Age-Dependent Ribosomal DNA Variations in Mice

被引:23
作者
Watada, Eriko [1 ,2 ]
Li, Sihan [4 ]
Hori, Yutaro [1 ]
Fujiki, Katsunori [1 ]
Shirahige, Katsuhiko [1 ,3 ]
Inada, Toshifumi [4 ]
Kobayashi, Takehiko [1 ,2 ,3 ]
机构
[1] Univ Tokyo, Inst Quantitat Biosci, Tokyo, Japan
[2] Univ Tokyo, Dept Biol Sci, Tokyo, Japan
[3] Univ Tokyo, Collaborat Res Inst Innovat Microbiol, Tokyo, Japan
[4] Tohoku Univ, Grad Sch Pharmaceut Sci, Sendai, Miyagi, Japan
基金
日本学术振兴会;
关键词
ribosomal RNA gene; rDNA copy number; DNA methylation; senescence; genome instability; mouse; mutation rate; yeast life span; RNA GENES; SACCHAROMYCES-CEREVISIAE; CHROMATIN STRUCTURES; CELLULAR SENESCENCE; REPLICATION FORK; RDNA REPEATS; YEAST; TRANSCRIPTION; RECOMBINATION; CELLS;
D O I
10.1128/MCB.00368-20
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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-mousespecific 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.
引用
收藏
页数:17
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