Genome-wide dynamic nascent transcript profiles reveal that most paused RNA polymerases terminate.

Rudradeep Mukherjee, Michael J Guertin
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Abstract

We present a simple model for analyzing and interpreting data from kinetic experiments that measure engaged RNA polymerase occupancy. The framework represents the densities of nascent transcripts within the pause region and the gene body as steady-state values determined by four key transcriptional processes: initiation, pause release, premature termination, and elongation. We validate the model's predictions using data from experiments that rapidly inhibit initiation and pause release. The model successfully classified factors based on the steps in early transcription that they regulate, confirming TBP and ZNF143 as initiation factors and HSF and GR as pause release factors. We found that most paused polymerases terminate and paused polymerases are short-lived with half lives less than a minute. We make this model available as software to serve as a quantitative tool for determining the kinetic mechanisms of transcriptional regulation.

全基因组动态新生转录本图谱显示,大多数暂停的 RNA 聚合酶都会终止。
我们提出了一个简单的模型,用于分析和解释动力学实验中测量参与RNA聚合酶占用的数据。该框架代表了暂停区域和基因体内新生转录本的密度,作为由四个关键转录过程决定的稳态值:起始,暂停释放,过早终止和延伸。我们使用实验数据验证了模型的预测,这些数据可以快速抑制起始和暂停释放。该模型成功地根据其调控的早期转录步骤对因子进行分类,确认TBP和ZNF143为起始因子,HSF和GR为暂停释放因子。我们发现大多数暂停聚合酶终止,暂停聚合酶的半衰期不到一分钟。我们将该模型作为软件提供,作为确定转录调控动力学机制的定量工具。
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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