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Genomic diversity, lifestyles and evolutionary origins of DPANN archaea
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Archaea-a primary domain of life besides Bacteria-have for a long time been regarded as peculiar organisms that play marginal roles in biogeochemical cycles. However, this picture changed with the discovery of a large diversity of archaea in non-extreme environments enabled by the use of cultivation-independent methods. These approaches have allowed the reconstruction of genomes of uncultivated microorganisms and revealed that archaea are diverse and broadly distributed in the biosphere and seemingly include a large diversity of putative symbiotic organisms, most of which belong to the tentative archaeal superphylum referred to as DPANN. This archaeal group encompasses at least 10 different lineages and includes organisms with extremely small cell and genome sizes and limited metabolic capabilities. Therefore, many members of DPANN may be obligately dependent on symbiotic interactions with other organisms and may even include novel parasites. In this contribution, we review the current knowledge of the gene repertoires and lifestyles of members of this group and discuss their placement in the tree of life, which is the basis for our understanding of the deep microbial roots and the role of symbiosis in the evolution of life on Earth.
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“These artifacts are expected to particularly affect microbial lineages comprised predominantly of symbiotic members such as the CPR bacteria and DPANN archaea, as genomes of known symbionts are often compositionally biased and characterized by faster evolutionary rates (Dombrowski et al. 2019).”
From The Emergence of Life (2019) · cites this paper as Dombrowski et al. 2019
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“These absences are present across related lineages, suggesting a genuine loss, rather than metagenome-assembled genome incompleteness.”
From ATP synthase evolution on a cross-braced dated tree of life (2023) · cites this paper as [59]
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“This finding suggests that ATP synthases are not as essential as previously assumed32,33,45,65 with loss in DPANN and CPR lineages likely being the result of genome streamlining processes consistent with their predicted host-dependent lifestyles58,59.”
From ATP synthase evolution on a cross-braced dated tree of life (2023) · cites this paper as [59]
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Guindon, S., Dufayard, J.-F., Lefort, V., Anisimova, M., Hordijk, W., & Gascuel, O. (2010) · Systematic Biology · doi:10.1093/sysbio/syq010 · Cited by 18,376
Towards a natural system of organisms: proposal for the domains Archaea, Bacteria, and Eucarya.
Woese, C. R., Kandler, O., & Wheelis, M. L. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.12.4576 · Cited by 6,128
Ultrafast Approximation for Phylogenetic Bootstrap
Minh, B. Q., Nguyen, M. A. T., & von Haeseler, A. (2013) · Molecular Biology and Evolution · doi:10.1093/molbev/mst024 · Cited by 4,844
Phylogenetic structure of the prokaryotic domain: The primary kingdoms
Woese, C. R., & Fox, G. E. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.11.5088 · Cited by 4,131
A standardized bacterial taxonomy based on genome phylogeny substantially revises the tree of life
Parks, D. H., Chuvochina, M., Waite, D. W., Rinke, C., Skarshewski, A., Chaumeil, P.-A., & Hugenholtz, P. (2018) · Nature Biotechnology · doi:10.1038/nbt.4229 · Cited by 3,603
Archaea in coastal marine environments.
