Article Contents
ARTICLE   Open Access     Cite

Radiating pattern revealed by a deep learning model traces the evolutionary dynamics of the Archaea domain

More Information
  • Corresponding author: wyz@sjtu.edu.cn
  • DownLoad: Full size image
    1. Early diversification of archaea remains unsettled due to uncertainty from conventional phylogenomics.

      By integrating deep learning and traditional phylogenomics, we revealed archaeal evolutionary patterns.

      Early diversification of DPANN potentially linked to acetate metabolism in lower temperature environments.

      The other archaea might share an ancestor with methyl-reducing methanogenesis and carbon fixation.

      From domain-wide radiating patterns to genus-level adaptation, our framework offers comprehensive insights.

  • Archaea, one of the primary domains of life, have coevolved with Earth for billions of years and play critical roles in biogeochemical cycles across diverse ecosystems. However, resolving deep archaeal phylogeny is confounded by among-site heterogeneity and compositional biases, which together exacerbate long-branch attraction in lineages like DPANN. Here, using variational autoencoders and other deep learning models along with phylogenomics, we re-evaluated archaeal evolution and identified a radiating evolutionary landscape of three major archaeal superphyla, DPANN, TACK-Asgard and Euryarchaeota. Our integrated results also support the scenario in which DPANN evolved as an early monophyletic lineage, potentially relying on acetate-related metabolism under lower temperature conditions, whereas TACK-Asgard and Euryarchaeota possibly share a hydrogen-dependent methyl-reducing methanogen ancestor with the complete Wood–Ljungdahl pathway in higher temperature habitats. Environmental factors, including temperature, oxygen, and salinity, have kept influencing subsequent archaeal evolution in distinct patterns, highlighting the interplay between environmental factors and evolutionary trajectories of this ancient domain. By demonstrating that deep learning can be systematically integrated with phylogenomics to generate testable hypotheses on ancient metabolisms and environmental adaptation, this work provides a new analytical insight for archaeal evolutionary studies.
  • 加载中
  • [1] Woese C. R. and Fox G. E. (1977). Phylogenetic structure of the prokaryotic domain: The primary kingdoms. Proc. Natl. Acad. Sci. USA 74:5088−5090. DOI:10.1073/pnas.74.11.5088

    View in Article CrossRef Google Scholar

    [2] Woese C. R., Magrum L. J. and Fox G. E. (1978). Archaebacteria. J. Mol. Evol. 11:245−251. DOI:10.1007/BF01734485

    View in Article CrossRef Google Scholar

    [3] Woese C. R., Kandler O. and Wheelis M. L. (1990). Towards a natural system of organisms: Proposal for the domains Archaea, Bacteria, and Eucarya. Proc. Natl. Acad. Sci. USA 87:4576−4579. DOI:10.1073/pnas.87.12.4576

    View in Article CrossRef Google Scholar

    [4] Martin W. F. and Sousa F. L. (2015). Early microbial evolution: The age of anaerobes. Cold Spring Harb. Perspect. Biol. 8:a018127. DOI:10.1101/cshperspect.a018127

    View in Article CrossRef Google Scholar

    [5] Ueno Y., Yamada K., Yoshida N., et al. (2006). Evidence from fluid inclusions for microbial methanogenesis in the early Archaean era. Nature 440:516−519. DOI:10.1038/nature04584

    View in Article CrossRef Google Scholar

    [6] Schopf J. W., Kitajima K., Spicuzza M. J., et al. (2018). SIMS analyses of the oldest known assemblage of microfossils document their taxon-correlated carbon isotope compositions. Proc. Natl. Acad. Sci. USA 115:53−58. DOI:10.1073/pnas.1718063115

    View in Article CrossRef Google Scholar

    [7] Baker B. J., De Anda V., Seitz K. W., et al. (2020). Diversity, ecology and evolution of archaea. Nat. Microbiol. 5:887−900. DOI:10.1038/s41564-020-0715-z

    View in Article CrossRef Google Scholar

    [8] Tahon G., Geesink P. and Ettema T. J. G. (2021). Expanding archaeal diversity and phylogeny: Past, present, and future. Annu. Rev. Microbiol. 75:359−381. DOI:10.1146/annurev-micro-040921-050212

    View in Article CrossRef Google Scholar

    [9] Berghuis B. A., Yu F. B., Schulz F., et al. (2019). Hydrogenotrophic methanogenesis in archaeal phylum Verstraetearchaeota reveals the shared ancestry of all methanogens. Proc. Natl. Acad. Sci. USA 116:5037−5044. DOI:10.1073/pnas.1815631116

    View in Article CrossRef Google Scholar

    [10] Borrel G., Adam P. S., McKay L. J., et al. (2019). Wide diversity of methane and short-chain alkane metabolisms in uncultured archaea. Nat. Microbiol. 4:603−613. DOI:10.1038/s41564-019-0363-3

