Kruger K, Grabowski P J, Zaug A J, Sands J, Gottschling D E, Cech T R
Cell. 1982 Nov;31(1):147-57. doi: 10.1016/0092-8674(82)90414-7.
In the macronuclear rRNA genes of Tetrahymena thermophila, a 413 bp intervening sequence (IVS) interrupts the 26S rRNA-coding region. A restriction fragment of the rDNA containing the IVS and portions of the adjacent rRNA sequences (exons) was inserted downstream from the lac UV5 promoter in a recombinant plasmid. Transcription of this template by purified Escherichia coli RNA polymerase in vitro produced a shortened version of the pre-rRNA, which was then deproteinized. When incubated with monovalent and divalent cations and a guanosine factor, this RNA underwent splicing. The reactions that were characterized included the precise excision of the IVS, attachment of guanosine to the 5' end of the IVS, covalent cyclization of the IVS and ligation of the exons. We conclude that splicing activity is intrinsic to the structure of the RNA, and that enzymes, small nuclear RNAs and folding of the pre-rRNA into an RNP are unnecessary for these reactions. We propose that the IVS portion of the RNA has several enzyme-like properties that enable it to break and reform phosphodiester bonds. The finding of autocatalytic rearrangements of RNA molecules has implications for the mechanism and the evolution of other reactions that involve RNA.
在嗜热四膜虫的大核rRNA基因中,一段413bp的间隔序列(IVS)中断了26S rRNA编码区。将包含IVS和相邻rRNA序列(外显子)部分的rDNA限制性片段插入重组质粒中lac UV5启动子的下游。用纯化的大肠杆菌RNA聚合酶在体外转录该模板,产生了一个缩短版的前体rRNA,然后将其脱蛋白。当与单价和二价阳离子以及鸟苷因子一起孵育时,该RNA进行剪接。所表征的反应包括IVS的精确切除、鸟苷与IVS 5'端的连接、IVS的共价环化以及外显子的连接。我们得出结论,剪接活性是RNA结构所固有的,并且这些反应不需要酶、小核RNA以及前体rRNA折叠成RNP。我们提出,RNA的IVS部分具有几种类似酶的特性,使其能够断裂和重新形成磷酸二酯键。RNA分子自催化重排的发现对涉及RNA的其他反应的机制和进化具有启示意义。