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调控子复合物亚基的需求在果蝇翅缘区分了三类 Notch 靶基因。

Requirements for mediator complex subunits distinguish three classes of notch target genes at the Drosophila wing margin.

机构信息

Kimmel Center for Biology and Medicine of the Skirball Institute, NYU School of Medicine, Department of Cell Biology, New York, New York, USA.

出版信息

Dev Dyn. 2011 Sep;240(9):2051-9. doi: 10.1002/dvdy.22705. Epub 2011 Jul 25.

DOI:10.1002/dvdy.22705
PMID:21793099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3192913/
Abstract

Spatial and temporal gene regulation relies on a combinatorial code of sequence-specific transcription factors that must be integrated by the general transcriptional machinery. A key link between the two is the mediator complex, which consists of a core complex that reversibly associates with the accessory kinase module. We show here that genes activated by Notch signaling at the dorsal-ventral boundary of the Drosophila wing disc fall into three classes that are affected differently by the loss of kinase module subunits. One class requires all four kinase module subunits for activation, while the others require only Med12 and Med13, either for activation or for repression. These distinctions do not result from different requirements for the Notch coactivator Mastermind or the corepressors Hairless and Groucho. We propose that interactions with the kinase module through distinct cofactors allow the DNA-binding protein Suppressor of Hairless to carry out both its activator and repressor functions.

摘要

时空基因调控依赖于序列特异性转录因子的组合密码,这些转录因子必须被通用转录机制整合。两者之间的一个关键环节是中介复合物,它由一个核心复合物组成,该核心复合物与辅助激酶模块可逆地结合。我们在这里表明,在果蝇翅盘的背腹边界处由 Notch 信号激活的基因分为三类,它们受激酶模块亚基缺失的影响不同。一类基因的激活需要四个激酶模块亚基,而其他基因只需要 Med12 和 Med13,无论是激活还是抑制。这些区别不是由于 Notch 共激活因子 Mastermind 或核心抑制物 Hairless 和 Groucho 的不同要求造成的。我们提出,通过不同的辅助因子与激酶模块的相互作用,使得 DNA 结合蛋白 Suppressor of Hairless 能够发挥其激活和抑制功能。

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Dev Dyn. 2011 Sep;240(9):2051-9. doi: 10.1002/dvdy.22705. Epub 2011 Jul 25.
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本文引用的文献

1
Notch-dependent expression of the archipelago ubiquitin ligase subunit in the Drosophila eye.果蝇眼中原癌基因 Notch 依赖性表达的穹窿泛素连接酶亚基。
Development. 2011 Jan;138(2):251-60. doi: 10.1242/dev.054429. Epub 2010 Dec 9.
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Differential regulation of transcription through distinct Suppressor of Hairless DNA binding site architectures during Notch signaling in proneural clusters.在神经前体细胞簇中的 Notch 信号传导过程中,通过不同的 Suppressor of Hairless DNA 结合位点结构对转录进行差异调控。
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Structural and mechanistic insights into cooperative assembly of dimeric Notch transcription complexes.二聚体 Notch 转录复合物协同组装的结构和机制见解。
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The metazoan Mediator co-activator complex as an integrative hub for transcriptional regulation.后生动物中介体共激活复合物作为转录调控的整合中心。
Nat Rev Genet. 2010 Nov;11(11):761-72. doi: 10.1038/nrg2901. Epub 2010 Oct 13.
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Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling.Med12 对于早期小鼠发育以及经典 Wnt 和 Wnt/PCP 信号通路至关重要。
Development. 2010 Aug;137(16):2723-31. doi: 10.1242/dev.053660. Epub 2010 Jul 14.
6
A genome-wide RNA interference screen identifies a differential role of the mediator CDK8 module subunits for GATA/ RUNX-activated transcription in Drosophila.全基因组 RNA 干扰筛选鉴定了果蝇中 GATA/RUNX 激活转录的中介 CDK8 模块亚基的差异作用。
Mol Cell Biol. 2010 Jun;30(11):2837-48. doi: 10.1128/MCB.01625-09. Epub 2010 Apr 5.
7
The human Mediator complex: a versatile, genome-wide regulator of transcription.人类中介体复合物:一种通用的、全基因组转录调控因子。
Trends Biochem Sci. 2010 Jun;35(6):315-22. doi: 10.1016/j.tibs.2010.02.004. Epub 2010 Mar 17.
8
Cyclin-dependent kinase 8 positively cooperates with Mediator to promote thyroid hormone receptor-dependent transcriptional activation.周期蛋白依赖性激酶 8 与中介体协同正向促进甲状腺激素受体依赖性转录激活。
Mol Cell Biol. 2010 May;30(10):2437-48. doi: 10.1128/MCB.01541-09. Epub 2010 Mar 15.
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CDK8 is a positive regulator of transcriptional elongation within the serum response network.CDK8 是血清反应网络中转录延伸的正调控因子。
Nat Struct Mol Biol. 2010 Feb;17(2):194-201. doi: 10.1038/nsmb.1752. Epub 2010 Jan 24.
10
Nuclear CDKs drive Smad transcriptional activation and turnover in BMP and TGF-beta pathways.细胞核周期蛋白依赖性激酶驱动骨形态发生蛋白(BMP)和转化生长因子-β(TGF-β)信号通路中的Smad转录激活和周转。
Cell. 2009 Nov 13;139(4):757-69. doi: 10.1016/j.cell.2009.09.035.