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核糖开关对嘌呤的感应

Purine sensing by riboswitches.

作者信息

Kim Jane N, Breaker Ronald R

机构信息

Department of Molecular, Cellular and Developmental Biology, Yale University, P.O. Box 208103, New Haven, CT 06520-8103, USA.

出版信息

Biol Cell. 2008 Jan;100(1):1-11. doi: 10.1042/BC20070088.

Abstract

Structured mRNA elements called riboswitches control gene expression by binding to small metabolites. Over a dozen riboswitch classes have been characterized that target a broad range of molecules and vary widely in size and secondary structure. Four of the known riboswitch classes recognize purines or modified purines. Three of these classes are closely related in conserved sequence and secondary structure, but members of these classes selectively recognize guanine, adenine or 2'-deoxyguanosine. Members of the fourth riboswitch class adopt a distinct structure to form a selective binding pocket for the guanine analogue preQ(1) (7-aminomethyl-7-deazaguanine). All four classes of purine-sensing riboswitches are most likely to recognize their respective metabolites by utilizing a riboswitch residue to make a canonical Watson-Crick base-pair with the ligand. This review will provide a summary of the purine-sensing riboswitches, as well as discuss the complex functions and applications of these RNAs.

摘要

一种被称为核糖开关的结构化信使核糖核酸(mRNA)元件通过与小分子代谢物结合来控制基因表达。目前已鉴定出超过十二种类别的核糖开关,它们靶向多种分子,在大小和二级结构上差异很大。已知的核糖开关类别中有四类识别嘌呤或修饰嘌呤。其中三类在保守序列和二级结构上密切相关,但这些类别的成员选择性地识别鸟嘌呤、腺嘌呤或2'-脱氧鸟苷。第四类核糖开关的成员采用独特的结构形成一个对鸟嘌呤类似物preQ(1)(7-氨基甲基-7-脱氮鸟嘌呤)具有选择性的结合口袋。所有四类嘌呤感应核糖开关很可能通过利用一个核糖开关残基与配体形成典型的沃森-克里克碱基对来识别它们各自的代谢物。本综述将对嘌呤感应核糖开关进行总结,并讨论这些核糖核酸的复杂功能和应用。

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