Identity and geometry of a base triple in 16S rRNA determined by comparative sequence analysis and molecular modeling

被引:7
作者
Babin, P
Dolan, M
Wollenzien, P
Gutell, RR
机构
[1] N Carolina State Univ, Dept Biochem, Raleigh, NC 27695 USA
[2] Univ Texas, Inst Cell & Mol Biol, Austin, TX 78712 USA
[3] Univ Texas, Sch Biol Sci, Austin, TX 78712 USA
关键词
16S rRNA; base triple; comparative sequence analysis; molecular modeling;
D O I
10.1017/S1355838299990659
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Comparative sequence analysis complements experimental methods for the determination of RNA three-dimensional structure, This approach is based on the concept that different sequences within the same gene family form similar higher-order structures. The large number of rRNA sequences with sufficient variation, along with improved covariation algorithms, are providing us with the opportunity to identify new base triples in 16S rRNA. The three-dimensional conformations for one of our strongest candidates involving U121 (C124:G237) and/or U121 (U125:A236) (Escherichia coli sequence and numbering) are analyzed here with different molecular modeling tools. Molecular modeling shows that U121 interacts with C124 in the U121 (C124:G237) base triple. This arrangement maintains isomorphic structures for the three most frequent sequence motifs (approximately 93% of known bacterial and archaeal sequences), is consistent with chemical reactivity of U121 in E. coli ribosomes, and is geometrically favorable. Further, the restricted set of observed canonical (GU, AU, CC) base-pair types at positions 124:237 and 125:236 is consistent with the fact that the canonical base-pair sets (for both base pairs) that are not observed in nature prevent the formation of the 121 (124:237) base triple, The analysis described here serves as a general scheme for the prediction of specific secondary and tertiary structure base pairing where there is a network of correlated base changes.
引用
收藏
页码:1430 / 1439
页数:10
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