| Literature DB >> 33177075 |
Shiran Gabay-Maskit1, Luis Daniel Cruz-Zaragoza2, Nadav Shai1, Miriam Eisenstein1, Chen Bibi1, Nir Cohen1, Tobias Hansen2, Eden Yifrach1, Nofar Harpaz1, Ruth Belostotsky3, Wolfgang Schliebs2, Maya Schuldiner4, Ralf Erdmann5, Einat Zalckvar4.
Abstract
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.Entities:
Keywords: Glyoxylate cycle; Malate dehydrogenase; Peroxisomes; Pex5; Piggybacking; Protein targeting
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Year: 2020 PMID: 33177075 PMCID: PMC7758625 DOI: 10.1242/jcs.244376
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285