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Genome-wide proteomic profiling reveals the role of dominance protein expression in heterosis in immature maize ears

Heterosis refers to the phenomenon in which hybrid progeny show superior performance relative to their parents. Early maize ear development shows strong heterosis in ear architecture traits and greatly affects grain yield. To explore the underlying molecular mechanisms, genome-wide proteomics of imm...

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Autores principales: Hu, Xiaojiao, Wang, Hongwu, Li, Kun, Wu, Yujin, Liu, Zhifang, Huang, Changling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700959/
https://www.ncbi.nlm.nih.gov/pubmed/29170427
http://dx.doi.org/10.1038/s41598-017-15985-3
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author Hu, Xiaojiao
Wang, Hongwu
Li, Kun
Wu, Yujin
Liu, Zhifang
Huang, Changling
author_facet Hu, Xiaojiao
Wang, Hongwu
Li, Kun
Wu, Yujin
Liu, Zhifang
Huang, Changling
author_sort Hu, Xiaojiao
collection PubMed
description Heterosis refers to the phenomenon in which hybrid progeny show superior performance relative to their parents. Early maize ear development shows strong heterosis in ear architecture traits and greatly affects grain yield. To explore the underlying molecular mechanisms, genome-wide proteomics of immature ears of maize hybrid ZD909 and its parents were analyzed using tandem mass tag (TMT) technology. A total of 9,713 proteins were identified in all three genotypes. Among them, 3,752 (38.6%) proteins were differentially expressed between ZD909 and its parents. Multiple modes of protein action were discovered in the hybrid, while dominance expression patterns accounted for 63.6% of the total differentially expressed proteins (DEPs). Protein pathway enrichment analysis revealed that high parent dominance proteins mainly participated in carbon metabolism and nitrogen assimilation processes. Our results suggested that the dominant expression of favorable alleles related to C/N metabolism in the hybrid may be essential for ZD909 ear growth and heterosis formation. Integrated analysis of proteomic and quantitative trait locus (QTL) data further support our DEP identification and provide useful information for the discovery of genes associated with ear development. Our study provides comprehensive insight into the molecular mechanisms underlying heterosis in immature maize ears from a proteomic perspective.
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spelling pubmed-57009592017-11-30 Genome-wide proteomic profiling reveals the role of dominance protein expression in heterosis in immature maize ears Hu, Xiaojiao Wang, Hongwu Li, Kun Wu, Yujin Liu, Zhifang Huang, Changling Sci Rep Article Heterosis refers to the phenomenon in which hybrid progeny show superior performance relative to their parents. Early maize ear development shows strong heterosis in ear architecture traits and greatly affects grain yield. To explore the underlying molecular mechanisms, genome-wide proteomics of immature ears of maize hybrid ZD909 and its parents were analyzed using tandem mass tag (TMT) technology. A total of 9,713 proteins were identified in all three genotypes. Among them, 3,752 (38.6%) proteins were differentially expressed between ZD909 and its parents. Multiple modes of protein action were discovered in the hybrid, while dominance expression patterns accounted for 63.6% of the total differentially expressed proteins (DEPs). Protein pathway enrichment analysis revealed that high parent dominance proteins mainly participated in carbon metabolism and nitrogen assimilation processes. Our results suggested that the dominant expression of favorable alleles related to C/N metabolism in the hybrid may be essential for ZD909 ear growth and heterosis formation. Integrated analysis of proteomic and quantitative trait locus (QTL) data further support our DEP identification and provide useful information for the discovery of genes associated with ear development. Our study provides comprehensive insight into the molecular mechanisms underlying heterosis in immature maize ears from a proteomic perspective. Nature Publishing Group UK 2017-11-23 /pmc/articles/PMC5700959/ /pubmed/29170427 http://dx.doi.org/10.1038/s41598-017-15985-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hu, Xiaojiao
Wang, Hongwu
Li, Kun
Wu, Yujin
Liu, Zhifang
Huang, Changling
Genome-wide proteomic profiling reveals the role of dominance protein expression in heterosis in immature maize ears
title Genome-wide proteomic profiling reveals the role of dominance protein expression in heterosis in immature maize ears
title_full Genome-wide proteomic profiling reveals the role of dominance protein expression in heterosis in immature maize ears
title_fullStr Genome-wide proteomic profiling reveals the role of dominance protein expression in heterosis in immature maize ears
title_full_unstemmed Genome-wide proteomic profiling reveals the role of dominance protein expression in heterosis in immature maize ears
title_short Genome-wide proteomic profiling reveals the role of dominance protein expression in heterosis in immature maize ears
title_sort genome-wide proteomic profiling reveals the role of dominance protein expression in heterosis in immature maize ears
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700959/
https://www.ncbi.nlm.nih.gov/pubmed/29170427
http://dx.doi.org/10.1038/s41598-017-15985-3
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