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MBE Advance Access originally published online on May 21, 2004
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Mol. Biol. Evol. 21(8):1572-1582. 2004
DOI: 10.1093/molbev/msh161
© 2004 by the Society for Molecular Biology and Evolution. ISSN: 0737-4038

Comparison of Diverse Protein Sequences of the Nuclear-Encoded Subunits of Cytochrome C Oxidase Suggests Conservation of Structure Underlies Evolving Functional Sites

Jayatri Das*, Stephen T. Miller{dagger} and David L. Stern*

* Department of Ecology and Evolutionary Biology
{dagger} Department of Molecular Biology, Princeton University, Princeton, New Jersey

E-mail: jdas{at}princeton.edu.

Interspecific comparisons of protein sequences can reveal regions of evolutionary conservation that are under purifying selection because of functional constraints. Interpreting these constraints requires combining evolutionary information with structural, biochemical, and physiological data to understand the biological function of conserved regions. We take this integrative approach to investigate the evolution and function of the nuclear-encoded subunits of cytochrome c oxidase (COX). We find that the nuclear-encoded subunits evolved subsequent to the origin of mitochondria and the subunit composition of the holoenzyme varies across diverse taxa that include animals, yeasts, and plants. By mapping conserved amino acids onto the crystal structure of bovine COX, we show that conserved residues are structurally organized into functional domains. These domains correspond to some known functional sites as well as to other uncharacterized regions. We find that amino acids that are important for structural stability are conserved at frequencies higher than expected within each taxon, and groups of conserved residues cluster together at distances of less than 5 Å more frequently than do randomly selected residues. We, therefore, suggest that selection is acting to maintain the structural foundation of COX across taxa, whereas active sites vary or coevolve within lineages.

Key Words: cytochrome c oxidase • nuclear-encoded • evolution • structure • mitochondria


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