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转录因子搜索其基因组结合位点的速度-特异性权衡。

Speed-Specificity Trade-Offs in the Transcription Factors Search for Their Genomic Binding Sites.

机构信息

Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel.

Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel.

出版信息

Trends Genet. 2021 May;37(5):421-432. doi: 10.1016/j.tig.2020.12.001. Epub 2021 Jan 5.

Abstract

Transcription factors (TFs) regulate gene expression by binding DNA sequences recognized by their DNA-binding domains (DBDs). DBD-recognized motifs are short and highly abundant in genomes. The ability of TFs to bind a specific subset of motif-containing sites, and to do so rapidly upon activation, is fundamental for gene expression in all eukaryotes. Despite extensive interest, our understanding of the TF-target search process is fragmented; although binding specificity and detection speed are two facets of this same process, trade-offs between them are rarely addressed. In this opinion article, we discuss potential speed-specificity trade-offs in the context of existing models. We further discuss the recently described 'distributed specificity' paradigm, suggesting that intrinsically disordered regions (IDRs) promote specificity while reducing the TF-target search time.

摘要

转录因子 (TFs) 通过结合其 DNA 结合域 (DBD) 识别的 DNA 序列来调节基因表达。DBD 识别的基序很短,在基因组中高度丰富。TF 能够结合特定的一组包含基序的位点,并且在激活后快速结合,这对于所有真核生物的基因表达都是至关重要的。尽管人们对此非常感兴趣,但我们对 TF-靶标搜索过程的理解仍然很零碎;尽管结合特异性和检测速度是同一过程的两个方面,但很少涉及它们之间的权衡。在这篇观点文章中,我们将根据现有的模型讨论潜在的速度-特异性权衡。我们进一步讨论了最近描述的“分布式特异性”范例,表明无序区域 (IDR) 促进特异性的同时减少了 TF-靶标搜索时间。

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