bioRxivCell BiologyPreprint
Reducing mitochondrial ribosomal gene expression does not alter metabolic health or lifespan in mice
K. Reid, E. G. Daniels, G. Vasam, R. Kamble, G. E. Janssens, M. Hu, A. E. Green, R. H. Houtkooper, K. J. Menzies
Abstract
Maintaining mitochondrial function is critical to an improved health span and lifespan. Introducing mild stress by inhibiting mitochondrial translation invokes the mitochondrial unfolded protein response (UPRmt) and increases lifespan in several animal models. Notably, lower mitochondrial ribosomal protein (MRP) expression also correlates with increased lifespan in a reference population of mice. In this study, we tested whether partially reducing the expression of a critical MRP, Mrpl54, reduced mitochondrial DNA-encoded protein content, induced the UPRmt, and affected lifespan or metabolic health using germline heterozygous Mrpl54 mice. Despite reduced Mrpl54 expression in multiple organs and a reduction in mitochondrial-encoded protein expression in myoblasts, we identified few significant differences between male or female Mrpl54+/- and wild type mice in initial body composition, respiratory parameters, energy intake and expenditure, or ambulatory motion. We also observed no differences in glucose or insulin tolerance, treadmill endurance, cold tolerance, heart rate, or blood pressure. There were no differences in median life expectancy or maximum lifespan. Overall, we demonstrate that genetic manipulation of Mrpl54 expression reduces mitochondrial-encoded protein content but is not sufficient to improve healthspan in otherwise healthy and unstressed mice.
- organism: mouse
- assay: bulk RNA-seq
- research focus: cell type annotation
- research focus: metabolism & bioenergetics
- research focus: cancer & tumor microenvironment
- approach: experimental assay
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