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本文引用的文献

1
Perspectives on the RNA polymerase II core promoter.RNA聚合酶II核心启动子的研究视角
Biochem Soc Trans. 2006 Dec;34(Pt 6):1047-50. doi: 10.1042/BST0341047.
2
A core promoter element downstream of the TATA box that is recognized by TFIIB.位于TATA框下游的一种核心启动子元件,可被TFIIB识别。
Genes Dev. 2005 Oct 15;19(20):2418-23. doi: 10.1101/gad.342405.
3
Kinetic and mechanistic analysis of the RNA polymerase II transcrption reaction at the human interleukin-2 promoter.人白细胞介素-2启动子处RNA聚合酶II转录反应的动力学和机制分析
J Mol Biol. 2001 Dec 14;314(5):993-1006. doi: 10.1006/jmbi.2000.5215.
4
Enhanceosomes.增强体
Curr Opin Genet Dev. 2001 Apr;11(2):205-8. doi: 10.1016/s0959-437x(00)00180-5.
5
The role of high-mobility group I(Y) proteins in expression of IL-2 and T cell proliferation.高迁移率族I(Y)蛋白在白细胞介素-2表达和T细胞增殖中的作用
J Immunol. 2000 Mar 15;164(6):3157-68. doi: 10.4049/jimmunol.164.6.3157.
6
Stimulus-specific assembly of enhancer complexes on the tumor necrosis factor alpha gene promoter.肿瘤坏死因子α基因启动子上增强子复合物的刺激特异性组装。
Mol Cell Biol. 2000 Mar;20(6):2239-47. doi: 10.1128/MCB.20.6.2239-2247.2000.
7
Mechanism by which the IFN-beta enhanceosome activates transcription.干扰素-β增强体激活转录的机制。
Proc Natl Acad Sci U S A. 1999 Nov 9;96(23):13108-13. doi: 10.1073/pnas.96.23.13108.
8
Stabilization of interleukin-2 mRNA by the c-Jun NH2-terminal kinase pathway.通过c-Jun氨基末端激酶途径稳定白细胞介素-2信使核糖核酸
Science. 1998 Jun 19;280(5371):1945-9. doi: 10.1126/science.280.5371.1945.
9
Generality of a functional initiator consensus sequence.功能性引发剂共有序列的通用性。
Gene. 1996 Dec 5;182(1-2):13-22. doi: 10.1016/s0378-1119(96)00438-6.
10
A dynamic assembly of diverse transcription factors integrates activation and cell-type information for interleukin 2 gene regulation.多种转录因子的动态组装整合激活信息和细胞类型信息以调控白细胞介素2基因。
Proc Natl Acad Sci U S A. 1996 Sep 3;93(18):9358-65. doi: 10.1073/pnas.93.18.9358.

人类白细胞介素-2启动子调控区和核心区的序列及结构限制的表征

Characterization of the sequence and architectural constraints of the regulatory and core regions of the human interleukin-2 promoter.

作者信息

Weaver Jessica R, Good Kristi, Walters Ryan D, Kugel Jennifer F, Goodrich James A

机构信息

Department of Chemistry and Biochemistry, University of Colorado at Boulder, 215 UCB, Boulder, CO 80309-0215, USA.

出版信息

Mol Immunol. 2007 Apr;44(11):2813-9. doi: 10.1016/j.molimm.2007.01.027. Epub 2007 Mar 6.

DOI:10.1016/j.molimm.2007.01.027
PMID:17337059
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1924494/
Abstract

The cytokine interleukin-2 (IL-2) is produced by T cells when they recognize a foreign antigen. Transcription of the IL-2 gene is tightly controlled by the combined actions of multiple transcriptional activators. However, the contribution of sequences in the IL-2 core promoter and the architecture of the IL-2 regulatory region to setting levels of IL-2 transcription are not understood. We have probed these properties of the human IL-2 promoter to understand how the regulatory and core promoter regions cooperate in response to T cell stimulation, thereby setting high levels of inducible transcription. We found that the IL-2 core promoter contains a TATA box that is critical for inducible expression. Moreover, the spacing and orientation between the IL-2 regulatory and core promoter regions is important for setting the level of transcription. The regulatory region of the IL-2 promoter is capable of mediating high levels of expression even when the helical phasing between transcription factor binding sites is perturbed. Although long considered an enhancer, our studies indicate that the regulatory region in the IL-2 promoter is better considered as a proximal regulatory element, since it lacks multiple properties associated with enhancer elements.

摘要

细胞因子白细胞介素-2(IL-2)由T细胞识别外来抗原时产生。IL-2基因的转录受到多种转录激活因子联合作用的严格调控。然而,IL-2核心启动子中的序列以及IL-2调控区域的结构对IL-2转录水平的影响尚不清楚。我们探究了人类IL-2启动子的这些特性,以了解调控区域和核心启动子区域如何协同响应T细胞刺激,从而实现高水平的诱导型转录。我们发现,IL-2核心启动子包含一个对诱导型表达至关重要的TATA盒。此外,IL-2调控区域与核心启动子区域之间的间距和方向对于设定转录水平很重要。即使转录因子结合位点之间的螺旋相位受到干扰,IL-2启动子的调控区域仍能介导高水平的表达。尽管长期以来被认为是一种增强子,但我们的研究表明,IL-2启动子中的调控区域更应被视为近端调控元件,因为它缺乏与增强子元件相关的多种特性。