Department of Biochemistry, Duke University School of Medicine, Durham, North Carolina 27710; email:
Department of Pharmacology, Weill Medical College, Cornell University, New York, New York 10065; email:
Annu Rev Cell Dev Biol. 2017 Oct 6;33:319-342. doi: 10.1146/annurev-cellbio-100616-060758. Epub 2017 Jul 31.
In recent years, mA has emerged as an abundant and dynamically regulated modification throughout the transcriptome. Recent technological advances have enabled the transcriptome-wide identification of mA residues, which in turn has provided important insights into the biology and regulation of this pervasive regulatory mark. Also central to our current understanding of mA are the discovery and characterization of mA readers, writers, and erasers. Over the last few years, studies into the function of these proteins have led to important discoveries about the regulation and function of mA. However, during this time our understanding of these proteins has also evolved considerably, sometimes leading to the reversal of early concepts regarding the reading, writing and erasing of mA. In this review, we summarize recent advances in mA research, and we highlight how these new findings have reshaped our understanding of how mA is regulated in the transcriptome.
近年来,m6A 作为一种丰富且动态调控的转录后修饰在整个转录组中广泛存在。最近的技术进步使得 m6A 残基的全转录组鉴定成为可能,这反过来又为理解这种普遍存在的调控标记的生物学和调控机制提供了重要线索。m6A 研究的另一个核心内容是 m6A 阅读蛋白、写作蛋白和擦除蛋白的发现和特征鉴定。在过去的几年中,对这些蛋白功能的研究导致了关于 m6A 阅读、写作和擦除调控和功能的重要发现。然而,在此期间,我们对这些蛋白的理解也有了很大的发展,有时导致了早期关于 m6A 阅读、写作和擦除概念的反转。在这篇综述中,我们总结了 m6A 研究的最新进展,并强调了这些新发现如何重塑我们对 m6A 在转录组中调控方式的理解。