Facilitating RNA structure prediction with microarrays

被引:36
作者
Kierzek, E
Kierzek, R
Turner, DH
Catrina, IE
机构
[1] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
[2] Univ Rochester, Dept Pediat, Sch Med & Dent, Rochester, NY 14642 USA
[3] Univ Rochester, Ctr Pediat Biomed Res, Sch Med & Dent, Rochester, NY 14642 USA
[4] Polish Acad Sci, Inst Bioorgan Chem, PL-61704 Poznan, Poland
关键词
D O I
10.1021/bi051409+
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
Determining RNA secondary structure is important for understanding structure-function relationships and identifying potential drug targets. This paper reports the use of microarrays with heptamer 2'-O-methyl oligoribonucleotides to probe the secondary structure of an RNA and thereby improve the prediction of that secondary structure. When experimental constraints from hybridization results are added to a free-energy minimization algorithm, the prediction of the secondary structure of Escherichia coli 5S rRNA improves from 27 to 92% of the known canonical base pairs. Optimization of buffer conditions for hybridization and application of 2'-O-methyl-2-thiouridine to enhance binding and improve discrimination between AU and GU pairs are also described. The results suggest that probing RNA with oligonucleotide microarrays can facilitate determination of secondary structure.
引用
收藏
页码:581 / 593
页数:13
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