Identification of the Zeo1 Protein as a Candidate Structural Homolog of {\alpha}-Synuclein in Budding Yeast

TL;DR

This study identifies Zeo1 as a potential structural homolog of α-synuclein in yeast, revealing biochemical similarities and suggesting new avenues for understanding neurodegenerative disease mechanisms through cross-species protein analysis.

Contribution

The paper introduces Zeo1 as a novel structural homolog of α-synuclein in yeast, providing insights into disease pathways using comparative proteome-wide structure prediction.

Findings

Zeo1 overexpression is toxic in yeast and localizes to lipid membranes.

Zeo1 shares biochemical similarities with α-synuclein.

PKC1 rescues toxicities induced by both Zeo1 and α-synuclein.

Abstract

Human {\alpha}-synuclein (SNCA) is a 140-amino-acid protein belonging to the three-member synuclein family. It has been extensively studied due to its misfolding/aggregation in and genetic linkage to neurodegenerative diseases, especially Parkinson's disease (PD). To better understand its biology, models of SNCA toxicity have been developed in budding yeast over the past decade, which have yielded insights into the protein's modes of action in specific pathways and potential therapeutic targets. Given that the synuclein gene family is not present in yeast, an extensive homology search was undertaken to determine if any yeast protein may possess structural homology to SNCA and whose native biology may shed more light on SNCA's pathomechanism in eukaryotes. We identified Zeo1, a membrane-associated protein involved in the cell wall integrity (CWI) pathway, as a candidate structural homolog. We show that Zeo1 overexpression is toxic in yeast and, similar to SNCA, localizes to lipid membranes. A number of biochemical similarities between Zeo1 and SNCA also become apparent in light of this potential structural connection. Moreover, the yeast PKC1 gene, a kinase acting as a downstream signaling hub in the CWI pathway, rescues both SNCA- and Zeo1-induced toxicities. Using the same homology search methods that identified Zeo1, we show that Pkc1 has a hybrid structural similarity to PINK1 and PARIS, two mitochondrial PD-implicated proteins not generally linked directly to synuclein-specific pathobiology. Overall, this proof-of-concept study shows the potential utility of hitherto uncharacterized cross-species structural homologs, identified using comparative proteome-wide structure prediction algorithms, in shedding light on abstruse connections among disease-relevant proteins.