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细菌小非编码RNA的鉴定:实验方法

Identification of bacterial small non-coding RNAs: experimental approaches.

作者信息

Altuvia Shoshy

机构信息

Department of Molecular Genetics and Biotechnology, The Hebrew University-Hadassah Medical School, Jerusalem 91120, Israel.

出版信息

Curr Opin Microbiol. 2007 Jun;10(3):257-61. doi: 10.1016/j.mib.2007.05.003. Epub 2007 Jun 5.

Abstract

Almost 140 bacterial small RNAs (sRNAs; sometimes referred to as non-coding RNAs) have been discovered in the past six years. The majority of these sRNAs were discovered in Escherichia coli, and a smaller subset was characterized in other bacteria, many of which were pathogenic. Many of these genes were identified as a result of systematic screens using computational prediction of sRNAs and experimental-based approaches, including microarray and shotgun cloning. A smaller number of sRNAs were discovered by direct labeling or by functional genetic screens. Many of the discovered genes, ranging in size from 50 to 500 nucleotides, are conserved and located in intergenic regions, in-between open reading frames. The expression of many of these genes is growth phase dependent or stress related. As each search employed specific parameters, this led to the identification of genes with distinct characteristics. Consequently, unique sRNAs such as those that are species-specific, sRNA genes that are transcribed under unique conditions or genes located on the antisense strand of protein-encoding genes, were probably missed.

摘要

在过去六年里,已发现了近140种细菌小RNA(sRNA;有时被称为非编码RNA)。这些sRNA大多是在大肠杆菌中发现的,一小部分在其他细菌中得到了表征,其中许多是致病菌。这些基因中有许多是通过使用sRNA的计算预测和基于实验的方法(包括微阵列和鸟枪法克隆)进行系统筛选而鉴定出来的。通过直接标记或功能遗传筛选发现的sRNA数量较少。许多已发现的基因大小在50到500个核苷酸之间,是保守的,位于基因间区域,即开放阅读框之间。这些基因中的许多基因的表达依赖于生长阶段或与应激相关。由于每次搜索都采用了特定参数,这导致了具有不同特征的基因的鉴定。因此,可能遗漏了一些独特的sRNA,如物种特异性的sRNA、在独特条件下转录的sRNA基因或位于蛋白质编码基因反义链上的基因。

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