Meng Wei-Ying, Wang Zi-Xin, Zhang Yunfang, Hou Yujun, Xue Jian-Huang
Key Laboratory of Spine and Spinal Cord Injury Repair and Regeneration of Ministry of Education, Tongji Hospital affiliated to Tongji University, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, Shanghai Key Laboratory of Signaling and Disease Research, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, China.
J Biol Chem. 2024 Apr;300(4):106791. doi: 10.1016/j.jbc.2024.106791. Epub 2024 Feb 23.
DNA modifications add another layer of complexity to the eukaryotic genome to regulate gene expression, playing critical roles as epigenetic marks. In eukaryotes, the study of DNA epigenetic modifications has been confined to 5mC and its derivatives for decades. However, rapid developing approaches have witnessed the expansion of DNA modification reservoirs during the past several years, including the identification of 6mA, 5gmC, 4mC, and 4acC in diverse organisms. However, whether these DNA modifications function as epigenetic marks requires careful consideration. In this review, we try to present a panorama of all the DNA epigenetic modifications in eukaryotes, emphasizing recent breakthroughs in the identification of novel DNA modifications. The characterization of their roles in transcriptional regulation as potential epigenetic marks is summarized. More importantly, the pathways for generating or eliminating these DNA modifications, as well as the proteins involved are comprehensively dissected. Furthermore, we briefly discuss the potential challenges and perspectives, which should be taken into account while investigating novel DNA modifications.
DNA修饰为真核生物基因组增添了另一层复杂性以调控基因表达,作为表观遗传标记发挥着关键作用。在真核生物中,几十年来DNA表观遗传修饰的研究一直局限于5-甲基胞嘧啶(5mC)及其衍生物。然而,在过去几年中,快速发展的方法见证了DNA修饰库的扩展,包括在多种生物中鉴定出6-甲基腺嘌呤(6mA)、5-羟甲基胞嘧啶(5gmC)、4-甲基胞嘧啶(4mC)和4-乙酰胞嘧啶(4acC)。然而,这些DNA修饰是否作为表观遗传标记发挥作用需要仔细考量。在本综述中,我们试图呈现真核生物中所有DNA表观遗传修饰的全景,强调在新型DNA修饰鉴定方面的最新突破。总结了它们作为潜在表观遗传标记在转录调控中的作用特征。更重要的是,全面剖析了产生或消除这些DNA修饰的途径以及相关蛋白。此外,我们简要讨论了在研究新型DNA修饰时应考虑的潜在挑战和前景。