scholarly journals Advances in quantitative biology methods for studying replicative aging in Saccharomyces cerevisiae

2020 ◽  
Vol 4 ◽  
pp. 151-160 ◽  
Author(s):  
Richard O'Laughlin ◽  
Meng Jin ◽  
Yang Li ◽  
Lorraine Pillus ◽  
Lev S. Tsimring ◽  
...  
2020 ◽  
Vol 48 (14) ◽  
pp. 7883-7898 ◽  
Author(s):  
Iñigo Prada-Luengo ◽  
Henrik D Møller ◽  
Rasmus A Henriksen ◽  
Qian Gao ◽  
Camilla Eggert Larsen ◽  
...  

Abstract Circular DNA can arise from all parts of eukaryotic chromosomes. In yeast, circular ribosomal DNA (rDNA) accumulates dramatically as cells age, however little is known about the accumulation of other chromosome-derived circles or the contribution of such circles to genetic variation in aged cells. We profiled circular DNA in Saccharomyces cerevisiae populations sampled when young and after extensive aging. Young cells possessed highly diverse circular DNA populations but 94% of the circular DNA were lost after ∼15 divisions, whereas rDNA circles underwent massive accumulation to >95% of circular DNA. Circles present in both young and old cells were characterized by replication origins including circles from unique regions of the genome and repetitive regions: rDNA and telomeric Y’ regions. We further observed that circles can have flexible inheritance patterns: [HXT6/7circle] normally segregates to mother cells but in low glucose is present in up to 50% of cells, the majority of which must have inherited this circle from their mother. Interestingly, [HXT6/7circle] cells are eventually replaced by cells carrying stable chromosomal HXT6 HXT6/7 HXT7 amplifications, suggesting circular DNAs are intermediates in chromosomal amplifications. In conclusion, the heterogeneity of circular DNA offers flexibility in adaptation, but this heterogeneity is remarkably diminished with age.


2011 ◽  
Vol 50 (8) ◽  
pp. 963-970 ◽  
Author(s):  
Yuen T. Lam ◽  
May T. Aung-Htut ◽  
Yu L. Lim ◽  
Hongyuan Yang ◽  
Ian W. Dawes

2006 ◽  
Vol 53 (4) ◽  
pp. 833-835 ◽  
Author(s):  
Tomasz Biliński ◽  
Grzegorz Bartosz

Mammalian somatic cells and also cells of the yeast Saccharomyces cerevisiae are capable of undergoing a limited number of divisions. Reaching the division limit is referred to, apparently not very fortunately, as replicative aging. A common feature of S. cerevisiae cells and fibroblasts approaching the limit of cell divisions in vitro is attaining giant volumes. In yeast cells this phenomenon is an inevitable consequence of budding so it is not causally related to aging. Therefore, reaching a critically large cell volume may underlie the limit of cell divisions. A similar phenomenon may limit the number of cell divisions of cultured mammalian cells. The term replicative (generative) aging may be therefore illegitimate.


2014 ◽  
Vol 1 (1) ◽  
pp. 37-42 ◽  
Author(s):  
Maksim Sorokin ◽  
◽  
Dmitry Knorre ◽  
Fedor Severin ◽  
◽  
...  

2008 ◽  
Vol 63 (1) ◽  
pp. 21-34 ◽  
Author(s):  
G. Yiu ◽  
A. McCord ◽  
A. Wise ◽  
R. Jindal ◽  
J. Hardee ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document