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同源等位基因共享转录机制导致早期胚胎转录减少。

Shared Transcriptional Machinery at Homologous Alleles Leads to Reduced Transcription in Early Embryos.

作者信息

Deng Hao, Lim Bomyi

机构信息

Department of Chemical and Biomolecular Engineering, University of Pennsylvania, Philadelphia, PA, United States.

出版信息

Front Cell Dev Biol. 2022 Jul 11;10:912838. doi: 10.3389/fcell.2022.912838. eCollection 2022.

DOI:10.3389/fcell.2022.912838
PMID:35898395
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9311490/
Abstract

The mechanism by which transcriptional machinery is recruited to enhancers and promoters to regulate gene expression is one of the most challenging and extensively studied questions in modern biology. We explored the possibility that interallelic interactions between two homologous alleles might affect gene regulation. Using an MS2- and PP7-based, allele-specific live imaging assay, we visualized transcripts of a reporter gene in hemizygous and homozygous embryos. Surprisingly, each homozygous allele produced fewer RNAs than the corresponding hemizygous allele, suggesting the possibility of allelic competition in homozygotes. However, the competition was not observed when the enhancer-promoter interaction was weakened by placing the reporter construct in a different chromosome location or by moving the enhancer further away from the promoter. Moreover, the reporter gene showed reduced transcriptional activity when a partial transcription unit (either an enhancer or reporter gene only) was in the homologous position. We propose that the transcriptional machinery that binds both the enhancer and promoter regions, such as RNA Pol II or preinitiation complexes, may be responsible for the allelic competition. We showed that the degree of allelic interference increased over developmental time as more Pol II was needed to activate zygotic genes. Such allelic competition was observed for an endogenous gene as well. Our study provides new insights into the role of 3D interallelic interactions in gene regulation.

摘要

转录机制被招募到增强子和启动子以调控基因表达的方式,是现代生物学中最具挑战性且研究广泛的问题之一。我们探究了两个同源等位基因之间的等位基因间相互作用可能影响基因调控的可能性。利用基于MS2和PP7的等位基因特异性活细胞成像分析方法,我们在半合子和纯合子胚胎中观察了报告基因的转录本。令人惊讶的是,每个纯合等位基因产生的RNA比相应的半合子等位基因少,这表明纯合子中存在等位基因竞争的可能性。然而,当通过将报告基因构建体置于不同染色体位置或使增强子远离启动子来削弱增强子 - 启动子相互作用时,未观察到竞争现象。此外,当部分转录单元(仅增强子或仅报告基因)处于同源位置时,报告基因的转录活性降低。我们提出,结合增强子和启动子区域的转录机制,如RNA聚合酶II或起始前复合物,可能是等位基因竞争的原因。我们发现,随着激活合子基因需要更多的聚合酶II,等位基因干扰程度在发育过程中增加。对于一个内源基因也观察到了这种等位基因竞争。我们的研究为三维等位基因间相互作用在基因调控中的作用提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf0/9311490/0ad779ca1a30/fcell-10-912838-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf0/9311490/70690e0fd02d/fcell-10-912838-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf0/9311490/4e87f3bddcff/fcell-10-912838-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf0/9311490/0c10ce8ef445/fcell-10-912838-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf0/9311490/0ad779ca1a30/fcell-10-912838-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf0/9311490/70690e0fd02d/fcell-10-912838-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf0/9311490/4e87f3bddcff/fcell-10-912838-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf0/9311490/0c10ce8ef445/fcell-10-912838-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf0/9311490/0ad779ca1a30/fcell-10-912838-g004.jpg

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Nature. 2022 May;605(7911):754-760. doi: 10.1038/s41586-022-04680-7. Epub 2022 May 4.
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Nonlinear control of transcription through enhancer-promoter interactions.通过增强子-启动子相互作用的转录非线性控制。
Nature. 2022 Apr;604(7906):571-577. doi: 10.1038/s41586-022-04570-y. Epub 2022 Apr 13.
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Molecular competition can shape enhancer activity in the embryo.分子竞争能够塑造胚胎中的增强子活性。
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