    View in Article CrossRef Google Scholar

    [11] Spang A., Caceres E. F. and Ettema T. J. G. (2017). Genomic exploration of the diversity, ecology, and evolution of the archaeal domain of life. Science 357:eaaf3883. DOI:10.1126/science.aaf3883

    View in Article CrossRef Google Scholar

    [12] Rinke C., Chuvochina M., Mussig A. J., et al. (2021). A standardized archaeal taxonomy for the Genome Taxonomy Database. Nat. Microbiol. 6:946−959. DOI:10.1038/s41564-021-00918-8

    View in Article CrossRef Google Scholar

    [13] Moi D., Bernard C., Steinegger M., et al. (2025). Structural phylogenetics unravels the evolutionary diversification of communication systems in gram-positive bacteria and their viruses. Nat. Struct. & Mol. Biol. 32:2492−2502. DOI:10.1038/s41594-025-01649-8

    View in Article CrossRef Google Scholar

    [14] Greener J. G., Moffat L. and Jones D. T. (2018). Design of metalloproteins and novel protein folds using variational autoencoders. Sci. Rep. 8:16189. DOI:10.1038/s41598-018-34533-1

    View in Article CrossRef Google Scholar

    [15] Hie B. L., Yang K. K. and Kim P. S. (2022). Evolutionary velocity with protein language models predicts evolutionary dynamics of diverse proteins. Cell Syst. 13:274−285,e276. DOI:10.1016/j.cels.2022.01.003

    View in Article CrossRef Google Scholar

    [16] Lu A. X., Yan W., Yang K. K., et al. (2024). Tokenized and continuous embedding compressions of protein sequence and structure. bioRxiv:2024.2008.2006.606920. DOI:10.1101/2024.08.06.606920.

    View in Article Google Scholar

    [17] Detlefsen N. S., Hauberg S. and Boomsma W. (2022). Learning meaningful representations of protein sequences. Nat. Commun. 13:1914. DOI:10.1038/s41467-022-29443-w

    View in Article CrossRef Google Scholar

    [18] Ding X., Zou Z. and Brooks C. L. III (2019). Deciphering protein evolution and fitness landscapes with latent space models. Nat. Commun. 10:5644. DOI:10.1038/s41467-019-13633-0

    View in Article Google Scholar

    [19] Ziegler C., Martin J., Sinner C., et al. (2023). Latent generative landscapes as maps of functional diversity in protein sequence space. Nat. Commun. 14:2222. DOI:10.1038/s41467-023-37958-z

    View in Article CrossRef Google Scholar

    [20] Guy L. and Ettema T. J. (2011). The archaeal 'TACK' superphylum and the origin of eukaryotes. Trends Microbiol. 19:580−587. DOI:10.1016/j.tim.2011.09.002

    View in Article CrossRef Google Scholar

    [21] Rinke C., Schwientek P., Sczyrba A., et al. (2013). Insights into the phylogeny and coding potential of microbial dark matter. Nature 499:431−437. DOI:10.1038/nature12352

    View in Article CrossRef Google Scholar

    [22] Williams T. A., Szollosi G. J., Spang A., et al. (2017). Integrative modeling of gene and genome evolution roots the archaeal tree of life. Proc. Natl. Acad. Sci. USA 114:E4602−E4611. DOI:10.1073/pnas.1618463114

    View in Article CrossRef Google Scholar

    [23] Baker B. A., McCarthy C. G. P., Lopez-Garcia P., et al. (2025). Phylogenomic analyses indicate the archaeal superphylum DPANN originated from free-living euryarchaeal-like ancestors. Nat. Microbiol. 10:1593−1604. DOI:10.1038/s41564-025-02024-5

    View in Article CrossRef Google Scholar

    [24] Mei R., Kaneko M., Imachi H., et al. (2023). The origin and evolution of methanogenesis and archaea are intertwined. PNAS Nexus 2:pgad023. DOI:10.1093/pnasnexus/pgad023

    View in Article CrossRef Google Scholar

    [25] Garcia P. S., Gribaldo S. and Borrel G. (2022). Diversity and evolution of methane-related pathways in archaea. Annu. Rev. Microbiol. 76:727−755. DOI:10.1146/annurev-micro-041020-024935

    View in Article CrossRef Google Scholar

    [26] Adam P. S., Borrel G. and Gribaldo S. (2019). An archaeal origin of the Wood-Ljungdahl H(4)MPT branch and the emergence of bacterial methylotrophy. Nat. Microbiol. 4:2155−2163. DOI:10.1038/s41564-019-0534-2

    View in Article CrossRef Google Scholar

    [27] Berg I. A., Kockelkorn D., Ramos-Vera W. H., et al. (2010). Autotrophic carbon fixation in archaea. Nat. Rev. Microbiol. 8:447−460. DOI:10.1038/nrmicro2365

