1. Academic Validation
  2. Autophagy inducers lead to transient accumulation of autophagosomes in Arabidopsis roots

Autophagy inducers lead to transient accumulation of autophagosomes in Arabidopsis roots

  • Plant Cell Rep. 2022 Feb;41(2):463-471. doi: 10.1007/s00299-021-02821-2.
Jeong Hun Kim 1 Hyera Jung 1 Ye Eun Choi 1 Taijoon Chung 2
Affiliations

Affiliations

  • 1 Department of Biological Sciences, Pusan National University, 63 Beon-gil 2, Busandaehag-ro, Geumjeong-gu, Busan, 46241, Republic of Korea.
  • 2 Department of Biological Sciences, Pusan National University, 63 Beon-gil 2, Busandaehag-ro, Geumjeong-gu, Busan, 46241, Republic of Korea. [email protected].
Abstract

This study reveals that plant roots show a rapid termination of Autophagy induction, offering a plant model for studying how excessive Autophagy is deterred. In eukaryotes, Autophagy is an intracellular mechanism that is important for recycling nutrients by degrading various macromolecules and organelles in vacuoles and lysosomes. Autophagy is induced when the nutrient supply to plant cells is limited. The protein kinase target of rapamycin (TOR) complex negatively regulates Autophagy when nutrients are present in adequate amounts. The TOR inhibitor AZD8055 is an Autophagy inducer that is useful for studying starvation-induced Autophagy in plant cells. The mechanism by which AZD8055 increases the autophagic flux in plant cells has not been studied in detail. Here, we show that AZD8055-induced Autophagy requires phosphatidylinositol 3-kinase activity and canonical AUTOPHAGY-RELATED (ATG) genes in Arabidopsis thaliana. Autophagic flux rapidly increased in seedlings treated with AZD8055. Unexpectedly, Autophagy induction was transient in root cells and terminated earlier than in cotyledon cells. Transient induction is partly caused by a temporary effect of AZD8055 on phagophore initiation. These findings indicate a TOR-independent mechanism for terminating Autophagy induction, thereby paving the way for elucidating how excess Autophagy is prevented in plant roots.

Keywords

ATG5; ATG8; Phosphoinositide; atg2.

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