Abstract

BackgroundProgrammed cell death (PCD) is a necessary part of the life of multi-cellular organisms. A type of plant PCD is the defensive hypersensitive response (HR) elicited via recognition of a pathogen by host resistance (R) proteins. The lethal, recessive accelerated cell death 11 (acd11) mutant exhibits HR-like accelerated cell death, and cell death execution in acd11 shares genetic requirements for HR execution triggered by one subclass of R proteins.Methodology/Principal FindingsTo identify genes required for this PCD pathway, we conducted a genetic screen for suppressors of acd11, here called lazarus (laz) mutants. In addition to known suppressors of R protein-mediated HR, we isolated 13 novel complementation groups of dominant and recessive laz mutants. Here we describe laz1, which encodes a protein with a domain of unknown function (DUF300), and demonstrate that LAZ1 contributes to HR PCD conditioned by the Toll/interleukin-1 (TIR)-type R protein RPS4 and by the coiled-coil (CC)-type R protein RPM1. Using a yeast-based topology assay, we also provide evidence that LAZ1 is a six transmembrane protein with structural similarities to the human tumor suppressor TMEM34. Finally, we demonstrate by transient expression of reporter fusions in protoplasts that localization of LAZ1 is distributed between the cytosol, the plasma membrane and FM4–64 stained vesicles.Conclusions/SignificanceOur findings indicate that LAZ1 functions as a regulator or effector of plant PCD associated with the HR, in addition to its role in acd11-related death. Furthermore, the similar topology of a plant and human DUF300 proteins suggests similar functions in PCD across the eukaryotic kingdoms, although a direct role for TMEM34 in cell death control remains to be established. Finally, the subcellular localization pattern of LAZ1 suggests that it may have transport functions for yet unknown, death-related signaling molecules at the plasma membrane and/or endosomal compartments. In summary, our results validate the utility of the large-scale suppressor screen to identify novel components with functions in plant PCD, which may also have implications for deciphering cell death mechanisms in other organisms.

Highlights

  • Programmed cell death (PCD) is critical to normal growth and development as well as immune responses [1]

  • Test crosses showed that laz1-1 was allelic to three other recessive mutants. laz1-1, laz12 and laz1-3 exhibited similar suppression of acd11 cell death (Figure 1A). laz1-4 suppression appeared weaker, which may be due to the nature of this mutation as discussed below

  • Given that laz1-3 specific transcripts compared to the control (LAZ1) is mainly involved in the Enhanced Disease Susceptibility 1 (EDS1)-dependent pathway of pathogen-triggered hypersensitive response (HR), we investigated whether laz1 abolished Toll/Interleukin-1 Receptor (TIR)-nucleotide binding site (NB)-leucine rich repeats (LRR) R protein-mediated resistance in a similar manner as eds1

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Summary

Introduction

Programmed cell death (PCD) is critical to normal growth and development as well as immune responses [1]. An intensively studied type of plant PCD is the hypersensitive response (HR), a localized cell death reaction evoked following recognition of invading pathogens [2]. This response acts to limit pathogen growth to non-infected tissues. Other defense responses include expression of pathogenesis related (PR) genes, production of antimicrobial phytoalexins, and systemic acquired resistance. These immune responses are activated either by receptors that recognize pathogen associated molecular patterns (PAMPs), or via direct or indirect recognition of pathogen effectors by cognate resistance (R) proteins [3]. The lethal, recessive accelerated cell death 11 (acd11) mutant exhibits HR-like accelerated cell death, and cell death execution in acd shares genetic requirements for HR execution triggered by one subclass of R proteins

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