Stepwise conversion of a mesophilic to a thermophilic ribozyme

被引:10
作者
Fang, XW
Srividya, N
Golden, BL
Sosnick, TR
Pan, T
机构
[1] Univ Chicago, Dept Biochem & Mol Biol, Chicago, IL 60637 USA
[2] Purdue Univ, Dept Biochem, W Lafayette, IN 47907 USA
[3] Univ Chicago, Inst Biophys Dynam, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
ribozyme; folding; stability; cooperativity; thermophile;
D O I
10.1016/S0022-2836(03)00582-5
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
A fundamental question in RNA folding is the mechanism of thermodynamic stability. We investigated the equilibrium folding of a series of sequence variants in which one to three motifs of a 255-nucleotide mesophilic ribozyme were substituted with the corresponding motifs from its thermophilic homologue. Substitution of three crucial motifs individually or in groups results in a continual increase in the stability and folding cooperativity in a stepwise fashion. We find an unexpected relationship between stability and folding cooperativity. Without changing the folding cooperativity, RNAs having a similar native structure can only achieve moderate change in stability and likewise, without changing stability, RNAs having a similar native structure can only achieve moderate change in folding cooperativity. This intricate relationship must be included in the predictions of tertiary RNA stability. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:177 / 183
页数:7
相关论文
共 16 条
[1]   Hierarchy and dynamics of RNA folding [J].
Brion, P ;
Westhof, E .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 1997, 26 :113-137
[2]   The Ribonuclease P Database [J].
Brown, JW .
NUCLEIC ACIDS RESEARCH, 1999, 27 (01) :314-314
[3]   Comparative analysis of ribonuclease P RNA using gene sequences from natural microbial populations reveals tertiary structural elements [J].
Brown, JW ;
Nolan, JM ;
Haas, ES ;
Rubio, MAT ;
Major, F ;
Pace, NR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (07) :3001-3006
[4]   Comparative photocross-linking analysis of the tertiary structures of Escherichia coli and Bacillus subtilis RNase P RNAs [J].
Chen, JL ;
Nolan, JM ;
Harris, ME ;
Pace, NR .
EMBO JOURNAL, 1998, 17 (05) :1515-1525
[5]   A thermodynamic framework and cooperativity in the tertiary folding of a Mg2+-dependent ribozyme [J].
Fang, XW ;
Pan, T ;
Sosnick, TR .
BIOCHEMISTRY, 1999, 38 (51) :16840-16846
[6]   The thermodynamic origin of the stability of a thermophilic ribozyme [J].
Fang, XW ;
Golden, BL ;
Littrell, K ;
Shelton, V ;
Thiyagarajan, P ;
Pan, T ;
Sosnick, TR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (08) :4355-4360
[7]   Evolution of Tetrahymena ribozyme mutants with increased structural stability [J].
Guo, F ;
Cech, TR .
NATURE STRUCTURAL BIOLOGY, 2002, 9 (11) :855-861
[8]   FURTHER PERSPECTIVE ON THE CATALYTIC CORE AND SECONDARY STRUCTURE OF RIBONUCLEASE-P RNA [J].
HAAS, ES ;
BROWN, JW ;
PITULLE, C ;
PACE, NR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (07) :2527-2531
[9]   Structure of the UGAGAU hexaloop that braces Bacillus RNase P for action [J].
Leeper, TC ;
Martin, MB ;
Kim, H ;
Cox, S ;
Semenchenko, V ;
Schmidt, FJ ;
Van Doren, SR .
NATURE STRUCTURAL BIOLOGY, 2002, 9 (05) :397-403
[10]   Derivation of the three-dimensional architecture of bacterial ribonuclease P RNAs from comparative sequence analysis [J].
Massire, C ;
Jaeger, L ;
Westhof, E .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 279 (04) :773-793