David M. Rand and Lisa M. Kann
Department of Ecology and Evolutionary Biology
Brown University
Providence, RI 02912
email: David_Rand@Brown.edu
voice: (401) 863-2890
fax: (401) 863-2166
Keywords: mildly deleterious, mutation selection balance, nearly neutral,
non-neutral, strand bias
Abstract
Two patterns are presented that illustrate the interaction of
mutation and selection in the evolution of animal mtDNA: 1) variation among
taxa in the ratio of polymorphism to divergence (rpd) at silent and replacement
sites in protein-coding genes, and 2) strand-differences in polymorphism
and divergence at "silent" sites that suggest a mutation-selection balance
in the evolution of codon usage. Cytochrome b data from GenBank show
that about half of the species pairs tested have a significant excess of
amino acid polymorphism, relative to divergence. The remaining half
of species pairs do not depart from neutrality, but generally do show an
excess of amino acid polymorphism. Sequences from Drosophila pseudoobscura
displaying a signature of an expanding population show a slight, but non-significant,
deficiency of amino acid polymorphism suggestive of recently intensified
selection on mildly deleterious mutations. Genes whose reading frames
lie on the major coding strand of Drosophila mtDNA show a preponderance
of T -> C substitutions, while genes encoded on the minor strand experience
more A-> G than T-> C substitutions between species at both silent and
replacement sites. However, silent mutations at third codon positions
are introduced into the population in proportions opposite to those observed
as fixed differences between species (e.g., an excess of T -> C polymorphisms
are found at the ND5 gene on the minor coding strand). The high A+T
content of insect mtDNAs imposes strong codon usage bias favoring A-ending
and T-ending codons resulting in a distinct mutation-selection balance
for genes encoded on opposites strands. Thus, at both replacement
and silent sites, mutations that appear to be constrained in terms of divergence
between species are in excess within species. The data suggest that
mildly deleterious mutations are common in mitochondrial genes. A test
of this, and a competing, hypothesis is proposed that requires additional
sequence surveys of polymorphism and divergence. An important challenge
is to tease apart the impact of mutation and selection on levels of polymorphism
versus divergence in a genome that does not generally recombine.