Curran J F
Department of Biology, Wake Forest University, Winston-Salem, NC 27109.
Nucleic Acids Res. 1993 Apr 25;21(8):1837-43. doi: 10.1093/nar/21.8.1837.
The codon that is in-frame prior to +1 frameshifting at the E.coli prfB (RF2 gene) frameshift site is randomized to create thirty-two variants. These alleles vary 1000-fold in frameshift-dependent expression in fusions to lacZ. Frameshifting is more frequent at sites where the in-frame codon ends in uridine, as if third position wobble pairs to message uridine facilitate slippage into the +1 frame. Consistent with other studies of programmed frameshift sites, efficient frameshifting depends on stable message:tRNA base pairs after rephasing. For complexes with mispairs, frameshift frequency depends on the nature, number, and position of mispairs. Central purine:purine mispairs are especially inhibitory. Relative stabilities of +1 rephased complexes are estimated from published data on the stabilities of tRNA:tRNA complexes. Stability correlates with frameshifting over its entire range, which suggests that stability is an important determinant of the probability of translation of the rephased complex.
在大肠杆菌prfB(RF2基因)移码位点发生+1移码之前处于读框内的密码子被随机化,以产生32个变体。这些等位基因在与lacZ融合时,移码依赖性表达相差1000倍。当读框内密码子以尿苷结尾时,移码在这些位点更频繁发生,就好像第三位摆动配对到信使尿苷有助于滑入+1读框。与其他对程序性移码位点的研究一致,有效的移码取决于重相位后稳定的信使RNA:tRNA碱基对。对于有错配的复合物,移码频率取决于错配的性质、数量和位置。中心嘌呤:嘌呤错配尤其具有抑制作用。根据已发表的关于tRNA:tRNA复合物稳定性的数据估算+1重相位复合物的相对稳定性。稳定性在其整个范围内与移码相关,这表明稳定性是重相位复合物翻译概率的一个重要决定因素。