生物
减数分裂
遗传学
重编程
减数分裂细胞
表观遗传学
有性生殖
裂殖酵母
染色质
同源重组
细胞生物学
背景(考古学)
染色体分离
减数分裂II
遗传重组
波姆裂殖酵母
酿酒酵母
染色体
DNA
基因
重组
古生物学
出处
期刊:Development
[The Company of Biologists]
日期:2024-10-14
卷期号:151 (20)
被引量:1
摘要
ABSTRACT Meiosis is a hallmark of sexual reproduction because it represents the transition from one life cycle to the next and, in animals, meiosis produces gametes. Why meiosis evolved has been debated and most studies have focused on recombination of the parental alleles as the main function of meiosis. However, 40 years ago, Robin Holliday proposed that an essential function of meiosis is to oppose the consequence of successive mitoses that cause cellular aging. Cellular aging results from accumulated defective organelles and proteins and modifications of chromatin in the form of DNA methylation and histone modifications referred to collectively as epigenetic marks. Here, recent findings supporting the hypothesis that meiosis opposes cellular aging are reviewed and placed in the context of the diversity of the life cycles of eukaryotes, including animals, yeast, flowering plants and the bryophyte Marchantia.
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