Use of DNAzymes for site-specific analysis of ribonucleotide modifications

被引:40
作者
Hengesbach, Martin [1 ]
Meusburger, Madeleine
Lyko, Frank
Helm, Mark [1 ]
机构
[1] Univ Heidelberg, Inst Pharm & Mol Biotechnol, D-69120 Heidelberg, Germany
关键词
DNAzyme; tandem DNAzyme; modification; modified nucleotide; modification enzymes;
D O I
10.1261/rna.742708
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
Post-transcriptional ribonucleotide modifications are widespread and abundant processes that have not been analyzed adequately due to the lack of appropriate detection methods. Here, two methods for the analysis of modified nucleotides in RNA are presented that are based on the quantitative and site-specific DNAzyme-mediated cleavage of the target RNA at or near the site of modification. Quantitative RNA cleavage is achieved by cycling the DNAzyme and its RNA substrate through repeated periods of heating and cooling. In a first approach, DNAzyme-directed cleavage directly 5' of the residue in question allows radioactive labeling of the newly freed 5'-OH. After complete enzymatic hydrolysis, the modification status can be assessed by two-dimensional thin layer chromatography. In a second approach, oligoribonucleotide fragments comprising the modification site are excised from the full-length RNA in an endonucleolytic fashion, using a tandem DNAzyme. The excised fragment is isolated by electrophoresis and submitted to further conventional analysis. These results establish DNAzymes as valuable tools for the site-specific and highly sensitive detection of ribonucleotide modifications.
引用
收藏
页码:180 / 187
页数:8
相关论文
共 32 条
[1]   4 NEWLY LOCATED PSEUDOURIDYLATE RESIDUES IN ESCHERICHIA-COLI 23S RIBOSOMAL-RNA ARE ALL AT THE PEPTIDYLTRANSFERASE CENTER - ANALYSIS BY THE APPLICATION OF A NEW SEQUENCING TECHNIQUE [J].
BAKIN, A ;
OFENGAND, J .
BIOCHEMISTRY, 1993, 32 (37) :9754-9762
[2]  
Bakin AV, 1998, METH MOL B, V77, P297
[3]   A previously unidentified activity of yeast and mouse RNA:pseudouridine synthases 1 (Pus1p) on tRNAs [J].
Behm-Ansmant, Isabelle ;
Massenet, Severine ;
Immel, Francoise ;
Patton, Jeffrey R. ;
Motorin, Yuri ;
Branlant, Christiane .
RNA, 2006, 12 (08) :1583-1593
[4]   A pseudoknotted tRNA variant is a substrate for tRNA (cytosine-5)-methyltransferase from Xenopus laevis [J].
Brulé, H ;
Grosjean, H ;
Giegé, R ;
Florentz, C .
BIOCHIMIE, 1998, 80 (12) :977-985
[5]   Analysis of 2′-O-methylated nucleosides and pseudouridines in ribosomal RNAs using DNAzymes [J].
Buchhaupt, Markus ;
Pelfer, Christian ;
Entian, Karl-Dieter .
ANALYTICAL BIOCHEMISTRY, 2007, 361 (01) :102-108
[6]   Optimisation of the 10-23 DNAzyme-substrate pairing interactions enhanced RNA cleavage activity at purine-cytosine target sites [J].
Cairns, MJ ;
King, A ;
Sun, LQ .
NUCLEIC ACIDS RESEARCH, 2003, 31 (11) :2883-2889
[7]   Cloning and characterization of a mammalian pseudouridine synthase [J].
Chen, JG ;
Patton, JR .
RNA, 1999, 5 (03) :409-419
[8]   Dinucleotide junction cleavage versatility of 8-17 deoxyribozyme [J].
Cruz, RPG ;
Withers, JB ;
Li, YF .
CHEMISTRY & BIOLOGY, 2004, 11 (01) :57-67
[9]   A new and efficient DNA enzyme for the sequence-specific cleavage of RNA [J].
Feldman, AR ;
Sen, D .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 313 (02) :283-294
[10]   Methylation of tRNAAsP by the DNA methyltransferase homolog Dnmt2 [J].
Goll, MG ;
Kirpekar, F ;
Maggert, KA ;
Yoder, JA ;
Hsieh, CL ;
Zhang, XY ;
Golic, KG ;
Jacobsen, SE ;
Bestor, TH .
SCIENCE, 2006, 311 (5759) :395-398