How a neutral evolutionary ratchet can build cellular complexity
Language English Country England, Great Britain Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
Grant support
MOP-4124
Canadian Institutes of Health Research - Canada
MOP-42517
Canadian Institutes of Health Research - Canada
MOP-4467
Canadian Institutes of Health Research - Canada
ROP-85016
Canadian Institutes of Health Research - Canada
PubMed
21698757
DOI
10.1002/iub.489
Knihovny.cz E-resources
- MeSH
- Biological Evolution * MeSH
- RNA Editing MeSH
- Adaptation, Physiological MeSH
- Genetic Drift * MeSH
- Humans MeSH
- Models, Genetic MeSH
- Plants anatomy & histology genetics metabolism MeSH
- RNA Splicing MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
Complex cellular machines and processes are commonly believed to be products of selection, and it is typically understood to be the job of evolutionary biologists to show how selective advantage can account for each step in their origin and subsequent growth in complexity. Here, we describe how complex machines might instead evolve in the absence of positive selection through a process of "presuppression," first termed constructive neutral evolution (CNE) more than a decade ago. If an autonomously functioning cellular component acquires mutations that make it dependent for function on another, pre-existing component or process, and if there are multiple ways in which such dependence may arise, then dependence inevitably will arise and reversal to independence is unlikely. Thus, CNE is a unidirectional evolutionary ratchet leading to complexity, if complexity is equated with the number of components or steps necessary to carry out a cellular process. CNE can explain "functions" that seem to make little sense in terms of cellular economy, like RNA editing or splicing, but it may also contribute to the complexity of machines with clear benefit to the cell, like the ribosome, and to organismal complexity overall. We suggest that CNE-based evolutionary scenarios are in these and other cases less forced than the selectionist or adaptationist narratives that are generally told.
References provided by Crossref.org
Lessons from the deep: mechanisms behind diversification of eukaryotic protein complexes
A Uniquely Complex Mitochondrial Proteome from Euglena gracilis
Gene fragmentation and RNA editing without borders: eccentric mitochondrial genomes of diplonemids
Massive mitochondrial DNA content in diplonemid and kinetoplastid protists
From simple to supercomplex: mitochondrial genomes of euglenozoan protists
Unexpectedly Streamlined Mitochondrial Genome of the Euglenozoan Euglena gracilis
Dual core processing: MRB1 is an emerging kinetoplast RNA editing complex
Gene fragmentation: a key to mitochondrial genome evolution in Euglenozoa?