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连接I组核酶两个结构域的碱基三联体的诱变及比较序列分析。

Mutagenesis and comparative sequence analysis of a base triple joining the two domains of group I ribozymes.

作者信息

Tanner M A, Anderson E M, Gutell R R, Cech T R

机构信息

Department of Chemistry and Biochemistry, University of Colorado, Boulder 80309-0215, USA.

出版信息

RNA. 1997 Sep;3(9):1037-51.

Abstract

Tertiary interactions are important in the higher-order folding of catalytic RNAs. Recently, a base triple, joining the two major domains of the catalytic core, was determined in group I introns from the cyanobacterium Anabaena PCC7120 and the eukaryote Tetrahymena thermophila. This base triple involves the fifth base pair of P4 and the fifth base of the single-stranded region J8/7. We made base pair and single-nucleotide substitutions in the fifth base pair of P4, a G-C in the wild-type Anabaena intron, and tested them for self-splicing activity. The results suggest a hydrogen bonding model in which only the C of the base pair interacts directly with the fifth base of J8/7. Comparative sequence analysis was used to determine the different combinations of base triples that occur in approximately 450 natural group I introns identified to date. About 94% of the base triples analyzed are compatible with the proposed hydrogen bonding model. Disrupting this base triple in the Tetrahymena intron resulted in the disappearance of splicing intermediates (intron 3' exon and 5' exon), even though the first step of splicing was not affected. Restoration of the base triple by a compensatory mutation reverted the intermediates to wild-type levels. These results suggest that disruption of the base triple increases the rate of the second step of splicing or of a conformational change preceding the second step. Repositioning of the base triple to form a new set of interactions may be required for the second step of splicing.

摘要

三级相互作用在催化性RNA的高阶折叠中很重要。最近,在来自蓝藻鱼腥藻PCC7120和真核生物嗜热栖热菌的I组内含子中确定了一个连接催化核心两个主要结构域的碱基三联体。这个碱基三联体涉及P4的第五个碱基对和单链区域J8/7的第五个碱基。我们在野生型鱼腥藻内含子中P4的第五个碱基对(一个G-C碱基对)中进行了碱基对和单核苷酸替换,并测试了它们的自我剪接活性。结果表明了一种氢键模型,其中只有碱基对中的C与J8/7的第五个碱基直接相互作用。通过比较序列分析来确定在迄今已鉴定的约450个天然I组内含子中出现的不同碱基三联体组合。所分析的碱基三联体中约94%与所提出的氢键模型相符。破坏嗜热栖热菌内含子中的这个碱基三联体导致剪接中间体(内含子3'外显子和5'外显子)消失,尽管剪接的第一步不受影响。通过补偿性突变恢复碱基三联体可使中间体恢复到野生型水平。这些结果表明,碱基三联体的破坏增加了剪接第二步或第二步之前构象变化的速率。剪接的第二步可能需要重新定位碱基三联体以形成一组新的相互作用。

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