    View in Article CrossRef Google Scholar

    [28] Weiss M. C., Sousa F. L., Mrnjavac N., et al. (2016). The physiology and habitat of the last universal common ancestor. Nat. Microbiol. 1:16116. DOI:10.1038/nmicrobiol.2016.116

    View in Article CrossRef Google Scholar

    [29] Adam P. S., Kolyfetis G. E., Bornemann T. L. V., et al. (2022). Genomic remnants of ancestral methanogenesis and hydrogenotrophy in archaea drive anaerobic carbon cycling. Sci. Adv. 8:eabm9651. DOI:10.1126/sciadv.abm9651

    View in Article CrossRef Google Scholar

    [30] Wang Y., Wegener G., Williams T. A., et al. (2021). A methylotrophic origin of methanogenesis and early divergence of anaerobic multicarbon alkane metabolism. Sci. Adv. 7:eabj1453. DOI:10.1126/sciadv.abj1453

    View in Article CrossRef Google Scholar

    [31] Adam P. S., Borrel G. and Gribaldo S. (2018). Evolutionary history of carbon monoxide dehydrogenase/acetyl-CoA synthase, one of the oldest enzymatic complexes. Proc. Natl. Acad. Sci. USA 115:E1166−E1173. DOI:10.1073/pnas.1716667115

    View in Article CrossRef Google Scholar

    [32] Vulcano F., Hribovsek P., Denny E. O., et al. (2023). Potential for homoacetogenesis via the Wood-Ljungdahl pathway in Korarchaeia lineages from marine hydrothermal vents. Environ. Microbiol. Rep. 15:698−707. DOI:10.1111/1758-2229.13168

    View in Article CrossRef Google Scholar

    [33] He Y., Li M., Perumal V., et al. (2016). Genomic and enzymatic evidence for acetogenesis among multiple lineages of the archaeal phylum Bathyarchaeota widespread in marine sediments. Nat. Microbiol. 1:16035. DOI:10.1038/nmicrobiol.2016.35

    View in Article CrossRef Google Scholar

    [34] Schmidt M. and Schonheit P. (2013). Acetate formation in the photoheterotrophic bacterium Chloroflexus aurantiacus involves an archaeal type ADP-forming acetyl-CoA synthetase isoenzyme I. FEMS Microbiol. Lett. 349:171−179. DOI:10.1111/1574-6968.12312

    View in Article CrossRef Google Scholar

    [35] Jones C. P., Khan K. and Ingram-Smith C. (2017). Investigating the mechanism of ADP-forming acetyl-CoA synthetase from the protozoan parasite Entamoeba histolytica. FEBS Lett. 591:603−612. DOI:10.1002/1873-3468.12573

    View in Article CrossRef Google Scholar

    [36] Brasen C., Schmidt M., Grotzinger J., et al. (2008). Reaction mechanism and structural model of ADP-forming acetyl-CoA synthetase from the hyperthermophilic archaeon Pyrococcus furiosus: Evidence for a second active site histidine residue. J. Biol. Chem. 283:15409−15418. DOI:10.1074/jbc.M710218200

    View in Article CrossRef Google Scholar

    [37] Ouboter H. T., Arshad A., Berger S., et al. (2023). Acetate and acetyl-CoA metabolism of ANME-2 anaerobic archaeal methanotrophs. Appl. Environ. Microbiol. 89:e0036723. DOI:10.1128/aem.00367-23

    View in Article CrossRef Google Scholar

    [38] Kingma D. P. and Welling M. (2013). Auto-encoding variational Bayes. arXiv:1312.6114. DOI:10.48550/arXiv.1312.6114

    View in Article Google Scholar

    [39] Kingma D. P. and Welling M. (2019). An introduction to variational autoencoders. Found. Trends Mach. Learn. 12:4−89. DOI:10.1561/2200000056

    View in Article CrossRef Google Scholar

    [40] Zhu M., Song Y., Yuan Q., et al. (2024). Accurately predicting optimal conditions for microorganism proteins through geometric graph learning and language model. Commun. Biol. 7:1709. DOI:10.1038/s42003-024-07436-3

    View in Article CrossRef Google Scholar

    [41] Tan P., Li M., Zhang L., et al. (2023). TemPL: A novel deep learning model for zero-shot prediction of protein stability and activity based on temperature-guided language modeling. arXiv:2304.03780. DOI:10.48550/arXiv.2304.03780

    View in Article Google Scholar

    [42] Li G., Rabe K. S., Nielsen J., et al. (2019). Machine learning applied to predicting microorganism growth temperatures and enzyme catalytic optima. ACS Synth. Biol. 8:1411−1420. DOI:10.1021/acssynbio.9b00099

    View in Article CrossRef Google Scholar

    [43] Gado J. E., Beckham G. T. and Payne C. M. (2020). Improving enzyme optimum temperature prediction with resampling strategies and ensemble learning. J. Chem. Inf. Model. 60:4098−4107. DOI:10.1021/acs.jcim.0c00489

