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A piggybacking mechanism enables peroxisomal localization of the glyoxylate cycle enzyme Mdh2 in yeast

Eukaryotic cells have evolved organelles that allow the compartmentalization and regulation of metabolic processes. Knowledge of molecular mechanisms that allow temporal and spatial organization of enzymes within organelles is therefore crucial for understanding eukaryotic metabolism. Here, we show...

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Detalles Bibliográficos
Autores principales: Gabay-Maskit, Shiran, Cruz-Zaragoza, Luis Daniel, Shai, Nadav, Eisenstein, Miriam, Bibi, Chen, Cohen, Nir, Hansen, Tobias, Yifrach, Eden, Harpaz, Nofar, Belostotsky, Ruth, Schliebs, Wolfgang, Schuldiner, Maya, Erdmann, Ralf, Zalckvar, Einat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7758625/
https://www.ncbi.nlm.nih.gov/pubmed/33177075
http://dx.doi.org/10.1242/jcs.244376
Descripción
Sumario:Eukaryotic cells have evolved organelles that allow the compartmentalization and regulation of metabolic processes. Knowledge of molecular mechanisms that allow temporal and spatial organization of enzymes within organelles is therefore crucial for understanding eukaryotic metabolism. Here, we show that the yeast malate dehydrogenase 2 (Mdh2) is dually localized to the cytosol and to peroxisomes and is targeted to peroxisomes via association with Mdh3 and a Pex5-dependent piggybacking mechanism. This dual localization of Mdh2 contributes to our understanding of the glyoxylate cycle and provides a new perspective on compartmentalization of cellular metabolism, which is critical for the perception of metabolic disorders and aging.