DeLong, E. F. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5685 · Cited by 2,758
Insights into the phylogeny and coding potential of microbial dark matter
Rinke, C., Schwientek, P., Sczyrba, A., Ivanova, N. N., Anderson, I. J., Cheng, J.-F., Darling, A., Malfatti, S., Swan, B. K., Gies, E. A., et al. (2013) · Nature · doi:10.1038/nature12352 · Cited by 2,394
A new view of the tree of life
Hug, L. A., Baker, B. J., Anantharaman, K., Brown, C. T., Probst, A. J., Castelle, C. J., Butterfield, C. N., Hernsdorf, A. W., Amano, Y., Ise, K., et al. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.48 · Cited by 2,039
Genomics and Evolution of Heritable Bacterial Symbionts
Moran, N. A., McCutcheon, J. P., & Nakabachi, A. (2008) · Annual Review of Genetics · doi:10.1146/annurev.genet.41.110306.130119 · Cited by 1,771
A Bayesian Mixture Model for Across-Site Heterogeneities in the Amino-Acid Replacement Process
Lartillot, N., & Philippe, H. (2004) · Molecular Biology and Evolution · doi:10.1093/molbev/msh112 · Cited by 1,516
Complex archaea that bridge the gap between prokaryotes and eukaryotes
Spang, A., Saw, J. H., Jørgensen, S. L., Zaremba-Niedzwiedzka, K., Martijn, J., Lind, A. E., van Eijk, R., Schleper, C., Guy, L., & Ettema, T. J. G. (2015) · Nature · doi:10.1038/nature14447 · Cited by 1,324
Self-citationA Whole-Cell Computational Model Predicts Phenotype from Genotype
Karr, J. R., Sanghvi, J. C., Macklin, D. N., Gutschow, M. V., Jacobs, J. M., Bolival, B., Assad-Garcia, N., Glass, J. I., & Covert, M. W. (2012) · Cell · doi:10.1016/j.cell.2012.05.044 · Cited by 1,300
Mesophilic crenarchaeota: proposal for a third archaeal phylum, the Thaumarchaeota
Brochier‐Armanet, C., Boussau, B., Gribaldo, S., & Forterre, P. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1852 · Cited by 1,249
Asgard archaea illuminate the origin of eukaryotic cellular complexity
Zaremba-Niedzwiedzka, K., Caceres, E. F., Saw, J. H., Bäckström, D., Juzokaite, L., Vancaester, E., Seitz, K. W., Anantharaman, K., Starnawski, P., Kjeldsen, K. U., et al. (2017) · Nature · doi:10.1038/nature21031 · Cited by 1,226
Self-citationA review of long-branch attraction
Bergsten, J. (2005) · Cladistics · doi:10.1111/j.1096-0031.2005.00059.x · Cited by 1,162
Accelerated evolution and Muller’s Rachet in endosymbiotic bacteria
Moran, N. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.7.2873 · Cited by 1,017
Novel major archaebacterial group from marine plankton
Fuhrman, J. A., McCallum, K. L., & Davis, A. A. (1992) · Nature · doi:10.1038/356148a0 · Cited by 897
Eukaryotic evolution, changes and challenges
Embley, T. M., & Martin, W. (2006) · Nature · doi:10.1038/nature04546 · Cited by 867
A new phylum of Archaea represented by a nanosized hyperthermophilic symbiont
Huber, H., Hohn, M. J., Rachel, R., Fuchs, T., Wimmer, V. C., & STETTER, K. O. (2002) · Nature · doi:10.1038/417063a · Cited by 825
Is It Better to Add Taxa or Characters to a Difficult Phylogenetic Problem?
Graybeal, A. (1998) · Systematic Biology · doi:10.1080/106351598260996 · Cited by 745
Lartillot, N., Brinkmann, H., & Philippe, H. (2007) · BMC Evolutionary Biology · doi:10.1186/1471-2148-7-s1-s4 · Cited by 705
Major New Microbial Groups Expand Diversity and Alter our Understanding of the Tree of Life
Castelle, C. J., & Banfield, J. F. (2018) · Cell · doi:10.1016/j.cell.2018.02.016 · Cited by 595
New CRISPR–Cas systems from uncultivated microbes
Burstein, D. E., Harrington, L. B., Strutt, S. C., Probst, A. J., Anantharaman, K., Thomas, B. C., Doudna, J. A., & Banfield, J. F. (2016) · Nature · doi:10.1038/nature21059 · Cited by 583
Archaea and the origin of eukaryotes
Eme, L., Spang, A., Lombard, J., Stairs, C. W., & Ettema, T. J. G. (2017) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2017.133 · Cited by 575
