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Zscan4 在诱导多能干细胞生成过程中短暂地重新激活早期胚胎基因。

Zscan4 transiently reactivates early embryonic genes during the generation of induced pluripotent stem cells.

机构信息

Developmental Genomics and Aging Section, Laboratory of Genetics, National Institute on Aging, NIH , Baltimore, MD 21224, USA.

出版信息

Sci Rep. 2012;2:208. doi: 10.1038/srep00208. Epub 2012 Jan 4.

Abstract

The generation of induced pluripotent stem cells (iPSCs) by the forced expression of defined transcription factors in somatic cells holds great promise for the future of regenerative medicine. However, the initial reprogramming mechanism is still poorly understood. Here we show that Zscan4, expressed transiently in2-cell embryos and embryonic stem cells (ESCs), efficiently produces iPSCs from mouse embryo fibroblasts when coexpressed with Klf4, Oct4, and Sox2. Interestingly, the forced expression of Zscan4 is required onlyfor the first few days of iPSC formation. Microarray analysis revealed transient and early induction of preimplantation-specific genes in a Zscan4-dependent manner. Our work indicates that Zscan4 is a previously unidentified potent natural factor that facilitates the reprogramming process and reactivates early embryonic genes.

摘要

通过在体细胞中强制表达特定转录因子来生成诱导多能干细胞(iPSCs),为再生医学的未来带来了巨大的希望。然而,初始重编程机制仍知之甚少。在这里,我们表明 Zscan4 在 2 细胞胚胎和胚胎干细胞(ESCs)中短暂表达,当与 Klf4、Oct4 和 Sox2 共表达时,能够有效地从小鼠胚胎成纤维细胞中产生 iPSCs。有趣的是,Zscan4 的强制表达仅在 iPSC 形成的最初几天内是必需的。微阵列分析显示,Zscan4 以依赖于 Zscan4 的方式瞬时且早期诱导植入前特异性基因。我们的工作表明,Zscan4 是一种以前未被识别的强大天然因子,可促进重编程过程并重新激活早期胚胎基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee86/3250575/ca1fdfd8a1cc/srep00208-f1.jpg

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