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Intrachromosomal Looping Is Required for Activation of Endogenous Pluripotency Genes during Reprogramming

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机构: [1]Jilin Univ, Affiliated Hosp 1, Stem Cell & Canc Ctr, Changchun 130021, Peoples R China; [2]Shanghai Jiao Tong Univ, Sch Med, Peoples Hosp 9, Dept Ophthalmol, Shanghai 200025, Peoples R China; [3]Capital Med Univ, Beijing Childrens Hosp, Beijing Pediat Inst, Beijing 100045, Peoples R China; [4]Shenzhen Beike Cell Engn Res Inst, Shenzhen 518057, Peoples R China; [5]Stanford Univ, Sch Med, VA Palo Alto Hlth Care Syst, Palo Alto, CA 94304 USA; [6]GMR Epigenet, Palo Alto, CA 94303 USA; [7]Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England
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Generation of induced pluripotent stem cells (iPSCs) by defined factors is an extremely inefficient process, because there is a strong epigenetic block preventing cells from achieving pluripotency. Here we report that virally expressed factors bound to the promoters of their target genes to the same extent in both iPSCs and unreprogrammed cells (URCs). However, expression of endogenous pluripotentcy genes was observed only in iPSCs. Comparison of local chromatin structure of the OCT4 locus revealed that there was a cohesin-complex-mediated intrachromosomal loop that juxtaposes a downstream enhancer to the gene's promoter, enabling activation of endogenous stemness genes. None of these long-range interactions were observed in URCs. Knockdown of the cohesin-complex gene SMC1 by RNAi abolished the intrachromosomal interaction and affected pluripotency. These findings highlight the importance of the SMC1-orchestrated intrachromosomal loop as a critical epigenetic barrier to the induction of pluripotency.

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出版当年[2012]版:
大类 | 1 区 生物
小类 | 1 区 细胞与组织工程 1 区 细胞生物学
最新[2025]版:
大类 | 1 区 医学
小类 | 1 区 细胞与组织工程 1 区 细胞生物学
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出版当年[2011]版:
Q1 CELL & TISSUE ENGINEERING Q1 CELL BIOLOGY
最新[2024]版:
Q1 CELL & TISSUE ENGINEERING Q1 CELL BIOLOGY

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第一作者机构: [2]Shanghai Jiao Tong Univ, Sch Med, Peoples Hosp 9, Dept Ophthalmol, Shanghai 200025, Peoples R China; [5]Stanford Univ, Sch Med, VA Palo Alto Hlth Care Syst, Palo Alto, CA 94304 USA;
通讯作者:
通讯机构: [1]Jilin Univ, Affiliated Hosp 1, Stem Cell & Canc Ctr, Changchun 130021, Peoples R China; [5]Stanford Univ, Sch Med, VA Palo Alto Hlth Care Syst, Palo Alto, CA 94304 USA; [6]GMR Epigenet, Palo Alto, CA 94303 USA;
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