NuRD在造血基因表达中功能的保守机制。

Q3 Biochemistry, Genetics and Molecular Biology Enzymes Pub Date : 2023-01-01 Epub Date: 2023-08-30 DOI:10.1016/bs.enz.2023.07.006
Jonathan Lenz, Alexander Brehm
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引用次数: 0

摘要

核小体重塑和脱乙酰复合物(NuRD)在所有后生动物中普遍表达。它结合了核小体重塑和组蛋白脱乙酰活性,产生不可接近的染色质结构并抑制基因转录。NuRD参与分化过程中和分化细胞中各种谱系特异性基因表达程序的产生和维持。与大量谱系特异性转录因子的密切合作是使NuRD在许多不同的分化环境中发挥作用的关键。转录因子和NuRD之间这种相互作用的分子性质是复杂的,还没有被很好地理解。这篇综述以造血为范式,强调我们对转录因子和NuRD在分化过程中如何在分子水平上合作的理解的最新进展。脊椎动物和无脊椎动物系统的比较有助于确定指导转录因子和NuRD之间功能相互作用的保守和基本概念。我们还讨论了转录因子NuRD轴如何构成治疗血红蛋白病的潜在治疗靶点。
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Conserved mechanisms of NuRD function in hematopoetic gene expression.

The Nucleosome Remodeling and Deacetylating Complex (NuRD) is ubiquitously expressed in all metazoans. It combines nucleosome remodeling and histone deacetylating activities to generate inaccessible chromatin structures and to repress gene transcription. NuRD is involved in the generation and maintenance of a wide variety of lineage-specific gene expression programs during differentiation and in differentiated cells. A close cooperation with a large number of lineage-specific transcription factors is key to allow NuRD to function in many distinct differentiation contexts. The molecular nature of this interplay between transcription factors and NuRD is complex and not well understood. This review uses hematopoiesis as a paradigm to highlight recent advances in our understanding of how transcription factors and NuRD cooperate at the molecular level during differentiation. A comparison of vertebrate and invertebrate systems serves to identify the conserved and fundamental concepts guiding functional interactions between transcription factors and NuRD. We also discuss how the transcription factor-NuRD axis constitutes a potential therapeutic target for the treatment of hemoglobinopathies.

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来源期刊
Enzymes
Enzymes Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
4.30
自引率
0.00%
发文量
10
期刊最新文献
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