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本文引用的文献

1
Stb3 plays a role in the glucose-induced transition from quiescence to growth in Saccharomyces cerevisiae.Stb3 在酿酒酵母葡萄糖诱导的从静止到生长的转变中发挥作用。
Genetics. 2010 Jul;185(3):797-810. doi: 10.1534/genetics.110.116665. Epub 2010 Apr 12.
2
Life in the midst of scarcity: adaptations to nutrient availability in Saccharomyces cerevisiae.在资源匮乏的环境中生存:酿酒酵母对营养可用性的适应。
Curr Genet. 2010 Feb;56(1):1-32. doi: 10.1007/s00294-009-0287-1.
3
Protein kinase A and TORC1 activate genes for ribosomal biogenesis by inactivating repressors encoded by Dot6 and its homolog Tod6.蛋白激酶 A 和 TORC1 通过失活由 Dot6 和其同源物 Tod6 编码的阻遏物来激活核糖体生物发生的基因。
Proc Natl Acad Sci U S A. 2009 Nov 24;106(47):19928-33. doi: 10.1073/pnas.0907027106. Epub 2009 Nov 9.
4
Control of high osmolarity signalling in the yeast Saccharomyces cerevisiae.酵母酿酒酵母中高渗透压信号的控制。
FEBS Lett. 2009 Dec 17;583(24):4025-9. doi: 10.1016/j.febslet.2009.10.069.
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Growth control and ribosome biogenesis.生长控制与核糖体生物发生。
Curr Opin Cell Biol. 2009 Dec;21(6):855-63. doi: 10.1016/j.ceb.2009.09.002. Epub 2009 Sep 30.
6
The histone deacetylase Rpd3p is required for transient changes in genomic expression in response to stress.组蛋白去乙酰化酶Rpd3p是应激反应中基因组表达瞬时变化所必需的。
Genome Biol. 2009;10(5):R57. doi: 10.1186/gb-2009-10-5-r57. Epub 2009 May 26.
7
A glycolytic burst drives glucose induction of global histone acetylation by picNuA4 and SAGA.糖酵解爆发驱动picNuA4和SAGA对全局组蛋白乙酰化的葡萄糖诱导作用。
Nucleic Acids Res. 2009 Jul;37(12):3969-80. doi: 10.1093/nar/gkp270. Epub 2009 Apr 30.
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Microarray profiling of phage-display selections for rapid mapping of transcription factor-DNA interactions.用于转录因子 - DNA 相互作用快速图谱绘制的噬菌体展示筛选的微阵列分析
PLoS Genet. 2009 Apr;5(4):e1000449. doi: 10.1371/journal.pgen.1000449. Epub 2009 Apr 10.
9
High-resolution DNA-binding specificity analysis of yeast transcription factors.酵母转录因子的高分辨率DNA结合特异性分析
Genome Res. 2009 Apr;19(4):556-66. doi: 10.1101/gr.090233.108. Epub 2009 Jan 21.
10
Chromatin Central: towards the comparative proteome by accurate mapping of the yeast proteomic environment.染色质中心:通过精确绘制酵母蛋白质组环境迈向比较蛋白质组
Genome Biol. 2008;9(11):R167. doi: 10.1186/gb-2008-9-11-r167. Epub 2008 Nov 28.

相邻基因配对在酿酒酵母核糖体生物合成基因MPP10和YJR003C的协同表达中发挥作用。

Adjacent gene pairing plays a role in the coordinated expression of ribosome biogenesis genes MPP10 and YJR003C in Saccharomyces cerevisiae.

作者信息

Arnone James T, McAlear Michael A

机构信息

Department of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT 06459-0175, USA.

出版信息

Eukaryot Cell. 2011 Jan;10(1):43-53. doi: 10.1128/EC.00257-10. Epub 2010 Nov 29.

DOI:10.1128/EC.00257-10
PMID:21115740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3019797/
Abstract

The rRNA and ribosome biogenesis (RRB) regulon from Saccharomyces cerevisiae contains some 200 genes, the expression of which is tightly regulated under changing cellular conditions. RRB gene promoters are enriched for the RRPE and PAC consensus motifs, and a significant fraction of RRB genes are found as adjacent gene pairs. A genetic analysis of the MPP10 promoter revealed that both the RRPE and PAC motifs are important for coordinated expression of MPP10 following heat shock, osmotic stress, and glucose replenishment. The association of the RRPE binding factor Stb3 with the MPP10 promoter was found to increase after glucose replenishment and to decrease following heat shock. Similarly, bulk histone H3 clearing and histone H4K12 acetylation levels at the MPP10 promoter were found to increase or decrease following glucose replenishment or heat shock, respectively. Interestingly, substitutions in the PAC and RRPE sequences at the MPP10 promoter were also found to impact the regulated expression of the adjacent RRB gene YJR003, whose promoter lies in the opposite orientation and some 3.8 kb away. Furthermore, the regulated expression of YJR003C could be disrupted by inserting a reporter cassette that increased its distance from MPP10. Given that a high incidence of gene pairing was also found within the ribosomal protein (RP) and RRB regulons across different yeast species, our results indicate that immediately adjacent positioning of genes can be functionally significant for their coregulated expression.

摘要

来自酿酒酵母的核糖体RNA和核糖体生物合成(RRB)调控子包含约200个基因,其表达在不断变化的细胞条件下受到严格调控。RRB基因启动子富含RRPE和PAC共有基序,并且发现相当一部分RRB基因以相邻基因对的形式存在。对MPP10启动子的遗传分析表明,RRPE和PAC基序对于热休克、渗透胁迫和葡萄糖补充后MPP10的协同表达都很重要。发现RRPE结合因子Stb3与MPP10启动子的结合在葡萄糖补充后增加,而在热休克后减少。同样,发现MPP10启动子处的组蛋白H3整体清除和组蛋白H4K12乙酰化水平分别在葡萄糖补充或热休克后增加或减少。有趣的是,还发现MPP10启动子处PAC和RRPE序列的替换也会影响相邻RRB基因YJR003的调控表达,其启动子方向相反且相距约3.8 kb。此外,插入一个报告盒增加其与MPP10的距离会破坏YJR003C的调控表达。鉴于在不同酵母物种的核糖体蛋白(RP)和RRB调控子中也发现了高频率的基因配对,我们的结果表明基因的紧邻定位对它们的共调控表达可能具有功能重要性。