Systems genomics of salinity stress response in rice

Populations can adapt to stressful environments through changes in gene expression. However, the fitness effect of gene expression in mediating stress response and adaptation remains largely unexplored. Here, we use an integrative field dataset obtained from 780 plants of <i>Oryza sativa</i> ssp. <i>indica</i> (rice) grown in a field experiment under normal or moderate salt stress conditions to examine selection and evolution of gene expression variation under salinity stress conditions. We find that salinity stress induces increased selective pressure on gene expression. Further, we show that <i>trans</i>-eQTLs rather than <i>cis</i>-eQTLs are primarily associated with rice's gene expression under salinity stress, potentially via a few master-regulators. Importantly, and contrary to the expectations, we find that <i>cis-trans</i> reinforcement is more common than <i>cis-trans</i> compensation which may be reflective of rice diversification subsequent to domestication. We further identify genetic fixation as the likely mechanism underlying this compensation/reinforcement. Additionally, we show that <i>cis</i>- and <i>trans</i>-eQTLs are under balancing and purifying selection, respectively, giving us insights into the evolutionary dynamics of gene expression variation. By examining genomic, transcriptomic, and phenotypic variation across a rice population, we gain insights into the molecular and genetic landscape underlying adaptive salinity stress responses, which is relevant for other crops and other stresses.

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Publication Details

Journal
eLife
Published
2024-08-19
DOI
https://doi.org/10.7554/elife.99352
Citations
4
Primary Topic
Plant Stress Responses and Tolerance
Type
article
Field-Weighted Citation Impact
2.40

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article

Systems genomics of salinity stress response in rice

A.G. Sajise, Maricris Zaidem, Simon C. Groen, Michael D. Purugganan et al.
4 citations
eLife
Plant Stress Responses and Tolerance
2.40
article

Systems genomics of salinity stress response in rice

A.G. Sajise, Maricris Zaidem, Simon C. Groen, Michael D. Purugganan, Zoé Joly‐Lopez, Steven J. Franks, Rahul Satija, Mignon A. Natividad, Rakesh K. Singh, Sonal Gupta, Irina Ćalić, Georgina V. Vergara
article en
4 citations

Abstract

Populations can adapt to stressful environments through changes in gene expression. However, the fitness effect of gene expression in mediating stress response and adaptation remains largely unexplored. Here, we use an integrative field dataset obtained from 780 plants of <i>Oryza sativa</i> ssp. <i>indica</i> (rice) grown in a field experiment under normal or moderate salt stress conditions to examine selection and evolution of gene expression variation under salinity stress conditions. We find that salinity stress induces increased selective pressure on gene expression. Further, we show that <i>trans</i>-eQTLs rather than <i>cis</i>-eQTLs are primarily associated with rice's gene expression under salinity stress, potentially via a few master-regulators. Importantly, and contrary to the expectations, we find that <i>cis-trans</i> reinforcement is more common than <i>cis-trans</i> compensation which may be reflective of rice diversification subsequent to domestication. We further identify genetic fixation as the likely mechanism underlying this compensation/reinforcement. Additionally, we show that <i>cis</i>- and <i>trans</i>-eQTLs are under balancing and purifying selection, respectively, giving us insights into the evolutionary dynamics of gene expression variation. By examining genomic, transcriptomic, and phenotypic variation across a rice population, we gain insights into the molecular and genetic landscape underlying adaptive salinity stress responses, which is relevant for other crops and other stresses.

eLifeVol. 13
University of California, Riverside (US), University of the Philippines System (PH), Université du Québec à Montréal (CA), International Rice Research Institute (PH), Fordham University (US), University of Oxford (GB), Inari Agriculture (United States) (US), New York Genome Center (US), International Center for Biosaline Agriculture (AE), New York University (US)
National Science Foundation, Gordon and Betty Moore Foundation, Life Sciences Research Foundation, Fordham University, Zegar Family Foundation, York University, Canada Research Chairs, Heinrich-Heine-Universität Düsseldorf, National Institutes of Health, University of California, Riverside, Natural Sciences and Engineering Research Council of Canada, National Institute of General Medical Sciences
Zero hunger
Openalex Percentile: Top 11%
Plant Stress Responses and Tolerance
2.40
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