Williamson C L, Tierney W M, Kerker B J, Burke J M
Department of Chemistry, Williams College, Williamstown, Massachusetts 01267.
J Biol Chem. 1987 Oct 25;262(30):14672-82.
The intron within the Tetrahymena thermophila nuclear large rRNA precursor is the best studied example of group I self-splicing introns. In this paper, we examine the structural and functional roles of four internal sequence elements which are characteristic of group I introns in the RNA-catalyzed processing reactions. Oligonucleotide-directed mutagenesis was used to generate mutations in sequence elements 9R', 9L, 9R and 2 of the Tetrahymena intervening sequence. Self-splicing activities of variant precursor RNAs were characterized by in vitro splicing following transcription with T7 or SP6 RNA polymerase. First, we confirm the proposed base pairing of sequence elements 9R and 9R' by construction and analysis of compensatory mutations. Mutations in elements 9R (G272A C274G) and 9R' (G100C C102U) each disrupt the pairing and eliminate self-splicing activity. A compensatory 9R/9R' mutation (G100C C102U G272A C274G) restores pairing and normal splicing activity. We conclude that 9R X 9R' pairing is a requirement for self-splicing. Second, we show that self-splicing activity is very sensitive to both nucleotide sequence and RNA secondary structure in the pairing segments of elements 9L and 2. Mutations within these regions at positions 266, 268, 307, and 309 can increase as well as decrease activity relative to wild type. Third, a mutation in the highly conserved nonpairing segment of element 9L (U259A A261C) increases KM for GTP from 29 to 120 microM, but does not otherwise affect splicing activity. The primary consequence of this mutation is a decrease in GTP binding energy of approximately 0.9 kcal/mol. Last, we show that a mutation in the highly conserved nonpairing segment of element 2 (A301C A302G G303C) eliminates transesterification activity, but does not affect 3' splice site hydrolysis.
嗜热四膜虫核大核糖体RNA前体中的内含子是I类自剪接内含子中研究得最为透彻的例子。在本文中,我们研究了四个内部序列元件在RNA催化加工反应中的结构和功能作用,这些元件是I类内含子的特征。利用寡核苷酸定向诱变在嗜热四膜虫间隔序列的序列元件9R'、9L、9R和2中产生突变。通过用T7或SP6 RNA聚合酶转录后的体外剪接来表征变异前体RNA的自剪接活性。首先,我们通过构建和分析补偿性突变来证实序列元件9R和9R'之间推测的碱基配对。元件9R(G272A C274G)和9R'(G100C C102U)中的突变各自破坏了配对并消除了自剪接活性。一个补偿性的9R/9R'突变(G100C C102U G272A C274G)恢复了配对和正常的剪接活性。我们得出结论,9R×9R'配对是自剪接的必要条件。其次,我们表明自剪接活性对元件9L和2的配对区段中的核苷酸序列和RNA二级结构都非常敏感。相对于野生型,这些区域中位置为266、268、307和309处的突变既可以增加也可以降低活性。第三,元件9L高度保守的非配对区段中的一个突变(U259A A261C)使GTP的KM从29增加到120微摩尔,但在其他方面不影响剪接活性。该突变的主要后果是GTP结合能降低了约0.9千卡/摩尔。最后,我们表明元件2高度保守的非配对区段中的一个突变(A301C A302G G303C)消除了转酯活性,但不影响3'剪接位点水解。