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转录激活因子Cat8p对酿酒酵母双相转变期间碳代谢的重编程起主要作用。

The transcriptional activator Cat8p provides a major contribution to the reprogramming of carbon metabolism during the diauxic shift in Saccharomyces cerevisiae.

作者信息

Haurie V, Perrot M, Mini T, Jenö P, Sagliocco F, Boucherie H

机构信息

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

出版信息

J Biol Chem. 2001 Jan 5;276(1):76-85. doi: 10.1074/jbc.M008752200.

DOI:10.1074/jbc.M008752200
PMID:11024040
Abstract

In yeast, the transition between the fermentative and the oxidative metabolism, called the diauxic shift, is associated with major changes in gene expression and protein synthesis. The zinc cluster protein Cat8p is required for the derepression of nine genes under nonfermentative growth conditions (ACS1, FBP1, ICL1, IDP2, JEN1, MLS1, PCK1, SFC1, and SIP4). To investigate whether the transcriptional control mediated by Cat8p can be extended to other genes and whether this control is the main control for the changes in the synthesis of the respective proteins during the adaptation to growth on ethanol, we analyzed the transcriptome and the proteome of a cat8 Delta strain during the diauxic shift. In this report, we demonstrate that, in addition to the nine genes known as Cat8p-dependent, there are 25 other genes or open reading frames whose expression at the diauxic shift is altered in the absence of Cat8p. For all of the genes characterized here, the Cat8p-dependent control results in a parallel alteration in mRNA and protein synthesis. It appears that the biochemical functions of the proteins encoded by Cat8p-dependent genes are essentially related to the first steps of ethanol utilization, the glyoxylate cycle, and gluconeogenesis. Interestingly, no function involved in the tricarboxylic cycle and the oxidative phosphorylation seems to be controlled by Cat8p.

摘要

在酵母中,发酵代谢与氧化代谢之间的转变,即双相转变,与基因表达和蛋白质合成的重大变化相关。锌簇蛋白Cat8p是在非发酵生长条件下解除九个基因(ACS1、FBP1、ICL1、IDP2、JEN1、MLS1、PCK1、SFC1和SIP4)抑制所必需的。为了研究由Cat8p介导的转录控制是否可以扩展到其他基因,以及这种控制是否是适应乙醇生长过程中相应蛋白质合成变化的主要控制因素,我们分析了双相转变期间cat8Δ菌株的转录组和蛋白质组。在本报告中,我们证明,除了已知依赖于Cat8p的九个基因外,还有25个其他基因或开放阅读框,其在双相转变时的表达在没有Cat8p的情况下发生改变。对于此处表征的所有基因,依赖于Cat8p的控制导致mRNA和蛋白质合成的平行改变。似乎由依赖于Cat8p的基因编码的蛋白质的生化功能基本上与乙醇利用的第一步、乙醛酸循环和糖异生有关。有趣的是,三羧酸循环和氧化磷酸化中涉及的任何功能似乎都不受Cat8p的控制。

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