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Independent accretion of TIM22 complex subunits in the animal and fungal lineages

Background: The mitochondrial protein import complexes arose early in eukaryogenesis. Most of the components of the protein import pathways predate the last eukaryotic common ancestor. For example, the carrier-insertase TIM22 complex comprises the widely conserved Tim22 channel core. However, the au...

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Autores principales: Muñoz-Gómez, Sergio A., Snyder, Shannon N., Montoya, Samantha J., Wideman, Jeremy G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523481/
https://www.ncbi.nlm.nih.gov/pubmed/33014348
http://dx.doi.org/10.12688/f1000research.25904.1
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author Muñoz-Gómez, Sergio A.
Snyder, Shannon N.
Montoya, Samantha J.
Wideman, Jeremy G.
author_facet Muñoz-Gómez, Sergio A.
Snyder, Shannon N.
Montoya, Samantha J.
Wideman, Jeremy G.
author_sort Muñoz-Gómez, Sergio A.
collection PubMed
description Background: The mitochondrial protein import complexes arose early in eukaryogenesis. Most of the components of the protein import pathways predate the last eukaryotic common ancestor. For example, the carrier-insertase TIM22 complex comprises the widely conserved Tim22 channel core. However, the auxiliary components of fungal and animal TIM22 complexes are exceptions to this ancient conservation. Methods: Using comparative genomics and phylogenetic approaches, we identified precisely when each TIM22 accretion occurred. Results: In animals, we demonstrate that Tim29 and Tim10b arose early in the holozoan lineage. Tim29 predates the metazoan lineage being present in the animal sister lineages, choanoflagellate and filastereans, whereas the erroneously named Tim10b arose from a duplication of Tim9 at the base of metazoans. In fungi, we show that Tim54 has representatives present in every holomycotan lineage including microsporidians and fonticulids, whereas Tim18 and Tim12 appeared much later in fungal evolution. Specifically, Tim18 and Tim12 arose from duplications of Sdh3 and Tim10, respectively, early in the Saccharomycotina. Surprisingly, we show that Tim54 is distantly related to AGK suggesting that AGK and Tim54 are extremely divergent orthologues and the origin of AGK/Tim54 interaction with Tim22 predates the divergence of animals and fungi. Conclusions: We argue that the evolutionary history of the TIM22 complex is best understood as the neutral structural divergence of an otherwise strongly functionally conserved protein complex. This view suggests that many of the differences in structure/subunit composition of multi-protein complexes are non-adaptive. Instead, most of the phylogenetic variation of functionally conserved molecular machines, which have been under stable selective pressures for vast phylogenetic spans, such as the TIM22 complex, is most likely the outcome of the interplay of random genetic drift and mutation pressure.
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spelling pubmed-75234812020-10-01 Independent accretion of TIM22 complex subunits in the animal and fungal lineages Muñoz-Gómez, Sergio A. Snyder, Shannon N. Montoya, Samantha J. Wideman, Jeremy G. F1000Res Research Article Background: The mitochondrial protein import complexes arose early in eukaryogenesis. Most of the components of the protein import pathways predate the last eukaryotic common ancestor. For example, the carrier-insertase TIM22 complex comprises the widely conserved Tim22 channel core. However, the auxiliary components of fungal and animal TIM22 complexes are exceptions to this ancient conservation. Methods: Using comparative genomics and phylogenetic approaches, we identified precisely when each TIM22 accretion occurred. Results: In animals, we demonstrate that Tim29 and Tim10b arose early in the holozoan lineage. Tim29 predates the metazoan lineage being present in the animal sister lineages, choanoflagellate and filastereans, whereas the erroneously named Tim10b arose from a duplication of Tim9 at the base of metazoans. In fungi, we show that Tim54 has representatives present in every holomycotan lineage including microsporidians and fonticulids, whereas Tim18 and Tim12 appeared much later in fungal evolution. Specifically, Tim18 and Tim12 arose from duplications of Sdh3 and Tim10, respectively, early in the Saccharomycotina. Surprisingly, we show that Tim54 is distantly related to AGK suggesting that AGK and Tim54 are extremely divergent orthologues and the origin of AGK/Tim54 interaction with Tim22 predates the divergence of animals and fungi. Conclusions: We argue that the evolutionary history of the TIM22 complex is best understood as the neutral structural divergence of an otherwise strongly functionally conserved protein complex. This view suggests that many of the differences in structure/subunit composition of multi-protein complexes are non-adaptive. Instead, most of the phylogenetic variation of functionally conserved molecular machines, which have been under stable selective pressures for vast phylogenetic spans, such as the TIM22 complex, is most likely the outcome of the interplay of random genetic drift and mutation pressure. F1000 Research Limited 2020-08-28 /pmc/articles/PMC7523481/ /pubmed/33014348 http://dx.doi.org/10.12688/f1000research.25904.1 Text en Copyright: © 2020 Muñoz-Gómez SA et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Muñoz-Gómez, Sergio A.
Snyder, Shannon N.
Montoya, Samantha J.
Wideman, Jeremy G.
Independent accretion of TIM22 complex subunits in the animal and fungal lineages
title Independent accretion of TIM22 complex subunits in the animal and fungal lineages
title_full Independent accretion of TIM22 complex subunits in the animal and fungal lineages
title_fullStr Independent accretion of TIM22 complex subunits in the animal and fungal lineages
title_full_unstemmed Independent accretion of TIM22 complex subunits in the animal and fungal lineages
title_short Independent accretion of TIM22 complex subunits in the animal and fungal lineages
title_sort independent accretion of tim22 complex subunits in the animal and fungal lineages
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523481/
https://www.ncbi.nlm.nih.gov/pubmed/33014348
http://dx.doi.org/10.12688/f1000research.25904.1
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