Transcription elongation mechanisms that control gene expression in erythropoiesis.

2区 生物学 Q1 Biochemistry, Genetics and Molecular Biology
Current Topics in Developmental Biology Pub Date : 2026-01-01 Epub Date: 2026-06-23 DOI:10.1016/bs.ctdb.2026.06.004
Kaustav Mukherjee, James J Bieker
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引用次数: 0

Abstract

The regulation of RNA transcript abundance relies on the control of two key early steps in gene expression: transcription initiation and productive elongation. Although DNA-directed RNA polymerase provides the intrinsic catalytic activity required for RNA synthesis, its ability to effectively produce a transcript relies on accurate recruitment to specific DNA sites to initiate RNA polymerization, followed by release from promoter-proximal pausing into a productive elongation machine. These steps are governed by accessory factors that not only facilitate the assembly of a functional pre-initiation complex but also exert both negative and positive control over polymerase pause/elongation status. We describe experiments that have elucidated these mechanisms in the context of erythropoiesis.

调控红细胞生成过程中基因表达的转录延伸机制。
RNA转录丰度的调控依赖于基因表达的两个关键早期步骤的控制:转录起始和生产延伸。尽管DNA定向RNA聚合酶提供了RNA合成所需的内在催化活性,但其有效产生转录物的能力依赖于准确招募到特定DNA位点以启动RNA聚合,然后从启动子近端暂停释放到生产延伸机器。这些步骤是由辅助因素控制的,这些辅助因素不仅促进了功能性起始前复合物的组装,而且对聚合酶暂停/延伸状态施加了消极和积极的控制。我们描述了在红细胞生成的背景下阐明这些机制的实验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
91
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