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Unraveling regulatory divergence, heterotic malleability, and allelic imbalance switching in rice due to drought stress

The indica ecotypes, IR64, an elite drought-susceptible variety adapted to irrigated ecosystem, and Apo (IR55423-01 or NSIC RC9), a moderate drought-tolerant upland genotype together with their hybrid (IR64 × Apo) were exposed to non- and water-stress conditions. By sequencing (RNA-seq) these genoty...

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Autores principales: Ereful, Nelzo C., Laurena, Antonio, Liu, Li-Yu, Kao, Shu-Min, Tsai, Eric, Greenland, Andy, Powell, Wayne, Mackay, Ian, Leung, Hei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241847/
https://www.ncbi.nlm.nih.gov/pubmed/34188147
http://dx.doi.org/10.1038/s41598-021-92938-x
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author Ereful, Nelzo C.
Laurena, Antonio
Liu, Li-Yu
Kao, Shu-Min
Tsai, Eric
Greenland, Andy
Powell, Wayne
Mackay, Ian
Leung, Hei
author_facet Ereful, Nelzo C.
Laurena, Antonio
Liu, Li-Yu
Kao, Shu-Min
Tsai, Eric
Greenland, Andy
Powell, Wayne
Mackay, Ian
Leung, Hei
author_sort Ereful, Nelzo C.
collection PubMed
description The indica ecotypes, IR64, an elite drought-susceptible variety adapted to irrigated ecosystem, and Apo (IR55423-01 or NSIC RC9), a moderate drought-tolerant upland genotype together with their hybrid (IR64 × Apo) were exposed to non- and water-stress conditions. By sequencing (RNA-seq) these genotypes, we were able to map genes diverging in cis and/or trans factors. Under non-stress condition, cis dominantly explains (11.2%) regulatory differences, followed by trans (8.9%). Further analysis showed that water-limiting condition largely affects trans and cis + trans factors. On the molecular level, cis and/or trans regulatory divergence explains their genotypic differences and differential drought response. Between the two parental genotypes, Apo appears to exhibit more photosynthetic efficiency even under water-limiting condition and is ascribed to trans. Statistical analyses showed that regulatory divergence is significantly influenced by environmental conditions. Likewise, the mode of parental expression inheritance which drives heterosis (HET) is significantly affected by environmental conditions indicating the malleability of heterosis to external factors. Further analysis revealed that the HET class, dominance, was significantly enriched under water-stress condition. We also identified allelic imbalance switching in which several genes prefer IR64- (or Apo-) specific allele under non-stress condition but switched to Apo- (or IR64-) specific allele when exposed to water-stress condition.
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spelling pubmed-82418472021-07-06 Unraveling regulatory divergence, heterotic malleability, and allelic imbalance switching in rice due to drought stress Ereful, Nelzo C. Laurena, Antonio Liu, Li-Yu Kao, Shu-Min Tsai, Eric Greenland, Andy Powell, Wayne Mackay, Ian Leung, Hei Sci Rep Article The indica ecotypes, IR64, an elite drought-susceptible variety adapted to irrigated ecosystem, and Apo (IR55423-01 or NSIC RC9), a moderate drought-tolerant upland genotype together with their hybrid (IR64 × Apo) were exposed to non- and water-stress conditions. By sequencing (RNA-seq) these genotypes, we were able to map genes diverging in cis and/or trans factors. Under non-stress condition, cis dominantly explains (11.2%) regulatory differences, followed by trans (8.9%). Further analysis showed that water-limiting condition largely affects trans and cis + trans factors. On the molecular level, cis and/or trans regulatory divergence explains their genotypic differences and differential drought response. Between the two parental genotypes, Apo appears to exhibit more photosynthetic efficiency even under water-limiting condition and is ascribed to trans. Statistical analyses showed that regulatory divergence is significantly influenced by environmental conditions. Likewise, the mode of parental expression inheritance which drives heterosis (HET) is significantly affected by environmental conditions indicating the malleability of heterosis to external factors. Further analysis revealed that the HET class, dominance, was significantly enriched under water-stress condition. We also identified allelic imbalance switching in which several genes prefer IR64- (or Apo-) specific allele under non-stress condition but switched to Apo- (or IR64-) specific allele when exposed to water-stress condition. Nature Publishing Group UK 2021-06-29 /pmc/articles/PMC8241847/ /pubmed/34188147 http://dx.doi.org/10.1038/s41598-021-92938-x Text en © Crown 2021 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 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 Article
Ereful, Nelzo C.
Laurena, Antonio
Liu, Li-Yu
Kao, Shu-Min
Tsai, Eric
Greenland, Andy
Powell, Wayne
Mackay, Ian
Leung, Hei
Unraveling regulatory divergence, heterotic malleability, and allelic imbalance switching in rice due to drought stress
title Unraveling regulatory divergence, heterotic malleability, and allelic imbalance switching in rice due to drought stress
title_full Unraveling regulatory divergence, heterotic malleability, and allelic imbalance switching in rice due to drought stress
title_fullStr Unraveling regulatory divergence, heterotic malleability, and allelic imbalance switching in rice due to drought stress
title_full_unstemmed Unraveling regulatory divergence, heterotic malleability, and allelic imbalance switching in rice due to drought stress
title_short Unraveling regulatory divergence, heterotic malleability, and allelic imbalance switching in rice due to drought stress
title_sort unraveling regulatory divergence, heterotic malleability, and allelic imbalance switching in rice due to drought stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241847/
https://www.ncbi.nlm.nih.gov/pubmed/34188147
http://dx.doi.org/10.1038/s41598-021-92938-x
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