锌指转录因子在神经发育障碍中的分子机制研究进展

IF 2.9 Q3 NEUROSCIENCES IBRO Neuroscience Reports Pub Date : 2025-06-01 Epub Date: 2025-02-26 DOI:10.1016/j.ibneur.2025.02.010
Hailin Wang , Ying Yang , Ziwei Ni , Xiaoting Qiao , Yaqian Guo , Xiaomin Wang , Duo Cao , Yayun Wang , Cailian Ruan
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引用次数: 0

摘要

神经发育障碍(ndd)是一种异质性的早发性脑功能障碍,可能由遗传或获得性病因引起。这些障碍的特点是行为和认知缺陷,主要表现在儿童发育期间,因此可能损害个人在学习、运动和社交场合的表现。全面了解ndd的发病机制对于制定有针对性的治疗干预措施至关重要。锌指转录因子(Zinc-finger transcription factors, ZFPs)通过调节RNA聚合酶与DNA的结合,激活或抑制基因转录,在基因表达调控中发挥关键作用。近年来,ZFPs的BCL11基因家族因其在神经系统发育中的重要参与而引起了极大的关注。本文旨在阐明BCL11基因家族的结构和分子功能,探讨其对中枢神经系统发育的影响,并探讨其与神经发育障碍的关系。
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Advances in the molecular mechanisms of zinc-finger transcription factors in neurodevelopmental disorders
Neurodevelopmental disorders (NDDs) constitute a heterogeneous group of early-onset brain dysfunction disorders, which may arise from genetic or acquired etiologies. These disorders are characterized by behavioral and cognitive deficits that predominantly manifest during childhood development, thereby potentially impairing an individual's performance in learning, sports, and social situations. A comprehensive understanding of the pathogenesis of NDDs is crucial for the development of targeted therapeutic interventions. Zinc-finger transcription factors (ZFPs) play a pivotal role in regulating gene expression by modulating the binding of RNA polymerase to DNA, thereby either activating or repressing gene transcription. In recent years, the BCL11 gene family of ZFPs has garnered significant attention due to its critical involvement in nervous system development. This review aims to elucidate the structure and molecular functions of the BCL11 gene family, discuss its impact on the development of the central nervous system, and explore its association with neurodevelopmental disorders.
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来源期刊
IBRO Neuroscience Reports
IBRO Neuroscience Reports Neuroscience-Neuroscience (all)
CiteScore
2.80
自引率
0.00%
发文量
99
审稿时长
14 weeks
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