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Mol Cell Biol. 1995 Aug;15(8):4021-30. doi: 10.1128/MCB.15.8.4021.
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In vitro transcriptional activation by a metabolic intermediate: activation by Leu3 depends on alpha-isopropylmalate.代谢中间产物的体外转录激活:Leu3的激活依赖于α-异丙基苹果酸。
Science. 1992 Nov 13;258(5085):1143-5. doi: 10.1126/science.1439822.
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Development of a chromosomally integrated metabolite-inducible Leu3p-alpha-IPM "off-on" gene switch.开发一种整合在染色体上的代谢物诱导型 Leu3p-α-IPM“开-关”基因开关。
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本文引用的文献

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The acidic activation domains of the GCN4 and GAL4 proteins are not alpha helical but form beta sheets.GCN4和GAL4蛋白的酸性激活结构域不是α螺旋,而是形成β折叠。
Cell. 1993 Feb 26;72(4):587-94. doi: 10.1016/0092-8674(93)90077-4.
2
Genetic evidence that an activation domain of GAL4 does not require acidity and may form a beta sheet.GAL4激活结构域不需要酸性环境且可能形成β折叠的遗传证据。
Cell. 1993 Feb 26;72(4):575-85. doi: 10.1016/0092-8674(93)90076-3.
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Transcriptional regulator Leu3 of Saccharomyces cerevisiae: separation of activator and repressor functions.酿酒酵母转录调节因子Leu3:激活子与阻遏子功能的分离
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体内检测酵母亮氨酸3转录激活因子的亮氨酸非依赖性DNA位点占据情况。

Detection of leucine-independent DNA site occupancy of the yeast Leu3p transcriptional activator in vivo.

作者信息

Kirkpatrick C R, Schimmel P

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge 02139, USA.

出版信息

Mol Cell Biol. 1995 Aug;15(8):4021-30. doi: 10.1128/MCB.15.8.4021.

DOI:10.1128/MCB.15.8.4021
PMID:7623798
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC230641/
Abstract

The product of the Saccharomyces cerevisiae LEU3 gene, Leu3p, is a transcriptional activator which regulates leucine biosynthesis in response to intracellular levels of leucine through the biosynthetic intermediate alpha-isopropylmalate. We devised a novel assay to examine the DNA site occupancy of Leu3p under different growth conditions, using a reporter gene with internal Leu3p-binding sites. Expression of the reporter is inhibited by binding of nuclear Leu3p to these sites; inhibition is dependent on the presence of the sites in the reporter, on the integrity of the Leu3p DNA-binding domain, and, surprisingly, on the presence of a transcriptional activation domain in the inhibiting protein. By this assay, Leu3p was found to occupy its binding site under all conditions tested, including high and low levels of leucine and in the presence and absence of alpha-isopropylmalate. The localization of Leu3p to the nucleus was confirmed by immunofluorescence staining of cells expressing epitope-tagged Leu3p derivatives. We conclude that Leu3p regulates transcription in vivo without changing its intracellular localization and DNA site occupancy.

摘要

酿酒酵母LEU3基因的产物Leu3p是一种转录激活因子,它通过生物合成中间体α-异丙基苹果酸,响应细胞内亮氨酸水平来调节亮氨酸的生物合成。我们设计了一种新颖的检测方法,使用带有内部Leu3p结合位点的报告基因,来检测不同生长条件下Leu3p对DNA位点的占据情况。报告基因的表达会被核内Leu3p与这些位点的结合所抑制;抑制作用取决于报告基因中这些位点的存在、Leu3p DNA结合结构域的完整性,并且令人惊讶的是,还取决于抑制蛋白中转录激活结构域的存在。通过这种检测方法,发现Leu3p在所有测试条件下都占据其结合位点,包括亮氨酸水平的高低以及α-异丙基苹果酸的有无。通过对表达表位标签化Leu3p衍生物的细胞进行免疫荧光染色,证实了Leu3p在细胞核中的定位。我们得出结论,Leu3p在体内调节转录时不会改变其细胞内定位和DNA位点占据情况。