Cycling through developmental decisions: how cell cycle dynamics control pluripotency, differentiation and reprogramming

被引:119
作者
Soufi, Abdenour [1 ]
Dalton, Stephen [2 ,3 ]
机构
[1] Univ Edinburgh, MRC Ctr Regenerat Med, Inst Stem Cell Res, Edinburgh, Midlothian, Scotland
[2] Univ Georgia, Ctr Mol Med, Athens, GA 30602 USA
[3] Univ Georgia, Dept Biochem & Mol Biol, Athens, GA 30602 USA
来源
DEVELOPMENT | 2016年 / 143卷 / 23期
基金
英国医学研究理事会;
关键词
Stem cells; Cell cycle; Cell fate; Differentiation; Reprogramming; Pluripotency; NEURAL STEM-CELLS; TRANSCRIPTION FACTORS; HISTONE MODIFICATIONS; MITOTIC CHROMATIN; EMBRYONAL CARCINOMA; GENE-EXPRESSION; IN-VIVO; ASYMMETRIC DIVISION; GENOME REACTIVATION; HEART REGENERATION;
D O I
10.1242/dev.142075
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
A strong connection exists between the cell cycle and mechanisms required for executing cell fate decisions in a wide-range of developmental contexts. Terminal differentiation is often associated with cell cycle exit, whereas cell fate switches are frequently linked to cell cycle transitions in dividing cells. These phenomena have been investigated in the context of reprogramming, differentiation and trans-differentiation but the underpinning molecular mechanisms remain unclear. Most progress to address the connection between cell fate and the cell cycle has been made in pluripotent stem cells, in which the transition through mitosis and G1 phase is crucial for establishing a window of opportunity for pluripotency exit and the initiation of differentiation. This Review will summarize recent developments in this area and place them in a broader context that has implications for a wide range of developmental scenarios.
引用
收藏
页码:4301 / 4311
页数:11
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