Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY, USA.
Department of Microbiology, New York University School of Medicine, New York, NY, USA.
Mol Microbiol. 2021 Aug;116(2):361-365. doi: 10.1111/mmi.14723. Epub 2021 Apr 25.
Although riboswitches have long been known to regulate translation initiation and transcription termination, a growing body of evidence indicates that they can also control bacterial RNA lifetimes by acting directly to hasten or impede RNA degradation. Ligand binding to the aptamer domain of a riboswitch can accelerate RNA decay by triggering a conformational change that exposes sites to endonucleolytic cleavage or by catalyzing the self-cleavage of a prefolded ribozyme. Alternatively, the conformational change induced by ligand binding can protect RNA from degradation by blocking access to an RNA terminus or internal region that would otherwise be susceptible to attack by an exonuclease or endonuclease. Such changes in RNA longevity often accompany a parallel effect of the same riboswitch on translation or transcription. Consequently, a single riboswitch aptamer may govern the function of multiple effector elements (expression platforms) that are co-resident within a transcript and act independently of one another.
尽管核糖开关早已被证实可以调节翻译起始和转录终止,但越来越多的证据表明,它们还可以通过直接作用来加速或阻碍 RNA 降解,从而控制细菌 RNA 的寿命。配体与核糖开关的适体结构域结合,可以通过触发构象变化来加速 RNA 降解,这种构象变化会暴露出易被内切核酸酶切割的位点,或者通过催化预折叠核酶的自我切割来实现。或者,配体结合所诱导的构象变化可以通过阻止 RNA 末端或内部区域被外切核酸酶或内切核酸酶攻击,从而保护 RNA 免受降解。这种 RNA 寿命的变化通常伴随着同一核糖开关对翻译或转录的平行影响。因此,单个核糖开关适体可能控制多个效应元件(表达平台)的功能,这些效应元件共同存在于一个转录本中,并相互独立地发挥作用。