Decoding pluripotency: Genetic screens to interrogate the acquisition, maintenance, and exit of pluripotency

被引:9
|
作者
Li, Qing V. [1 ,2 ]
Rosen, Bess P. [1 ,3 ]
Huangfu, Danwei [1 ]
机构
[1] Sloan Kettering Inst, 1275 York Ave, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Louis Gerstner Jr Grad Sch Biomed Sci, 1275 York Ave, New York, NY 10021 USA
[3] Cornell Univ, Weill Grad Sch Med Sci, New York, NY 10021 USA
关键词
CRISPR; differentiation; embryonic stem cells; genetic screens; pluripotency; RNAi; EMBRYONIC STEM-CELLS; PROTEIN-INTERACTION NETWORK; SELF-RENEWAL; RNAI SCREEN; NAIVE PLURIPOTENCY; GROUND-STATE; SYSTEMATIC IDENTIFICATION; REGULATORY CIRCUITRY; FUNCTIONAL GENOMICS; ENHANCER ACTIVITY;
D O I
10.1002/wsbm.1464
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Pluripotent stem cells have the ability to unlimitedly self-renew and differentiate to any somatic cell lineage. A number of systems biology approaches have been used to define this pluripotent state. Complementary to systems level characterization, genetic screens offer a unique avenue to functionally interrogate the pluripotent state and identify the key players in pluripotency acquisition and maintenance, exit of pluripotency, and lineage differentiation. Here we review how genetic screens have helped us decode pluripotency regulation. We will summarize results from RNA interference (RNAi) based screens, discuss recent advances in CRISPR/Cas-based genetic perturbation methods, and how these advances have made it possible to more comprehensively interrogate pluripotency and differentiation through genetic screens. Such investigations will not only provide a better understanding of this unique developmental state, but may enhance our ability to use pluripotent stem cells as an experimental model to study human development and disease progression. Functional interrogation of pluripotency also provides a valuable roadmap for utilizing genetic perturbation to gain systems level understanding of additional cellular states, from later stages of development to pathological disease states. This article is categorized under: Developmental Biology > Stem Cell Biology and Regeneration Developmental Biology > Developmental Processes in Health and Disease Biological Mechanisms > Cell Fates
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页数:25
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