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本文引用的文献

1
Why are there still over 1000 uncharacterized yeast genes?为什么仍有1000多个未被鉴定的酵母基因?
Genetics. 2007 May;176(1):7-14. doi: 10.1534/genetics.107.074468. Epub 2007 Apr 15.
2
Hxk2 regulates the phosphorylation state of Mig1 and therefore its nucleocytoplasmic distribution.Hxk2调节Mig1的磷酸化状态,进而调节其在细胞核与细胞质之间的分布。
J Biol Chem. 2007 Feb 16;282(7):4485-4493. doi: 10.1074/jbc.M606854200. Epub 2006 Dec 18.
3
Genome-wide identification of genes required for growth of Saccharomyces cerevisiae under ethanol stress.全基因组范围内鉴定酿酒酵母在乙醇胁迫下生长所需的基因。
Yeast. 2006 Apr 15;23(5):351-9. doi: 10.1002/yea.1359.
4
Transcriptomic and proteomic approach for understanding the molecular basis of adaptation of Saccharomyces cerevisiae to wine fermentation.通过转录组学和蛋白质组学方法理解酿酒酵母适应葡萄酒发酵的分子基础。
Appl Environ Microbiol. 2006 Jan;72(1):836-47. doi: 10.1128/AEM.72.1.836-847.2006.
5
oPOSSUM: identification of over-represented transcription factor binding sites in co-expressed genes.oPOSSUM:共表达基因中过度富集的转录因子结合位点的鉴定
Nucleic Acids Res. 2005 Jun 2;33(10):3154-64. doi: 10.1093/nar/gki624. Print 2005.
6
Metabolite profiling for analysis of yeast stress response during very high gravity ethanol fermentations.用于分析超高浓度乙醇发酵过程中酵母应激反应的代谢物谱分析
Biotechnol Bioeng. 2005 Jun 20;90(6):703-14. doi: 10.1002/bit.20457.
7
Quantitative analysis of wine yeast gene expression profiles under winemaking conditions.酿酒条件下葡萄酒酵母基因表达谱的定量分析。
Yeast. 2005 Apr 15;22(5):369-83. doi: 10.1002/yea.1217.
8
A dynamic transcriptional network communicates growth potential to ribosome synthesis and critical cell size.一个动态转录网络将生长潜力传递给核糖体合成及关键细胞大小。
Genes Dev. 2004 Oct 15;18(20):2491-505. doi: 10.1101/gad.1228804. Epub 2004 Oct 1.
9
Bioconductor: open software development for computational biology and bioinformatics.生物导体:用于计算生物学和生物信息学的开源软件开发。
Genome Biol. 2004;5(10):R80. doi: 10.1186/gb-2004-5-10-r80. Epub 2004 Sep 15.
10
Expression of stress response genes in wine strains with different fermentative behavior.具有不同发酵行为的葡萄酒菌株中应激反应基因的表达
FEMS Yeast Res. 2004 May;4(7):699-710. doi: 10.1016/j.femsyr.2004.01.008.

葡萄酒发酵过程中酵母转录组的动态变化揭示了一种新的发酵应激反应。

Dynamics of the yeast transcriptome during wine fermentation reveals a novel fermentation stress response.

作者信息

Marks Virginia D, Ho Sui Shannan J, Erasmus Daniel, van der Merwe George K, Brumm Jochen, Wasserman Wyeth W, Bryan Jennifer, van Vuuren Hennie J J

机构信息

Wine Research Centre, University of British Columbia, Vancouver, Canada.

出版信息

FEMS Yeast Res. 2008 Feb;8(1):35-52. doi: 10.1111/j.1567-1364.2007.00338.x.

DOI:10.1111/j.1567-1364.2007.00338.x
PMID:18215224
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5065349/
Abstract

In this study, genome-wide expression analyses were used to study the response of Saccharomyces cerevisiae to stress throughout a 15-day wine fermentation. Forty per cent of the yeast genome significantly changed expression levels to mediate long-term adaptation to fermenting grape must. Among the genes that changed expression levels, a group of 223 genes was identified, which was designated as fermentation stress response (FSR) genes that were dramatically induced at various points during fermentation. FSR genes sustain high levels of induction up to the final time point and exhibited changes in expression levels ranging from four- to 80-fold. The FSR is novel; 62% of the genes involved have not been implicated in global stress responses and 28% of the FSR genes have no functional annotation. Genes involved in respiratory metabolism and gluconeogenesis were expressed during fermentation despite the presence of high concentrations of glucose. Ethanol, rather than nutrient depletion, seems to be responsible for entry of yeast cells into the stationary phase.

摘要

在本研究中,利用全基因组表达分析来研究酿酒酵母在为期15天的葡萄酒发酵过程中对压力的反应。40%的酵母基因组显著改变表达水平,以介导对发酵葡萄汁的长期适应。在表达水平发生变化的基因中,鉴定出一组223个基因,它们被指定为发酵应激反应(FSR)基因,在发酵过程中的不同时间点被显著诱导。FSR基因在直至最后时间点都维持高水平的诱导,并表现出4至80倍的表达水平变化。FSR是新发现的;62%的相关基因未涉及全局应激反应,28%的FSR基因没有功能注释。尽管存在高浓度葡萄糖,但参与呼吸代谢和糖异生的基因在发酵过程中仍有表达。乙醇而非营养物质耗尽似乎是酵母细胞进入静止期的原因。