Evidence map›Paper›PMID 40795276›Full record

ArticlePlant & cell physiology2025

Coincidence of the threshold temperature of seasonal switching for diel transcriptomic oscillations and growth.

Tomoaki Muranaka, Genki Yumoto, Mie N Honjo, Atsushi J Nagano, Ji Zhou, Hiroshi Kudoh

Abstract read
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Article in Plant & cell physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Tomoaki MuranakaCenter for Ecological Research, Kyoto University, Hirano 2-509-3, Otsu 520-2113, Japan.ORCID 0000-0002-9288-3722
Genki YumotoCenter for Ecological Research, Kyoto University, Hirano 2-509-3, Otsu 520-2113, Japan.ORCID 0000-0002-7137-4785
Mie N HonjoCenter for Ecological Research, Kyoto University, Hirano 2-509-3, Otsu 520-2113, Japan.ORCID 0000-0001-7613-293X
Atsushi J NaganoBioscience and Biotechnology Center, Nagoya University, Furo-cho, Chikusa, Nagoya 464-8601, Japan.ORCID 0000-0001-7891-5049
Ji ZhouData Sciences, Crop Science Centre, National Institute of Agricultural Botany, 93 Lawrence Weaver Road, Cambridge CB3 0LE, UK.ORCID 0000-0002-5752-5524
Hiroshi KudohCenter for Ecological Research, Kyoto University, Hirano 2-509-3, Otsu 520-2113, Japan.ORCID 0000-0001-9777-4886

Funding

Early-Career Scientists 23K14253Fellows JP19J22000Fellows JP20J00255JSPS Grant-in-Aid for Specially Promoted Research JP21H04977JST CREST JPMJCR15O1Transformative Research Areas 24H02304
6 · The paper itself

Abstract

Predicting plant responses to global warming is essential for ecosystem management and crop yields. As many genes are controlled by the circadian clock, understanding the effects of temperature on transcriptomic rhythmicity under natural conditions is necessary. Here, we detected diel rhythmic genes (DRGs) in Arabidopsis halleri in four seasons. In winter, the expression of most DRGs showed low amplitude but kept at high levels, consistent with the high enrichment of cold response genes. We defined 204 core DRGs that were rhythmic over at least three seasons. Using machine learning, sampling time was successfully decoded by these 204 core DRGs across a year. In the three-dimensional principal component space for core DRGs, the diel transcriptomes appeared as four circular orbits with different diameters arranged in seasonal order, shaping a cone-like structure. Each transcriptome was mapped to the surface of the cone. The geometrical distance from the cone axis to the single-time-point transcriptome was defined as the amplitude of the transcriptomic clock. The amplitude showed seasonal switching with a sudden rhythm attenuation at 7°C and lower. Additionally, field monitoring of the plant size revealed growth arrest at similar temperatures. These results imply cooperation in the temperature-dependent regulations of circadian rhythmicity and growth, highlighting the importance of the circadian clock in predicting plant responses to climate change.

Indexed as

ArabidopsisTemperatureTranscriptomeCircadian ClocksCircadian RhythmGene Expression Regulation, PlantSeasonsArabidopsis halleri subsp. gemmiferacircadian clockfield transcriptomephenologytemperature response

Identifiers

PMID40795276
PMCPMC12540251

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.