Self-citationCastelle, C. J., Wrighton, K. C., Thomas, B. C., Hug, L. A., Brown, C. T., Wilkins, M. J., Frischkorn, K. R., Tringe, S. G., Singh, A., Markillie, L. M., et al. (2015) · Current Biology · doi:10.1016/j.cub.2015.01.014 · Cited by 536
The genome of Nanoarchaeum equitans: Insights into early archaeal evolution and derived parasitism
Waters, E. R., Hohn, M. J., Ahel, I., Graham, D. E., Adams, M. D., Barnstead, M., Beeson, K. Y., Bibbs, L., Bolanos, R. A., Keller, M., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1735403100 · Cited by 522
The phage‐host arms race: Shaping the evolution of microbes
Stern, A., & Sorek, R. (2010) · BioEssays · doi:10.1002/bies.201000071 · Cited by 517
Environmental Diversity of Bacteria and Archaea
DeLong, E. F., & Pace, N. R. (2001) · Systematic Biology · doi:10.1080/10635150118513 · Cited by 512
Genetic Diversity of Archaea in Deep-Sea Hydrothermal Vent Environments
Takai, K., & Horikoshi, K. (1999) · Genetics · doi:10.1093/genetics/152.4.1285 · Cited by 487
Biosynthetic capacity, metabolic variety and unusual biology in the CPR and DPANN radiations
Castelle, C. J., Brown, C. T., Anantharaman, K., Probst, A. J., Huang, R. H., & Banfield, J. F. (2018) · Nature Reviews Microbiology · doi:10.1038/s41579-018-0076-2 · Cited by 454
Evolutionary microbial genomics: insights into bacterial host adaptation
Toft, C., & Andersson, S. G. E. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2798 · Cited by 424
Archaeal Diversity in Waters from Deep South African Gold Mines
Takai, K., Moser, D. P., DeFlaun, M. F., Onstott, T. C., & Fredrickson, J. K. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.21.5750-5760.2001 · Cited by 403
The growing tree of Archaea: new perspectives on their diversity, evolution and ecology
Adam, P. S., Borrel, G., Brochier‐Armanet, C., & Gribaldo, S. (2017) · The ISME Journal · doi:10.1038/ismej.2017.122 · Cited by 394
Narasingarao, P., Podell, S. B., Ugalde, J. A., Brochier‐Armanet, C., Emerson, J., Brocks, J. J., Heidelberg, K. B., Banfield, J. F., & Allen, E. E. (2011) · The ISME Journal · doi:10.1038/ismej.2011.78 · Cited by 364
Moran, N., & Bennett, G. (2014) · Annual Review of Microbiology · doi:10.1146/annurev-micro-091213-112901 · Cited by 357
Genomic exploration of the diversity, ecology, and evolution of the archaeal domain of life
Spang, A., Caceres, E. F., & Ettema, T. J. G. (2017) · Science · doi:10.1126/science.aaf3883 · Cited by 346
Self-citationEnigmatic, ultrasmall, uncultivated Archaea
Baker, B. J., Comolli, L. R., Dick, G. J., Hauser, L., Hyatt, D., Dill, B. D., Land, M., VerBerkmoes, N. C., Hettich, R. L., & Banfield, J. F. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914470107 · Cited by 337
Impact of genome reduction on bacterial metabolism and its regulation
Yus, E., Maier, T., Michalodimitrakis, K., van Noort, V., Yamada, T., Chen, W.-H., Wodke, J. A. H., Güell, M., Martínez, S., Bourgeois, R., et al. (2009) · Science · doi:10.1126/science.1177263 · Cited by 327
New Abundant Microbial Groups in Aquatic Hypersaline Environments
Ghai, R., Pašić, L., Fernández, A. B., Martín-Cuadrado, A.-B., Mizuno, C. M., McMahon, K. D., Papke, R. T., Stepanauskas, R., Rodriguez-Brito, B., Rohwer, F. L., et al. (2011) · Scientific Reports · doi:10.1038/srep00135 · Cited by 310
Probst, A. J., Ladd, B., Jarett, J. K., Geller‐McGrath, D., Sieber, C. M. K., Emerson, J., Anantharaman, K., Thomas, B. C., Malmstrom, R. R., Stieglmeier, M., et al. (2018) · Nature Microbiology · doi:10.1038/s41564-017-0098-y · Cited by 267
Trichomonas hydrogenosomes contain the NADH dehydrogenase module of mitochondrial complex I
Hrdy, I., Hirt, R. P., Dolezal, P., Bardonová, L., Foster, P. G., Tachezy, J., & Martin Embley, T. (2004) · Nature · doi:10.1038/nature03149 · Cited by 262
Insights into the ecology, evolution, and metabolism of the widespread Woesearchaeotal lineages
