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潜在RNA温度计的全基因组生物信息学预测与实验评估

Genome-wide bioinformatic prediction and experimental evaluation of potential RNA thermometers.

作者信息

Waldminghaus Torsten, Gaubig Lena C, Narberhaus Franz

机构信息

Lehrstuhl für Biologie der Mikroorganismen, Ruhr-Universität Bochum, Universitätsstrasse 150, NDEF 06/783, 44780, Bochum, Germany.

出版信息

Mol Genet Genomics. 2007 Nov;278(5):555-64. doi: 10.1007/s00438-007-0272-7. Epub 2007 Jul 24.

Abstract

Only recently, the fundamental role of regulatory RNAs in prokaryotes and eukaryotes has been appreciated. We developed a pipeline from bioinformatic prediction to experimental validation of new RNA thermometers. Known RNA thermometers are located in the 5'-untranslated region of certain heat shock or virulence genes and control translation by temperature-dependent base pairing of the ribosome binding site. We established the searchable database RNA-SURIBA (Structures of Untranslated Regions In BActeria). A structure-based search pattern reliably recognizes known RNA thermometers and predicts related structures upstream of annotated genes in complete genome sequences. The known ROSE(1) (Repression Of heat Shock gene Expression) thermometer and several other functional ROSE-like elements were correctly predicted. For further investigation, we chose a new candidate upstream of the phage shock gene D (pspD) in the pspABCDE operon of E. coli. We established a new reporter gene system that measures translational control at heat shock temperatures and we demonstrated that the upstream region of pspD does not confer temperature control to the phage shock gene. However, translational efficiency was modulated by a point mutation stabilizing the predicted hairpin. Testing other candidates by this structure prediction and validation process will lead to new insights into the requirements for biologically active RNA thermometers. The database is available on http://www.ruhr-uni-bochum.de/mikrobiologie/ .

摘要

直到最近,调控RNA在原核生物和真核生物中的基本作用才得到认识。我们开发了一套从生物信息学预测到新型RNA温度计实验验证的流程。已知的RNA温度计位于某些热休克或毒力基因的5'非翻译区,并通过核糖体结合位点的温度依赖性碱基配对来控制翻译。我们建立了可搜索的数据库RNA-SURIBA(细菌非翻译区结构)。基于结构的搜索模式能够可靠地识别已知的RNA温度计,并预测完整基因组序列中注释基因上游的相关结构。已知的ROSE(1)(热休克基因表达抑制)温度计和其他几个功能性ROSE样元件被正确预测。为了进一步研究,我们在大肠杆菌的pspABCDE操纵子中的噬菌体休克基因D(pspD)上游选择了一个新的候选元件。我们建立了一个新的报告基因系统,用于测量热休克温度下的翻译控制,并且我们证明pspD的上游区域不会赋予噬菌体休克基因温度控制。然而,翻译效率通过稳定预测发夹结构的点突变而受到调节。通过这种结构预测和验证过程测试其他候选元件将为生物活性RNA温度计的要求带来新的见解。该数据库可在http://www.ruhr-uni-bochum.de/mikrobiologie/上获取。

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