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Wrapping of DNA around the E.coli RNA polymerase open promoter complex.DNA围绕大肠杆菌RNA聚合酶开放启动子复合物的包裹。
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Complete genome sequence of an aerobic hyper-thermophilic crenarchaeon, Aeropyrum pernix K1.嗜热嗜酸栖热袍菌K1的全基因组序列
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DNA bending and wrapping around RNA polymerase: a "revolutionary" model describing transcriptional mechanisms.DNA围绕RNA聚合酶的弯曲与缠绕:一种描述转录机制的“革命性”模型。
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Evolutionary instability of operon structures disclosed by sequence comparisons of complete microbial genomes.通过完整微生物基因组的序列比较揭示的操纵子结构的进化不稳定性。
Mol Biol Evol. 1999 Mar;16(3):332-46. doi: 10.1093/oxfordjournals.molbev.a026114.
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Sequence analysis of a 32-kb region including the major ribosomal protein gene clusters from alkaliphilic Bacillus sp. strain C-125.对包含嗜碱芽孢杆菌C-125菌株主要核糖体蛋白基因簇的一个32千碱基区域进行序列分析。
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Structure and expression of elongation factor Tu from Bacillus stearothermophilus.嗜热脂肪芽孢杆菌延伸因子Tu的结构与表达
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嗜热脂肪芽孢杆菌中str操纵子的克隆、特性分析及延伸因子Tu的表达

Cloning and characterization of the str operon and elongation factor Tu expression in Bacillus stearothermophilus.

作者信息

Krásný L, Vacík T, Fucík V, Jonák J

机构信息

Department of Protein Biosynthesis, Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, 166 37 Prague 6, Czech Republic.

出版信息

J Bacteriol. 2000 Nov;182(21):6114-22. doi: 10.1128/JB.182.21.6114-6122.2000.

DOI:10.1128/JB.182.21.6114-6122.2000
PMID:11029432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC94746/
Abstract

The complete primary structure of the str operon of Bacillus stearothermophilus was determined. It was established that the operon is a five-gene transcriptional unit: 5'-ybxF (unknown function; homology to eukaryotic ribosomal protein L30)-rpsL (S12)-rpsG (S7)-fus (elongation factor G [EF-G])-tuf (elongation factor Tu [EF-Tu])-3'. The main operon promoter (strp) was mapped upstream of ybxF, and its strength was compared with the strength of the tuf-specific promoter (tufp) located in the fus-tuf intergenic region. The strength of the tufp region to initiate transcription is about 20-fold higher than that of the strp region, as determined in chloramphenicol acetyltransferase assays. Deletion mapping experiments revealed that the different strengths of the promoters are the consequence of a combined effect of oppositely acting cis elements, identified upstream of strp (an inhibitory region) and tufp (a stimulatory A/T-rich block). Our results suggest that the oppositely adjusted core promoters significantly contribute to the differential expression of the str operon genes, as monitored by the expression of EF-Tu and EF-G.

摘要

嗜热脂肪芽孢杆菌str操纵子的完整一级结构已被确定。已确定该操纵子是一个五基因转录单元:5'-ybxF(功能未知;与真核核糖体蛋白L30同源)-rpsL(S12)-rpsG(S7)-fus(延伸因子G [EF-G])-tuf(延伸因子Tu [EF-Tu])-3'。主要操纵子启动子(strp)被定位在ybxF上游,并将其强度与位于fus-tuf基因间区域的tuf特异性启动子(tufp)的强度进行了比较。在氯霉素乙酰转移酶测定中确定,tufp区域启动转录的强度比strp区域高约20倍。缺失定位实验表明,启动子强度不同是由位于strp上游(一个抑制区域)和tufp上游(一个富含A/T的刺激区域)的反向作用顺式元件共同作用的结果。我们的结果表明,如通过EF-Tu和EF-G的表达所监测到的,反向调节的核心启动子对str操纵子基因的差异表达有显著贡献。