Age-Dependent Ribosomal DNA Variations in Mice.
Eriko WatadaSihan LiYutaro HoriKatsunori FujikiKatsuhiko ShirahigeToshifumi InadaTakehiko KobayashiPublished in: Molecular and cellular biology (2020)
The rRNA gene, which consists of tandem repetitive arrays (ribosomal DNA [rDNA] repeat), is one of the most unstable regions in the genome. The rDNA repeat in the budding yeast Saccharomyces cerevisiae is known to become unstable as the cell ages. However, it is unclear how the rDNA repeat changes in aging mammalian cells. Using quantitative single-cell analyses, we identified age-dependent alterations in rDNA copy number and levels of methylation in mice. The degree of methylation and copy number of rDNA from bone marrow cells of 2-year-old mice were increased by comparison to levels in 4-week-old mice in two mouse strains, BALB/cA and C57BL/6. Moreover, the level of pre-rRNA transcripts was reduced in older BALB/cA mice. We also identified many sequence variations in the rDNA. Among them, three mutations were unique to old mice, and two of them were found in the conserved region in budding yeast. We established yeast strains with the old-mouse-specific mutations and found that they shortened the life span of the cells. Our findings suggest that rDNA is also fragile in mammalian cells and that alterations within this region have a profound effect on cellular function.
Keyphrases
- copy number
- genome wide
- saccharomyces cerevisiae
- high fat diet induced
- mitochondrial dna
- single cell
- dna methylation
- bone marrow
- induced apoptosis
- escherichia coli
- stem cells
- physical activity
- randomized controlled trial
- clinical trial
- wild type
- type diabetes
- single molecule
- insulin resistance
- adipose tissue
- rna seq
- signaling pathway
- transcription factor
- mass spectrometry
- metabolic syndrome
- high frequency
- cell proliferation
- circulating tumor
- oxidative stress
- high throughput
- autism spectrum disorder
- cell therapy