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肠道的转录辅因子调控网络

A Transcriptional Cofactor Regulatory Network for the Intestine.

作者信息

Horowitz Brent B, Nanda Shivani, Walhout Albertha J M

出版信息

bioRxiv. 2023 Jan 6:2023.01.05.522920. doi: 10.1101/2023.01.05.522920.

DOI:10.1101/2023.01.05.522920
PMID:36711629
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9881946/
Abstract

Chromatin modifiers and transcriptional cofactors (collectively referred to as CFs) work with DNA-binding transcription factors (TFs) to regulate gene expression. In multicellular eukaryotes, distinct tissues each execute their own gene expression program for accurate differentiation and subsequent functionality. While the function of TFs in differential gene expression has been studied in detail in many systems, the contribution of CFs has remained less explored. Here we uncovered the contributions of CFs to gene regulation in the intestine. We first annotated 366 CFs encoded by the genome and assembled a library of 335 RNAi clones. Using this library, we analyzed the effects of individually depleting these CFs on the expression of 19 fluorescent transcriptional reporters in the intestine and identified 216 regulatory interactions. We found that different CFs interact specifically with different promoters, and that both essential and intestinally expressed CFs exhibit the highest proportion of interactions. We did not find all members of CF complexes acting on the same set of reporters but instead found diversity in the promoter targets of each complex component. Finally, we found that previously identified activation mechanisms for the promoter use different CFs and TFs. Overall, we demonstrate that CFs function specifically rather than ubiquitously at intestinal promoters and provide an RNAi resource for reverse genetic screens.

摘要

染色质修饰因子和转录辅因子(统称为CFs)与DNA结合转录因子(TFs)共同作用来调节基因表达。在多细胞真核生物中,不同组织各自执行自身的基因表达程序以实现精确分化和后续功能。虽然TFs在差异基因表达中的功能已在许多系统中得到详细研究,但CFs的作用仍较少被探索。在此,我们揭示了CFs在肠道中对基因调控的贡献。我们首先注释了基因组编码的366个CFs,并构建了一个包含335个RNAi克隆的文库。利用该文库,我们分析了单独敲除这些CFs对肠道中19个荧光转录报告基因表达的影响,并鉴定出216种调控相互作用。我们发现不同的CFs与不同的启动子特异性相互作用,并且必需的和在肠道中表达的CFs表现出最高比例的相互作用。我们没有发现CF复合物的所有成员作用于同一组报告基因,而是发现每个复合物组分的启动子靶标存在多样性。最后,我们发现先前鉴定的启动子激活机制使用不同的CFs和TFs。总体而言,我们证明CFs在肠道启动子处特异性而非普遍发挥作用,并为反向遗传筛选提供了一种RNAi资源。