Cargando…

Adaptive Threonine Increase in Transmembrane Regions of Mitochondrial Proteins in Higher Primates

BACKGROUND: The mitochondrial (mt) gene tree of placental mammals reveals a very strong acceleration of the amino acid (AA) replacement rate and a change in AA compositional bias in the lineage leading to the higher primates (simians), in contrast to the nuclear gene tree. Whether this acceleration...

Descripción completa

Detalles Bibliográficos
Autores principales: Kitazoe, Yasuhiro, Kishino, Hirohisa, Hasegawa, Masami, Nakajima, Noriaki, Thorne, Jeffrey L., Tanaka, Masashi
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2553178/
https://www.ncbi.nlm.nih.gov/pubmed/18836526
http://dx.doi.org/10.1371/journal.pone.0003343
_version_ 1782159484342239232
author Kitazoe, Yasuhiro
Kishino, Hirohisa
Hasegawa, Masami
Nakajima, Noriaki
Thorne, Jeffrey L.
Tanaka, Masashi
author_facet Kitazoe, Yasuhiro
Kishino, Hirohisa
Hasegawa, Masami
Nakajima, Noriaki
Thorne, Jeffrey L.
Tanaka, Masashi
author_sort Kitazoe, Yasuhiro
collection PubMed
description BACKGROUND: The mitochondrial (mt) gene tree of placental mammals reveals a very strong acceleration of the amino acid (AA) replacement rate and a change in AA compositional bias in the lineage leading to the higher primates (simians), in contrast to the nuclear gene tree. Whether this acceleration and compositional bias were caused by adaptive evolution at the AA level or directional mutation pressure at the DNA level has been vigorously debated. METHODOLOGY/PRINCIPAL FINDINGS: Our phylogenetic analysis indicates that the rate acceleration in the simian lineage is accompanied by a marked increase in threonine (Thr) residues in the transmembrane helix regions of mt DNA-encoded proteins. This Thr increase involved the replacement of hydrophobic AAs in the membrane interior. Even after accounting for lack of independence due to phylogeny, a regression analysis reveals a statistical significant positive correlation between Thr composition and longevity in primates. CONCLUSION/SIGNIFICANCE: Because crucial roles of Thr and Ser in membrane proteins have been proposed to be the formation of hydrogen bonds enhancing helix-helix interactions, the Thr increase detected in the higher primates might be adaptive by serving to reinforce stability of mt proteins in the inner membrane. The correlation between Thr composition in the membrane interior and the longevity of animals is striking, especially because some mt functions are thought to be involved in aging.
format Text
id pubmed-2553178
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-25531782008-10-06 Adaptive Threonine Increase in Transmembrane Regions of Mitochondrial Proteins in Higher Primates Kitazoe, Yasuhiro Kishino, Hirohisa Hasegawa, Masami Nakajima, Noriaki Thorne, Jeffrey L. Tanaka, Masashi PLoS One Research Article BACKGROUND: The mitochondrial (mt) gene tree of placental mammals reveals a very strong acceleration of the amino acid (AA) replacement rate and a change in AA compositional bias in the lineage leading to the higher primates (simians), in contrast to the nuclear gene tree. Whether this acceleration and compositional bias were caused by adaptive evolution at the AA level or directional mutation pressure at the DNA level has been vigorously debated. METHODOLOGY/PRINCIPAL FINDINGS: Our phylogenetic analysis indicates that the rate acceleration in the simian lineage is accompanied by a marked increase in threonine (Thr) residues in the transmembrane helix regions of mt DNA-encoded proteins. This Thr increase involved the replacement of hydrophobic AAs in the membrane interior. Even after accounting for lack of independence due to phylogeny, a regression analysis reveals a statistical significant positive correlation between Thr composition and longevity in primates. CONCLUSION/SIGNIFICANCE: Because crucial roles of Thr and Ser in membrane proteins have been proposed to be the formation of hydrogen bonds enhancing helix-helix interactions, the Thr increase detected in the higher primates might be adaptive by serving to reinforce stability of mt proteins in the inner membrane. The correlation between Thr composition in the membrane interior and the longevity of animals is striking, especially because some mt functions are thought to be involved in aging. Public Library of Science 2008-10-06 /pmc/articles/PMC2553178/ /pubmed/18836526 http://dx.doi.org/10.1371/journal.pone.0003343 Text en Kitazoe et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kitazoe, Yasuhiro
Kishino, Hirohisa
Hasegawa, Masami
Nakajima, Noriaki
Thorne, Jeffrey L.
Tanaka, Masashi
Adaptive Threonine Increase in Transmembrane Regions of Mitochondrial Proteins in Higher Primates
title Adaptive Threonine Increase in Transmembrane Regions of Mitochondrial Proteins in Higher Primates
title_full Adaptive Threonine Increase in Transmembrane Regions of Mitochondrial Proteins in Higher Primates
title_fullStr Adaptive Threonine Increase in Transmembrane Regions of Mitochondrial Proteins in Higher Primates
title_full_unstemmed Adaptive Threonine Increase in Transmembrane Regions of Mitochondrial Proteins in Higher Primates
title_short Adaptive Threonine Increase in Transmembrane Regions of Mitochondrial Proteins in Higher Primates
title_sort adaptive threonine increase in transmembrane regions of mitochondrial proteins in higher primates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2553178/
https://www.ncbi.nlm.nih.gov/pubmed/18836526
http://dx.doi.org/10.1371/journal.pone.0003343
work_keys_str_mv AT kitazoeyasuhiro adaptivethreonineincreaseintransmembraneregionsofmitochondrialproteinsinhigherprimates
AT kishinohirohisa adaptivethreonineincreaseintransmembraneregionsofmitochondrialproteinsinhigherprimates
AT hasegawamasami adaptivethreonineincreaseintransmembraneregionsofmitochondrialproteinsinhigherprimates
AT nakajimanoriaki adaptivethreonineincreaseintransmembraneregionsofmitochondrialproteinsinhigherprimates
AT thornejeffreyl adaptivethreonineincreaseintransmembraneregionsofmitochondrialproteinsinhigherprimates
AT tanakamasashi adaptivethreonineincreaseintransmembraneregionsofmitochondrialproteinsinhigherprimates