Liu, X., Li, M., Castelle, C. J., Probst, A. J., Zhou, Z., Pan, J., Liu, Y., Banfield, J. F., & Gu, J. (2018) · Microbiome · doi:10.1186/s40168-018-0488-2 · Cited by 258
Koskinen, K., Pausan, M.-R., Perras, A., Beck, M., Bang, C., Mora, M., Schilhabel, A., Schmitz, R. A., & Moissl‐Eichinger, C. (2017) · mBio · doi:10.1128/mbio.00824-17 · Cited by 241
Archaeal Type III RuBisCOs Function in a Pathway for AMP Metabolism
Sato, T., Atomi, H., & Imanaka, T. (2007) · Science · doi:10.1126/science.1135999 · Cited by 237
Integrative modeling of gene and genome evolution roots the archaeal tree of life
Williams, T. A., Szöllősi, G. J., Spang, A., Foster, P. G., Heaps, S. E., Boussau, B., Ettema, T. J. G., & Embley, T. M. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1618463114 · Cited by 233
Self-citationA Site- and Time-Heterogeneous Model of Amino Acid Replacement
Blanquart, S., & Lartillot, N. (2008) · Molecular Biology and Evolution · doi:10.1093/molbev/msn018 · Cited by 217
Vavourakis, C. D., Ghai, R., Rodríguez‐Valera, F., Sorokin, D. Y., Tringe, S. G., Hugenholtz, P., & Muyzer, G. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00211 · Cited by 203
Sequence evolution in bacterial endosymbionts having extreme base compositions
Clark, M. A., Moran, N. A., & Baumann, P. (1999) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a026071 · Cited by 202
Nanoarchaeum equitans creates functional tRNAs from separate genes for their 5′- and 3′-halves
Randau, L., Münch, R., Hohn, M. J., Jahn, D., & Söll, D. G. (2005) · Nature · doi:10.1038/nature03233 · Cited by 201
Tropism switching in Bordetella bacteriophage defines a family of diversity-generating retroelements
Doulatov, S. R., Hodes, A., Dai, L., Mandhana, N., Liu, M., Deora, R., Simons, R. W., Zimmerly, S., & Miller, J. F. (2004) · Nature · doi:10.1038/nature02833 · Cited by 198
Leeuwenhoek, A. V. (1677) · Philosophical Transactions of the Royal Society of London · doi:10.1098/rstl.1677.0003 · Cited by 179
Tracing the evolution of gene loss in obligate bacterial symbionts
Moran, N. A. (2003) · Current Opinion in Microbiology · doi:10.1016/j.mib.2003.08.001 · Cited by 177
On Reduced Amino Acid Alphabets for Phylogenetic Inference
Susko, E., & Roger, A. J. (2007) · Molecular Biology and Evolution · doi:10.1093/molbev/msm144 · Cited by 177
Wurch, L. L., Giannone, R., Belisle, B. S., Swift, C., Utturkar, S., Hettich, R., Reysenbach, A., & Podar, M. (2016) · Nature Communications · doi:10.1038/ncomms12115 · Cited by 174
Brochier‐Armanet, C., Gribaldo, S., Zivanovic, Y., Confalonieri, F., & Forterre, P. (2005) · Genome biology · doi:10.1186/gb-2005-6-5-r42 · Cited by 168
Petitjean, C., Deschamps, P., López‐García, P., & Moreira, D. (2014) · Genome Biology and Evolution · doi:10.1093/gbe/evu274 · Cited by 161
Three-dimensional analysis of the structure and ecology of a novel, ultra-small archaeon
Comolli, L. R., Baker, B. J., Downing, K. H., Siegerist, C. E., & Banfield, J. F. (2008) · The ISME Journal · doi:10.1038/ismej.2008.99 · Cited by 150
Biology of a widespread uncultivated archaeon that contributes to carbon fixation in the subsurface
Probst, A. J., Weinmaier, T., Raymann, K., Perras, A., Emerson, J. B., Rattei, T., Wanner, G., Klingl, A., Berg, I. A., Yoshinaga, M., et al. (2014) · Nature Communications · doi:10.1038/ncomms6497 · Cited by 135
Jahn, U., Gallenberger, M., Paper, W., Junglas, B., Eisenreich, W., STETTER, K. O., Rachel, R., & Huber, H. (2007) · Journal of Bacteriology · doi:10.1128/jb.01731-07 · Cited by 125
A genomic analysis of the archaeal system Ignicoccus hospitalis-Nanoarchaeum equitans
Podar, M., Anderson, I., Makarova, K. S., Elkins, J. G., Ivanova, N., Wall, M. A., Lykidis, A., Mavromatis, K., Sun, H., Hudson, M. E., et al. (2008) · Genome biology · doi:10.1186/gb-2008-9-11-r158 · Cited by 119
