Phylogenetic analyses with systematic taxon sampling show that mitochondria branch within Alphaproteobacteria.
Journal
Nature ecology & evolution
ISSN: 2397-334X
Titre abrégé: Nat Ecol Evol
Pays: England
ID NLM: 101698577
Informations de publication
Date de publication:
09 2020
09 2020
Historique:
received:
07
09
2019
accepted:
29
05
2020
pubmed:
15
7
2020
medline:
20
11
2020
entrez:
15
7
2020
Statut:
ppublish
Résumé
Though it is well accepted that mitochondria originated from an alphaproteobacteria-like ancestor, the phylogenetic relationship of the mitochondrial endosymbiont to extant Alphaproteobacteria is yet unresolved. The focus of much debate is whether the affinity between mitochondria and fast-evolving alphaproteobacterial lineages reflects true homology or artefacts. Approaches such as site exclusion have been claimed to mitigate compositional heterogeneity between taxa, but this comes at the cost of information loss, and the reliability of such methods is so far unproven. Here we demonstrate that site-exclusion methods produce erratic phylogenetic estimates of mitochondrial origin. Thus, previous phylogenetic hypotheses on the origin of mitochondria based on pretreated datasets should be re-evaluated. We applied alternative strategies to reduce phylogenetic noise by systematic taxon sampling while keeping site substitution information intact. Cross-validation based on a series of trees placed mitochondria robustly within Alphaproteobacteria, sharing an ancient common ancestor with Rickettsiales and currently unclassified marine lineages.
Identifiants
pubmed: 32661403
doi: 10.1038/s41559-020-1239-x
pii: 10.1038/s41559-020-1239-x
doi:
Banques de données
figshare
['10.6084/m9.figshare.12347216']
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1213-1219Commentaires et corrections
Type : CommentIn
Type : CommentIn
Références
Ku, C. et al. Endosymbiotic origin and differential loss of eukaryotic genes. Nature 524, 427–432 (2015).
doi: 10.1038/nature14963
Thiergart, T., Landan, G., Schenk, M., Dagan, T. & Martin, W. F. An evolutionary network of genes present in the eukaryote common ancestor polls genomes on eukaryotic and mitochondrial origin. Genome Biol. Evol. 4, 466–485 (2012).
doi: 10.1093/gbe/evs018
Abhishek, A., Bavishi, A., Bavishi, A. & Choudhary, M. Bacterial genome chimaerism and the origin of mitochondria. Can. J. Microbiol. 57, 49–61 (2011).
doi: 10.1139/W10-099
Atteia, A. et al. A proteomic survey of Chlamydomonas reinhardtii mitochondria sheds new light on the metabolic plasticity of the organelle and on the nature of the alpha-proteobacterial mitochondrial ancestor. Mol. Biol. Evol. 26, 1533–1548 (2009).
doi: 10.1093/molbev/msp068
Roger, A. J., Muñoz-Gómez, S. A. & Kamikawa, R. The origin and diversification of mitochondria. Curr. Biol. 27, R1177–R1192 (2017).
doi: 10.1016/j.cub.2017.09.015
Derelle, R. & Lang, B. F. Rooting the eukaryotic tree with mitochondrial and bacterial proteins. Mol. Biol. Evol. 29, 1277–1289 (2012).
doi: 10.1093/molbev/msr295
Wang, Z. & Wu, M. An integrated phylogenomic approach toward pinpointing the origin of mitochondria. Sci. Rep. 5, 7949 (2015).
doi: 10.1038/srep07949
Viklund, J., Ettema, T. J. & Andersson, S. G. Independent genome reduction and phylogenetic reclassification of the oceanic SAR11 clade. Mol. Biol. Evol. 29, 599–615 (2012).
doi: 10.1093/molbev/msr203
Esser, C. et al. A genome phylogeny for mitochondria among alpha-proteobacteria and a predominantly eubacterial ancestry of yeast nuclear genes. Mol. Biol. Evol. 21, 1643–1660 (2004).
doi: 10.1093/molbev/msh160
Fitzpatrick, D. A., Creevey, C. J. & McInerney, J. O. Genome phylogenies indicate a meaningful alpha-proteobacterial phylogeny and support a grouping of the mitochondria with the Rickettsiales. Mol. Biol. Evol. 23, 74–85 (2006).
doi: 10.1093/molbev/msj009
Rodríguez-Ezpeleta, N. & Embley, T. M. The SAR11 group of alpha-proteobacteria is not related to the origin of mitochondria. PLoS ONE 7, e30520 (2012).
