Mutational Bias Plays an Important Role in Shaping Longevity-Related Amino Acid Content in Mammalian mtDNA-Encoded Proteins
Author(s) -
Juan Carlos Aledo,
Héctor Valverde,
João Pedro de Magalhães
Publication year - 2012
Publication title -
journal of molecular evolution
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.693
H-Index - 123
eISSN - 1432-1432
pISSN - 0022-2844
DOI - 10.1007/s00239-012-9510-7
Subject(s) - biology , methionine , longevity , amino acid , mitochondrial dna , threonine , genetics , cysteine , proteome , mitochondrion , gene , biochemistry , serine , phosphorylation , enzyme
During the course of evolution, amino acid shifts might have resulted in mitochondrial proteomes better endowed to resist oxidative stress. However, owing to the problem of distinguishing between functional constraints/adaptations in protein sequences and mutation-driven biases in the composition of these sequences, the adaptive value of such amino acid shifts remains under discussion. We have analyzed the coding sequences of mtDNA from 173 mammalian species, dissecting the effect of nucleotide composition on amino acid usages. We found remarkable cysteine avoidance in mtDNA-encoded proteins. However, no effect of longevity on cysteine content could be detected. On the other hand, nucleotide compositional shifts fully accounted for threonine usages. In spite of a strong effect of mutational bias on methionine abundances, our results suggest a role of selection in determining the composition of methionine. Whether this selective effect is linked or not to protection against oxidative stress is still a subject of debate.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom