There is considerable variation in the rate at which different genes evolve. Why is
this? Classically it has been considered that the density of functionally important
sites must predict rates of protein evolution.
Likewise, amino acid choice is usually assumed to reflect optimal protein function
and codon choice is random. Here I briefly review evidence suggesting that this
view is too simplistic. In particular I concentrate on how selection acting during the
proteins production history can also affect gene evolutionary rates as well as amino
acid and codon choice.
Exploring the role of selection at the DNA and RNA level, I specifically address how
the need 1) to specify exonic splice enhancer motifs in pre-mRNA and 2) to ensure
nucleosome positioning on DNA, impacts amino acid choice, codon choice and rates
of evolution at both synonymous and non-synonymous sites.