Ortiz‐Álvarez, R., & Casamayor, E. O. (2015) · Environmental Microbiology Reports · doi:10.1111/1758-2229.12370 · Cited by 116
Metabolic versatility of small archaea Micrarchaeota and Parvarchaeota
Chen, L.-X., Méndez-García, C., Dombrowski, N., Servín-Garcidueñas, L. E., Eloe-Fadrosh, E., Fang, B.-Z., Luo, Z.-H., Tan, S., Zhi, X.-Y., Hua, Z., et al. (2017) · The ISME Journal · doi:10.1038/s41396-017-0002-z · Cited by 115
Self-citationPodar, M., Makarova, K. S., Graham, D. E., Wolf, Y. I., Koonin, E. V., & Reysenbach, A. (2013) · Biology Direct · doi:10.1186/1745-6150-8-9 · Cited by 111
‘ARMAN’ archaea depend on association with euryarchaeal host in culture and in situ
Golyshina, O. V., Toshchakov, S. V., Makarova, K. S., Gavrilov, S. N., Korzhenkov, A. A., Cono, V. L., Arcadi, E., Nechitaylo, T. Y., Ferrer, M., Kublanov, I. V., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00104-7 · Cited by 108
Jahn, U., Summons, R., Sturt, H. F., Grosjean, E., & Huber, H. (2004) · Archives of Microbiology · doi:10.1007/s00203-004-0725-x · Cited by 108
The C-type lectin fold as an evolutionary solution for massive sequence variation
McMahon, S. A., Miller, J. L., Lawton, J. A., Kerkow, D. E., Hodes, A., Martı́-Renom, M. A., Doulatov, S. R., Eswar, N., Šali, A., Miller, J. F., et al. (2005) · Nature Structural & Molecular Biology · doi:10.1038/nsmb992 · Cited by 106
Rudolph, C., Wanner, G., & Huber, R. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.5.2336-2344.2001 · Cited by 102
Youssef, N. H., Rinke, C., Stepanauskas, R., Farag, I., Woyke, T., & Elshahed, M. S. (2014) · The ISME Journal · doi:10.1038/ismej.2014.141 · Cited by 97
Küper, U., Meyer, C., Müller, V., Rachel, R., & Huber, H. (2010) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0911711107 · Cited by 96
Durbin, A. M., & Teske, A. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00168 · Cited by 94
Raymann, K., Forterre, P., Brochier‐Armanet, C., & Gribaldo, S. (2014) · Genome Biology and Evolution · doi:10.1093/gbe/evu004 · Cited by 91
Dissecting the energy metabolism in Mycoplasma pneumoniae through genome-scale metabolic modeling
Wodke, J. A. H., Puchałka, J., Lluch‐Senar, M., Marcos, J., Yus, E., Godinho, M., Gutiérrez‐Gallego, R., dos Santos, V. A. P. M., Serrano, L., Klipp, E., et al. (2013) · Molecular Systems Biology · doi:10.1038/msb.2013.6 · Cited by 89
John, E. S., Liu, Y., Podar, M., Stott, M. B., Meneghin, J., Chen, Z., Lagutin, K., Mitchell, K., & Reysenbach, A. (2018) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2018.08.005 · Cited by 89
A pentose bisphosphate pathway for nucleoside degradation in Archaea
Aono, R., Sato, T., Imanaka, T., & Atomi, H. (2015) · Nature Chemical Biology · doi:10.1038/nchembio.1786 · Cited by 87
Giulio, M. D. (2005) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2005.09.023 · Cited by 84
Retroelement guided protein diversification abounds in vast lineages of bacteria and archaea
Paul, B., Burstein, D., Castelle, C., Handa, S., Arambula, D., Czornyj, E., Thomas, B., Ghosh, P., Miller, J. F., Banfield, J., et al. (2017) · Nature Microbiology · doi:10.1038/nmicrobiol.2017.45 · Cited by 82
Exploring microbial dark matter to resolve the deep archaeal ancestry of eukaryotes
Saw, J. H. W., Spang, A., Zaremba-Niedźwiedzka, K., Juzokaite, L., Dodsworth, J. A., Murugapiran, S. K., Colman, D. R., Takacs‐Vesbach, C. D., Hedlund, B. P., Guy, L., et al. (2015) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2014.0328 · Cited by 80
Self-citationA Complex Endomembrane System in the Archaeon Ignicoccus hospitalis Tapped by Nanoarchaeum equitans
Heimerl, T., Flechsler, J., Pickl, C., Heinz, V., Salecker, B., Zweck, J., Wanner, G., Geimer, S., Samson, R. Y., Bell, S. D., et al. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01072 · Cited by 78
Targeted diversity generation by intraterrestrial archaea and archaeal viruses
