Endocycles: a recurrent evolutionary innovation for post-mitotic cell growth

内复制 有丝分裂 生物 染色质 细胞生物学 多倍体 细胞周期 细胞分裂 遗传学 细胞 基因组 DNA 基因
作者
Bruce A. Edgar,Norman Zielke,Crisanto Gutiérrez
出处
期刊:Nature Reviews Molecular Cell Biology [Nature Portfolio]
卷期号:15 (3): 197-210 被引量:332
标识
DOI:10.1038/nrm3756
摘要

Endocycling cells successively replicate their genomes without segregating chromosomes during mitosis and thereby become polyploid. Lack of chromosome segregation typically results from downregulation of mitotic cyclin-dependent kinase activity. Endocycles probably evolved many times, and the various endocycle mechanisms found in nature highlight the versatility of the cell cycle control machinery. In endoreplication cell cycles, known as endocycles, cells successively replicate their genomes without segregating chromosomes during mitosis and thereby become polyploid. Such cycles, for which there are many variants, are widespread in protozoa, plants and animals. Endocycling cells can achieve ploidies of >200,000 C (chromatin-value); this increase in genomic DNA content allows a higher genomic output, which can facilitate the construction of very large cells or enhance macromolecular secretion. These cells execute normal S phases, using a G1–S regulatory apparatus similar to the one used by mitotic cells, but their capability to segregate chromosomes has been suppressed, typically by downregulation of mitotic cyclin-dependent kinase activity. Endocycles probably evolved many times, and the various endocycle mechanisms found in nature highlight the versatility of the cell cycle control machinery.
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