Pyle A M, Moran S, Strobel S A, Chapman T, Turner D H, Cech T R
Department of Chemistry and Biochemistry, University of Colorado, Boulder 80309.
Biochemistry. 1994 Nov 22;33(46):13856-63. doi: 10.1021/bi00250a040.
There is a phylogenetically conserved G.U pair at the 5'-splice site of group I introns. When this is mutagenized to a G-C pair, splicing of these introns is greatly reduced. We have used a ribozyme derived from the Tetrahymena group I intron to compare the binding and reactivity of oligonucleotides that form either a G.U or a G-C pair at this position. Ribozyme binding of oligonucleotides at 42 degrees C was measured by native gel electrophoresis and equilibrium dialysis. Binding of GGCCCUCC (C(-1)P), which base-pairs with the ribozyme guide sequence to form a G-C at the cleavage site, was 10-fold weaker than the binding of GGCCCUCU (U(-1)P), which maintains the conserved G.U pair at the cleavage site. This is surprising since a terminal G-C enhances the binding between oligonucleotides by 20-fold relative to a terminal G.U. Thermal denaturation studies indicate that C(-1)P and several analogs with deoxy substitutions bind the guide-sequence oligonucleotide, GGAGGGAAA, as strongly as they bind the ribozyme. In contrast, U(-1)P binds 240-fold more strongly to the ribozyme than to GGAGGGAAA, a difference that is decreased by deoxy substitutions. Thus, while U(-1)P binds the ribozyme through a combination of base-pairing and specific 2-OH and other tertiary interactions, C(-1)P may bind by base-pairing alone. The substrate GGCCCUCCAAAAA (C(-1)S) is cleaved 100-fold more slowly than GGCCCUCUAAAAA (U(-1)S) and also has a higher propensity to be cleaved at the wrong nucleotide position.(ABSTRACT TRUNCATED AT 250 WORDS)
在I组内含子的5'剪接位点存在一个系统发育保守的G.U碱基对。当将此碱基对诱变形成G-C碱基对时,这些内含子的剪接会大幅减少。我们使用了一种源自嗜热四膜虫I组内含子的核酶,来比较在此位置形成G.U或G-C碱基对的寡核苷酸的结合和反应性。通过非变性凝胶电泳和平衡透析测定了42℃时寡核苷酸与核酶的结合情况。与核酶引导序列碱基配对在切割位点形成G-C的GGCCCUCC(C(-1)P)的结合力,比在切割位点维持保守G.U碱基对的GGCCCUCU(U(-1)P)的结合力弱10倍。这很令人惊讶,因为相对于末端G.U,末端G-C会使寡核苷酸之间的结合增强20倍。热变性研究表明,C(-1)P和几个具有脱氧取代的类似物与引导序列寡核苷酸GGAGGGAAA的结合强度,与它们和核酶的结合强度一样。相比之下,U(-1)P与核酶的结合力比对GGAGGGAAA的结合力强240倍,这种差异会因脱氧取代而减小。因此,虽然U(-1)P通过碱基配对以及特定的2'-OH和其他三级相互作用的组合与核酶结合,但C(-1)P可能仅通过碱基配对结合。底物GGCCCUCCAAAAA(C(-1)S)的切割速度比GGCCCUCUAAAAA(U(-1)S)慢100倍,并且在错误核苷酸位置被切割的倾向也更高。(摘要截短于250字)