Metal ion-induced site-selective RNA hydrolysis by use of acridine-bearing oligonucleotide as cofactor

被引:52
作者
Kuzuya, A [1 ]
Mizoguchi, R [1 ]
Morisawa, F [1 ]
Machida, K [1 ]
Komiyama, M [1 ]
机构
[1] Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan
关键词
D O I
10.1021/ja025653p
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New types of noncovalent ribozyme-mimics for site-selective RNA scission are prepared by combining metal ions with oligonucleotides bearing an acridine. Lanthanide(III) ions and various divalent metal ions (Zn(II), Mn(II), Cu(II), Ni(II), Co(II), Mg(II), and Ca(II)) are employed without being bound to any sequence-recognizing moiety. The modified oligonucleotide forms a heteroduplex with the substrate RNA, and selectively activates the phosphodiester linkages in front of the acridine. As a result, these linkages are preferentially hydrolyzed over the others, even though the metal ions are not fixed anywhere. The scission is efficient under physiological conditions, irrespective of the sequence at the target site. Site-selective RNA scission is also successful with the combination of an oligonucleotide bearing an acridine at its terminus, another unmodified oligonucleotide, and the metal ion. In a proposed mechanism, the acridine pushes the unpaired ribonucleotide out of the heteroduplex and changes the conformation of RNA at the target site for the sequence-selective activation.
引用
收藏
页码:6887 / 6894
页数:8
相关论文
共 36 条
[1]  
ALBERT A, 1966, ACRIDINES, P434
[2]   Oligonucleotide-europium complex conjugate designed to cleave the 5′ cap structure of the ICAM-1 transcript potentiates antisense activity in cells [J].
Baker, BF ;
Lot, SS ;
Kringel, J ;
Cheng-Flournoy, S ;
Villiet, P ;
Sasmor, HM ;
Siwkowski, AM ;
Chappell, LL ;
Morrow, JR .
NUCLEIC ACIDS RESEARCH, 1999, 27 (06) :1547-1551
[3]   Cleavage of yeast tRNAPhe with complementary oligonucleotide conjugated to a small ribonuclease mimic [J].
Beloglazova, NG ;
Sil'nikov, VN ;
Zenkova, MA ;
Vlassov, VV .
FEBS LETTERS, 2000, 481 (03) :277-280
[4]   In vitro selection of catalytic polynucleotides [J].
Breaker, RR .
CHEMICAL REVIEWS, 1997, 97 (02) :371-390
[5]   THE CHEMISTRY OF SELF-SPLICING RNA AND RNA ENZYMES [J].
CECH, TR .
SCIENCE, 1987, 236 (4808) :1532-1539
[6]   Molecular design for a pinpoint RNA scission. Interposition of oligoamines between two DNA oligomers [J].
Endo, M ;
Azuma, Y ;
Saga, Y ;
Kuzuya, A ;
Kawai, G ;
Komiyama, M .
JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (04) :846-852
[7]   Recognition of hairpin-containing single-stranded DNA by oligonucleotides containing internal acridine derivatives [J].
François, JC ;
Hélène, C .
BIOCONJUGATE CHEMISTRY, 1999, 10 (03) :439-446
[8]   The acridine ring selectively intercalated into a DNA helix at various types of abasic sites: Double strand formation and photophysical properties [J].
Fukui, K ;
Tanaka, K .
NUCLEIC ACIDS RESEARCH, 1996, 24 (20) :3962-3967
[9]   Towards artificial ribonucleases: The sequence-specific cleavage of RNA in a duplex [J].
Hall, J ;
Husken, D ;
Haner, R .
NUCLEIC ACIDS RESEARCH, 1996, 24 (18) :3522-3526
[10]   On the apparently anomalous distance dependence of charge-transfer rates in 9-amino-6-chloro-2-methoxyacridine-modified DNA [J].
Hess, S ;
Götz, M ;
Davis, WB ;
Michel-Beyerle, ME .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (41) :10046-10055