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转录因子靶位搜索和非特异性结合位点背景下的基因调控。

Transcription factor target site search and gene regulation in a background of unspecific binding sites.

机构信息

Institute of Biophysics, Ulm University, Albert-Einstein-Allee 11, Ulm 89081, Germany.

Institute of Biophysics, Ulm University, Albert-Einstein-Allee 11, Ulm 89081, Germany.

出版信息

J Theor Biol. 2018 Oct 7;454:91-101. doi: 10.1016/j.jtbi.2018.05.037. Epub 2018 Jun 2.

Abstract

Response time and transcription level are vital parameters of gene regulation. They depend on how fast transcription factors (TFs) find and how efficient they occupy their specific target sites. It is well known that target site search is accelerated by TF binding to and sliding along unspecific DNA and that unspecific associations alter the occupation frequency of a gene. However, whether target site search time and occupation frequency can be optimized simultaneously is mostly unclear. We developed a transparent and intuitively accessible state-based formalism to calculate search times to target sites on and occupation frequencies of promoters of arbitrary state structure. Our formalism is based on dissociation rate constants experimentally accessible in live cell experiments. To demonstrate our approach, we consider promoters activated by a single TF, by two coactivators or in the presence of a competitive inhibitor. We find that target site search time and promoter occupancy differentially vary with the unspecific dissociation rate constant. Both parameters can be harmonized by adjusting the specific dissociation rate constant of the TF. However, while measured DNA residence times of various eukaryotic TFs correspond to a fast search time, the occupation frequencies of target sites are generally low. Cells might tolerate low target site occupancies as they enable timely gene regulation in response to a changing environment.

摘要

反应时间和转录水平是基因调控的重要参数。它们取决于转录因子 (TFs) 找到特定靶标位点的速度和效率。众所周知,TF 与非特异性 DNA 结合并沿其滑动可加速靶标搜索,非特异性结合改变了基因的占据频率。然而,目标搜索时间和占据频率是否可以同时优化,目前尚不清楚。我们开发了一种透明且直观的基于状态的形式主义方法,用于计算任意状态结构的启动子上的靶标搜索时间和占据频率。我们的形式主义方法基于在活细胞实验中可获得的离解速率常数。为了验证我们的方法,我们考虑了由单个 TF、两个共激活因子或竞争性抑制剂激活的启动子。我们发现,非特异性离解速率常数会导致靶标搜索时间和启动子占据的差异。通过调整 TF 的特异性离解速率常数,可以协调这两个参数。然而,尽管各种真核 TF 的测量 DNA 停留时间对应于快速搜索时间,但靶标位点的占据频率通常较低。细胞可能容忍低靶标占据,因为它们能够及时响应环境变化进行基因调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/080b/6103292/a2bd2a1ff071/gr1.jpg

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