Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, Center for Reproductive Sciences and Department of Urology, University of California San Francisco, San Francisco, CA, USA.
Curr Opin Genet Dev. 2013 Oct;23(5):548-55. doi: 10.1016/j.gde.2013.06.005. Epub 2013 Aug 12.
Cells are constantly changing their state of equilibrium in response to internal and external stimuli. These changes in cell identity are driven by highly coordinated modulation of gene expression. This coordinated regulation is achieved in large part due to changes in the structure and composition of the chromatin, driven by epigenetic modulators. Recent discoveries in cellular and genomic reprogramming have highlighted the importance of chromatin modifications to reach and uphold the fidelity of target cell states. In this review, we focus on the latest work addressing the mechanisms surrounding the epigenetic regulation of various types of reprogramming, including somatic cell nuclear transfer (SCNT), cell fusion and transcription factor-induced and microRNA-induced pluripotency. The studies covered herein showcase the interplay between these epigenetic pathways, and highlight the importance of furthering our understanding of these connections to form a clearer picture of the mechanisms underlying stable cell fate transitions.
细胞不断地响应内部和外部刺激来改变其平衡状态。这些细胞身份的变化是由基因表达的高度协调调控驱动的。这种协调调控在很大程度上是由于染色质结构和组成的变化,这些变化是由表观遗传调节剂驱动的。细胞和基因组重编程方面的最新发现强调了染色质修饰对于达到和维持靶细胞状态保真度的重要性。在这篇综述中,我们重点介绍了最新的研究工作,这些工作涉及到围绕各种类型的重编程的表观遗传调控的机制,包括体细胞核移植(SCNT)、细胞融合以及转录因子诱导和 microRNA 诱导的多能性。本文涵盖的研究展示了这些表观遗传途径之间的相互作用,并强调了进一步了解这些联系的重要性,以便更清楚地了解稳定的细胞命运转变的机制。