Paul, B. G., Bagby, S. C., Czornyj, E., Arambula, D. G., Handa, S., Sczyrba, A., Ghosh, P., Miller, J. F., & Valentine, D. L. (2015) · Nature Communications · doi:10.1038/ncomms7585 · Cited by 77
Junglas, B., Briegel, A., Burghardt, T., Walther, P., Wirth, R., Huber, H., & Rachel, R. (2008) · Archives of Microbiology · doi:10.1007/s00203-008-0402-6 · Cited by 77
Unveiling viral–host interactions within the ‘microbial dark matter’
Martínez‐García, M., Santos, F., Moreno‐Paz, M., Parro, V., & Antón, J. (2014) · Nature Communications · doi:10.1038/ncomms5542 · Cited by 76
Giannone, R., Huber, H., Karpinets, T., Heimerl, T., Küper, U., Rachel, R., Keller, M., Hettich, R., & Podar, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022942 · Cited by 74
Sediment‐associated microdiversity within the Marine Group I Crenarchaeota
Durbin, A. M., & Teske, A. (2010) · Environmental Microbiology Reports · doi:10.1111/j.1758-2229.2010.00163.x · Cited by 74
Munson-McGee, J. H., Field, E. K., Bateson, M. M., Rooney, C., Stepanauskas, R., & Young, M. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.01539-15 · Cited by 68
Inter-species interconnections in acid mine drainage microbial communities
Comolli, L. R., & Banfield, J. F. (2014) · Frontiers in Microbiology · doi:10.3389/fmicb.2014.00367 · Cited by 65
Omic Approaches in Microbial Ecology: Charting the Unknown
Baker, B. J., & Dick, G. J. (2013) · Microbe Magazine · doi:10.1128/microbe.8.353.1 · Cited by 65
New substitution models for rooting phylogenetic trees
Williams, T. A., Heaps, S. E., Cherlin, S., Nye, T. M. W., Boys, R. J., & Embley, T. M. (2015) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2014.0336 · Cited by 61 · cited 1×
“While site- and branch-heterogeneous models have been described (Blanquart and Lartillot 2008; Heaps et al. 2014; Williams et al. 2015; Cherlin et al. 2018) and implemented, they are currently computationally intractable even on modestly”
Self-citationExtreme halophilic archaea derive from two distinct methanogen Class II lineages.
Aouad, M., Taib, N., Oudart, A., Lecocq, M., Gouy, M., & Brochier-Armanet, C. (2018) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2018.04.011 · Cited by 61
Gene Transfers from Nanoarchaeota to an Ancestor of Diplomonads and Parabasalids
Andersson, J. O. (2004) · Molecular Biology and Evolution · doi:10.1093/molbev/msh254 · Cited by 60
Tackling the minority: sulfate-reducing bacteria in an archaea-dominated subsurface biofilm
Probst, A. J., Holman, H. N., DeSantis, T. Z., Andersen, G. L., Birarda, G., Bechtel, H. A., Piceno, Y. M., Sonnleitner, M., Venkateswaran, K. J., & Moissl‐Eichinger, C. (2012) · The ISME Journal · doi:10.1038/ismej.2012.133 · Cited by 60
The complete set of tRNA species in Nanoarchaeum equitans
Randau, L., Pearson, M., & Söll, D. G. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.04.051 · Cited by 60
Characterisation of a stable laboratory co-culture of acidophilic nanoorganisms
Krause, S., Bremges, A., Münch, P. C., McHardy, A. C., & Gescher, J. (2017) · Scientific Reports · doi:10.1038/s41598-017-03315-6 · Cited by 58
Jarett, J. K., Nayfach, S., Podar, M., Inskeep, W. P., Ivanova, N., Munson-McGee, J. H., Schulz, F., Young, M., Jay, Z. J., Beam, J. P., et al. (2018) · Microbiome · doi:10.1186/s40168-018-0539-8 · Cited by 54
Lewalter, K., & Müller, V. (2006) · Biochimica et Biophysica Acta · doi:10.1016/j.bbabio.2006.04.027 · Cited by 48
Archaeal communities of Arctic methane-containing permafrost
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Giannone, R. J., Wurch, L. L., Heimerl, T., Martin, S., Yang, Z. K., Huber, H., Rachel, R., Hettich, R. L., & Podar, M. (2014) · The ISME Journal · doi:10.1038/ismej.2014.112 · Cited by 46
Narrowe, A. B., Spang, A., Stairs, C. W., Caceres, E., Baker, B. J., Miller, C. S., & Ettema, T. J. G. (2018) · Genome Biology and Evolution · doi:10.1093/gbe/evy154 · Cited by 42
