2021
DOI: 10.3389/fcell.2020.619126
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Genomic Instability and Cellular Senescence: Lessons From the Budding Yeast

Abstract: Aging is a complex biological process that occurs in all living organisms. Aging is initiated by the gradual accumulation of biomolecular damage in cells leading to the loss of cellular function and ultimately death. Cellular senescence is one such pathway that leads to aging. The accumulation of nucleic acid damage and genetic alterations that activate permanent cell-cycle arrest triggers the process of senescence. Cellular senescence can result from telomere erosion and ribosomal DNA instability. In this rev… Show more

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Cited by 20 publications
(17 citation statements)
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“…When SIRT7 is knocked out, the copy number of rDNA is reduced by 50%. [216][217][218] SIRT7 also promotes RNA polymerase binding to the rDNA promoter region and coding region by catalyzing the deacetylation of RNA pol I. 219 Moreover, SIRT7 maintains rDNA repeat stability and nucleolar integrity through the recruitment of DNA methyltransferase 1 and SIRT1.…”
Section: Ribosomes Aging and Neurodegenerative Diseasesmentioning
confidence: 99%
“…When SIRT7 is knocked out, the copy number of rDNA is reduced by 50%. [216][217][218] SIRT7 also promotes RNA polymerase binding to the rDNA promoter region and coding region by catalyzing the deacetylation of RNA pol I. 219 Moreover, SIRT7 maintains rDNA repeat stability and nucleolar integrity through the recruitment of DNA methyltransferase 1 and SIRT1.…”
Section: Ribosomes Aging and Neurodegenerative Diseasesmentioning
confidence: 99%
“…Model organisms have a relatively shorter generation time and life spans that range from weeks to months, and their smaller sizes are advantageous for laboratory high throughput ageing experiments. Additionally, unicellular organisms such as yeast allow us to study the molecular mechanisms of ageing and senescence at the cellular level [5].…”
Section: Introductionmentioning
confidence: 99%
“…Loss of proteostasis, deregulated nutrient sensing, mitochondrial dysfunction, altered intercellular communication, and stem cell exhaustion can all contribute to cellular senescence and inflammation. Cellular senescence can impact genomic instability and telomere attrition. Epigenetic alterations can affect gene expression, including the expression of genes that regulate cell growth and senescence. , For example, certain epigenetic changes can lead to the upregulation of p16 and p21, two proteins that promote cellular senescence One of the consequences of loss of proteostasis is the accumulation of misfolded and damaged proteins.…”
Section: Mechanisms and Physiology Of Agingmentioning
confidence: 99%