    View in Article CrossRef Google Scholar

    [44] Barnum T. P., Crits-Christoph A., Molla M., et al. (2024). Predicting microbial growth conditions from amino acid composition. bioRxiv:2024.2003.2022.586313. DOI:10.1101/2024.03.22.586313

    View in Article Google Scholar

    [45] Gado J. E., Knotts M., Shaw A. Y., et al. (2025). Machine learning prediction of enzyme optimum pH. Nat. Mach. Intell. 7:716−729. DOI:10.1038/s42256-025-01026-6

    View in Article CrossRef Google Scholar

    [46] Hu S., Wang X., Wang Z., et al. (2024). HPClas: A data-driven approach for identifying halophilic proteins based on catBoost. mLife 3:515−526. DOI:10.1002/mlf2.12125

    View in Article CrossRef Google Scholar

    [47] Davin A. A., Woodcroft B. J., Soo R. M., et al. (2025). A geological timescale for bacterial evolution and oxygen adaptation. Science 388:eadp1853. DOI:10.1126/science.adp1853

    View in Article CrossRef Google Scholar

    [48] Flamholz A. I., Goldford J. E., Richter P. A., et al. (2024). Annotation-free prediction of microbial dioxygen utilization. mSystems 9:e0076324. DOI:10.1128/msystems.00763-24

    View in Article CrossRef Google Scholar

    [49] Groussin M., Boussau B., Charles S., et al. (2013). The molecular signal for the adaptation to cold temperature during early life on Earth. Biol. Lett. 9:20130608. DOI:10.1098/rsbl.2013.0608

    View in Article CrossRef Google Scholar

    [50] Groussin M., Boussau B. and Gouy M. (2013). A branch-heterogeneous model of protein evolution for efficient inference of ancestral sequences. Syst. Biol. 62:523−538. DOI:10.1093/sysbio/syt016

    View in Article CrossRef Google Scholar

    [51] Hyatt D., Chen G. L., Locascio P. F., et al. (2010). Prodigal: Prokaryotic gene recognition and translation initiation site identification. BMC Bioinform. 11:119. DOI:10.1186/1471-2105-11-119

    View in Article CrossRef Google Scholar

    [52] Camacho C., Coulouris G., Avagyan V., et al. (2009). BLAST+: Architecture and applications. BMC Bioinform. 10:421. DOI:10.1186/1471-2105-10-421

    View in Article CrossRef Google Scholar

    [53] Katoh K. and Standley D. M. (2013). MAFFT multiple sequence alignment software version 7: Improvements in performance and usability. Mol. Biol. Evol. 30:772−780. DOI:10.1093/molbev/mst010

    View in Article CrossRef Google Scholar

    [54] Capella-Gutierrez S., Silla-Martinez J. M. and Gabaldon T. (2009). trimAl: A tool for automated alignment trimming in large-scale phylogenetic analyses. Bioinformatics 25:1972−1973. DOI:10.1093/bioinformatics/btp348

    View in Article CrossRef Google Scholar

    [55] Price M. N., Dehal P. S. and Arkin A. P. (2010). FastTree 2--approximately maximum-likelihood trees for large alignments. PLOS ONE 5:e9490. DOI:10.1371/journal.pone.0009490

    View in Article Google Scholar

    [56] Nguyen L. T., Schmidt H. A., von Haeseler A., et al. (2015). IQ-TREE: A fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol. Biol. Evol. 32:268−274. DOI:10.1093/molbev/msu300

    View in Article CrossRef Google Scholar

    [57] Kalyaanamoorthy S., Minh B. Q., Wong T. K. F., et al. (2017). ModelFinder: Fast model selection for accurate phylogenetic estimates. Nat. Methods. 14:587−589. DOI:10.1038/nmeth.4285

    View in Article CrossRef Google Scholar

    [58] Mirdita M., Schutze K., Moriwaki Y., et al. (2022). ColabFold: Making protein folding accessible to all. Nat. Methods 19:679−682. DOI:10.1038/s41592-022-01488-1

    View in Article CrossRef Google Scholar

    [59] Zhang C., Shine M., Pyle A. M., et al. (2022). US-align: Universal structure alignments of proteins, nucleic acids, and macromolecular complexes. Nat. Methods 19:1109−1115. DOI:10.1038/s41592-022-01585-1

    View in Article CrossRef Google Scholar

    [60] Wang Y., Wegener G., Hou J., et al. (2019). Expanding anaerobic alkane metabolism in the domain of Archaea. Nat. Microbiol. 4:595−602. DOI:10.1038/s41564-019-0364-2

    View in Article CrossRef Google Scholar

    [61] Leng H., Wang Y., Zhao W., et al. (2023). Identification of a deep-branching thermophilic clade sheds light on early bacterial evolution. Nat. Commun. 14:4354. DOI:10.1038/s41467-023-39960-x

