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Asymmetric gene expression in grain development of reciprocal crosses between tetraploid and hexaploid wheats

Production of viable progeny from interploid crosses requires precise regulation of gene expression from maternal and paternal chromosomes, yet the transcripts contributed to hybrid seeds from polyploid parent species have rarely been explored. To investigate the genome-wide maternal and paternal co...

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Autores principales: Jia, Zhen, Gao, Peng, Yin, Feifan, Quilichini, Teagen D., Sheng, Huajin, Song, Jingpu, Yang, Hui, Gao, Jie, Chen, Ting, Yang, Bo, Kochian, Leon V., Zou, Jitao, Patterson, Nii, Yang, Qingyong, Gillmor, C. Stewart, Datla, Raju, Li, Qiang, Xiang, Daoquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789062/
https://www.ncbi.nlm.nih.gov/pubmed/36564439
http://dx.doi.org/10.1038/s42003-022-04374-w
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author Jia, Zhen
Gao, Peng
Yin, Feifan
Quilichini, Teagen D.
Sheng, Huajin
Song, Jingpu
Yang, Hui
Gao, Jie
Chen, Ting
Yang, Bo
Kochian, Leon V.
Zou, Jitao
Patterson, Nii
Yang, Qingyong
Gillmor, C. Stewart
Datla, Raju
Li, Qiang
Xiang, Daoquan
author_facet Jia, Zhen
Gao, Peng
Yin, Feifan
Quilichini, Teagen D.
Sheng, Huajin
Song, Jingpu
Yang, Hui
Gao, Jie
Chen, Ting
Yang, Bo
Kochian, Leon V.
Zou, Jitao
Patterson, Nii
Yang, Qingyong
Gillmor, C. Stewart
Datla, Raju
Li, Qiang
Xiang, Daoquan
author_sort Jia, Zhen
collection PubMed
description Production of viable progeny from interploid crosses requires precise regulation of gene expression from maternal and paternal chromosomes, yet the transcripts contributed to hybrid seeds from polyploid parent species have rarely been explored. To investigate the genome-wide maternal and paternal contributions to polyploid grain development, we analyzed the transcriptomes of developing embryos, from zygote to maturity, alongside endosperm in two stages of development, using reciprocal crosses between tetraploid and hexaploid wheats. Reciprocal crosses between species with varied levels of ploidy displayed broad impacts on gene expression, including shifts in alternative splicing events in select crosses, as illustrated by active splicing events, enhanced protein synthesis and chromatin remodeling. Homoeologous gene expression was repressed on the univalent D genome in pentaploids, but this suppression was attenuated in crosses with a higher ploidy maternal parent. Imprinted genes were identified in endosperm and early embryo tissues, supporting predominant maternal effects on early embryogenesis. By systematically investigating the complex transcriptional networks in reciprocal-cross hybrids, this study presents a framework for understanding the genomic incompatibility and transcriptome shock that results from interspecific hybridization and uncovers the transcriptional impacts on hybrid seeds created from agriculturally-relevant polyploid species.
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spelling pubmed-97890622022-12-25 Asymmetric gene expression in grain development of reciprocal crosses between tetraploid and hexaploid wheats Jia, Zhen Gao, Peng Yin, Feifan Quilichini, Teagen D. Sheng, Huajin Song, Jingpu Yang, Hui Gao, Jie Chen, Ting Yang, Bo Kochian, Leon V. Zou, Jitao Patterson, Nii Yang, Qingyong Gillmor, C. Stewart Datla, Raju Li, Qiang Xiang, Daoquan Commun Biol Article Production of viable progeny from interploid crosses requires precise regulation of gene expression from maternal and paternal chromosomes, yet the transcripts contributed to hybrid seeds from polyploid parent species have rarely been explored. To investigate the genome-wide maternal and paternal contributions to polyploid grain development, we analyzed the transcriptomes of developing embryos, from zygote to maturity, alongside endosperm in two stages of development, using reciprocal crosses between tetraploid and hexaploid wheats. Reciprocal crosses between species with varied levels of ploidy displayed broad impacts on gene expression, including shifts in alternative splicing events in select crosses, as illustrated by active splicing events, enhanced protein synthesis and chromatin remodeling. Homoeologous gene expression was repressed on the univalent D genome in pentaploids, but this suppression was attenuated in crosses with a higher ploidy maternal parent. Imprinted genes were identified in endosperm and early embryo tissues, supporting predominant maternal effects on early embryogenesis. By systematically investigating the complex transcriptional networks in reciprocal-cross hybrids, this study presents a framework for understanding the genomic incompatibility and transcriptome shock that results from interspecific hybridization and uncovers the transcriptional impacts on hybrid seeds created from agriculturally-relevant polyploid species. Nature Publishing Group UK 2022-12-23 /pmc/articles/PMC9789062/ /pubmed/36564439 http://dx.doi.org/10.1038/s42003-022-04374-w Text en © Crown 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jia, Zhen
Gao, Peng
Yin, Feifan
Quilichini, Teagen D.
Sheng, Huajin
Song, Jingpu
Yang, Hui
Gao, Jie
Chen, Ting
Yang, Bo
Kochian, Leon V.
Zou, Jitao
Patterson, Nii
Yang, Qingyong
Gillmor, C. Stewart
Datla, Raju
Li, Qiang
Xiang, Daoquan
Asymmetric gene expression in grain development of reciprocal crosses between tetraploid and hexaploid wheats
title Asymmetric gene expression in grain development of reciprocal crosses between tetraploid and hexaploid wheats
title_full Asymmetric gene expression in grain development of reciprocal crosses between tetraploid and hexaploid wheats
title_fullStr Asymmetric gene expression in grain development of reciprocal crosses between tetraploid and hexaploid wheats
title_full_unstemmed Asymmetric gene expression in grain development of reciprocal crosses between tetraploid and hexaploid wheats
title_short Asymmetric gene expression in grain development of reciprocal crosses between tetraploid and hexaploid wheats
title_sort asymmetric gene expression in grain development of reciprocal crosses between tetraploid and hexaploid wheats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789062/
https://www.ncbi.nlm.nih.gov/pubmed/36564439
http://dx.doi.org/10.1038/s42003-022-04374-w
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