Szekely E, Belford H G, Greer C L
Department of Biological Chemistry, California College of Medicine, University of California, Irvine 92717.
J Biol Chem. 1988 Sep 25;263(27):13839-47.
Predicted single-stranded structure at the 3' splice site is a conserved feature among intervening sequences (IVSs) in eukaryotic nuclear tRNA precursors. The role of 3' splice site structure in splicing was examined through hexanucleotide insertions at a central intron position in the Saccharomyces cerevisiae tRNA gene. These insertions were designed to alter the structure at the splice site without changing its sequence. Endonuclease cleavage of pre-tRNA substrates was then measured in vitro, and suppressor activity was examined in vivo. A precursor with fully double-stranded structure at the 3' splice site was not cleaved by endonuclease. The introduction of one unpaired nucleotide at the 3' splice site was sufficient to restore cleavage, although at a reduced rate. We have also observed that guanosine at the antepenultimate position provides a second consensus feature among IVSs in tRNA precursors. Point mutations at this position were found to affect splicing although there was no specific requirement for guanosine. These and previous results suggest that elements of secondary and/or tertiary structure at the 3' end of IVSs are primary determinants in pre-tRNA splice site utilization whereas specific sequence requirements are limited.
真核细胞核tRNA前体中,内含子序列(IVSs)3'剪接位点处预测的单链结构是一个保守特征。通过在酿酒酵母tRNA基因的中央内含子位置插入六核苷酸,研究了3'剪接位点结构在剪接过程中的作用。这些插入设计用于改变剪接位点的结构而不改变其序列。然后在体外测量前体tRNA底物的核酸内切酶切割,并在体内检测抑制活性。在3'剪接位点具有完全双链结构的前体不能被核酸内切酶切割。在3'剪接位点引入一个未配对的核苷酸足以恢复切割,尽管切割速率降低。我们还观察到,倒数第二个位置的鸟苷是tRNA前体IVSs中的第二个共有特征。发现该位置的点突变会影响剪接,尽管对鸟苷没有特定要求。这些结果以及之前的结果表明,IVSs 3'端的二级和/或三级结构元件是前体tRNA剪接位点利用的主要决定因素,而特定的序列要求有限。