4.8 Article

ERF108 from Poncirus trifoliata (L.) Raf. functions in cold tolerance by modulating raffinose synthesis through transcriptional regulation of PtrRafS

Journal

PLANT JOURNAL
Volume 108, Issue 3, Pages 705-724

Publisher

WILEY
DOI: 10.1111/tpj.15465

Keywords

trifoliate orange; ethylene-responsive factor; cold stress; raffinose synthase; sugar accumulation; transcriptional regulation

Categories

Funding

  1. National Key Research and Development Program of China [2018YFD1000302]
  2. National Natural Science Foundation of China [31772273, 31972377]
  3. Hubei Provincial Natural Science Foundation for Innovative Group [2017CFA018]

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The study identified a cold-responsive transcription factor PtrERF108 from trifoliate orange, which enhances cold tolerance in plants by modulating the synthesis of raffinose. PtrERF108, through regulating its direct target PtrRafS, increases raffinose synthesis and influences the cold tolerance of plants under cold conditions.
Ethylene-responsive factors (ERFs) are plant-specific transcription factors involved in cold stress response, and raffinose is known to accumulate in plants exposed to cold. However, it remains elusive whether ERFs function in cold tolerance by modulating raffinose synthesis. Here, we identified a cold-responsive PtrERF108 from trifoliate orange (Poncirus trifoliata (L.) Raf.), a cold-tolerant plant closely related to citrus. PtrERF108 is localized in the nucleus and has transcriptional activation activity. Overexpression of PtrERF108 conferred enhanced cold tolerance of transgenic lemon, whereas virus-induced gene silencing (VIGS)-mediated knockdown of PtrERF108 in trifoliate orange greatly elevated cold sensitivity. Transcriptome profiling showed that PtrERF108 overexpression caused extensive reprogramming of genes associated with signaling transduction, physiological processes and metabolic pathways. Among them, a raffinose synthase (RafS)-encoding gene, PtrRafS, was confirmed as a direct target of PtrERF108. RafS activity and raffinose content were significantly increased in PtrERF108-overexpressing transgenic plants, but prominently decreased in the VIGS plants under cold conditions. Meanwhile, exogenous replenishment of raffinose could recover the cold tolerance of PtrERF108-silenced plants, whereas VIGS-mediated knockdown of PtrRafS resulted in cold-sensitive phenotype. Taken together, the current results demonstrate that PtrERF108 plays a positive role in cold tolerance by modulation of raffinose synthesis via regulating PtrRafS. Our findings reveal a new transcriptional module composed of ERF108-RafS underlying cold-induced raffinose accumulation in plants.

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