A protein that guards cells against aging-related problems by protecting a particularly vulnerable set of genes has been identified by researchers from Stanford University and the VA Palo Alto Health Care System (VAPAHCS).
The genes that encode components of the ribosome — the protein-making machine of the cell — are abundant and constantly in use. Most organisms, including humans, have many copies of ribosomal genes (collectively called ribosomal DNA, or rDNA), some of which are kept silent as backups in case the active copies of ribosomal genes are damaged.
This is important because rDNA is essential but unstable — prone to mutation and rearrangement.
“Ribosomal DNA is one of the major hotspots for instability in the genome,”
said Silvana Paredes, the research scientist who led the study.
Working in Katrin Chua’s laboratory, which is jointly affiliated with Stanford and the Geriatric Research Education and Clinical Center at the VAPAHCS, Paredes examined the relationship between aging, rDNA, and a protein called sirtuin 7 (SIRT7). SIRT7 helps modify the proteins that DNA winds around, which affects whether genes are turned on or off.
Paredes found that SIRT7 was important for keeping parts of the rDNA turned off.
This function turned out to be crucial for preventing aging-related deterioration in the cell. When SIRT7 was removed, the rDNA genes became damaged. The cells stopped dividing and exhibited other symptoms of damage and age.
Such senescent cells accumulate in tissues in aging-related conditions as diverse as cancer, diabetes, heart disease, arthritis, and neurodegeneration; studies in mice have suggested that removing senescent cells can prevent some of these conditions. Identifying SIRT7 as a protein that keeps cells healthy could therefore lead to therapies that prevent cellular senescence.
“By identifying rDNA instability as an underlying trigger of senescence of human cells and demonstrating the central role of SIRT7 in protecting against this process, our studies not only provide important insights into basic mechanisms of aging, but also identify potential molecular targets for aging-related disease processes,”
The work was supported in part by a grant from the NIA, National Institutes of Health; a Department of Veterans Affairs merit award; and the Paul F. Glenn Laboratories.
Silvana Paredes, Maria Angulo-Ibanez, Luisa Tasselli, Scott M. Carlson, Wei Zheng, Tie-Mei Li, and Katrin F. Chua
The epigenetic regulator SIRT7 guards against mammalian cellular senescence induced by ribosomal DNA instability
J. Biol. Chem. 2018 293: 11242-. doi:10.1074/jbc.AC118.003325
Image: In the absence of SIRT7, a human primary cell displays multiple nucleoli. DNA was stained with DAPI (turquoise) and nucleolus was stained with anti-fibrillarin (red). Credit: Silvana Paredes