Self-citation“Altiarchaeales”: Uncultivated Archaea from the Subsurface
Probst, A. J., & Moissl‐Eichinger, C. (2015) · Life · doi:10.3390/life5021381 · Cited by 37
Culture Independent Genomic Comparisons Reveal Environmental Adaptations for Altiarchaeales
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Close Encounters of the Third Domain: The Emerging Genomic View of Archaeal Diversity and Evolution
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Quest for Ancestors of Eukaryal Cells Based on Phylogenetic Analyses of Aminoacyl-tRNA Synthetases
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Bayesian modelling of compositional heterogeneity in molecular phylogenetics
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“Although several DPANN archaea encode subunits of putative ATP synthases, these protein complexes might not always be functional as suggested by the structural and biophysical investigations of the A3B3 core complex of N. equitans (Mohanty et al. 2015).”
BackgroundInfluentialThe Effect of Nonreversibility on Inferring Rooted Phylogenies
Cherlin, S., Heaps, S., Nye, T., Boys, R., Williams, T., & Embley, T. (2015) · Molecular biology and evolution · doi:10.1093/molbev/msx294 · Cited by 12
Self-citation
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Innovations to culturing the uncultured microbial majority
Lewis, W. H., Tahon, G., Geesink, P., Sousa, D. Z., & Ettema, T. J. G. (2020) · Nature Reviews Microbiology · doi:10.1038/s41579-020-00458-8 · Cited by 639
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Viral community-wide auxiliary metabolic genes differ by lifestyles, habitats, and hosts
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Unexpected host dependency of Antarctic Nanohaloarchaeota
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Self-citationReductive evolution and unique predatory mode in the CPR bacterium Vampirococcus lugosii
Moreira, D., Zivanovic, Y., López‐Archilla, A. I., Iniesto, M., & López‐García, P. (2021) · Nature Communications · doi:10.1038/s41467-021-22762-4 · Cited by 126
Metadata
- Authors
- Dombrowski, N., Lee, J.-H., Williams, T. A., Offre, P., & Spang, A.
- Affiliations
- Utrecht University (NL)
- Uppsala University (SE)
- University of Bristol (GB)
- Corresponding author
- Spang, Anja
- Venue
- FEMS Microbiology Letters
- Publisher
- Oxford University Press (OUP)
- Published
- 2019-01-01
- Volume
- 366
- Issue
- 2
- ISSN
- 0378-1097 (ISSN-L)
- 1574-6968
- PMC
- PMC6349945
- OpenAlex
- W2910961041
- Cited by
- 230
- References
- 110
- Citations by year
- 2026: 20 · 2025: 25 · 2024: 34 · 2023: 30 · 2022: 43 · 2021: 39 · 2020: 28 · 2019: 11
- FWCI
- 2.19
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- FEMS Microbiology Letters (publishedVersion, cc-by)
- NIOZ Publications (Royal Netherlands Institute for Sea Research) (publishedVersion, other-oa)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Bristol Research (University of Bristol) (publishedVersion, cc-by)
- Flanders Marine Institute (Flanders Marine Institute) (submittedVersion, other-oa)
- KTH Publication Database DiVA (KTH Royal Institute of Technology) (submittedVersion, other-oa)
- Explore Bristol Research (submittedVersion, cc-by)
- Funders
- Swedish Research Council (2016-03559)
- Netherlands Organisation for Scientific Research
- Royal Society University Research
- Topics
- Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Protist diversity and phylogeny
- Keywords
- DPANN archaea, genomic diversity, symbiosis, obligate symbionts, gene repertoire, tree of life, unculturable microorganisms
- MeSH terms
- Archaea, Phylogeny, Genetic Variation, Evolution, Molecular, Genome, Archaeal
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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