Abstract

Plant autophagy plays an important role in delaying senescence, nutrient recycling, and stress responses. Functional analysis of plant autophagy has almost exclusively focused on the proteins required for the core process of autophagosome assembly, but little is known about the proteins involved in other important processes of autophagy, including autophagy cargo recognition and sequestration. In this study, we report functional genetic analysis of Arabidopsis NBR1, a homolog of mammalian autophagy cargo adaptors P62 and NBR1. We isolated two nbr1 knockout mutants and discovered that they displayed some but not all of the phenotypes of autophagy-deficient atg5 and atg7 mutants. Like ATG5 and ATG7, NBR1 is important for plant tolerance to heat, oxidative, salt, and drought stresses. The role of NBR1 in plant tolerance to these abiotic stresses is dependent on its interaction with ATG8. Unlike ATG5 and ATG7, however, NBR1 is dispensable in age- and darkness-induced senescence and in resistance to a necrotrophic pathogen. A selective role of NBR1 in plant responses to specific abiotic stresses suggest that plant autophagy in diverse biological processes operates through multiple cargo recognition and delivery systems. The compromised heat tolerance of atg5, atg7, and nbr1 mutants was associated with increased accumulation of insoluble, detergent-resistant proteins that were highly ubiquitinated under heat stress. NBR1, which contains an ubiquitin-binding domain, also accumulated to high levels with an increasing enrichment in the insoluble protein fraction in the autophagy-deficient mutants under heat stress. These results suggest that NBR1-mediated autophagy targets ubiquitinated protein aggregates most likely derived from denatured or otherwise damaged nonnative proteins generated under stress conditions.

Highlights

  • Autophagy is an evolutionary conserved mechanism for degradation of cytoplasmic constituents including proteins and organelle materials [1,2,3]

  • Arabidopsis NBR1 is a homolog of mammalian autophagy cargo adaptors P62 and NBR1

  • NBR1 contains an ubiquitin-binding domain, and the compromised stress tolerance of autophagy mutants was associated with increased accumulation of NBR1 and ubiquitin-positive cellular protein aggregates in the insoluble protein fraction under stress conditions

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Summary

Introduction

Autophagy is an evolutionary conserved mechanism for degradation of cytoplasmic constituents including proteins and organelle materials [1,2,3]. An isolation membrane forms, elongates and sequesters cytoplasmic constituents including organelles. The edges of the membrane fuse to form a double-membrane vesicle termed autophagosome, which can fuse with the lysosomes or vacuoles to deliver the content for degradation [4]. Saccharomuces cerevisiae, where autophagy has been well studied, there are more than 30 autophagy-related (ATG) proteins identified [5]. The products of these ATG genes are involved in the induction of autophagy, autophagosome nucleation, elongation, maturation and fusion with vacuoles. Most of the ATG genes initially discovered in yeast have been detected and analyzed in other eukaryotes, suggesting the highly conserved nature of the core autophagy process

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