of the genetic basis of resistance to Goss’s wilt by using a combined approach of genome-wide association mapping and gene co-expression network analysis. Genome-wide association analysis was accomplished using a diversity panel consisting of 555 maize inbred lines and a set of 450 recombinant inbred lines (RILs) from three bi-parental mapping populations, providing the most comprehensive screening of Goss’s wilt resistance to date. Three SNPs in the diversity panel and 10 SNPs in the combined dataset, including the diversity panel and RILs, were found to be significantly associated with Goss’s wilt resistance. Each significant SNP explained 1–5% of the phenotypic variation for Goss’s wilt (total of 8–11%). To augment the results of genome-wide association mapping and help identify candidate genes, a time course RNA sequencing experiment was conducted using resistant (N551) and susceptible (B14A) maize inbred lines. Gene co-expression network analysis of this time course experiment identified one module of 141 correlated genes that showed differential regulation in response to Cmn inoculations in both resistant and susceptible lines. SNPs inside and flanking these genes explained 13.3% of the phenotypic variation. Among 1,000 random samples of genes, only 8% of samples explained more phenotypic variance for Goss’s wilt resistance than those implicated by the co-expression network analysis. While a statistically significant enrichment was not observed (P < 0.05), these results suggest a possible role for these genes in quantitative resistance at the field level and warrant more research on combining gene co-expression network analysis with quantitative genetic analyses to dissect complex disease resistance traits. The results of the GWAS and co-expression analysis both support the complex nature of resistance to this important disease of maize. Genetics Society of America 2019-07-30 /pmc/articles/PMC6778796/ /pubmed/31362973 http://dx.doi.org/10.1534/g3.119.400347 Text en Copyright © 2019 Singh et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Singh, Amritpal
Li, Guangyong
Brohammer, Alex B.
Jarquin, Diego
Hirsch, Candice N.
Alfano, James R.
Lorenz, Aaron J.
Genome-Wide Association and Gene Co-expression Network Analyses Reveal Complex Genetics of Resistance to Goss’s Wilt of Maize
title Genome-Wide Association and Gene Co-expression Network Analyses Reveal Complex Genetics of Resistance to Goss’s Wilt of Maize
title_full Genome-Wide Association and Gene Co-expression Network Analyses Reveal Complex Genetics of Resistance to Goss’s Wilt of Maize
title_fullStr Genome-Wide Association and Gene Co-expression Network Analyses Reveal Complex Genetics of Resistance to Goss’s Wilt of Maize
title_full_unstemmed Genome-Wide Association and Gene Co-expression Network Analyses Reveal Complex Genetics of Resistance to Goss’s Wilt of Maize
title_short Genome-Wide Association and Gene Co-expression Network Analyses Reveal Complex Genetics of Resistance to Goss’s Wilt of Maize
title_sort genome-wide association and gene co-expression network analyses reveal complex genetics of resistance to goss’s wilt of maize
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6778796/
https://www.ncbi.nlm.nih.gov/pubmed/31362973
http://dx.doi.org/10.1534/g3.119.400347
work_keys_str_mv AT singhamritpal genomewideassociationandgenecoexpressionnetworkanalysesrevealcomplexgeneticsofresistancetogossswiltofmaize
AT liguangyong genomewideassociationandgenecoexpressionnetworkanalysesrevealcomplexgeneticsofresistancetogossswiltofmaize
AT brohammeralexb genomewideassociationandgenecoexpressionnetworkanalysesrevealcomplexgeneticsofresistancetogossswiltofmaize
AT jarquindiego genomewideassociationandgenecoexpressionnetworkanalysesrevealcomplexgeneticsofresistancetogossswiltofmaize
AT hirschcandicen genomewideassociationandgenecoexpressionnetworkanalysesrevealcomplexgeneticsofresistancetogossswiltofmaize
AT alfanojamesr genomewideassociationandgenecoexpressionnetworkanalysesrevealcomplexgeneticsofresistancetogossswiltofmaize
AT lorenzaaronj genomewideassociationandgenecoexpressionnetworkanalysesrevealcomplexgeneticsofresistancetogossswiltofmaize