Cargando…

Transcriptome shock invokes disruption of parental expression-conserved genes in tetraploid wheat

Allopolyploidy often triggers phenotypic novelty and gene expression remolding in the resulting polyploids. In this study, we employed multiple phenotypic and genetic approaches to investigate the nature and consequences of allotetraploidization between A- and S-subgenome of tetraploid wheat. Result...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Huakun, Gou, Xiaowan, Zhang, Ai, Wang, Xutong, Zhao, Na, Dong, Yuzhu, Li, Linfeng, Liu, Bao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873831/
https://www.ncbi.nlm.nih.gov/pubmed/27198893
http://dx.doi.org/10.1038/srep26363
_version_ 1782432950610034688
author Zhang, Huakun
Gou, Xiaowan
Zhang, Ai
Wang, Xutong
Zhao, Na
Dong, Yuzhu
Li, Linfeng
Liu, Bao
author_facet Zhang, Huakun
Gou, Xiaowan
Zhang, Ai
Wang, Xutong
Zhao, Na
Dong, Yuzhu
Li, Linfeng
Liu, Bao
author_sort Zhang, Huakun
collection PubMed
description Allopolyploidy often triggers phenotypic novelty and gene expression remolding in the resulting polyploids. In this study, we employed multiple phenotypic and genetic approaches to investigate the nature and consequences of allotetraploidization between A- and S-subgenome of tetraploid wheat. Results showed that karyotype of the nascent allopolyploid plants (AT2) is stable but they showed clear novelty in multiple morphological traits which might have positively contributed to the initial establishment of the tetraploids. Further microarray-based transcriptome profiling and gene-specific cDNA-pyrosequencing have documented that transcriptome shock was exceptionally strong in AT2, but a substantial proportion of the induced expression changes was rapidly stabilized in early generations. Meanwhile, both additive and nonadditive expression genes showed extensive homeolog expression remodeling and which have led to the subgenome expression dominance in leaf and young inflorescence of AT2. Through comparing the homeolog-expressing patterns between synthetic and natural tetraploid wheats, it appears that the shock-induced expression changes at both the total expression level and subgenome homeolog partitioning are evolutionarily persistent. Together, our study shed new light on how gene expression changes have rapidly occurred at the initial stage following allotetraploidization, as well as their evolutionary relevance, which may have implications for wheat improvements.
format Online
Article
Text
id pubmed-4873831
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-48738312016-06-03 Transcriptome shock invokes disruption of parental expression-conserved genes in tetraploid wheat Zhang, Huakun Gou, Xiaowan Zhang, Ai Wang, Xutong Zhao, Na Dong, Yuzhu Li, Linfeng Liu, Bao Sci Rep Article Allopolyploidy often triggers phenotypic novelty and gene expression remolding in the resulting polyploids. In this study, we employed multiple phenotypic and genetic approaches to investigate the nature and consequences of allotetraploidization between A- and S-subgenome of tetraploid wheat. Results showed that karyotype of the nascent allopolyploid plants (AT2) is stable but they showed clear novelty in multiple morphological traits which might have positively contributed to the initial establishment of the tetraploids. Further microarray-based transcriptome profiling and gene-specific cDNA-pyrosequencing have documented that transcriptome shock was exceptionally strong in AT2, but a substantial proportion of the induced expression changes was rapidly stabilized in early generations. Meanwhile, both additive and nonadditive expression genes showed extensive homeolog expression remodeling and which have led to the subgenome expression dominance in leaf and young inflorescence of AT2. Through comparing the homeolog-expressing patterns between synthetic and natural tetraploid wheats, it appears that the shock-induced expression changes at both the total expression level and subgenome homeolog partitioning are evolutionarily persistent. Together, our study shed new light on how gene expression changes have rapidly occurred at the initial stage following allotetraploidization, as well as their evolutionary relevance, which may have implications for wheat improvements. Nature Publishing Group 2016-05-20 /pmc/articles/PMC4873831/ /pubmed/27198893 http://dx.doi.org/10.1038/srep26363 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhang, Huakun
Gou, Xiaowan
Zhang, Ai
Wang, Xutong
Zhao, Na
Dong, Yuzhu
Li, Linfeng
Liu, Bao
Transcriptome shock invokes disruption of parental expression-conserved genes in tetraploid wheat
title Transcriptome shock invokes disruption of parental expression-conserved genes in tetraploid wheat
title_full Transcriptome shock invokes disruption of parental expression-conserved genes in tetraploid wheat
title_fullStr Transcriptome shock invokes disruption of parental expression-conserved genes in tetraploid wheat
title_full_unstemmed Transcriptome shock invokes disruption of parental expression-conserved genes in tetraploid wheat
title_short Transcriptome shock invokes disruption of parental expression-conserved genes in tetraploid wheat
title_sort transcriptome shock invokes disruption of parental expression-conserved genes in tetraploid wheat
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873831/
https://www.ncbi.nlm.nih.gov/pubmed/27198893
http://dx.doi.org/10.1038/srep26363
work_keys_str_mv AT zhanghuakun transcriptomeshockinvokesdisruptionofparentalexpressionconservedgenesintetraploidwheat
AT gouxiaowan transcriptomeshockinvokesdisruptionofparentalexpressionconservedgenesintetraploidwheat
AT zhangai transcriptomeshockinvokesdisruptionofparentalexpressionconservedgenesintetraploidwheat
AT wangxutong transcriptomeshockinvokesdisruptionofparentalexpressionconservedgenesintetraploidwheat
AT zhaona transcriptomeshockinvokesdisruptionofparentalexpressionconservedgenesintetraploidwheat
AT dongyuzhu transcriptomeshockinvokesdisruptionofparentalexpressionconservedgenesintetraploidwheat
AT lilinfeng transcriptomeshockinvokesdisruptionofparentalexpressionconservedgenesintetraploidwheat
AT liubao transcriptomeshockinvokesdisruptionofparentalexpressionconservedgenesintetraploidwheat