Reprogramming: identifying the mechanisms that safeguard cell identity

被引:41
作者
Brumbaugh, Justin [1 ]
Di Stefano, Bruno [2 ,3 ,4 ,5 ,6 ]
Hochedlinger, Konrad [2 ,3 ,4 ,5 ,6 ]
机构
[1] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
[2] Massachusetts Gen Hosp, Dept Mol Biol, 185 Cambridge St, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Ctr Regenerat Med, 185 Cambridge St, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Canc Ctr, 185 Cambridge St, Boston, MA 02114 USA
[5] Harvard Med Sch, Dept Genet, 77 Ave Louis Pasteur, Boston, MA 02115 USA
[6] Harvard Stem Cell Inst, 350 Massachusetts Ave, Cambridge, MA 02138 USA
来源
DEVELOPMENT | 2019年 / 146卷 / 23期
基金
美国国家卫生研究院;
关键词
Reprogramming; Cell identity; Safeguarding; EMBRYONIC STEM-CELLS; HISTONE VARIANT MACROH2A; MESSENGER-RNA METHYLATION; PRIMORDIAL GERM-CELLS; ALTERNATIVE POLYADENYLATION; HEMATOPOIETIC STEM; DNA METHYLATION; SELF-RENEWAL; NUCLEAR TRANSFER; TRANSPOSABLE ELEMENTS;
D O I
10.1242/dev.182170
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Development and homeostasis rely upon concerted regulatory pathways to establish the specialized cell types needed for tissue function. Once a cell type is specified, the processes that restrict and maintain cell fate are equally important in ensuring tissue integrity. Over the past decade, several approaches to experimentally reprogram cell fate have emerged. Importantly, efforts to improve and understand these approaches have uncovered novel molecular determinants that reinforce lineage commitment and help resist cell fate changes. In this Review, we summarize recent studies that have provided insights into the various chromatin factors, post-transcriptional processes and features of genomic organization that safeguard cell identity in the context of reprogramming to pluripotency. We also highlight how these factors function in other experimental, physiological and pathological cell fate transitions, including direct lineage conversion, pluripotency-to-totipotency reversion and cancer.
引用
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页数:17
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