N6-腺苷甲基化与 LINE-1 的调控机制

Q3 Medicine 遗传 Pub Date : 2024-03-20 DOI:10.16288/j.yczz.23-248
Ao Zhang, Shan Cen, Xiao-Yu Li
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引用次数: 0

摘要

长穿插元件-1(LINE-1)是人类基因组中唯一的自主转座子,它的逆转录会导致细胞基因组结构和功能的改变,导致各种严重疾病的发生。作为LINE-1逆转录过程中的核心关键中间环节,宿主对LINE-1 mRNA的修饰直接影响着LINE-1的转位。N6-腺苷甲基化(m6A)是真核RNA上最丰富的表观遗传修饰,具有动态可逆性。m6A修饰也存在于LINE-1 mRNA上,它参与调控整个LINE-1复制周期,影响LINE-1逆转录及其邻近基因的表达,进而影响基因组稳定性、细胞自我更新和分化潜能,在人类发育和疾病中发挥着重要作用。在这篇综述中,我们总结了LINE-1 m6A修饰的研究进展,包括其修饰位置、模式和相关机制,希望能为相关疾病的机制研究和治疗提供新的视角。
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N6-adenosine methylation and the regulatory mechanism on LINE-1.

Long interspersed elements-1(LINE-1) is the only autonomous transposon in human genome,and its retrotransposition results in change of cellular genome structure and function, leading occurrence of various severe diseases. As a central key intermediated component during life cycle of LINE-1 retrotransposition, the host modification of LINE-1 mRNA affects the LINE-1 transposition directly. N6-adenosine methylation(m6A), the most abundant epigenetic modification on eukaryotic RNA, is dynamically reversible. m6A modification is also found on LINE-1 mRNA, and it participants regulation of the whole LINE-1 replication cycle, with affecting LINE-1 retrotransposition as well as its adjacent genes expression, followed by influencing genomic stability, cellular self-renewal, and differentiation potential, which plays important roles in human development and diseases. In this review, we summarize the research progress in LINE-1 m6A modification, including its modification positions, patterns and related mechanisms, hoping to provide a new sight on the mechanism research and treatment of related diseases.

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来源期刊
遗传
遗传 Medicine-Medicine (all)
CiteScore
2.50
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0.00%
发文量
6699
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