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本文引用的文献

1
Histone acetylation in chromatin structure and transcription.染色质结构与转录中的组蛋白乙酰化作用
Nature. 1997 Sep 25;389(6649):349-52. doi: 10.1038/38664.
2
Plasmid pIP501 encoded transcriptional repressor CopR binds asymmetrically at two consecutive major grooves of the DNA.质粒pIP501编码的转录阻遏物CopR在DNA的两个连续大沟处不对称结合。
J Mol Biol. 1997 Jun 27;269(5):684-93. doi: 10.1006/jmbi.1997.1083.
3
Oct-1, silencer sequence, and GC box regulate thyroid hormone receptor beta1 promoter.
Mol Cell Endocrinol. 1997 Jun 20;130(1-2):153-65. doi: 10.1016/s0303-7207(97)00085-3.
4
RING1 is associated with the polycomb group protein complex and acts as a transcriptional repressor.RING1与多梳蛋白复合体相关联,并作为转录抑制因子发挥作用。
Mol Cell Biol. 1997 Jul;17(7):4105-13. doi: 10.1128/MCB.17.7.4105.
5
Molecular architecture of the hsp70 promoter after deletion of the TATA box or the upstream regulation region.删除TATA盒或上游调控区域后hsp70启动子的分子结构。
Mol Cell Biol. 1997 Jul;17(7):3799-808. doi: 10.1128/MCB.17.7.3799.
6
Histones, nucleosomes and the roles of chromatin structure in transcriptional control.组蛋白、核小体以及染色质结构在转录调控中的作用。
Biochem Soc Trans. 1997 May;25(2):354-8. doi: 10.1042/bst0250354.
7
Gene silencing by chicken ovalbumin upstream promoter-transcription factor I (COUP-TFI) is mediated by transcriptional corepressors, nuclear receptor-corepressor (N-CoR) and silencing mediator for retinoic acid receptor and thyroid hormone receptor (SMRT).鸡卵清蛋白上游启动子转录因子I(COUP-TFI)介导的基因沉默是由转录共抑制因子、核受体共抑制因子(N-CoR)以及维甲酸受体和甲状腺激素受体沉默介质(SMRT)介导的。
Mol Endocrinol. 1997 Jun;11(6):714-24. doi: 10.1210/mend.11.6.0002.
8
Differential effects of nuclear receptor corepressor (N-CoR) expression levels on retinoic acid receptor-mediated repression support the existence of dynamically regulated corepressor complexes.核受体共抑制因子(N-CoR)表达水平对视黄酸受体介导的抑制作用的差异影响支持了动态调节的共抑制因子复合物的存在。
Mol Endocrinol. 1997 Jun;11(6):682-92. doi: 10.1210/mend.11.6.0018.
9
Two different negative regulatory elements control the transcription of T-cell activation gene 3 in activated mast cells.两种不同的负调控元件控制活化肥大细胞中T细胞活化基因3的转录。
Biochem J. 1997 Apr 15;323 ( Pt 2)(Pt 2):511-9. doi: 10.1042/bj3230511.
10
The neuron-restrictive silencer element: a dual enhancer/silencer crucial for patterned expression of a nicotinic receptor gene in the brain.神经元限制性沉默元件:一种对大脑中烟碱受体基因的模式化表达至关重要的双重增强子/沉默子。
Proc Natl Acad Sci U S A. 1997 May 27;94(11):5906-11. doi: 10.1073/pnas.94.11.5906.

转录控制以及沉默子在真核生物转录调控中的作用。

Transcriptional control and the role of silencers in transcriptional regulation in eukaryotes.

作者信息

Ogbourne S, Antalis T M

机构信息

Queensland Cancer Fund Experimental Oncology Program, The Queensland Institute of Medical Research, Brisbane, 4029 Queensland, Australia.

出版信息

Biochem J. 1998 Apr 1;331 ( Pt 1)(Pt 1):1-14. doi: 10.1042/bj3310001.

DOI:10.1042/bj3310001
PMID:9512455
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1219314/
Abstract

Mechanisms controlling transcription and its regulation are fundamental to our understanding of molecular biology and, ultimately, cellular biology. Our knowledge of transcription initiation and integral factors such as RNA polymerase is considerable, and more recently our understanding of the involvement of enhancers and complexes such as holoenzyme and mediator has increased dramatically. However, an understanding of transcriptional repression is also essential for a complete understanding of promoter structure and the regulation of gene expression. Transcriptional repression in eukaryotes is achieved through 'silencers', of which there are two types, namely 'silencer elements' and 'negative regulatory elements' (NREs). Silencer elements are classical, position-independent elements that direct an active repression mechanism, and NREs are position-dependent elements that direct a passive repression mechanism. In addition, 'repressors' are DNA-binding trasncription factors that interact directly with silencers. A review of the recent literature reveals that it is the silencer itself and its context within a given promoter, rather than the interacting repressor, that determines the mechanism of repression. Silencers form an intrinsic part of many eukaryotic promoters and, consequently, knowledge of their interactive role with enchancers and other transcriptional elements is essential for our understanding of gene regulation in eukaryotes.

摘要

控制转录及其调控的机制是我们理解分子生物学乃至细胞生物学的基础。我们对转录起始以及诸如RNA聚合酶等整合因子已有相当多的了解,最近我们对增强子以及诸如全酶和中介体等复合物参与情况的理解也有了显著增加。然而,对于转录抑制的理解对于全面理解启动子结构和基因表达调控同样至关重要。真核生物中的转录抑制是通过“沉默子”实现的,沉默子有两种类型,即“沉默子元件”和“负调控元件”(NREs)。沉默子元件是经典的、位置独立的元件,指导一种主动抑制机制,而NREs是位置依赖的元件,指导一种被动抑制机制。此外,“阻遏物”是与沉默子直接相互作用的DNA结合转录因子。对近期文献的综述表明,决定抑制机制的是沉默子本身及其在给定启动子中的背景,而非相互作用的阻遏物。沉默子是许多真核生物启动子的固有组成部分,因此,了解它们与增强子及其他转录元件的相互作用对于我们理解真核生物中的基因调控至关重要。