    View in Article CrossRef Google Scholar

    [62] Moody E. R. R., Mahendrarajah T. A., Dombrowski N., et al. (2022). An estimate of the deepest branches of the tree of life from ancient vertically evolving genes. eLife 11:e66695. DOI:10.7554/eLife.66695

    View in Article CrossRef Google Scholar

    [63] Huang W.-C., Dombrowski N., Mahendrarajah T. A., et al. (2025). Phylogenetic reconciliation supports a methanogenic ancestor of the archaea and a derived origin for host-associated lineages. bioRxiv:2025.11.11.687807. DOI:10.1101/2025.11.11.687807

    View in Article Google Scholar

    [64] Williams T. A. and Heaps S. E. (2014). An introduction to phylogenetics and the tree of life. In New Approaches to Prokaryotic Systematics, Goodfellow M., Sutcliffe I., and Chun J. (eds) (Academic Press), pp:13-44. DOI:10.1016/bs.mim.2014.05.001

    View in Article Google Scholar

    [65] de la Paz J. A., Nartey C. M., Yuvaraj M., et al. (2020). Epistatic contributions promote the unification of incompatible models of neutral molecular evolution. Proc. Natl. Acad. Sci. USA 117:5873−5882. DOI:10.1073/pnas.1913071117

    View in Article CrossRef Google Scholar

    [66] Rodriguez-Rivas J., Croce G., Muscat M., et al. (2022). Epistatic models predict mutable sites in SARS-CoV-2 proteins and epitopes. Proc. Natl. Acad. Sci. USA 119:e2113118119. DOI:10.1073/pnas.2113118119

    View in Article CrossRef Google Scholar

    [67] Bisardi M., Rodriguez-Rivas J., Zamponi F., et al. (2022). Modeling sequence-space exploration and emergence of epistatic signals in protein evolution. Mol. Biol. Evol. 39:msab321. DOI:10.1093/molbev/msab321

    View in Article CrossRef Google Scholar

    [68] Duchene D. A., Mather N., Van Der Wal C., et al. (2022). Excluding loci with substitution saturation improves inferences from phylogenomic data. Syst. Biol. 71:676−689. DOI:10.1093/sysbio/syab075

    View in Article CrossRef Google Scholar

    [69] Jermiin L. S. and Misof B. (2020). Measuring historical and compositional signals in phylogenetic data. bioRxiv:2020.2001.2003.894097. DOI:10.1101/2020.01.03.894097

    View in Article Google Scholar

    [70] Philippe H., Brinkmann H., Lavrov D. V., et al. (2011). Resolving difficult phylogenetic questions: Why more sequences are not enough. PLOS Biol. 9:e1000602. DOI:10.1371/journal.pbio.1000602

    View in Article CrossRef Google Scholar

    [71] Manuel C., Sakalli E., Schmidt H. A., et al. (2025). When the past fades: Detecting phylogenetic signal with SatuTe. Mol. Biol. Evol. 42:msaf090. DOI:10.1093/molbev/msaf090

    View in Article CrossRef Google Scholar

    [72] Felsenstein J. (1978). Cases in which parsimony or compatibility methods will be positively misleading. Syst. Zool. 27:401−410. DOI:10.2307/2412923

    View in Article CrossRef Google Scholar

    [73] Susko E. and Roger A. J. (2021). Long branch attraction biases in phylogenetics. Syst. Biol. 70:838−843. DOI:10.1093/sysbio/syab001

    View in Article CrossRef Google Scholar

    [74] Roch S., Nute M. and Warnow T. (2019). Long-branch attraction in species tree estimation: Inconsistency of partitioned likelihood and topology-based summary methods. Syst. Biol. 68:281−297. DOI:10.1093/sysbio/syy061

    View in Article CrossRef Google Scholar

    [75] Ingram-Smith C., Woods B. I. and Smith K. S. (2006). Characterization of the acyl substrate binding pocket of acetyl-CoA synthetase. Biochemistry 45:11482−11490. DOI:10.1021/bi061023e

    View in Article CrossRef Google Scholar

    [76] Musfeldt M. and Schonheit P. (2002). Novel type of ADP-forming acetyl coenzyme A synthetase in hyperthermophilic archaea: Heterologous expression and characterization of isoenzymes from the sulfate reducer Archaeoglobus fulgidus and the methanogen Methanococcus jannaschii. J. Bacteriol. 184:636−644. DOI:10.1128/JB.184.3.636-644.2002

    View in Article CrossRef Google Scholar

    [77] Brasen C. and Schonheit P. (2005). AMP-forming acetyl-CoA synthetase from the extremely halophilic archaeon Haloarcula marismortui: Purification, identification and expression of the encoding gene, and phylogenetic affiliation. Extremophiles 9:355−365. DOI:10.1007/s00792-005-0449-0

    View in Article CrossRef Google Scholar

    [78] Liang M. H., Qv X. Y., Jin H. H., et al. (2016). Characterization and expression of AMP-forming acetyl-CoA synthetase from Dunaliella tertiolecta and its response to nitrogen starvation stress. Sci. Rep. 6:23445. DOI:10.1038/srep23445

