Abstract

Dictyostelium discoideum amoebas display colonial multicellularity where starving amoebas aggregate to form migrating slugs and fruiting bodies consisting of spores and three supporting cell types. To resolve the cell signalling mechanism that control sporulation, we use insertional mutagenesis of amoebas transformed with fusion constructs of spore genes and red fluorescent protein. We identified the defective gene in a mutant lacking spore gene expression as the autophagy gene Atg7. Directed knock-out of atg7 and of autophagy genes like atg5 and atg9 yielded a similar phenotype, with lack of viable spores and excessive differentiation of stalk cells. The atg7-, atg5- and atg9- cells were specifically defective in cAMP induction of prespore genes, but showed enhanced cAMP stimulation of prestalk genes at the same developmental stage. The lack of prespore gene induction in the autophagy mutants was not due to deleterious effects of loss of autophagy on known components of the cAMP pathway, such as cAMP receptors and their cAMP-induced phosphorylation and internalization, PKA and the transcription factors SpaA and GbfA, or to lack of NH3 production by proteolysis, which was previously suggested to stimulate the spore pathway. Our continued mutagenesis approach is the most likely to yield the intriguing link between autophagy and prespore gene induction.

Highlights

  • Autophagy is an ancient survival strategy that allows eukaryotic cells to survive starvation by enclosing and digesting cytosolic components and organelles

  • Further analysis showed that the atg7- mutant was impaired in cAMP induction of prespore gene expression, but not in cAMP-induction of different classes of prestalk genes and in stalk cell differentiation (Fig. 5)

  • Closer investigation of mutants lacking Atg5 and Atg9 revealed that they were defective in cAMPinduced prespore gene expression, indicating that the defect in atg7mutants was due to loss of autophagy and not to a role of Atg7, unrelated to autophagy

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Summary

Introduction

Autophagy is an ancient survival strategy that allows eukaryotic cells to survive starvation by enclosing and digesting cytosolic components and organelles. Autophagy initiates with the formation of crescent-shaped double-membraned structures called phagophores, which enclose cellular contents and fuse at their termini to form an autophagosome vesicle. The autophagosome subsequently fuses with a primary lysosome to form an autolysosome where both the inner membrane and captured cargo are degraded and the catabolites are fed back into the cell by integral membrane permeases. Autophagy initiates when amino acid starvation blocks phosphorylation of Atg by the Target of Rapamycin C1 (TORC1) kinase, which prevents Atg from forming a complex with Atgs 1, 17, 29 and 31 and to initiate a phagophore assembly site (PAS). The transmembrane protein Atg and its associates Atgs and 27 direct membrane to the PAS to cause phagophore expansion. Two ubiquitin-like conjugation systems composed of Atgs 5, 7, 10, 12 and 16 and Atgs 3, 4, 7 and 8 further regulate vesicle expansion (Feng et al, 2014; Mizushima et al, 2011; Yin et al, 2016)

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