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多重增强子干扰揭示了雌激素受体 α 结合增强子对基因调控的协同控制。

Multiplex Enhancer Interference Reveals Collaborative Control of Gene Regulation by Estrogen Receptor α-Bound Enhancers.

机构信息

Department of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.

Department of Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA.

出版信息

Cell Syst. 2017 Oct 25;5(4):333-344.e5. doi: 10.1016/j.cels.2017.08.011. Epub 2017 Sep 27.

DOI:10.1016/j.cels.2017.08.011
PMID:28964699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5679353/
Abstract

Multiple regulatory regions have the potential to regulate a single gene, yet how these elements combine to affect gene expression remains unclear. To uncover the combinatorial relationships between enhancers, we developed Enhancer-interference (Enhancer-i), a CRISPR interference-based approach that uses 2 different repressive domains, KRAB and SID, to prevent enhancer activation simultaneously at multiple regulatory regions. We applied Enhancer-i to promoter-distal estrogen receptor α binding sites (ERBS), which cluster around estradiol-responsive genes and therefore may collaborate to regulate gene expression. Targeting individual sites revealed predominant ERBS that are completely required for the transcriptional response, indicating a lack of redundancy. Simultaneous interference of different ERBS combinations identified supportive ERBS that contribute only when predominant sites are active. Using mathematical modeling, we find strong evidence for collaboration between predominant and supportive ERBS. Overall, our findings expose a complex functional hierarchy of enhancers, where multiple loci bound by the same transcription factor combine to fine-tune the expression of target genes.

摘要

多个调控区域有可能调节单个基因,但这些元件如何组合来影响基因表达尚不清楚。为了揭示增强子之间的组合关系,我们开发了增强子干扰(Enhancer-i),这是一种基于 CRISPR 干扰的方法,使用 2 种不同的抑制结构域 KRAB 和 SID,同时防止多个调控区域的增强子激活。我们将 Enhancer-i 应用于启动子远端雌激素受体α结合位点(ERBS),这些位点聚集在雌二醇反应基因周围,因此可能协同作用以调节基因表达。针对单个位点的研究表明,大多数 ERBS 完全是转录反应所必需的,这表明它们之间不存在冗余性。不同 ERBS 组合的同时干扰确定了仅在主要位点活跃时才起作用的支持性 ERBS。使用数学模型,我们发现主要 ERBS 和支持性 ERBS 之间存在协作的有力证据。总的来说,我们的研究结果揭示了增强子的复杂功能层次结构,其中由同一转录因子结合的多个位点结合起来微调靶基因的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be47/5679353/da9c1d5a10fa/nihms902356f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be47/5679353/3ce476a7917b/nihms902356f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be47/5679353/e6ddc093c1c1/nihms902356f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be47/5679353/8b2a38905059/nihms902356f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be47/5679353/7e41fb5af295/nihms902356f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be47/5679353/da9c1d5a10fa/nihms902356f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be47/5679353/3ce476a7917b/nihms902356f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be47/5679353/e6ddc093c1c1/nihms902356f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be47/5679353/8b2a38905059/nihms902356f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be47/5679353/7e41fb5af295/nihms902356f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be47/5679353/da9c1d5a10fa/nihms902356f5.jpg

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