Consecutive GA pairs stabilize medium-size RNA internal loops

被引:21
作者
Chen, G
Turner, DH [1 ]
机构
[1] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
[2] Univ Rochester, Sch Med & Dent, Dept Pediat, Rochester, NY 14642 USA
[3] Univ Rochester, Sch Med & Dent, Ctr Pediat Biomed Res, Rochester, NY 14642 USA
关键词
D O I
10.1021/bi052060t
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
Internal loops in RNA are important for folding and function. Consecutive noncanonical pairs can form in internal loops having at least two nucleotides on each side. Thermodynamic and structural insights into such internal loops should improve approximations for their stabilities and predictions of secondary and three-dimensional structures. Most natural internal loops are purine rich. A series of oligoribonucleotides that form purine-rich internal loops of 5-10 nucleotides, including kink-turn loops, were studied by UV melting, exchangeable proton and phosphorus NMR. Three consecutive GA pairs with the motif (5'YGGA)/(3 ' RAAG) or (GGAR3 ')/(AAGY5 ') (i.e., (5 ' GGA3 ')/(3 ' AAG5 ') closed on at least one side with a CG, UA, or UG pair with Y representing C or U and R representing A or G) stabilize internal loops having 6-10 nucleoticles. Certain motifs with two consecutive GA pairs are also stabilizing. In internal loops with three or more nucleotides on each side, the motif (5'UG)/(3 ' GA) has stability similar to (5'CG)/(3 ' GA). A revised model for predicting stabilities of internal loops with 6-10 nucleotides is derived by multiple linear regression. Loops with 2 x 3 nucleotides are predicted well by a previous thermodynamic model.
引用
收藏
页码:4025 / 4043
页数:19
相关论文
共 103 条
[91]   SYNTHESIS, DEPROTECTION, ANALYSIS AND PURIFICATION OF RNA AND RIBOZYMES [J].
WINCOTT, F ;
DIRENZO, A ;
SHAFFER, C ;
GRIMM, S ;
TRACZ, D ;
WORKMAN, C ;
SWEEDLER, D ;
GONZALEZ, C ;
SCARINGE, S ;
USMAN, N .
NUCLEIC ACIDS RESEARCH, 1995, 23 (14) :2677-2684
[92]   The GA motif: An RNA element common to bacterial antitermination systems, rRNA, and eukaryotic RNAs [J].
Winkler, WC ;
Grundy, FJ ;
Murphy, BA ;
Henkin, TM .
RNA, 2001, 7 (08) :1165-1172
[93]   RNA folding causes secondary structure rearrangement [J].
Wu, M ;
Tinoco, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (20) :11555-11560
[94]   Solution structure of (rGGC(AG)under-bar-GCC)(2) by two-dimensional NMR and the iterative relaxation matrix approach [J].
Wu, M ;
SantaLucia, J ;
Turner, DH .
BIOCHEMISTRY, 1997, 36 (15) :4449-4460
[95]  
Wuchty S, 1999, BIOPOLYMERS, V49, P145, DOI 10.1002/(SICI)1097-0282(199902)49:2<145::AID-BIP4>3.3.CO
[96]  
2-7
[97]  
XIA T, 1999, PREBIOTIC CHEM MOL F, P21
[98]   Thermodynamics of nonsymmetric tandem mismatches adjacent to G center dot C base pairs in RNA [J].
Xia, TB ;
McDowell, JA ;
Turner, DH .
BIOCHEMISTRY, 1997, 36 (41) :12486-12497
[99]   Thermodynamic parameters for an expanded nearest-neighbor model for formation of RNA duplexes with Watson-Crick base pairs [J].
Xia, TB ;
SantaLucia, J ;
Burkard, ME ;
Kierzek, R ;
Schroeder, SJ ;
Jiao, XQ ;
Cox, C ;
Turner, DH .
BIOCHEMISTRY, 1998, 37 (42) :14719-14735
[100]   Stem of SL1 RNA in HIV-1: Structure and nucleocapsid protein binding for a 1 x 3 internal loop [J].
Yuan, YQ ;
Kerwood, DJ ;
Paoletti, AC ;
Shubsda, MF ;
Borer, PN .
BIOCHEMISTRY, 2003, 42 (18) :5259-5269