    View in Article CrossRef Google Scholar

    [79] Kuprat T., Ortjohann M., Johnsen U., et al. (2021). Glucose metabolism and acetate switch in archaea: The enzymes in Haloferax volcanii. J. Bacteriol. 203:e00690−20. DOI:10.1128/JB.00690-20

    View in Article CrossRef Google Scholar

    [80] Fournier G. P. and Gogarten J. P. (2008). Evolution of acetoclastic methanogenesis in Methanosarcina via horizontal gene transfer from cellulolytic Clostridia. J. Bacteriol. 190:1124−1127. DOI:10.1128/JB.01382-07

    View in Article CrossRef Google Scholar

    [81] Rothman D. H., Fournier G. P., French K. L., et al. (2014). Methanogenic burst in the end-Permian carbon cycle. Proc. Natl. Acad. Sci. USA 111:5462−5467. DOI:10.1073/pnas.1318106111

    View in Article CrossRef Google Scholar

    [82] He C., Keren R., Whittaker M. L., et al. (2021). Genome-resolved metagenomics reveals site-specific diversity of episymbiotic CPR bacteria and DPANN archaea in groundwater ecosystems. Nat. Microbiol. 6:354−365. DOI:10.1038/s41564-020-00840-5

    View in Article CrossRef Google Scholar

    [83] Gong W., Hao B., Wei Z., et al. (2008). Structure of the alpha2epsilon2 Ni-dependent CO dehydrogenase component of the Methanosarcina barkeri acetyl-CoA decarbonylase/synthase complex. Proc. Natl. Acad. Sci. USA 105:9558−9563. DOI:10.1073/pnas.0800415105

    View in Article CrossRef Google Scholar

    [84] Schwank K., Bornemann T. L. V., Dombrowski N., et al. (2019). An archaeal symbiont-host association from the deep terrestrial subsurface. ISME J. 13:2135−2139. DOI:10.1038/s41396-019-0421-0

    View in Article CrossRef Google Scholar

    [85] Probst A. J. and Moissl-Eichinger C. (2015). "Altiarchaeales": Uncultivated archaea from the subsurface. Life (Basel) 5:1381−1395. DOI:10.3390/life5021381

    View in Article CrossRef Google Scholar

    [86] Weiss M. C., Preiner M., Xavier J. C., et al. (2018). The last universal common ancestor between ancient Earth chemistry and the onset of genetics. PLOS Genet. 14:e1007518. DOI:10.1371/journal.pgen.1007518

    View in Article CrossRef Google Scholar

    [87] Kurth J. M., Nobu M. K., Tamaki H., et al. (2021). Methanogenic archaea use a bacteria-like methyltransferase system to demethoxylate aromatic compounds. ISME J. 15:3549−3565. DOI:10.1038/s41396-021-01025-6

    View in Article CrossRef Google Scholar

    [88] Bueno de Mesquita C. P., Wu D. and Tringe S. G. (2023). Methyl-based methanogenesis: An ecological and genomic review. Microbiol. Mol. Biol. Rev. 87:e0002422. DOI:10.1128/mmbr.00024-22

    View in Article CrossRef Google Scholar

    [89] Dombrowski N., Teske A. P. and Baker B. J. (2018). Expansive microbial metabolic versatility and biodiversity in dynamic Guaymas Basin hydrothermal sediments. Nat. Commun. 9:4999. DOI:10.1038/s41467-018-07418-0

    View in Article CrossRef Google Scholar

    [90] Hoedt E. C., Parks D. H., Volmer J. G., et al. (2018). Culture- and metagenomics-enabled analyses of the Methanosphaera genus reveals their monophyletic origin and differentiation according to genome size. ISME J. 12:2942−2953. DOI:10.1038/s41396-018-0225-7

    View in Article CrossRef Google Scholar

    [91] Sprenger W. W., Hackstein J. H. and Keltjens J. T. (2007). The competitive success of Methanomicrococcus blatticola, a dominant methylotrophic methanogen in the cockroach hindgut, is supported by high substrate affinities and favorable thermodynamics. FEMS Microbiol. Ecol. 60:266−275. DOI:10.1111/j.1574-6941.2007.00287.x

    View in Article CrossRef Google Scholar

    [92] Thomas C. M., Taib N., Gribaldo S., et al. (2021). Comparative genomic analysis of Methanimicrococcus blatticola provides insights into host adaptation in archaea and the evolution of methanogenesis. ISME Commun. 1:47. DOI:10.1038/s43705-021-00050-y

    View in Article CrossRef Google Scholar

    [93] Preiner M., Xavier J. C., Sousa F. L., et al. (2018). Serpentinization: Connecting geochemistry, ancient metabolism and industrial hydrogenation. Life (Basel) 8:41. DOI:10.3390/life8040041

