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大量管家基因和组织特异性调控元件的高组成性活性取决于ETS蛋白的一个子集。

High constitutive activity of a broad panel of housekeeping and tissue-specific -regulatory elements depends on a subset of ETS proteins.

作者信息

Curina Alessia, Termanini Alberto, Barozzi Iros, Prosperini Elena, Simonatto Marta, Polletti Sara, Silvola Alessio, Soldi Monica, Austenaa Liv, Bonaldi Tiziana, Ghisletti Serena, Natoli Gioacchino

机构信息

Department of Experimental Oncology, European Institute of Oncology (IEO), 20139 Milan, Italy.

Humanitas Clinical and Research Center, 20089 Rozzano-Milan, Italy.

出版信息

Genes Dev. 2017 Feb 15;31(4):399-412. doi: 10.1101/gad.293134.116. Epub 2017 Mar 8.

DOI:10.1101/gad.293134.116
PMID:28275002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5358759/
Abstract

Enhancers and promoters that control the transcriptional output of terminally differentiated cells include cell type-specific and broadly active housekeeping elements. Whether the high constitutive activity of these two groups of -regulatory elements relies on entirely distinct or instead also on shared regulators is unknown. By dissecting the -regulatory repertoire of macrophages, we found that the ELF subfamily of ETS proteins selectively bound within 60 base pairs (bp) from the transcription start sites of highly active housekeeping genes. ELFs also bound constitutively active, but not poised, macrophage-specific enhancers and promoters. The role of ELFs in promoting high-level constitutive transcription was suggested by multiple evidence: ELF sites enabled robust transcriptional activation by endogenous and minimal synthetic promoters, ELF recruitment was stabilized by the transcriptional machinery, and ELF proteins mediated recruitment of transcriptional and chromatin regulators to core promoters. These data suggest that the co-optation of a limited number of highly active transcription factors represents a broadly adopted strategy to equip both cell type-specific and housekeeping -regulatory elements with the ability to efficiently promote transcription.

摘要

控制终末分化细胞转录输出的增强子和启动子包括细胞类型特异性和广泛活跃的管家元件。这两类调控元件的高组成活性是完全依赖于截然不同的调节因子,还是也依赖于共享的调节因子,目前尚不清楚。通过剖析巨噬细胞的调控元件库,我们发现ETS蛋白的ELF亚家族选择性地结合在高活性管家基因转录起始位点60个碱基对(bp)范围内。ELF也结合组成型活跃但未就绪的巨噬细胞特异性增强子和启动子。多项证据表明ELF在促进高水平组成型转录中发挥作用:ELF位点能够通过内源性和最小合成启动子实现强大的转录激活,转录机制稳定了ELF的招募,并且ELF蛋白介导转录和染色质调节因子向核心启动子的招募。这些数据表明,选择有限数量的高活性转录因子是一种广泛采用的策略,使细胞类型特异性和管家调控元件都具备有效促进转录的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc7f/5358759/4fc31e695c58/399f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc7f/5358759/21998b0a2775/399f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc7f/5358759/4fc31e695c58/399f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc7f/5358759/21998b0a2775/399f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc7f/5358759/4fc31e695c58/399f04.jpg

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