Comparing the yeast retrograde response and NF-κB stress responses: implications for aging
Visish Srinivasan
Department of Biology, Drexel University, Philadelphia, PA 19104, USA
Search for more papers by this authorAndres Kriete
School of Biomedical Engineering, Science and Health Systems, Drexel University, 3141 Chestnut St., Philadelphia, PA 19104, USA
Search for more papers by this authorAhmet Sacan
School of Biomedical Engineering, Science and Health Systems, Drexel University, 3141 Chestnut St., Philadelphia, PA 19104, USA
Search for more papers by this authorS. Michal Jazwinski
Tulane Center for Aging and Department of Medicine, Tulane University, 1430 Tulane Ave., New Orleans, LA 70112, USA
Search for more papers by this authorVisish Srinivasan
Department of Biology, Drexel University, Philadelphia, PA 19104, USA
Search for more papers by this authorAndres Kriete
School of Biomedical Engineering, Science and Health Systems, Drexel University, 3141 Chestnut St., Philadelphia, PA 19104, USA
Search for more papers by this authorAhmet Sacan
School of Biomedical Engineering, Science and Health Systems, Drexel University, 3141 Chestnut St., Philadelphia, PA 19104, USA
Search for more papers by this authorS. Michal Jazwinski
Tulane Center for Aging and Department of Medicine, Tulane University, 1430 Tulane Ave., New Orleans, LA 70112, USA
Search for more papers by this authorSummary
The mitochondrial retrograde response has been extensively described in Saccharomyces cerevisiae, where it has been found to extend life span during times of mitochondrial dysfunction, damage or low nutrient levels. In yeast, the retrograde response genes (RTG) convey these stress responses to the nucleus to change the gene expression adaptively. Similarly, most classes of higher organisms have been shown to have some version of a central stress-mediating transcription factor, NF-κB. There have been several modifications along the phylogenetic tree as NF-κB has taken a larger role in managing cellular stresses. Here, we review similarities and differences in mechanisms and pathways between RTG genes in yeast and NF-κB as seen in more complex organisms. We perform a structural homology search and reveal similarities of Rtg proteins with eukaryotic transcription factors involved in development and metabolism. NF-κB shows more sophisticated functions when compared to RTG genes including participation in immune responses and induction of apoptosis under high levels of ROS-induced mitochondrial and nuclear DNA damage. Involvement of NF-κB in chromosomal stability, coregulation of mitochondrial respiration, and cross talk with the TOR (target of rapamycin) pathway points to a conserved mechanism also found in yeast.
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