Agris Paul F
Department of Molecular and Structural Biochemistry, 128 Polk Hall, Campus Box 7622, North Carolina State University, Raleigh, North Carolina 27695-7622, USA.
EMBO Rep. 2008 Jul;9(7):629-35. doi: 10.1038/embor.2008.104. Epub 2008 Jun 13.
The biosynthesis of RNA includes its post-transcriptional modifications, and the crucial functions of these modifications have supported their conservation within all three kingdoms. For example, the modifications located within or adjacent to the anticodon of the transfer RNA (tRNA) enhance the accuracy of codon binding, maintain the translational reading frame and enable translocation of the tRNA from the A-site to the P-site of the ribosome. Although composed of different chemistries, the more than 70 known modifications of tRNA have in common their ability to reduce conformational dynamics, and to bring order to the internal loops and hairpin structures of RNA. The modified nucleosides of the anticodon domain of tRNA restrict its dynamics and shape its architecture; therefore, the need of the ribosome to constrain or remodel each tRNA to fit the decoding site is diminished. This concept reduces an entropic penalty for translation and provides a physicochemical basis for the conservation of RNA modifications in general.
RNA的生物合成包括其转录后修饰,这些修饰的关键功能支持了它们在所有三个生物界中的保守性。例如,位于转运RNA(tRNA)反密码子内或其附近的修饰提高了密码子结合的准确性,维持了翻译阅读框,并使tRNA能够从核糖体的A位点转移到P位点。尽管tRNA的70多种已知修饰由不同的化学组成,但它们都具有减少构象动力学并使RNA的内环和发夹结构有序化的能力。tRNA反密码子结构域的修饰核苷限制了其动力学并塑造了其结构;因此,核糖体将每个tRNA约束或重塑以适应解码位点的需求就减少了。这一概念减少了翻译中的熵罚,并为RNA修饰的保守性提供了一般的物理化学基础。