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古菌盒式H/ACA蛋白在依赖向导RNA和不依赖向导RNA的假尿苷形成中的不同作用。

Differential roles of archaeal box H/ACA proteins in guide RNA-dependent and independent pseudouridine formation.

作者信息

Gurha Priyatansh, Joardar Archi, Chaurasia Priyasri, Gupta Ramesh

机构信息

Department of Biochemistry and Molecular Biology, Southern Illinois University, Carbondale, Illinois 62901-4413, USA.

出版信息

RNA Biol. 2007 Oct;4(2):101-9. doi: 10.4161/rna.4.2.5177. Epub 2007 Oct 16.

Abstract

RNA-guided pseudouridine (Psi) synthesis in Archaea and Eukarya requires a four-protein one-RNA containing box H/ACA ribonucleoprotein (RNP) complex. The proteins in the archaeal RNP are aCbf5, aNop10, aGar1 and L7Ae. Pyrococcus aCbf5-aNop10 is suggested to be the minimal catalytic core in this synthesis and the activity is enhanced by L7Ae and aGar1. The protein aCbf5 is homologous to eukaryal Cbf5 (dyskerin, NAP57) as well as to bacterial TruB and eukaryal Pus4; the last two produce YPsi55 in tRNAs in a guide RNA-independent manner. Here, using recombinant Methanocaldococcus jannaschii proteins, we report that aCbf5 and aGar1 together can function as a tRNA Psi55 synthase in a guide RNA-independent manner. This activity is enhanced by aNop10, but not by L7Ae. The aCbf5 alone can also produce Psi55 in tRNAs that contain the canonical 3'-CCA sequence and this activity is stimulated by aGar1. These results suggest that the roles of accessory proteins are different in guide RNA-dependent and independent Psi synthesis by aCbf5. The presence of conserved C (or U) and A at tRNA positions 56 and 58, respectively, which are required for TruB/Pus4 activity, is not essential for aCbf5-mediated Psi55 formation. Conserved A58 in tRNA normally forms a tertiary reverse Hoogstein base pair with an equally conserved U54. This base pair is recognized by TruB. Apparently aCbf5 does not require this base pair to recognize U55 for conversion to Psi55.

摘要

古菌和真核生物中由RNA引导的假尿苷(Ψ)合成需要一个包含四种蛋白质和一种RNA的盒式H/ACA核糖核蛋白(RNP)复合物。古菌RNP中的蛋白质是aCbf5、aNop10、aGar1和L7Ae。有人提出嗜热栖热菌的aCbf5-aNop10是这种合成中的最小催化核心,L7Ae和aGar1可增强其活性。蛋白质aCbf5与真核生物的Cbf5(戴斯科林,NAP57)以及细菌的TruB和真核生物的Pus4同源;后两者以不依赖引导RNA的方式在tRNA中产生Ψ55。在这里,我们使用重组詹氏甲烷球菌蛋白报告称,aCbf5和aGar1一起可以以不依赖引导RNA的方式作为tRNA Ψ55合成酶发挥作用。aNop10可增强这种活性,但L7Ae不能。单独的aCbf5也可以在含有典型3'-CCA序列的tRNA中产生Ψ55,并且这种活性受到aGar1的刺激。这些结果表明,辅助蛋白在aCbf5依赖引导RNA和不依赖引导RNA的Ψ合成中的作用不同。TruB/Pus4活性所需的tRNA第56和58位分别存在保守的C(或U)和A,对于aCbf5介导的Ψ55形成并非必不可少。tRNA中保守的A58通常与同样保守的U54形成三级反向Hoogstein碱基对。这个碱基对被TruB识别。显然,aCbf5不需要这个碱基对来识别U55以将其转化为Ψ55。

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