Cargando…

Transgressive and parental dominant gene expression and cytosine methylation during seed development in Brassica napus hybrids

KEY MESSAGE: Transcriptomic and epigenomic profiling of gene expression and small RNAs during seed and seedling development reveals expression and methylation dominance levels with implications on early stage heterosis in oilseed rape. ABSTRACT: The enhanced performance of hybrids through heterosis...

Descripción completa

Detalles Bibliográficos
Autores principales: Orantes-Bonilla, Mauricio, Wang, Hao, Lee, Huey Tyng, Golicz, Agnieszka A., Hu, Dandan, Li, Wenwen, Zou, Jun, Snowdon, Rod J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113308/
https://www.ncbi.nlm.nih.gov/pubmed/37071201
http://dx.doi.org/10.1007/s00122-023-04345-7
_version_ 1785027811544662016
author Orantes-Bonilla, Mauricio
Wang, Hao
Lee, Huey Tyng
Golicz, Agnieszka A.
Hu, Dandan
Li, Wenwen
Zou, Jun
Snowdon, Rod J.
author_facet Orantes-Bonilla, Mauricio
Wang, Hao
Lee, Huey Tyng
Golicz, Agnieszka A.
Hu, Dandan
Li, Wenwen
Zou, Jun
Snowdon, Rod J.
author_sort Orantes-Bonilla, Mauricio
collection PubMed
description KEY MESSAGE: Transcriptomic and epigenomic profiling of gene expression and small RNAs during seed and seedling development reveals expression and methylation dominance levels with implications on early stage heterosis in oilseed rape. ABSTRACT: The enhanced performance of hybrids through heterosis remains a key aspect in plant breeding; however, the underlying mechanisms are still not fully elucidated. To investigate the potential role of transcriptomic and epigenomic patterns in early expression of hybrid vigor, we investigated gene expression, small RNA abundance and genome-wide methylation in hybrids from two distant Brassica napus ecotypes during seed and seedling developmental stages using next-generation sequencing. A total of 31117, 344, 36229 and 7399 differentially expressed genes, microRNAs, small interfering RNAs and differentially methylated regions were identified, respectively. Approximately 70% of the differentially expressed or methylated features displayed parental dominance levels where the hybrid followed the same patterns as the parents. Via gene ontology enrichment and microRNA-target association analyses during seed development, we found copies of reproductive, developmental and meiotic genes with transgressive and paternal dominance patterns. Interestingly, maternal dominance was more prominent in hypermethylated and downregulated features during seed formation, contrasting to the general maternal gamete demethylation reported during gametogenesis in angiosperms. Associations between methylation and gene expression allowed identification of putative epialleles with diverse pivotal biological functions during seed formation. Furthermore, most differentially methylated regions, differentially expressed siRNAs and transposable elements were in regions that flanked genes without differential expression. This suggests that differential expression and methylation of epigenomic features may help maintain expression of pivotal genes in a hybrid context. Differential expression and methylation patterns during seed formation in an F(1) hybrid provide novel insights into genes and mechanisms with potential roles in early heterosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00122-023-04345-7.
format Online
Article
Text
id pubmed-10113308
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-101133082023-04-20 Transgressive and parental dominant gene expression and cytosine methylation during seed development in Brassica napus hybrids Orantes-Bonilla, Mauricio Wang, Hao Lee, Huey Tyng Golicz, Agnieszka A. Hu, Dandan Li, Wenwen Zou, Jun Snowdon, Rod J. Theor Appl Genet Original Article KEY MESSAGE: Transcriptomic and epigenomic profiling of gene expression and small RNAs during seed and seedling development reveals expression and methylation dominance levels with implications on early stage heterosis in oilseed rape. ABSTRACT: The enhanced performance of hybrids through heterosis remains a key aspect in plant breeding; however, the underlying mechanisms are still not fully elucidated. To investigate the potential role of transcriptomic and epigenomic patterns in early expression of hybrid vigor, we investigated gene expression, small RNA abundance and genome-wide methylation in hybrids from two distant Brassica napus ecotypes during seed and seedling developmental stages using next-generation sequencing. A total of 31117, 344, 36229 and 7399 differentially expressed genes, microRNAs, small interfering RNAs and differentially methylated regions were identified, respectively. Approximately 70% of the differentially expressed or methylated features displayed parental dominance levels where the hybrid followed the same patterns as the parents. Via gene ontology enrichment and microRNA-target association analyses during seed development, we found copies of reproductive, developmental and meiotic genes with transgressive and paternal dominance patterns. Interestingly, maternal dominance was more prominent in hypermethylated and downregulated features during seed formation, contrasting to the general maternal gamete demethylation reported during gametogenesis in angiosperms. Associations between methylation and gene expression allowed identification of putative epialleles with diverse pivotal biological functions during seed formation. Furthermore, most differentially methylated regions, differentially expressed siRNAs and transposable elements were in regions that flanked genes without differential expression. This suggests that differential expression and methylation of epigenomic features may help maintain expression of pivotal genes in a hybrid context. Differential expression and methylation patterns during seed formation in an F(1) hybrid provide novel insights into genes and mechanisms with potential roles in early heterosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00122-023-04345-7. Springer Berlin Heidelberg 2023-04-18 2023 /pmc/articles/PMC10113308/ /pubmed/37071201 http://dx.doi.org/10.1007/s00122-023-04345-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Orantes-Bonilla, Mauricio
Wang, Hao
Lee, Huey Tyng
Golicz, Agnieszka A.
Hu, Dandan
Li, Wenwen
Zou, Jun
Snowdon, Rod J.
Transgressive and parental dominant gene expression and cytosine methylation during seed development in Brassica napus hybrids
title Transgressive and parental dominant gene expression and cytosine methylation during seed development in Brassica napus hybrids
title_full Transgressive and parental dominant gene expression and cytosine methylation during seed development in Brassica napus hybrids
title_fullStr Transgressive and parental dominant gene expression and cytosine methylation during seed development in Brassica napus hybrids
title_full_unstemmed Transgressive and parental dominant gene expression and cytosine methylation during seed development in Brassica napus hybrids
title_short Transgressive and parental dominant gene expression and cytosine methylation during seed development in Brassica napus hybrids
title_sort transgressive and parental dominant gene expression and cytosine methylation during seed development in brassica napus hybrids
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10113308/
https://www.ncbi.nlm.nih.gov/pubmed/37071201
http://dx.doi.org/10.1007/s00122-023-04345-7
work_keys_str_mv AT orantesbonillamauricio transgressiveandparentaldominantgeneexpressionandcytosinemethylationduringseeddevelopmentinbrassicanapushybrids
AT wanghao transgressiveandparentaldominantgeneexpressionandcytosinemethylationduringseeddevelopmentinbrassicanapushybrids
AT leehueytyng transgressiveandparentaldominantgeneexpressionandcytosinemethylationduringseeddevelopmentinbrassicanapushybrids
AT goliczagnieszkaa transgressiveandparentaldominantgeneexpressionandcytosinemethylationduringseeddevelopmentinbrassicanapushybrids
AT hudandan transgressiveandparentaldominantgeneexpressionandcytosinemethylationduringseeddevelopmentinbrassicanapushybrids
AT liwenwen transgressiveandparentaldominantgeneexpressionandcytosinemethylationduringseeddevelopmentinbrassicanapushybrids
AT zoujun transgressiveandparentaldominantgeneexpressionandcytosinemethylationduringseeddevelopmentinbrassicanapushybrids
AT snowdonrodj transgressiveandparentaldominantgeneexpressionandcytosinemethylationduringseeddevelopmentinbrassicanapushybrids