ZN手指转录因子的抑制作用

Tianlai Chen, Zihong Chen
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引用次数: 0

摘要

锌指是最丰富的蛋白基序之一,在细胞增殖、迁移和分化中起着关键作用。新兴的研究集中在锌指转录因子在相关疾病中的作用,发现它们参与激活致癌转录,HIV逆转录和细菌感染。因此,研究和了解锌指转录因子如何被选择性抑制是很重要的。这篇综述的目的是描述锌指抑制是如何在化学和生物学框架内发生的。综述了配合物的合成、抑制机制和选择性。细胞利用磷酸化和乙酰化作用,通过调节锌指转录因子的空间结构和化学性质来自我抑制锌指转录因子。此外,我们还提出了转录后修饰的潜在调控位点、治疗方法和对动物试验的关注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Inhibition of ZN Finger Transcription Factors
Zinc fingers are among the most abundant protein motifs and play a pivotal role in cell proliferation, migration, and differentiation. Emerging studies have focused on the zinc finger transcription factors role in related diseases and discovered they are involved in activating oncogenic transcription, HIV reverse transcription, and bacterium infection. Hence, it is important to investigate and understand how zinc finger transcription factors can be selectively inhibited. The aim of this minireview is to describe how Zn Finger inhibition occurs within both a chemical and biological framework. Complexes Synthesis, inhibition mechanism, and selectivity are comprehensively reviewed. Cells utilize phosphorylation and acetylation to self-inhibit the zinc finger transcription factors by adjusting spatial structure and chemical properties. Also, we propose potential regulation sites of post transcription modification, therapeutic treatments and concerns over animal trials.
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