Title Induction of Pluripotency in Mouse Somatic Cells with Lineage Specifiers
Authors Shu, Jian
Wu, Chen
Wu, Yetao
Li, Zhiyuan
Shao, Sida
Zhao, Wenhui
Tang, Xing
Yang, Huan
Shen, Lijun
Zuo, Xiaohan
Yang, Weifeng
Shi, Yan
Chi, Xiaochun
Zhang, Hongquan
Gao, Ge
Shu, Youmin
Yuan, Kehu
He, Weiwu
Tang, Chao
Zhao, Yang
Deng, Hongkui
Affiliation Peking Univ, Coll Life Sci, MOE Key Lab Cell Proliferat & Differentiat, Beijing 100871, Peoples R China.
Peking Univ, Ctr Quantitat Biol, Beijing 100871, Peoples R China.
Peking Univ, Peking Tsinghua Ctr Life Sci, Beijing 100871, Peoples R China.
Peking Univ, Ctr Bioinformat, State Key Lab Prot & Plant Gene Res, Coll Life Sci, Beijing 100871, Peoples R China.
Peking Univ, Sch Basic Med Sci, Lab Stem Cells Dev & Reprod Med, Beijing 100191, Peoples R China.
Peking Univ, Shenzhen Grad Sch, Sch Chem Biol & Biotechnol, Lab Chem Genom, Shenzhen 518055, Peoples R China.
Univ Calif San Francisco, Biophys Grad Program, San Francisco, CA 94158 USA.
OriGene Technol, Rockville, MD 20850 USA.
Keywords EMBRYONIC STEM-CELLS
HUMAN FIBROBLASTS
PRIMITIVE ENDODERM
DIRECT CONVERSION
GROUND-STATE
SELF-RENEWAL
DIFFERENTIATION
GENERATION
OCT4
EXPRESSION
Issue Date 2013
Publisher cell
Citation CELL.2013,153,(5),963-975.
Abstract The reprogramming factors that induce pluripotency have been identified primarily from embryonic stem cell (ESC)-enriched, pluripotency-associated factors. Here, we report that, during mouse somatic cell reprogramming, pluripotency can be induced with lineage specifiers that are pluripotency rivals to suppress ESC identity, most of which are not enriched in ESCs. We found that OCT4 and SOX2, the core regulators of pluripotency, can be replaced by lineage specifiers that are involved in mesendo-dermal (ME) specification and in ectodermal (ECT) specification, respectively. OCT4 and its substitutes attenuated the elevated expression of a group of ECT genes, whereas SOX2 and its substitutes curtailed a group of ME genes during reprogramming. Surprisingly, the two counteracting lineage specifiers can synergistically induce pluripotency in the absence of both OCT4 and SOX2. Our study suggests a "seesaw model'' in which a balance that is established using pluripotency factors and/or counteracting lineage specifiers can facilitate reprogramming.
URI http://hdl.handle.net/20.500.11897/162479
ISSN 0092-8674
DOI 10.1016/j.cell.2013.05.001
Indexed SCI(E)
PubMed
Appears in Collections: 生命科学学院
基础医学院
化学生物学与生物技术学院
细胞增殖分化调控机理研究教育部重点实验室

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