Mlf mediates proteotoxic response via formation of cellular foci for protein folding and degradation in Giardia

PLoS Pathog. 2024 Oct 21;20(10):e1012617. doi: 10.1371/journal.ppat.1012617. eCollection 2024 Oct.

Abstract

Myeloid leukemia factor 1 (Mlf1) was identified as a proto-oncoprotein that affects hematopoietic differentiation in humans. However, its cellular function remains elusive, spanning roles from cell cycle regulation to modulation of protein aggregate formation and participation in ciliogenesis. Given that structurally conserved homologs of Mlf1 can be found across the eukaryotic tree of life, we decided to characterize its cellular role underlying this phenotypic pleiotropy. Using a model of the unicellular eukaryote Giardia intestinalis, we demonstrate that its Mlf1 homolog (GiMlf) mainly localizes to two types of cytosolic foci: microtubular structures, where it interacts with Hsp40, and ubiquitin-rich, membraneless compartments, found adjacent to mitochondrion-related organelles known as mitosomes, containing the 26S proteasome regulatory subunit 4. Upon cellular stress, GiMlf either relocates to the affected compartment or disperses across the cytoplasm, subsequently accumulating into enlarged foci during the recovery phase. In vitro assays suggest that GiMlf can be recruited to membranes through its affinity for signaling phospholipids. Importantly, cytosolic foci diminish in the gimlf knockout strain, which exhibits extensive proteomic changes indicative of compromised proteostasis. Consistent with data from other cellular systems, we propose that Mlf acts in the response to proteotoxic stress by mediating the formation of function-specific foci for protein folding and degradation.

MeSH terms

  • Giardia lamblia* / metabolism
  • Humans
  • Protein Folding*
  • Proteolysis*
  • Protozoan Proteins* / genetics
  • Protozoan Proteins* / metabolism

Substances

  • Protozoan Proteins

Grants and funding

This work was supported by project START (START/SCI/012, MŠMT), Project name: Grant schemes at Charles University, Reg. number: CZ.02.2.69/0.0/0.0/19_073/0016935) to MVi, LA and VD and by a grant from Czech Science Foundation 20-25417S to PD. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.