Fitness effects of new mutations and adaptive evolution in house mice
dc.contributor.advisor
Keightley, Peter
en
dc.contributor.advisor
Sharp, Paul
en
dc.contributor.advisor
Halligan, Daniel
en
dc.contributor.author
Kousathanas, Athanasios
en
dc.contributor.sponsor
Biotechnology and Biological Sciences Research Council (BBSRC)
en
dc.date.accessioned
2013-12-10T10:03:30Z
dc.date.available
2013-12-10T10:03:30Z
dc.date.issued
2013-11-28
dc.description.abstract
Knowledge of the distribution of fitness effects of new mutations (DFE) can enable
us to quantify the amount of genetic change between species that is driven by natural
selection and contributes to adaptive evolution. The primary focus of this thesis is the
study of methods to infer the DFE and the study of adaptive evolution in the house
mouse subspecies Mus musculus castaneus.
Firstly, I extended previous methodology to model the DFE based on
polymorphism data. Methods that have previously been used to infer the DFE from
polymorphism data have relied on the assumption of a unimodal distribution. I
developed new models that can be used to fit DFEs of arbitrary complexity, and
found that multimodality can be detected by these models given enough data. I used
these new models to analyse polymorphism data from Drosophila melanogaster and
M. m. castaneus, and found evidence for a unimodal DFE for D. melanogaster and a
bimodal DFE for M. m. castaneus.
Secondly, I investigated the contribution of change in coding and non-coding
DNA to evolutionary adaptation. I used a polymorphism dataset of ~80 loci from M.
m. castaneus sequenced in 15 individuals to investigate selection in protein-coding
genes and putatively regulatory DNA close to these genes. I found that, although
protein-coding genes are much more selectively constrained than non-coding DNA,
they experience similar rates of adaptive substitution. These results suggest that
change in functional non-coding DNA sequences might be as important as
protein-coding genes to evolutionary adaptation.
Thirdly, I used whole genome data from 10 M. m. castaneus individuals to
compare the rate of adaptive substitution in autosomal and X-linked genes. I found
that, on average, X-linked genes have a 1.8 times faster rate of adaptive substitution
than autosomal genes. I also found that faster-X evolution is more pronounced for
male-specific genes. I used previously developed theory to show that these
observations can be explained if new advantageous mutations are recessive, with an
average dominance coefficient less than or equal to 0.25. These results can help to
explain the long-studied phenomenon of the large effect of the X chromosome in
speciation.
en
dc.identifier.uri
http://hdl.handle.net/1842/8250
dc.language.iso
en
dc.publisher
The University of Edinburgh
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dc.relation.hasversion
Kousathanas A, Oliver F, Halligan DL, Keightley PD. 2011. Positive and negative selection on noncoding DNA close to protein-coding genes in wild house mice. Molecular Biology and Evolution 28: 1183 –1191.
en
dc.relation.hasversion
Kousathanas A, Keightley PD. 2013. A comparison of models to infer the distribution of fitness effects of new mutations. Genetics 193: 1197–1208.
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dc.subject
house mice
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dc.subject
adaptive evolution
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dc.subject
X chromosome
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dc.subject
fitness effects
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dc.title
Fitness effects of new mutations and adaptive evolution in house mice
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dc.type
Thesis or Dissertation
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dc.type.qualificationlevel
Doctoral
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dc.type.qualificationname
PhD Doctor of Philosophy
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