dictyNews
Electronic Edition
Volume 47, number 9
April 23, 2021
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Abstracts
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Inferring adaptive codon preference to understand sources of
selection shaping codon usage bias
Janaina Lima de Oliveira1,2a, Atahualpa Castillo Morales2a,
Laurence D. Hurst2, Araxi O. Urrutia2, Christopher R. L.
Thompson3*, Jason B. Wolf2*
1. Instituto de Biologia, Universidade Federal da Bahia, Salvador,
Bahia, 40170-115, Brazil
2. Milner Centre for Evolution and Department of Biology and
Biochemistry, University of Bath, Claverton Down, Bath, BA2 7AY, UK
3. Centre for Life’s Origins and Evolution, Department of Genetics,
Evolution and Environment, University College London, Darwin
Building, Gower Street, London, WC1E 6BT, UK
aThese authors contributed equally to this work
*Correspondence to:
[log in to unmask] & [log in to unmask]
Molecular Biology and Evolution, in press
Alternative synonymous codons are often used at unequal
frequencies. Classically, studies of such codon usage bias (CUB)
attempted to separate the impact of neutral from selective forces by
assuming that deviations from a predicted neutral equilibrium capture
selection. However, GC biased gene conversion (gBGC) can also
cause deviation from a neutral null. Alternatively, selection has been
inferred from CUB in highly expressed genes, but the accuracy of
this approach has not been extensively tested, and gBGC can
interfere with such extrapolations (e.g. if expression and gene
conversion rates covary). It is therefore critical to examine
deviations from a mutational null in a species with no gBGC. To
achieve this goal, we implement such an analysis in the highly AT
rich genome of Dictyostelium discoideum, where we find no evidence
of gBGC. We infer neutral CUB under mutational equilibrium to
quantify ‘adaptive codon preference’, a nontautologous genome wide
quantitative measure of the relative selection strength driving CUB.
We observe signatures of purifying selection consistent with
selection favouring adaptive codon preference. Preferred codons are
not GC rich, underscoring the independence from gBGC. Expression-
associated ‘preference’ largely matches adaptive codon preference
but does not wholly capture the influence of selection shaping
patterns across all genes, suggesting selective constraints
associated specifically with high expression. We observe patterns
consistent with effects on mRNA translation and stability shaping
adaptive codon preference. Thus, our approach to quantifying
adaptive codon preference provides a framework for inferring the
sources of selection that shape CUB across different contexts
within the genome.
submitted by: Chris Thompson [[log in to unmask]]
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