Laun Peter, Bruschi Carlo V, Dickinson J Richard, Rinnerthaler Mark, Heeren Gino, Schwimbersky Richard, Rid Raphaela, Breitenbach Michael
Department of Cell Biology, Division of Genetics, University of Salzburg, Austria.
Nucleic Acids Res. 2007;35(22):7514-26. doi: 10.1093/nar/gkm919. Epub 2007 Nov 6.
Yeast mother cell-specific ageing is characterized by a limited capacity to produce daughter cells. The replicative lifespan is determined by the number of cell cycles a mother cell has undergone, not by calendar time, and in a population of cells its distribution follows the Gompertz law. Daughter cells reset their clock to zero and enjoy the full lifespan characteristic for the strain. This kind of replicative ageing of a cell population based on asymmetric cell divisions is investigated as a model for the ageing of a stem cell population in higher organisms. The simple fact that the daughter cells can reset their clock to zero precludes the accumulation of chromosomal mutations as the cause of ageing, because semiconservative replication would lead to the same mutations in the daughters. However, nature is more complicated than that because, (i) the very last daughters of old mothers do not reset the clock; and (ii) mutations in mitochondrial DNA could play a role in ageing due to the large copy number in the cell and a possible asymmetric distribution of damaged mitochondrial DNA between mother and daughter cell. Investigation of the loss of heterozygosity in diploid cells at the end of their mother cell-specific lifespan has shown that genomic rearrangements do occur in old mother cells. However, it is not clear if this kind of genomic instability is causative for the ageing process. Damaged material other than DNA, for instance misfolded, oxidized or otherwise damaged proteins, seem to play a major role in ageing, depending on the balance between production and removal through various repair processes, for instance several kinds of proteolysis and autophagy. We are reviewing here the evidence for genetic change and its causality in the mother cell-specific ageing process of yeast.
酵母母细胞特异性衰老的特征是产生子细胞的能力有限。复制寿命由母细胞经历的细胞周期数决定,而非日历时间,并且在一群细胞中其分布遵循冈珀茨定律。子细胞将其时钟重置为零,并享有该菌株特有的完整寿命。基于不对称细胞分裂的这种细胞群体复制性衰老被作为高等生物中干细胞群体衰老的模型进行研究。子细胞能将其时钟重置为零这一简单事实排除了染色体突变作为衰老原因的可能性,因为半保留复制会在子细胞中导致相同的突变。然而,实际情况更为复杂,因为:(i)老龄母细胞的最后一批子细胞不会重置时钟;(ii)线粒体DNA中的突变可能在衰老中起作用,这是由于细胞中线粒体DNA的拷贝数众多,以及受损线粒体DNA在母细胞和子细胞之间可能存在不对称分布。对二倍体细胞在其母细胞特异性寿命结束时杂合性丧失的研究表明,老龄母细胞中确实会发生基因组重排。然而,这种基因组不稳定性是否是衰老过程的原因尚不清楚。除DNA之外的受损物质,例如错误折叠、氧化或以其他方式受损的蛋白质,似乎在衰老中起主要作用,这取决于通过各种修复过程(例如几种蛋白水解和自噬)进行的产生与清除之间的平衡。我们在此综述酵母母细胞特异性衰老过程中基因变化及其因果关系的证据。