Cargando…
Transcriptome profiling of two maize inbreds with distinct responses to Gibberella ear rot disease to identify candidate resistance genes
BACKGROUND: Gibberella ear rot (GER) is one of the most economically important fungal diseases of maize in the temperate zone due to moldy grain contaminated with health threatening mycotoxins. To develop resistant genotypes and control the disease, understanding the host-pathogen interaction is ess...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5807830/ https://www.ncbi.nlm.nih.gov/pubmed/29426290 http://dx.doi.org/10.1186/s12864-018-4513-4 |
_version_ | 1783299354136674304 |
---|---|
author | Kebede, Aida Z. Johnston, Anne Schneiderman, Danielle Bosnich, Whynn Harris, Linda J. |
author_facet | Kebede, Aida Z. Johnston, Anne Schneiderman, Danielle Bosnich, Whynn Harris, Linda J. |
author_sort | Kebede, Aida Z. |
collection | PubMed |
description | BACKGROUND: Gibberella ear rot (GER) is one of the most economically important fungal diseases of maize in the temperate zone due to moldy grain contaminated with health threatening mycotoxins. To develop resistant genotypes and control the disease, understanding the host-pathogen interaction is essential. RESULTS: RNA-Seq-derived transcriptome profiles of fungal- and mock-inoculated developing kernel tissues of two maize inbred lines were used to identify differentially expressed transcripts and propose candidate genes mapping within GER resistance quantitative trait loci (QTL). A total of 1255 transcripts were significantly (P ≤ 0.05) up regulated due to fungal infection in both susceptible and resistant inbreds. A greater number of transcripts were up regulated in the former (1174) than the latter (497) and increased as the infection progressed from 1 to 2 days after inoculation. Focusing on differentially expressed genes located within QTL regions for GER resistance, we identified 81 genes involved in membrane transport, hormone regulation, cell wall modification, cell detoxification, and biosynthesis of pathogenesis related proteins and phytoalexins as candidate genes contributing to resistance. Applying droplet digital PCR, we validated the expression profiles of a subset of these candidate genes from QTL regions contributed by the resistant inbred on chromosomes 1, 2 and 9. CONCLUSION: By screening global gene expression profiles for differentially expressed genes mapping within resistance QTL regions, we have identified candidate genes for gibberella ear rot resistance on several maize chromosomes which could potentially lead to a better understanding of Fusarium resistance mechanisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4513-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5807830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58078302018-02-15 Transcriptome profiling of two maize inbreds with distinct responses to Gibberella ear rot disease to identify candidate resistance genes Kebede, Aida Z. Johnston, Anne Schneiderman, Danielle Bosnich, Whynn Harris, Linda J. BMC Genomics Research Article BACKGROUND: Gibberella ear rot (GER) is one of the most economically important fungal diseases of maize in the temperate zone due to moldy grain contaminated with health threatening mycotoxins. To develop resistant genotypes and control the disease, understanding the host-pathogen interaction is essential. RESULTS: RNA-Seq-derived transcriptome profiles of fungal- and mock-inoculated developing kernel tissues of two maize inbred lines were used to identify differentially expressed transcripts and propose candidate genes mapping within GER resistance quantitative trait loci (QTL). A total of 1255 transcripts were significantly (P ≤ 0.05) up regulated due to fungal infection in both susceptible and resistant inbreds. A greater number of transcripts were up regulated in the former (1174) than the latter (497) and increased as the infection progressed from 1 to 2 days after inoculation. Focusing on differentially expressed genes located within QTL regions for GER resistance, we identified 81 genes involved in membrane transport, hormone regulation, cell wall modification, cell detoxification, and biosynthesis of pathogenesis related proteins and phytoalexins as candidate genes contributing to resistance. Applying droplet digital PCR, we validated the expression profiles of a subset of these candidate genes from QTL regions contributed by the resistant inbred on chromosomes 1, 2 and 9. CONCLUSION: By screening global gene expression profiles for differentially expressed genes mapping within resistance QTL regions, we have identified candidate genes for gibberella ear rot resistance on several maize chromosomes which could potentially lead to a better understanding of Fusarium resistance mechanisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4513-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-09 /pmc/articles/PMC5807830/ /pubmed/29426290 http://dx.doi.org/10.1186/s12864-018-4513-4 Text en © The Author(s). 2018 Open AccessThis article is 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 you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kebede, Aida Z. Johnston, Anne Schneiderman, Danielle Bosnich, Whynn Harris, Linda J. Transcriptome profiling of two maize inbreds with distinct responses to Gibberella ear rot disease to identify candidate resistance genes |
title | Transcriptome profiling of two maize inbreds with distinct responses to Gibberella ear rot disease to identify candidate resistance genes |
title_full | Transcriptome profiling of two maize inbreds with distinct responses to Gibberella ear rot disease to identify candidate resistance genes |
title_fullStr | Transcriptome profiling of two maize inbreds with distinct responses to Gibberella ear rot disease to identify candidate resistance genes |
title_full_unstemmed | Transcriptome profiling of two maize inbreds with distinct responses to Gibberella ear rot disease to identify candidate resistance genes |
title_short | Transcriptome profiling of two maize inbreds with distinct responses to Gibberella ear rot disease to identify candidate resistance genes |
title_sort | transcriptome profiling of two maize inbreds with distinct responses to gibberella ear rot disease to identify candidate resistance genes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5807830/ https://www.ncbi.nlm.nih.gov/pubmed/29426290 http://dx.doi.org/10.1186/s12864-018-4513-4 |
work_keys_str_mv | AT kebedeaidaz transcriptomeprofilingoftwomaizeinbredswithdistinctresponsestogibberellaearrotdiseasetoidentifycandidateresistancegenes AT johnstonanne transcriptomeprofilingoftwomaizeinbredswithdistinctresponsestogibberellaearrotdiseasetoidentifycandidateresistancegenes AT schneidermandanielle transcriptomeprofilingoftwomaizeinbredswithdistinctresponsestogibberellaearrotdiseasetoidentifycandidateresistancegenes AT bosnichwhynn transcriptomeprofilingoftwomaizeinbredswithdistinctresponsestogibberellaearrotdiseasetoidentifycandidateresistancegenes AT harrislindaj transcriptomeprofilingoftwomaizeinbredswithdistinctresponsestogibberellaearrotdiseasetoidentifycandidateresistancegenes |