    View in Article CrossRef Google Scholar

    [94] Belthle K. S., Martin W. F. and Tuysuz H. (2024). Synergistic effects of silica-supported iron-cobalt catalysts for CO(2) reduction to prebiotic organics. ChemCatChem 16:e202301218. DOI:10.1002/cctc.202301218

    View in Article CrossRef Google Scholar

    [95] Preiner M., Igarashi K., Muchowska K. B., et al. (2020). A hydrogen-dependent geochemical analogue of primordial carbon and energy metabolism. Nat. Ecol. Evol. 4:534−542. DOI:10.1038/s41559-020-1125-6

    View in Article CrossRef Google Scholar

    [96] Zhou Z., Zhang C. J., Liu P. F., et al. (2022). Non-syntrophic methanogenic hydrocarbon degradation by an archaeal species. Nature 601:257−262. DOI:10.1038/s41586-021-04235-2

    View in Article CrossRef Google Scholar

    [97] Hahn C. J., Laso-Perez R., Vulcano F., et al. (2020). "Candidatus Ethanoperedens," a thermophilic genus of archaea mediating the anaerobic oxidation of ethane. mBio 11:e00600−20. DOI:10.1128/mBio.00600-20

    View in Article CrossRef Google Scholar

    [98] Kohtz A. J., Nupp S. and Hatzenpichler R. (2025). Cultivation of Methanonezhaarchaeia, the third class of methanogens within the phylum Thermoproteota. Sci. Adv. 11:eaea0936. DOI:10.1126/sciadv.aea0936

    View in Article CrossRef Google Scholar

    [99] Spang A., Stairs C. W., Dombrowski N., et al. (2019). Proposal of the reverse flow model for the origin of the eukaryotic cell based on comparative analyses of Asgard archaeal metabolism. Nat. Microbiol. 4:1138−1148. DOI:10.1038/s41564-019-0406-9

    View in Article CrossRef Google Scholar

    [100] Rao Y. Z., Li Y. X., Li Z. W., et al. (2026). Horizontal gene transfer and gene loss drove the divergent evolution of host dependency in Micrarchaeota. Natl. Sci. Rev. 13:nwaf542. DOI:10.1093/nsr/nwaf542

    View in Article CrossRef Google Scholar

    [101] Sakai H. D., Nur N., Kato S., et al. (2022). Insight into the symbiotic lifestyle of DPANN archaea revealed by cultivation and genome analyses. Proc. Natl. Acad. Sci. USA 119:e2115449119. DOI:10.1073/pnas.2115449119

    View in Article CrossRef Google Scholar

    [102] Reysenbach A. L. (2015). Thermoprotei class. nov. In Bergey's manual of systematics of archaea and bacteria, Whitman W. B. (ed) (Wiley), pp:1-1. DOI:10.1002/9781118960608.cbm00018

    View in Article Google Scholar

    [103] Hou J., Wang Y., Zhu P., et al. (2023). Taxonomic and carbon metabolic diversification of Bathyarchaeia during its coevolution history with early Earth surface environment. Sci. Adv. 9:eadf5069. DOI:10.1126/sciadv.adf5069

    View in Article CrossRef Google Scholar

    [104] Qi Y. L., Evans P. N., Li Y. X., et al. (2021). Comparative genomics reveals thermal adaptation and a high metabolic diversity in "Candidatus Bathyarchaeia". mSystems 6:e0025221. DOI:10.1128/mSystems.00252-21

    View in Article CrossRef Google Scholar

    [105] Kerou M., Eloy Alves R. J. and Schleper C. (2016). Nitrososphaeria. In Bergey's manual of systematics of archaea and bacteria, Whitman W. B. (ed) (Wiley), pp:1-8. DOI:10.1002/9781118960608.cbm00055.

    View in Article Google Scholar

    [106] Ren M. and Wang J. (2022). Phylogenetic divergence and adaptation of Nitrososphaeria across lake depths and freshwater ecosystems. ISME J. 16:1491−1501. DOI:10.1038/s41396-022-01199-7

    View in Article CrossRef Google Scholar

    [107] Ren M., Feng X., Huang Y., et al. (2019). Phylogenomics suggests oxygen availability as a driving force in Thaumarchaeota evolution. ISME J. 13:2150−2161. DOI:10.1038/s41396-019-0418-8

    View in Article CrossRef Google Scholar

    [108] Oren A., Ventosa A. and Kamekura M. (2017). Halobacteria. In Bergey's manual of systematics of archaea and bacteria, Whitman W. B. (ed) (Wiley), pp:1-5. DOI:10.1002/9781118960608.cbm00026.pub2.

