Assembly of core helices and rapid tertiary folding of a small bacterial group I ribozyme

被引:113
作者
Rangan, P
Masquida, B
Westhof, E
Woodson, SA
机构
[1] Johns Hopkins Univ, TC Jenkins Dept Biophys, Baltimore, MD 21218 USA
[2] Univ Strasbourg 1, Ctr Natl Rech Sci, Unite Propre Rech 9002, Inst Biol Mol & Cellulaire, F-67084 Strasbourg, France
关键词
RNA modeling; RNA structure; metal ions; hydroxyl radical footprinting;
D O I
10.1073/pnas.0337743100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Compact but non-native intermediates have been implicated in the hierarchical folding of several large RNAs, but there is little information on their structure. In this article, ribonuclease and hydroxyl radical cleavage protection assays showed that base pairing of core helices stabilize a compact state of a small group I ribozyme from Azoarcus pre-tRNA(ile). Base pairing of the ribozyme core requires 10-fold less Mg2+ than stable tertiary interactions, indicating that assembly of helices in the catalytic core represents a distinct phase that precedes the formation of native tertiary structure. Tertiary folding occurs in <100 ms at 37degreesC. Such rapid folding is unprecedented among group I ribozymes and illustrates the association between structural complexity and folding time. A 3D model of the Azoarcus ribozyme was constructed by identifying homologous sequence motifs in rRNA. The model reveals distinct structural features, such as a large interface between the P4-P6 and P3-P9 domains, that may explain the unusual stability of the Azoarcus ribozyme and the cooperativity of folding.
引用
收藏
页码:1574 / 1579
页数:6
相关论文
共 52 条
[1]   The complete atomic structure of the large ribosomal subunit at 2.4 Å resolution [J].
Ban, N ;
Nissen, P ;
Hansen, J ;
Moore, PB ;
Steitz, TA .
SCIENCE, 2000, 289 (5481) :905-920
[2]   Analysis of the cooperative thermal unfolding of the td intron of bacteriophage T4 [J].
Brion, P ;
Michel, F ;
Schroeder, R ;
Westhof, E .
NUCLEIC ACIDS RESEARCH, 1999, 27 (12) :2494-2502
[3]   Crystal structure of a group I ribozyme domain: Principles of RNA packing [J].
Cate, JH ;
Gooding, AR ;
Podell, E ;
Zhou, KH ;
Golden, BL ;
Kundrot, CE ;
Cech, TR ;
Doudna, JA .
SCIENCE, 1996, 273 (5282) :1678-1685
[4]   VISUALIZING THE HIGHER-ORDER FOLDING OF A CATALYTIC RNA MOLECULE [J].
CELANDER, DW ;
CECH, TR .
SCIENCE, 1991, 251 (4992) :401-407
[5]   FREQUENT USE OF THE SAME TERTIARY MOTIF BY SELF-FOLDING RNAS [J].
COSTA, M ;
MICHEL, F .
EMBO JOURNAL, 1995, 14 (06) :1276-1285
[6]   Folding mechanism of the Tetrahymena ribozyme P4-P6 domain [J].
Deras, ML ;
Brenowitz, M ;
Ralston, CY ;
Chance, MR ;
Woodson, SA .
BIOCHEMISTRY, 2000, 39 (36) :10975-10985
[7]   A TERTIARY INTERACTION IN THE TETRAHYMENA INTRON CONTRIBUTES TO SELECTION OF THE 5' SPLICE-SITE [J].
DOWNS, WD ;
CECH, TR .
GENES & DEVELOPMENT, 1994, 8 (10) :1198-1211
[8]   SELF-SPLICING OF THE TETRAHYMENA PRE-RIBOSOMAL-RNA IS DECREASED BY MISFOLDING DURING TRANSCRIPTION [J].
EMERICK, VL ;
WOODSON, SA .
BIOCHEMISTRY, 1993, 32 (50) :14062-14067
[9]   FINGERPRINTING THE FOLDING OF A GROUP-I PRECURSOR RNA [J].
EMERICK, VL ;
WOODSON, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (21) :9675-9679
[10]   Mg2+-dependent compaction and folding of yeast tRNAPhe and the catalytic domain of the B-subtilis RNase P RNA determined by small-angle X-ray scattering [J].
Fang, XW ;
Littrell, K ;
Yang, X ;
Henderson, SJ ;
Siefert, S ;
Thiyagarajan, P ;
Pan, T ;
Sosnick, TR .
BIOCHEMISTRY, 2000, 39 (36) :11107-11113