Sensing metabolic signals with nascent RNA transcripts: The T box and S box riboswitches as paradigms

被引:21
作者
Henkin, T. M. [1 ]
Grundy, F. J.
机构
[1] Ohio State Univ, Dept Microbiol, Columbus, OH 43210 USA
[2] Ohio State Univ, RNA Grp, Columbus, OH 43210 USA
关键词
D O I
10.1101/sqb.2006.71.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent studies in a variety of bacterial systems have revealed a number of regulatory systems in which the 5' region of a gene plays a key role in regulation of the downstream coding sequences. These RNA regions act in cis to determine if the full-length transcript will be synthesized or if the coding sequence(s) will be translated. Each class of system includes all RNA element whose structure is modulated in response to a specific regulatory signal, and the signals measured can include small molecules, small RNAs (including tRNA), and physical parameters such as temperature. Multiple sets of genes can be regulated by a particular mechanism, and multiple systems of this type, each of which responds to a specific signal, can be present in a single organism. In addition, different classes of RNA elements call be found that respond to a particular signal, indicating the existence of multiple alternate solutions to the same regulatory problem. The T box and S box systems, which respond to uncharged tRNA and S-adenosylmethionine (SAM), respectively, provide paradigms of two systems of this type.
引用
收藏
页码:231 / 237
页数:7
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