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Temperature-dependent growth contributes to long-term cold sensing

Author

Listed:
  • Yusheng Zhao

    (Norwich Research Park)

  • Rea L. Antoniou-Kourounioti

    (Norwich Research Park)

  • Grant Calder

    (Norwich Research Park
    University of York)

  • Caroline Dean

    (Norwich Research Park)

  • Martin Howard

    (Norwich Research Park)

Abstract

Temperature is a key factor in the growth and development of all organisms1,2. Plants have to interpret temperature fluctuations, over hourly to monthly timescales, to align their growth and development with the seasons. Much is known about how plants respond to acute thermal stresses3,4, but the mechanisms that integrate long-term temperature exposure remain unknown. The slow, winter-long upregulation of VERNALIZATION INSENSITIVE 3 (VIN3)5–7, a PHD protein that functions with Polycomb repressive complex 2 to epigenetically silence FLOWERING LOCUS C (FLC) during vernalization, is central to plants interpreting winter progression5,6,8–11. Here, by a forward genetic screen, we identify two dominant mutations of the transcription factor NTL8 that constitutively activate VIN3 expression and alter the slow VIN3 cold induction profile. In the wild type, the NTL8 protein accumulates slowly in the cold, and directly upregulates VIN3 transcription. Through combining computational simulation and experimental validation, we show that a major contributor to this slow accumulation is reduced NTL8 dilution due to slow growth at low temperatures. Temperature-dependent growth is thus exploited through protein dilution to provide the long-term thermosensory information for VIN3 upregulation. Indirect mechanisms involving temperature-dependent growth, in addition to direct thermosensing, may be widely relevant in long-term biological sensing of naturally fluctuating temperatures.

Suggested Citation

  • Yusheng Zhao & Rea L. Antoniou-Kourounioti & Grant Calder & Caroline Dean & Martin Howard, 2020. "Temperature-dependent growth contributes to long-term cold sensing," Nature, Nature, vol. 583(7818), pages 825-829, July.
  • Handle: RePEc:nat:nature:v:583:y:2020:i:7818:d:10.1038_s41586-020-2485-4
    DOI: 10.1038/s41586-020-2485-4
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    Cited by:

    1. Diederik S. Laman Trip & Théo Maire & Hyun Youk, 2022. "Slowest possible replicative life at frigid temperatures for yeast," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    2. Enrico Coen & Przemyslaw Prusinkiewicz, 2024. "Developmental timing in plants," Nature Communications, Nature, vol. 15(1), pages 1-13, December.

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