Johansen Steinar, Einvik Christer, Nielsen Henrik
RNA Research Group, Department of Molecular Biotechnology, Institute of Medical Biology, University of Tromsø, 037 Tromsø, Norway.
Biochimie. 2002 Sep;84(9):905-12. doi: 10.1016/s0300-9084(02)01443-8.
The group I-like ribozyme GIR1 is a unique example of a naturally occurring ribozyme with an evolved biological function. GIR1 generates the 5'-end of a nucleolar encoded messenger RNA involved in intron mobility. GIR1 is found as a cis-cleaving ribozyme within two very different rDNA group I introns (twin-ribozyme introns) in distantly related organisms. The Didymium GIR1 (DiGIR1) and Naegleria GIR1 (NaGIR1) share fundamental features in structural organization and reactivity, and display significant differences when compared to the related group I splicing ribozymes. GIR1 lacks the characteristic P1 segment present in all group I splicing ribozymes, it has a novel core organization, and it catalyses two site-specific hydrolytic cleavages rather than splicing. DiGIR1 and NaGIR1 appear to have originated from eubacterial group I introns in order to fulfil a common biological challenge: the expression of a protein encoding gene in a nucleolar context.
I类样核酶GIR1是具有进化生物学功能的天然存在核酶的独特例子。GIR1产生参与内含子移动性的核仁编码信使RNA的5'端。在远缘相关生物体的两个非常不同的rDNA I类内含子(双核酶内含子)中,GIR1作为顺式切割核酶被发现。地木耳GIR1(DiGIR1)和纳氏虫GIR1(NaGIR1)在结构组织和反应性方面具有基本特征,与相关的I类剪接核酶相比存在显著差异。GIR1缺乏所有I类剪接核酶中存在的特征性P1片段,具有新颖的核心结构,并且催化两个位点特异性水解切割而非剪接。DiGIR1和NaGIR1似乎起源于真细菌I类内含子,以应对共同的生物学挑战:在核仁环境中表达蛋白质编码基因。