Shaping space: the possible and the attainable in RNA genotype-phenotype mapping

被引:121
作者
Fontana, W
Schuster, P
机构
[1] Univ Vienna, Inst Theoret Chem, A-1090 Vienna, Austria
[2] Int Inst Appl Syst Anal, A-2361 Laxenburg, Austria
[3] Santa Fe Inst, Santa Fe, NM 87501 USA
基金
奥地利科学基金会;
关键词
D O I
10.1006/jtbi.1998.0771
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Understanding which phenotypes are accessible from which genotypes is fundamental for understanding the evolutionary process. This notion of acessibility can be used to define a relation of nearness among phenotypes, independently of their similarity. Because of neutrality, phenotypes denote equivalence classes of genotypes. The definition of neighborhood relations among phenotypes relies, therefore, on the statistics of neighborhood relations among equivalence classes of genotypes in genotype space. The folding of RNA sequences (genotypes) into secondary structures (phenotypes) is an ideal case to implement these concepts. We study the extent to which the folding of RNA sequences induces a "statistical topology" on the set of minimum free energy secondary structures. The resulting nearness relation suggests a notion of "continuous" structure transformation. We can, then, rationalize major transitions in evolutionary trajectories at the level of RNA structures by identifying those transformations which are irreducibly discontinuous. This is shown by means of computer simulations. The statistical topology organizing the set of RNA shapes explains why neutral drift in sequence space plays a key role in evolutionary optimization. (C) 1998 Academic Press.
引用
收藏
页码:491 / 515
页数:25
相关论文
共 23 条
[1]  
Buss L, 1987, The evolution of individuality
[2]   STRUCTURALLY COMPLEX AND HIGHLY-ACTIVE RNA LIGASES DERIVED FROM RANDOM RNA SEQUENCES [J].
EKLAND, EH ;
SZOSTAK, JW ;
BARTEL, DP .
SCIENCE, 1995, 269 (5222) :364-370
[3]   RNA SELECTION - APTAMERS ACHIEVE THE DESIRED RECOGNITION [J].
ELLINGTON, AD .
CURRENT BIOLOGY, 1994, 4 (05) :427-429
[4]   A COMPUTER-MODEL OF EVOLUTIONARY OPTIMIZATION [J].
FONTANA, W ;
SCHUSTER, P .
BIOPHYSICAL CHEMISTRY, 1987, 26 (2-3) :123-147
[5]   Continuity in evolution: On the nature of transitions [J].
Fontana, W ;
Schuster, P .
SCIENCE, 1998, 280 (5368) :1451-1455
[6]   Why are some protein structures so common? [J].
Govindarajan, S ;
Goldstein, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) :3341-3345
[7]  
GOVINDARAJAN S, 1997, IN PRESS FOLDABILITY
[8]   Analysis of RNA sequence structure maps by exhaustive enumeration .1. Neutral networks [J].
Gruner, W ;
Giegerich, R ;
Strothmann, D ;
Reidys, C ;
Weber, J ;
Hofacker, IL ;
Stadler, PF ;
Schuster, P .
MONATSHEFTE FUR CHEMIE, 1996, 127 (04) :355-374
[9]   Analysis of RNA sequence structure maps by exhaustive enumeration .2. structures of neutral networks and shape space covering [J].
Gruner, W ;
Giegerich, R ;
Strothmann, D ;
Reidys, C ;
Weber, J ;
Hofacker, IL ;
Stadler, PF ;
Schuster, P .
MONATSHEFTE FUR CHEMIE, 1996, 127 (04) :375-389
[10]   FAST FOLDING AND COMPARISON OF RNA SECONDARY STRUCTURES [J].
HOFACKER, IL ;
FONTANA, W ;
STADLER, PF ;
BONHOEFFER, LS ;
TACKER, M ;
SCHUSTER, P .
MONATSHEFTE FUR CHEMIE, 1994, 125 (02) :167-188