Annual transcriptome dynamics in natural environments reveals plant seasonal adaptation

As most organisms have evolved in seasonal environments, their environmental responses should be adapted to seasonal transitions. Here we show that the combination of temperature and day length shapes the seasonal dynamics of the transcriptome and adaptation to seasonal environments in a natural hab...

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Published inNature plants Vol. 5; no. 1; pp. 74 - 83
Main Authors Nagano, Atsushi J., Kawagoe, Tetsuhiro, Sugisaka, Jiro, Honjo, Mie N., Iwayama, Koji, Kudoh, Hiroshi
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.01.2019
Nature Publishing Group
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Abstract As most organisms have evolved in seasonal environments, their environmental responses should be adapted to seasonal transitions. Here we show that the combination of temperature and day length shapes the seasonal dynamics of the transcriptome and adaptation to seasonal environments in a natural habitat of a perennial plant Arabidopsis halleri subsp. gemmifera . Weekly transcriptomes for two years and bihourly diurnal transcriptomes on the four equinoxes/solstices, identified 2,879 and 7,185 seasonally- and diurnally-oscillating genes, respectively. Dominance of annual temperature changes for defining seasonal oscillations of gene expressions was indicated by controlled environment experiments manipulating the natural 1.5-month lag of temperature behind day length. We found that plants have higher fitness in ‘natural’ chambers than in ‘unnatural’ chambers simulating in-phase and anti-phase oscillations between temperature and day length. Seasonal temperature responses were disturbed in unnatural chambers. Our results demonstrate how plants use multiple types of environmental information to adapt to seasonal environments. A study examined transcriptome dynamics of Arabidopsis halleri weekly for two years and bihourly for the four equinoxes/solstices, revealing that the change of temperature rather than day length dominantly defines the seasonal transcriptome oscillations.
AbstractList As most organisms have evolved in seasonal environments, their environmental responses should be adapted to seasonal transitions. Here we show that the combination of temperature and day length shapes the seasonal dynamics of the transcriptome and adaptation to seasonal environments in a natural habitat of a perennial plant Arabidopsis halleri subsp. gemmifera . Weekly transcriptomes for two years and bihourly diurnal transcriptomes on the four equinoxes/solstices, identified 2,879 and 7,185 seasonally- and diurnally-oscillating genes, respectively. Dominance of annual temperature changes for defining seasonal oscillations of gene expressions was indicated by controlled environment experiments manipulating the natural 1.5-month lag of temperature behind day length. We found that plants have higher fitness in ‘natural’ chambers than in ‘unnatural’ chambers simulating in-phase and anti-phase oscillations between temperature and day length. Seasonal temperature responses were disturbed in unnatural chambers. Our results demonstrate how plants use multiple types of environmental information to adapt to seasonal environments. A study examined transcriptome dynamics of Arabidopsis halleri weekly for two years and bihourly for the four equinoxes/solstices, revealing that the change of temperature rather than day length dominantly defines the seasonal transcriptome oscillations.
As most organisms have evolved in seasonal environments, their environmental responses should be adapted to seasonal transitions. Here we show that the combination of temperature and day length shapes the seasonal dynamics of the transcriptome and adaptation to seasonal environments in a natural habitat of a perennial plant Arabidopsis halleri subsp. gemmifera. Weekly transcriptomes for two years and bihourly diurnal transcriptomes on the four equinoxes/solstices, identified 2,879 and 7,185 seasonally- and diurnally-oscillating genes, respectively. Dominance of annual temperature changes for defining seasonal oscillations of gene expressions was indicated by controlled environment experiments manipulating the natural 1.5-month lag of temperature behind day length. We found that plants have higher fitness in 'natural' chambers than in 'unnatural' chambers simulating in-phase and anti-phase oscillations between temperature and day length. Seasonal temperature responses were disturbed in unnatural chambers. Our results demonstrate how plants use multiple types of environmental information to adapt to seasonal environments.
As most organisms have evolved in seasonal environments, their environmental responses should be adapted to seasonal transitions. Here we show that the combination of temperature and day length shapes the seasonal dynamics of the transcriptome and adaptation to seasonal environments in a natural habitat of a perennial plant Arabidopsis halleri subsp. gemmifera. Weekly transcriptomes for two years and bihourly diurnal transcriptomes on the four equinoxes/solstices, identified 2,879 and 7,185 seasonally- and diurnally-oscillating genes, respectively. Dominance of annual temperature changes for defining seasonal oscillations of gene expressions was indicated by controlled environment experiments manipulating the natural 1.5-month lag of temperature behind day length. We found that plants have higher fitness in 'natural' chambers than in 'unnatural' chambers simulating in-phase and anti-phase oscillations between temperature and day length. Seasonal temperature responses were disturbed in unnatural chambers. Our results demonstrate how plants use multiple types of environmental information to adapt to seasonal environments.As most organisms have evolved in seasonal environments, their environmental responses should be adapted to seasonal transitions. Here we show that the combination of temperature and day length shapes the seasonal dynamics of the transcriptome and adaptation to seasonal environments in a natural habitat of a perennial plant Arabidopsis halleri subsp. gemmifera. Weekly transcriptomes for two years and bihourly diurnal transcriptomes on the four equinoxes/solstices, identified 2,879 and 7,185 seasonally- and diurnally-oscillating genes, respectively. Dominance of annual temperature changes for defining seasonal oscillations of gene expressions was indicated by controlled environment experiments manipulating the natural 1.5-month lag of temperature behind day length. We found that plants have higher fitness in 'natural' chambers than in 'unnatural' chambers simulating in-phase and anti-phase oscillations between temperature and day length. Seasonal temperature responses were disturbed in unnatural chambers. Our results demonstrate how plants use multiple types of environmental information to adapt to seasonal environments.
Author Nagano, Atsushi J.
Sugisaka, Jiro
Iwayama, Koji
Kawagoe, Tetsuhiro
Honjo, Mie N.
Kudoh, Hiroshi
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  organization: Center for Ecological Research, Kyoto University
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Snippet As most organisms have evolved in seasonal environments, their environmental responses should be adapted to seasonal transitions. Here we show that the...
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crossref
springer
SourceType Aggregation Database
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Enrichment Source
Publisher
StartPage 74
SubjectTerms 38/91
631/208
631/449
Adaptation
Adaptation, Physiological - genetics
Arabidopsis - genetics
Arabidopsis - physiology
Arabidopsis Proteins - genetics
Biomedical and Life Sciences
Chambers
Circadian Rhythm - genetics
Ecosystem
Environmental information
Equinoxes
Flowers - genetics
Gene Expression Profiling
Gene Expression Regulation, Plant
Interrupted Time Series Analysis
Life Sciences
Natural environment
Oscillations
Photoperiod
Plant Sciences
Seasonal variations
Seasons
Solstices
Temperature
Transcriptomes
Title Annual transcriptome dynamics in natural environments reveals plant seasonal adaptation
URI https://link.springer.com/article/10.1038/s41477-018-0338-z
https://www.ncbi.nlm.nih.gov/pubmed/30617252
https://www.proquest.com/docview/2165648348
https://www.proquest.com/docview/2165058939
Volume 5
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