Inoue T, Sullivan F X, Cech T R
Cell. 1985 Dec;43(2 Pt 1):431-7. doi: 10.1016/0092-8674(85)90173-4.
The dinucleotide CpUOH, when incubated with self-splicing Tetrahymena pre-rRNA in the absence of GTP, functions as a 5' exon. It cleaves the precursor exactly at the 3' splice site and becomes covalently ligated to the 3' exon. Other oligonucleotides with sequences that resemble CUCUCU, the sequence at the 3' end of the 5' exon, can add to the 3' exon in this reaction. Such splicing in trans is most readily explained by a site within the intervening sequence that binds the last few nucleotides of the 5' exon. This binding site functions in splice site recognition and is also part of the active site of the ribozyme. The mechanism by which 5' splice sites are selected in Tetrahymena rRNA and group I mitochondrial RNA splicing is like that used in nuclear mRNA splicing, in that it involves specific pairing of bases adjacent to the splice site with a complementary RNA sequence.
二核苷酸CpUOH在没有GTP的情况下与自我剪接的四膜虫前体rRNA一起温育时,可作为5'外显子发挥作用。它恰好在3'剪接位点处切割前体,并与3'外显子形成共价连接。其他具有与5'外显子3'端序列CUCUCU相似序列的寡核苷酸可在该反应中添加到3'外显子上。这种反式剪接最容易通过间隔序列中与5'外显子最后几个核苷酸结合的位点来解释。该结合位点在剪接位点识别中起作用,也是核酶活性位点的一部分。四膜虫rRNA和I组线粒体RNA剪接中选择5'剪接位点的机制与核mRNA剪接中使用的机制类似,即它涉及剪接位点相邻碱基与互补RNA序列的特异性配对。