Cargando…
Compensatory mutations cause excess of antagonistic epistasis in RNA secondary structure folding
BACKGROUND: The rate at which fitness declines as an organism's genome accumulates random mutations is an important variable in several evolutionary theories. At an intuitive level, it might seem natural that random mutations should tend to interact synergistically, such that the rate of mean f...
Autores principales: | , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2003
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC149451/ https://www.ncbi.nlm.nih.gov/pubmed/12590655 http://dx.doi.org/10.1186/1471-2148-3-3 |
_version_ | 1782120639597903872 |
---|---|
author | Wilke, Claus O Lenski, Richard E Adami, Christoph |
author_facet | Wilke, Claus O Lenski, Richard E Adami, Christoph |
author_sort | Wilke, Claus O |
collection | PubMed |
description | BACKGROUND: The rate at which fitness declines as an organism's genome accumulates random mutations is an important variable in several evolutionary theories. At an intuitive level, it might seem natural that random mutations should tend to interact synergistically, such that the rate of mean fitness decline accelerates as the number of random mutations is increased. However, in a number of recent studies, a prevalence of antagonistic epistasis (the tendency of multiple mutations to have a mitigating rather than reinforcing effect) has been observed. RESULTS: We studied in silico the net amount and form of epistatic interactions in RNA secondary structure folding by measuring the fraction of neutral mutants as a function of mutational distance d. We found a clear prevalence of antagonistic epistasis in RNA secondary structure folding. By relating the fraction of neutral mutants at distance d to the average neutrality at distance d, we showed that this prevalence derives from the existence of many compensatory mutations at larger mutational distances. CONCLUSIONS: Our findings imply that the average direction of epistasis in simple fitness landscapes is directly related to the density with which fitness peaks are distributed in these landscapes. |
format | Text |
id | pubmed-149451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-1494512003-02-25 Compensatory mutations cause excess of antagonistic epistasis in RNA secondary structure folding Wilke, Claus O Lenski, Richard E Adami, Christoph BMC Evol Biol Research Article BACKGROUND: The rate at which fitness declines as an organism's genome accumulates random mutations is an important variable in several evolutionary theories. At an intuitive level, it might seem natural that random mutations should tend to interact synergistically, such that the rate of mean fitness decline accelerates as the number of random mutations is increased. However, in a number of recent studies, a prevalence of antagonistic epistasis (the tendency of multiple mutations to have a mitigating rather than reinforcing effect) has been observed. RESULTS: We studied in silico the net amount and form of epistatic interactions in RNA secondary structure folding by measuring the fraction of neutral mutants as a function of mutational distance d. We found a clear prevalence of antagonistic epistasis in RNA secondary structure folding. By relating the fraction of neutral mutants at distance d to the average neutrality at distance d, we showed that this prevalence derives from the existence of many compensatory mutations at larger mutational distances. CONCLUSIONS: Our findings imply that the average direction of epistasis in simple fitness landscapes is directly related to the density with which fitness peaks are distributed in these landscapes. BioMed Central 2003-02-05 /pmc/articles/PMC149451/ /pubmed/12590655 http://dx.doi.org/10.1186/1471-2148-3-3 Text en Copyright © 2003 Wilke et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Article Wilke, Claus O Lenski, Richard E Adami, Christoph Compensatory mutations cause excess of antagonistic epistasis in RNA secondary structure folding |
title | Compensatory mutations cause excess of antagonistic epistasis in RNA secondary structure folding |
title_full | Compensatory mutations cause excess of antagonistic epistasis in RNA secondary structure folding |
title_fullStr | Compensatory mutations cause excess of antagonistic epistasis in RNA secondary structure folding |
title_full_unstemmed | Compensatory mutations cause excess of antagonistic epistasis in RNA secondary structure folding |
title_short | Compensatory mutations cause excess of antagonistic epistasis in RNA secondary structure folding |
title_sort | compensatory mutations cause excess of antagonistic epistasis in rna secondary structure folding |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC149451/ https://www.ncbi.nlm.nih.gov/pubmed/12590655 http://dx.doi.org/10.1186/1471-2148-3-3 |
work_keys_str_mv | AT wilkeclauso compensatorymutationscauseexcessofantagonisticepistasisinrnasecondarystructurefolding AT lenskiricharde compensatorymutationscauseexcessofantagonisticepistasisinrnasecondarystructurefolding AT adamichristoph compensatorymutationscauseexcessofantagonisticepistasisinrnasecondarystructurefolding |