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Sathe, J.

Publications and source records attributed to Sathe, J..

2 recordsLinked to original sources

The yeast mitochondrial Porin represses Snf1/AMP Kinase signaling to attenuate viral replication

Although fungi are broadly infected with mycoviruses, the antiviral mechanisms fungal cells use to oppose viral replication are not well understood. Here we discover a new mitochondrially controlled signaling mechanism in the budding yeast Saccharomyces cerevisiae that limits replication of L-A, an RNA mycovirus that endemically infects this organism. We show that Por1, the mitochondrial voltage dependent anion channel, prevents hyper-replication of L-A in stationary phase cells that have exhausted media nutrients. By investigating known stationary phase regulators, we find that deletion of the AMP-activated Kinase homolog SNF1 reverses hyper-replication of L-A observed in por1{Delta} cells. This epistatic relationship suggests that Por1 negatively regulates Snf1 in stationary phase cells and derepressed Snf1 promotes L-A hyper-replication. We confirm this model, first demonstrating that POR1 prevents the accumulation of activated Snf1 throughout stationary phase. By investigating Snf1 signaling targets we show that this POR1-SNF1 regulatory mechanism acts in stationary phase cells to limit amino acid availability that sustain L-A replication. POR1-SNF1 signaling represents a novel physiological control mechanism to limit viral replication in a eukaryotic cell.

genetics↗

Cell clusters are programmed towards a reductive metabolic 1 state by adherence junctions

Solitary cells form stable clusters via cell-cell adhesion using adherens junctions. The role of these junctions in early cell-state changes as cells form clusters is unclear. Here, we uncover that the formation of cadherin junctions as cells cluster drives a ubiquitous metabolic reprogramming. This reprogramming enhances the pentose phosphate pathway (PPP) and NADPH production to augment a reductive state. Consequently, cell clusters stabilized by cadherin junctions have reduced intracellular reactive oxygen species (ROS), are resistant to exogenous ROS-inducing agents, and have reduced apoptotic markers. Mechanistically, this metabolic reprogramming is driven by the cadherin-dependent activation of NRF2. Blocking the cadherin junction-dependent metabolic program reverses clustered cells to resemble the solitary cell state, increasing cell death and enhancing sensitivity to exogenous ROS. These insights suggest a biochemical basis for adherens junctions mediating a reductive metabolic program as solitary cells form clusters, with implications for understanding multicellular organization and collective cell behavior.

cell biology↗