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多梳反应元件的多任务处理

Multitasking by Polycomb response elements.

作者信息

Jaensch Elizabeth S, Kundu Sharmistha, Kingston Robert E

机构信息

Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, 02114, USA.

出版信息

Genes Dev. 2017 Jun 1;31(11):1069-1072. doi: 10.1101/gad.303206.117.

DOI:10.1101/gad.303206.117
PMID:28717045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5538430/
Abstract

Development requires the expression of master regulatory genes necessary to specify a cell lineage. Equally significant is the stable and heritable silencing of master regulators that would specify alternative lineages. This regulated gene silencing is carried out by Polycomb group (PcG) proteins, which must be correctly recruited only to the subset of their target loci that requires lineage-specific silencing. A recent study by Erceg and colleagues (pp. 590-602) expands on a key aspect of that targeting: The same DNA elements that recruit PcG complexes to a repressed locus also encode transcriptional enhancers that function in different lineages where that locus must be expressed. Thus, PcG targeting elements overlap with enhancers.

摘要

发育需要表达指定细胞谱系所必需的主调控基因。同样重要的是,那些会指定其他谱系的主调控因子要实现稳定且可遗传的沉默。这种受调控的基因沉默是由多梳蛋白家族(PcG)蛋白执行的,这些蛋白必须仅被正确招募到其需要谱系特异性沉默的目标基因座子集中。Erceg及其同事最近的一项研究(第590 - 602页)扩展了这种靶向的一个关键方面:将PcG复合物招募到一个抑制基因座的相同DNA元件,同时也编码转录增强子,这些增强子在该基因座必须表达的不同谱系中发挥作用。因此,PcG靶向元件与增强子重叠。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0537/5538430/a1c0e66c8a1d/1069f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0537/5538430/a1c0e66c8a1d/1069f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0537/5538430/a1c0e66c8a1d/1069f01.jpg

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本文引用的文献

1
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Genes Dev. 2017 Mar 15;31(6):590-602. doi: 10.1101/gad.292870.116. Epub 2017 Apr 5.
2
Causal role for inheritance of H3K27me3 in maintaining the OFF state of a HOX gene.H3K27me3的遗传在维持HOX基因的关闭状态中的因果作用。
Science. 2017 Apr 7;356(6333). doi: 10.1126/science.aai8236. Epub 2017 Mar 16.
3
Propagation of Polycomb-repressed chromatin requires sequence-specific recruitment to DNA.
三种类型的人类 PRC2 和 MLL1/2-Trithorax 复合物的反应元件。
Nucleic Acids Res. 2018 Sep 28;46(17):8848-8864. doi: 10.1093/nar/gky595.
多梳抑制染色质的传播需要序列特异性招募到 DNA。
Science. 2017 Apr 7;356(6333):85-88. doi: 10.1126/science.aai8266. Epub 2017 Mar 16.
4
PRC2 Facilitates the Regulatory Topology Required for Poised Enhancer Function during Pluripotent Stem Cell Differentiation.PRC2 促进多能干细胞分化过程中启动子增强子功能所需的调控拓扑结构。
Cell Stem Cell. 2017 May 4;20(5):689-705.e9. doi: 10.1016/j.stem.2017.02.004. Epub 2017 Mar 9.
5
A distal intergenic region controls pancreatic endocrine differentiation by acting as a transcriptional enhancer and as a polycomb response element.一个远端基因间区域通过作为转录增强子和多梳反应元件来控制胰腺内分泌分化。
PLoS One. 2017 Feb 22;12(2):e0171508. doi: 10.1371/journal.pone.0171508. eCollection 2017.
6
Polycomb Repressive Complex 1 Generates Discrete Compacted Domains that Change during Differentiation.多梳抑制复合体1产生在分化过程中发生变化的离散紧密结构域。
Mol Cell. 2017 Feb 2;65(3):432-446.e5. doi: 10.1016/j.molcel.2017.01.009.
7
Interdependence of PRC1 and PRC2 for recruitment to Polycomb Response Elements.PRC1与PRC2在招募至多梳反应元件过程中的相互依赖性。
Nucleic Acids Res. 2016 Dec 1;44(21):10132-10149. doi: 10.1093/nar/gkw701. Epub 2016 Aug 23.
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An Evolutionary Conserved Epigenetic Mark of Polycomb Response Elements Implemented by Trx/MLL/COMPASS.由Trx/MLL/COMPASS实现的多梳反应元件的进化保守表观遗传标记。
Mol Cell. 2016 Jul 21;63(2):318-328. doi: 10.1016/j.molcel.2016.06.018.
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Non-canonical PRC1.1 Targets Active Genes Independent of H3K27me3 and Is Essential for Leukemogenesis.非经典 PRC1.1 靶点独立于 H3K27me3 作用于活性基因,并且对白血病发生至关重要。
Cell Rep. 2016 Jan 12;14(2):332-46. doi: 10.1016/j.celrep.2015.12.034. Epub 2015 Dec 31.
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The quest for mammalian Polycomb response elements: are we there yet?对哺乳动物多梳应答元件的探索:我们找到了吗?
Chromosoma. 2016 Jun;125(3):471-96. doi: 10.1007/s00412-015-0539-4. Epub 2015 Oct 9.