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转录因子特异性限制了 DNA 结合基序的数量。

Transcription factor specificity limits the number of DNA-binding motifs.

机构信息

Facultad de Ciencias Exactas y Naturales, Laboratorio de Fisiología de Proteínas, Consejo Nacional de lnvestigaciones Cientificas y Técnicas, Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales (IQUIBICEN), Universidad de Buenos Aires, Buenos Aires, Argentina.

Marine and Coastal Sciences Department, Rutgers University, New Brunswick, New Jersey, United States of America.

出版信息

PLoS One. 2022 Jan 28;17(1):e0263307. doi: 10.1371/journal.pone.0263307. eCollection 2022.

Abstract

We study the limits imposed by transcription factor specificity on the maximum number of binding motifs that can coexist in a gene regulatory network, using the SwissRegulon Fantom5 collection of 684 human transcription factor binding sites as a model. We describe transcription factor specificity using regular expressions and find that most human transcription factor binding site motifs are separated in sequence space by one to three motif-discriminating positions. We apply theorems based on the pigeonhole principle to calculate the maximum number of transcription factors that can coexist given this degree of specificity, which is in the order of ten thousand and would fully utilize the space of DNA subsequences. Taking into account an expanded DNA alphabet with modified bases can further raise this limit by several orders of magnitude, at a lower level of sequence space usage. Our results may guide the design of transcription factors at both the molecular and system scale.

摘要

我们研究了转录因子特异性对基因调控网络中可以共存的最大结合基序数量的限制,使用瑞士 Regulon Fantom5 收集的 684 个人类转录因子结合位点作为模型。我们使用正则表达式描述转录因子特异性,并发现大多数人类转录因子结合位点序列在序列空间中通过一个到三个区分基序的位置分开。我们应用基于鸽笼原理的定理来计算在这种特异性下可以共存的最大转录因子数量,这是数量级为万的,并且可以充分利用 DNA 子序列的空间。考虑到具有修饰碱基的扩展 DNA 字母表,可以在较低的序列空间使用水平上,将该限制提高几个数量级。我们的结果可以指导分子和系统尺度上的转录因子设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d40a/8797260/9f7df05567fa/pone.0263307.g001.jpg

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