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Dynamic effects of interacting genes underlying rice flowering-time phenotypic plasticity and global adaptation
The phenotypic variation of living organisms is shaped by genetics, environment, and their interaction. Understanding phenotypic plasticity under natural conditions is hindered by the apparently complex environment and the interacting genes and pathways. Herein, we report findings from the dissectio...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263186/ https://www.ncbi.nlm.nih.gov/pubmed/32299830 http://dx.doi.org/10.1101/gr.255703.119 |
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author | Guo, Tingting Mu, Qi Wang, Jinyu Vanous, Adam E. Onogi, Akio Iwata, Hiroyoshi Li, Xianran Yu, Jianming |
author_facet | Guo, Tingting Mu, Qi Wang, Jinyu Vanous, Adam E. Onogi, Akio Iwata, Hiroyoshi Li, Xianran Yu, Jianming |
author_sort | Guo, Tingting |
collection | PubMed |
description | The phenotypic variation of living organisms is shaped by genetics, environment, and their interaction. Understanding phenotypic plasticity under natural conditions is hindered by the apparently complex environment and the interacting genes and pathways. Herein, we report findings from the dissection of rice flowering-time plasticity in a genetic mapping population grown in natural long-day field environments. Genetic loci harboring four genes originally discovered for their photoperiodic effects (Hd1, Hd2, Hd5, and Hd6) were found to differentially respond to temperature at the early growth stage to jointly determine flowering time. The effects of these plasticity genes were revealed with multiple reaction norms along the temperature gradient. By coupling genomic selection and the environmental index, accurate performance predictions were obtained. Next, we examined the allelic variation in the four flowering-time genes across the diverse accessions from the 3000 Rice Genomes Project and constructed haplotypes at both individual-gene and multigene levels. The geographic distribution of haplotypes revealed their preferential adaptation to different temperature zones. Regions with lower temperatures were dominated by haplotypes sensitive to temperature changes, whereas the equatorial region had a majority of haplotypes that are less responsive to temperature. By integrating knowledge from genomics, gene cloning and functional characterization, and environment quantification, we propose a conceptual model with multiple levels of reaction norms to help bridge the gaps among individual gene discovery, field-level phenotypic plasticity, and genomic diversity and adaptation. |
format | Online Article Text |
id | pubmed-7263186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72631862020-11-01 Dynamic effects of interacting genes underlying rice flowering-time phenotypic plasticity and global adaptation Guo, Tingting Mu, Qi Wang, Jinyu Vanous, Adam E. Onogi, Akio Iwata, Hiroyoshi Li, Xianran Yu, Jianming Genome Res Research The phenotypic variation of living organisms is shaped by genetics, environment, and their interaction. Understanding phenotypic plasticity under natural conditions is hindered by the apparently complex environment and the interacting genes and pathways. Herein, we report findings from the dissection of rice flowering-time plasticity in a genetic mapping population grown in natural long-day field environments. Genetic loci harboring four genes originally discovered for their photoperiodic effects (Hd1, Hd2, Hd5, and Hd6) were found to differentially respond to temperature at the early growth stage to jointly determine flowering time. The effects of these plasticity genes were revealed with multiple reaction norms along the temperature gradient. By coupling genomic selection and the environmental index, accurate performance predictions were obtained. Next, we examined the allelic variation in the four flowering-time genes across the diverse accessions from the 3000 Rice Genomes Project and constructed haplotypes at both individual-gene and multigene levels. The geographic distribution of haplotypes revealed their preferential adaptation to different temperature zones. Regions with lower temperatures were dominated by haplotypes sensitive to temperature changes, whereas the equatorial region had a majority of haplotypes that are less responsive to temperature. By integrating knowledge from genomics, gene cloning and functional characterization, and environment quantification, we propose a conceptual model with multiple levels of reaction norms to help bridge the gaps among individual gene discovery, field-level phenotypic plasticity, and genomic diversity and adaptation. Cold Spring Harbor Laboratory Press 2020-05 /pmc/articles/PMC7263186/ /pubmed/32299830 http://dx.doi.org/10.1101/gr.255703.119 Text en © 2020 Guo et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Guo, Tingting Mu, Qi Wang, Jinyu Vanous, Adam E. Onogi, Akio Iwata, Hiroyoshi Li, Xianran Yu, Jianming Dynamic effects of interacting genes underlying rice flowering-time phenotypic plasticity and global adaptation |
title | Dynamic effects of interacting genes underlying rice flowering-time phenotypic plasticity and global adaptation |
title_full | Dynamic effects of interacting genes underlying rice flowering-time phenotypic plasticity and global adaptation |
title_fullStr | Dynamic effects of interacting genes underlying rice flowering-time phenotypic plasticity and global adaptation |
title_full_unstemmed | Dynamic effects of interacting genes underlying rice flowering-time phenotypic plasticity and global adaptation |
title_short | Dynamic effects of interacting genes underlying rice flowering-time phenotypic plasticity and global adaptation |
title_sort | dynamic effects of interacting genes underlying rice flowering-time phenotypic plasticity and global adaptation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263186/ https://www.ncbi.nlm.nih.gov/pubmed/32299830 http://dx.doi.org/10.1101/gr.255703.119 |
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