McCown Phillip J, Winkler Wade C, Breaker Ronald R
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, USA.
Methods Mol Biol. 2012;848:113-29. doi: 10.1007/978-1-61779-545-9_8.
Among the nine classes of ribozymes that have been experimentally validated to date is the metabolite-responsive self-cleaving ribozyme called glmS. This RNA is almost exclusively located in the 5'-untranslated region of bacterial mRNAs that code for the production of GlmS proteins, which catalyze the synthesis of the aminosugar glucosamine-6-phosphate (GlcN6P). Each glmS ribozyme forms a conserved catalytic core that selectively binds GlcN6P and uses this metabolite as a cofactor to promote ribozyme self-cleavage. Metabolite-induced self-cleavage results in down-regulation of glmS gene expression, and thus the ribozyme functions as a key riboswitch component to permit feedback regulation of GlcN6P levels. Representatives of glmS ribozymes also serve as excellent experimental models to elucidate how RNAs fold to recognize small molecule ligands and promote chemical transformations.
在迄今为止已通过实验验证的九类核酶中,有一种名为glmS的代谢物响应性自我切割核酶。这种RNA几乎只位于编码GlmS蛋白的细菌mRNA的5'非翻译区,GlmS蛋白催化氨基糖6-磷酸葡萄糖胺(GlcN6P)的合成。每个glmS核酶形成一个保守的催化核心,该核心选择性地结合GlcN6P,并将这种代谢物用作辅助因子来促进核酶自我切割。代谢物诱导的自我切割导致glmS基因表达下调,因此该核酶作为关键的核糖开关组件发挥作用,以实现对GlcN6P水平的反馈调节。glmS核酶的代表也作为优秀的实验模型,用于阐明RNA如何折叠以识别小分子配体并促进化学转化。