DOT1L在神经发育和神经及精神障碍中的作用

IF 4.4 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Feiyan Shen , Linghui Zeng , Yanpan Gao
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引用次数: 0

摘要

端粒沉默1样干扰物(DOT1L)是哺乳动物中唯一的甲基转移酶,负责催化赖氨酸79 (H3K79)组蛋白H3的单甲基化、二甲基化和三甲基化,这种修饰对各种细胞过程至关重要,包括基因转录、细胞周期调节、DNA修复和发育。最近的研究越来越多地将DOT1L与神经系统联系起来,它在神经发育和神经元功能中起着至关重要的作用。它可以调节神经祖细胞的增殖和分化,促进神经元成熟,影响突触功能,这些都是正常的神经回路形成和大脑功能所必需的。此外,DOT1L的失调与几种神经系统疾病有关,突出了其在疾病病理中的潜在作用。DOT1L的异常表达或活性与认知缺陷和神经退行性疾病有关,强调了该酶在神经系统发育和维持中的重要性。本文综述了DOT1L在神经系统中的作用,强调了其在神经发育中的重要性,并探讨了其作为神经系统疾病治疗靶点的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DOT1L in neural development and neurological and psychotic disorders
Disruptor of Telomeric Silencing 1-Like (DOT1L) is the sole methyltransferase in mammals responsible for catalyzing the mono-, di-, and trimethylation of histone H3 at lysine 79 (H3K79), a modification crucial for various cellular processes, including gene transcription, cell cycle regulation, DNA repair, and development. Recent studies have increasingly linked DOT1L to the nervous system, where it plays a vital role in neurodevelopment and neuronal function. It has been shown to regulate the proliferation and differentiation of neural progenitor cells, promote neuronal maturation, and influence synaptic function, all of which are essential for proper neural circuit formation and brain function. Moreover, dysregulation of DOT1L has been associated with several neurological disorders, highlighting its potential role in disease pathology. Abnormal expression or activity of DOT1L has been implicated in cognitive deficits and neurodegenerative diseases, underscoring the enzyme's significance in both the development and maintenance of the nervous system. This review synthesizes recent findings on DOT1L's role in the nervous system, emphasizing its importance in neurodevelopment and exploring its potential as a therapeutic target for treating neurological disorders.
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来源期刊
Neurochemistry international
Neurochemistry international 医学-神经科学
CiteScore
8.40
自引率
2.40%
发文量
128
审稿时长
37 days
期刊介绍: Neurochemistry International is devoted to the rapid publication of outstanding original articles and timely reviews in neurochemistry. Manuscripts on a broad range of topics will be considered, including molecular and cellular neurochemistry, neuropharmacology and genetic aspects of CNS function, neuroimmunology, metabolism as well as the neurochemistry of neurological and psychiatric disorders of the CNS.
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