4.7 Article

Arabidopsis flowering integrator SOC1 transcriptionally regulates autophagy in response to long-term carbon starvation

期刊

JOURNAL OF EXPERIMENTAL BOTANY
卷 73, 期 19, 页码 6589-6599

出版社

OXFORD UNIV PRESS
DOI: 10.1093/jxb/erac298

关键词

Arabidopsis thaliana; ATG; autophagy; carbon starvation; SOC1; transcriptional regulation

资金

  1. National Natural Science Foundation of China [31900231, 32061160467, 31870171, 31701246, 32170362]
  2. Natural Science Foundation of Guangdong Province [2018A030310505]
  3. Fok YingTong Education Foundation for Young Teachers in the Higher Education Institutions of China [171014]
  4. Guangdong Natural Science Funds for Distinguished Young Scholars [2022B1515020026]

向作者/读者索取更多资源

SOC1 functions as a transcriptional repressor of autophagy by targeting the autophagy-related genes ATG4b, ATG7, and ATG18c. It negatively affects plant tolerance to long-term carbon starvation. This study highlights the important role of SOC1 in regulating plant autophagy and its cellular functions.
Autophagy is a highly conserved, self-digestion process that is essential for plant adaptations to various environmental stresses. Although the core components of autophagy in plants have been well established, the molecular basis for its transcriptional regulation remains to be fully characterized. In this study, we demonstrate that SUPPRESSOR OF OVEREXPRESSION OF CONSTANS1 (SOC1), a MADS-box family transcription factor that determines flowering transition in Arabidopsis, functions as a transcriptional repressor of autophagy. EMSAs, ChIP-qPCR assays, and dual-luciferase receptor assays showed that SOC1 can bind to the promoters of ATG4b, ATG7, and ATG18c via the conserved CArG box. qRT-PCR analysis showed that the three ATG genes ATG4b, ATG7, and ATG18c were up-regulated in the soc1-2 mutant. In line with this, the mutant also displayed enhanced autophagy activity, as revealed by increased autophagosome formation and elevated autophagic flux compared with the wild type. More importantly, SOC1 negatively affected the tolerance of plants to long-term carbon starvation, and this process requires a functional autophagy pathway. Finally, we found that SOC1 was repressed upon carbon starvation at both the transcriptional and protein levels. Overall, our study not only uncovers an important transcriptional mechanism that contributes to the regulation of plant autophagy in response to nutrient starvation, but also highlights novel cellular functions of the flowering integrator SOC1. SOC1 negatively regulates autophagy activity in Arabidopsis and plant tolerance to long-term carbon starvation by targeting the autophagy-related genes ATG4b, ATG7, and ATG18c.

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