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
[21]   MOLECULAR MECHANISM OF THERMAL UNFOLDING OF ESCHERICHIA-COLI FORMYLMETHIONINE TRANSFER-RNA [J].
CROTHERS, DM ;
COLE, PE ;
HILBERS, CW ;
SHULMAN, RG .
JOURNAL OF MOLECULAR BIOLOGY, 1974, 87 (01) :63-&
[22]  
Dieckmann T, 1996, RNA, V2, P628
[23]   A statistical sampling algorithm for RNA secondary structure prediction [J].
Ding, Y ;
Lawrence, CE .
NUCLEIC ACIDS RESEARCH, 2003, 31 (24) :7280-7301
[24]   A partition function algorithm for nucleic acid secondary structure including pseudoknots [J].
Dirks, RM ;
Pierce, NA .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 2003, 24 (13) :1664-1677
[25]   A universal mode of helix packing in RNA [J].
Doherty, EA ;
Batey, RT ;
Masquida, B ;
Doudna, JA .
NATURE STRUCTURAL BIOLOGY, 2001, 8 (04) :339-343
[26]   Solution structure of a consensus stem-loop D RNA domain that plays important roles in regulating translation and replication in enteroviruses and rhinoviruses [J].
Du, ZH ;
Yu, JH ;
Ulyanov, NB ;
Andino, R ;
James, TL .
BIOCHEMISTRY, 2004, 43 (38) :11959-11972
[27]   AA.AG@Helix.Ends:: A:A and A:G base-pairs at the ends of 16 S and 23 S rRNA helices [J].
Elgavish, T ;
Cannone, JJ ;
Lee, JC ;
Harvey, SC ;
Gutell, RR .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 310 (04) :735-753
[28]  
Fasman GD, 1975, HDB BIOCH MOL BIOL N, V1, P596
[29]   A pH controlled conformational switch in the cleavage site of the VS ribozyme substrate RNA [J].
Flinders, J ;
Dieckmann, T .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 308 (04) :665-679
[30]   NMR spectroscopy of RNA [J].
Fürtig, B ;
Richter, C ;
Wöhnert, J ;
Schwalbe, H .
CHEMBIOCHEM, 2003, 4 (10) :936-962