doi: 10.1371/journal.pone.0030520
Viale, A. M. & Arakaki, A. K. The chaperone connection to the origins of the eukaryotic organelles. FEBS Lett. 341, 146–151 (1994).
doi: 10.1016/0014-5793(94)80446-X
Castelli, M. et al. Deianiraea, an extracellular bacterium associated with the ciliate Paramecium, suggests an alternative scenario for the evolution of Rickettsiales. ISME J. 13, 2280–2294 (2019).
doi: 10.1038/s41396-019-0433-9
Brindefalk, B., Ettema, T. J., Viklund, J., Thollesson, M. & Andersson, S. G. A phylometagenomic exploration of oceanic alphaproteobacteria reveals mitochondrial relatives unrelated to the SAR11 clade. PLoS ONE 6, e24457 (2011).
doi: 10.1371/journal.pone.0024457
Thrash, J. C. et al. Phylogenomic evidence for a common ancestor of mitochondria and the SAR11 clade. Sci. Rep. 1, 13 (2011).
doi: 10.1038/srep00013
Georgiades, K., Madoui, M. A., Le, P., Robert, C. & Raoult, D. Phylogenomic analysis of Odyssella thessalonicensis fortifies the common origin of Rickettsiales, Pelagibacter ubique and Reclimonas americana mitochondrion. PLoS ONE 6, e24857 (2011).
doi: 10.1371/journal.pone.0024857
Martijn, J., Vosseberg, J., Guy, L., Offre, P. & Ettema, T. J. G. Deep mitochondrial origin outside the sampled alphaproteobacteria. Nature 557, 101–105 (2018).
doi: 10.1038/s41586-018-0059-5
Gray, M. W., Burger, G. & Lang, B. F. Mitochondrial evolution. Science 283, 1476–1481 (1999).
doi: 10.1126/science.283.5407.1476
Gawryluk, R. M. R. Evolutionary biology: A new home for the powerhouse? Curr. Biol. 28, R798–R800 (2018).
doi: 10.1016/j.cub.2018.05.073
Blanquart, S. & Lartillot, N. A Bayesian compound stochastic process for modeling nonstationary and nonhomogeneous sequence evolution. Mol. Biol. Evol. 23, 2058–2071 (2006).
doi: 10.1093/molbev/msl091
Muñoz-Gómez, S. A. et al. An updated phylogeny of the Alphaproteobacteria reveals that the parasitic Rickettsiales and Holosporales have independent origins. eLife 8, e42535 (2019).
Nguyen, L. T., Schmidt, H. A., von Haeseler, A. & Minh, B. Q. IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol. Biol. Evol. 32, 268–274 (2015).
doi: 10.1093/molbev/msu300
Jermiin, L. S., Jayaswal, V., Ababneh, F. M. & Robinson, J. Identifying optimal models of evolution. Methods Mol. Biol. 1525, 379–420 (2017).
doi: 10.1007/978-1-4939-6622-6_15
Capella-Gutiérrez, S., Silla-Martínez, J. M. & Gabaldón, T. trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses. Bioinformatics 25, 1972–1973 (2009).
doi: 10.1093/bioinformatics/btp348
Lartillot, N., Rodrigue, N., Stubbs, D. & Richer, J. PhyloBayes MPI: phylogenetic reconstruction with infinite mixtures of profiles in a parallel environment. Syst. Biol. 62, 611–615 (2013).
doi: 10.1093/sysbio/syt022
Kannan, S., Rogozin, I. B. & Koonin, E. V. MitoCOGs: clusters of orthologous genes from mitochondria and implications for the evolution of eukaryotes. BMC Evol. Biol. 14, 237 (2014).
doi: 10.1186/s12862-014-0237-5
Katoh, K. & Standley, D. M. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol. Biol. Evol. 30, 772–780 (2013).
doi: 10.1093/molbev/mst010
Eddy, S. R. Accelerated profile HMM searches. PLoS Comput. Biol. 7, e1002195 (2011).
doi: 10.1371/journal.pcbi.1002195
Criscuolo, A. & Gribaldo, S. BMGE (block mapping and gathering with entropy): a new software for selection of phylogenetic informative regions from multiple sequence alignments. BMC Evol. Biol. 10, 210 (2010).
doi: 10.1186/1471-2148-10-210
Fan, L. et al. Mitochondria and Alphaproteobacteria phylogenetic study alignments and tree files. figshare https://doi.org/10.6084/m9.figshare.12347216 (2020).