2013
DOI: 10.1038/cr.2013.72
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“TET-on” pluripotency

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Cited by 5 publications
(2 citation statements)
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“…The core reprogramming factors Oct4 and Sox2 are O-GlcNAcylated in ESCs, but the O-GlcNAc modification is rapidly removed upon differentiation (Jang et al 2012). Recently, 10-11 translocation 1-3 proteins functioning as DNA hydroxylases were reported to interact with O-linked GlcNAc transferase to mediate histone modifications and regulate gene expression (Wang et al 2013).…”
Section: Globo-series; Ssea-4mentioning
confidence: 99%
“…The core reprogramming factors Oct4 and Sox2 are O-GlcNAcylated in ESCs, but the O-GlcNAc modification is rapidly removed upon differentiation (Jang et al 2012). Recently, 10-11 translocation 1-3 proteins functioning as DNA hydroxylases were reported to interact with O-linked GlcNAc transferase to mediate histone modifications and regulate gene expression (Wang et al 2013).…”
Section: Globo-series; Ssea-4mentioning
confidence: 99%
“…However, TET family proteins have also been implicated in CRC development, as their dysregulation can alter the epigenetic landscape in colonocytes to promote malignant transformation [12]. TET enzymes were extensively linked to the regulation of pluripotency and self-renewal, two key features of cancer stem cells and hierarchical tumor heterogeneity [14,15]. DNA hypomethylation has also been associated with the increased mobility of transposable elements, which constitute a large proportion of the eukaryotic genome and Collectively, Ansari et al illuminate the importance of investigations evaluating dysbiosis at the molecular level, with specific regard to DNA methylation, as a causative driver of colorectal carcinogenesis.…”
mentioning
confidence: 99%