生物
重编程
表观遗传学
染色质
表观遗传学
诱导多能干细胞
二价染色质
细胞生物学
细胞分化
背景(考古学)
H3K4me3
遗传学
胚胎干细胞
染色质重塑
DNA甲基化
基因表达
基因
发起人
古生物学
作者
Rachel Herndon Klein,Paul S. Knoepfler
标识
DOI:10.1016/j.stemcr.2021.10.008
摘要
Many gene networks are shared between pluripotent stem cells and cancer; a concept exemplified by several DPPA factors such as DPPA2 and DPPA4, which are highly and selectively expressed in stem cells but also found to be reactivated in cancer. Despite their striking expression pattern, for many years the function of DPPA2 and DPPA4 remained a mystery; knockout of Dppa2 and Dppa4 did not affect pluripotency, but caused lung and skeletal defects late in development, long after Dppa2 and Dppa4 expression had been turned off. A number of recent papers have further clarified and defined the roles of these important factors, identifying roles in priming the chromatin and maintaining developmental competency through regulating both H3K4me3 and H3K27me3 at bivalent chromatin domains, and acting to remodel chromatin and facilitate reprogramming of somatic cells to induced pluripotency. These findings highlight an important regulatory role for DPPA2 and DPPA4 at the transitional boundary between pluripotency and differentiation and may have relevance to the functions of DPPA2 and 4 in the context of cancer cells as well.
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