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

被引:270
作者
Edgar, Bruce A. [1 ]
Zielke, Norman [1 ]
Gutierrez, Crisanto [2 ]
机构
[1] Ctr Mol Biol Heidelberg Alliance, German Canc Res Center, D-69120 Heidelberg, Germany
[2] CSIC UAM, Ctr Biol Mol Severo Ochoa, Madrid 28049, Spain
基金
欧洲研究理事会;
关键词
DEPENDENT KINASE INHIBITOR; REGENERATING RAT-LIVER; CYCLIN-E LEVELS; A-TYPE CYCLIN; S-PHASE; DNA-REPLICATION; TRANSCRIPTION FACTOR; FOLLICLE CELLS; DROSOPHILA EMBRYOGENESIS; ENDOREDUPLICATION CYCLES;
D O I
10.1038/nrm3756
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:197 / 210
页数:14
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