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本文引用的文献

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Mol Cell Biol. 2002 Oct;22(19):6735-49. doi: 10.1128/MCB.22.19.6735-6749.2002.
2
Regulation of an IMP dehydrogenase gene and its overexpression in drug-sensitive transcription elongation mutants of yeast.酵母药物敏感型转录延伸突变体中肌苷一磷酸脱氢酶基因的调控及其过表达
J Biol Chem. 2001 Aug 31;276(35):32905-16. doi: 10.1074/jbc.M105075200. Epub 2001 Jul 5.
3
Bacillus subtilis CodY represses early-stationary-phase genes by sensing GTP levels.枯草芽孢杆菌CodY通过感知鸟苷三磷酸(GTP)水平来抑制早期稳定期基因。
Genes Dev. 2001 May 1;15(9):1093-103. doi: 10.1101/gad.874201.
4
The TOR kinases link nutrient sensing to cell growth.TOR激酶将营养感知与细胞生长联系起来。
J Biol Chem. 2001 Mar 30;276(13):9583-6. doi: 10.1074/jbc.R000034200. Epub 2001 Feb 2.
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The rye mutants identify a role for Ssn/Srb proteins of the RNA polymerase II holoenzyme during stationary phase entry in Saccharomyces cerevisiae.黑麦突变体确定了酿酒酵母进入稳定期过程中RNA聚合酶II全酶的Ssn/Srb蛋白的作用。
Genetics. 2001 Jan;157(1):17-26. doi: 10.1093/genetics/157.1.17.
6
Genomic expression programs in the response of yeast cells to environmental changes.酵母细胞对环境变化响应中的基因组表达程序。
Mol Biol Cell. 2000 Dec;11(12):4241-57. doi: 10.1091/mbc.11.12.4241.
7
Transcriptional regulation of the yeast gmp synthesis pathway by its end products.酵母鸟苷酸合成途径受其终产物的转录调控。
J Biol Chem. 2001 Jan 12;276(2):1523-30. doi: 10.1074/jbc.M007926200.
8
Saccharomyces cerevisiae transcription elongation mutants are defective in PUR5 induction in response to nucleotide depletion.酿酒酵母转录延伸突变体在响应核苷酸耗竭时PUR5诱导方面存在缺陷。
Mol Cell Biol. 2000 Oct;20(20):7427-37. doi: 10.1128/MCB.20.20.7427-7437.2000.
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The NC2 repressor is dispensable in yeast mutated for the Sin4p component of the holoenzyme and plays roles similar to Mot1p in vivo.在全酶的Sin4p组分发生突变的酵母中,NC2阻遏物是可有可无的,并且在体内发挥与Mot1p类似的作用。
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Rapamycin-modulated transcription defines the subset of nutrient-sensitive signaling pathways directly controlled by the Tor proteins.雷帕霉素调节的转录作用定义了由Tor蛋白直接控制的营养敏感信号通路的子集。
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酵母IMD2基因的转录起始在营养限制条件下,通过其编码区中的一个序列被抑制。

Transcription initiation of the yeast IMD2 gene is abolished in response to nutrient limitation through a sequence in its coding region.

作者信息

Escobar-Henriques Mafalda, Collart Martine A, Daignan-Fornier Bertrand

机构信息

Institut de Biochimie et Génétique Cellulaires, CNRS UMR 5095, F-33077 Bordeaux Cedex, France.

出版信息

Mol Cell Biol. 2003 Sep;23(17):6279-90. doi: 10.1128/MCB.23.17.6279-6290.2003.

DOI:10.1128/MCB.23.17.6279-6290.2003
PMID:12917348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC180942/
Abstract

The yeast IMD2 to IMD4 and GUA1 genes, involved in GMP synthesis, are highly expressed in exponentially growing cells but are shut off when cells cease to grow upon nutrient limitation. We show for the IMD2 gene that this effect is not specific to certain carbon sources or to growth rate. Strikingly, the cis elements responsible for this nutritional response are contained within a 23-nucleotide sequence in the coding region of the IMD2 gene. Despite its very unusual location, this regulatory sequence mediates the repression of transcription initiation. From our data, we conclude that GMP synthesis is downregulated upon nutrient limitation through an active mechanism. We show that this transcriptional shutoff abolishes any possibility of the induction of IMD2, even under drastic conditions of guanylic nucleotide limitation. Taken together, these results indicate that low levels of guanylic nucleotides could be required for proper entry into stationary phase.

摘要

参与GMP合成的酵母IMD2至IMD4和GUA1基因在指数生长期细胞中高度表达,但当细胞在营养限制下停止生长时会关闭。我们发现,对于IMD2基因而言,这种效应并非特定于某些碳源或生长速率。引人注目的是,负责这种营养反应的顺式元件包含在IMD2基因编码区的一个23个核苷酸的序列中。尽管其位置非常特殊,但这个调控序列介导转录起始的抑制。根据我们的数据,我们得出结论,在营养限制下,GMP合成通过一种主动机制被下调。我们表明,这种转录关闭消除了IMD2诱导的任何可能性,即使在鸟苷酸限制的极端条件下也是如此。综上所述,这些结果表明,进入稳定期可能需要低水平的鸟苷酸。