METTL14 的 m6A mRNA 甲基化调控早期胰腺细胞分化。

Sevim Kahraman,Dario F De Jesus,Jiangbo Wei,Natalie K Brown,Zhongyu Zou,Jiang Hu,Mehdi Pirouz,Richard I Gregory,Chuan He,Rohit N Kulkarni
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引用次数: 0

摘要

N6-甲基腺苷(m6A)是mRNA中最丰富的化学修饰,在人类和小鼠胚胎干细胞的全能性、维持和分化中发挥着重要作用。我们最近报告说,m6A 在生理状态和 1 型及 2 型糖尿病中参与了出生后对β细胞功能的控制。然而,m6A调控人类和小鼠胰腺发育的确切机制尚待探索。在这里,我们发现在人类胰腺发育过程中,m6A 的结构是动态的,而 m6A 作者复合蛋白之一 METTL14 对人类和小鼠胰腺细胞的早期分化至关重要。
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m6A mRNA methylation by METTL14 regulates early pancreatic cell differentiation.
N6-methyladenosine (m6A) is the most abundant chemical modification in mRNA and plays important roles in human and mouse embryonic stem cell pluripotency, maintenance, and differentiation. We have recently reported that m6A is involved in the postnatal control of β-cell function in physiological states and in type 1 and 2 diabetes. However, the precise mechanisms by which m6A acts to regulate the development of human and mouse pancreas are unexplored. Here, we show that the m6A landscape is dynamic during human pancreas development, and that METTL14, one of the m6A writer complex proteins, is essential for the early differentiation of both human and mouse pancreatic cells.
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