Epigenetics of Reprogramming to Induced Pluripotency

被引:251
作者
Papp, Bernadett [1 ,2 ,3 ,4 ]
Plath, Kathrin [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Inst Mol Biol, Bioinformat Interdept Degree Program, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, Los Angeles, CA 90095 USA
关键词
EMBRYONIC STEM-CELLS; X-CHROMOSOME INACTIVATION; HUMAN SOMATIC-CELLS; SELF-RENEWAL; C-MYC; TRANSCRIPTION FACTORS; REGULATES PLURIPOTENCY; INTERACTION NETWORK; DNA METHYLATION; CHROMATIN;
D O I
10.1016/j.cell.2013.02.043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Reprogramming to induced pluripotent stem cells (iPSCs) proceeds in a stepwise manner with reprogramming factor binding, transcription, and chromatin states changing during transitions. Evidence is emerging that epigenetic priming events early in the process may be critical for pluripotency induction later. Chromatin and its regulators are important controllers of reprogramming, and reprogramming factor levels, stoichiometry, and extracellular conditions influence the outcome. The rapid progress in characterizing reprogramming is benefiting applications of iPSCs and is already enabling the rational design of novel reprogramming factor cocktails. However, recent studies have also uncovered an epigenetic instability of the X chromosome in human iPSCs that warrants careful consideration.
引用
收藏
页码:1324 / 1343
页数:20
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