    View in Article Google Scholar

    [109] Baker B. A., Gutierrez-Preciado A., Rodriguez Del Rio A., et al. (2024). Expanded phylogeny of extremely halophilic archaea shows multiple independent adaptations to hypersaline environments. Nat. Microbiol. 9:964−975. DOI:10.1038/s41564-024-01647-4

    View in Article CrossRef Google Scholar

    [110] Oren A. (2002). Diversity of halophilic microorganisms: Environments, phylogeny, physiology, and applications. J. Ind. Microbiol. Biotechnol. 28:56−63. DOI:10.1038/sj/jim/7000176

    View in Article CrossRef Google Scholar

    [111] Boussau B., Blanquart S., Necsulea A., et al. (2008). Parallel adaptations to high temperatures in the Archaean eon. Nature 456:942−945. DOI:10.1038/nature07393

    View in Article CrossRef Google Scholar

    [112] Jablonska J. and Tawfik D. S. (2021). The evolution of oxygen-utilizing enzymes suggests early biosphere oxygenation. Nat. Ecol. Evol. 5:442−448. DOI:10.1038/s41559-020-01386-9

    View in Article CrossRef Google Scholar

    [113] Lalonde S. V. and Konhauser K. O. (2015). Benthic perspective on Earth's oldest evidence for oxygenic photosynthesis. Proc. Natl. Acad. Sci. USA 112:995−1000. DOI:10.1073/pnas.1415718112

    View in Article CrossRef Google Scholar

    [114] Olson S. L., Kump L. R. and Kasting J. F. (2013). Quantifying the areal extent and dissolved oxygen concentrations of Archean oxygen oases. Chem. Geol. 362:35−43. DOI:10.1016/j.chemgeo.2013.08.012

    View in Article CrossRef Google Scholar

    [115] Forterre P. (2002). A hot story from comparative genomics: Reverse gyrase is the only hyperthermophile-specific protein. Trends Genet. 18:236−237. DOI:10.1016/s0168-9525(02)02650-1

    View in Article CrossRef Google Scholar

    [116] Forterre P., Mirambeau G., Jaxel C., et al. (1985). High positive supercoiling in vitro catalyzed by an ATP and polyethylene glycol-stimulated topoisomerase from Sulfolobus acidocaldarius. EMBO J. 4:2123−2128. DOI:10.1002/j.1460-2075.1985.tb03902.x

    View in Article CrossRef Google Scholar

    [117] Kikuchi A. and Asai K. (1984). Reverse gyrase--a topoisomerase which introduces positive superhelical turns into DNA. Nature 309:677-681. DOI:10.1038/309677a0.

    View in Article Google Scholar

    [118] Brochier-Armanet C. and Forterre P. (2007). Widespread distribution of archaeal reverse gyrase in thermophilic bacteria suggests a complex history of vertical inheritance and lateral gene transfers. Archaea 2:83−93. DOI:10.1155/2006/582916

    View in Article CrossRef Google Scholar

    [119] Catchpole R. J. and Forterre P. (2019). The evolution of reverse gyrase suggests a nonhyperthermophilic last universal common ancestor. Mol. Biol. Evol. 36:2737−2747. DOI:10.1093/molbev/msz180

    View in Article CrossRef Google Scholar

    [120] Jablonska J. and Tawfik D. S. (2019). The number and type of oxygen-utilizing enzymes indicates aerobic vs. anaerobic phenotype. Free Radic. Biol. Med. 140:84−92. DOI:10.1016/j.freeradbiomed.2019.03.031

    View in Article CrossRef Google Scholar

    [121] Sibbald S. J., Eme L., Archibald J. M., et al. (2020). Lateral gene transfer mechanisms and pan-genomes in eukaryotes. Trends Parasitol. 36:927−941. DOI:10.1016/j.pt.2020.07.014

    View in Article CrossRef Google Scholar

    [122] Soucy S. M., Huang J. and Gogarten J. P. (2015). Horizontal gene transfer: Building the web of life. Nat. Rev. Genet. 16:472−482. DOI:10.1038/nrg3962

    View in Article CrossRef Google Scholar

    [123] Stairs C. W., Eme L., Munoz-Gomez S. A., et al. (2018). Microbial eukaryotes have adapted to hypoxia by horizontal acquisitions of a gene involved in rhodoquinone biosynthesis. eLife 7:e34292. DOI:10.7554/eLife.34292

    View in Article CrossRef Google Scholar

    [124] Zhang J. and Yang J. R. (2015). Determinants of the rate of protein sequence evolution. Nat. Rev. Genet. 16:409−420. DOI:10.1038/nrg3950

    View in Article CrossRef Google Scholar

    [125] Yang J. R., Liao B. Y., Zhuang S. M., et al. (2012). Protein misinteraction avoidance causes highly expressed proteins to evolve slowly. Proc. Natl. Acad. Sci. USA 109:E831−840. DOI:10.1073/pnas.1117408109

    View in Article CrossRef Google Scholar

    [126] Echave J., Spielman S. J. and Wilke C. O. (2016). Causes of evolutionary rate variation among protein sites. Nat. Rev. Genet. 17:109−121. DOI:10.1038/nrg.2015.18

    View in Article CrossRef Google Scholar

    [127] Scanlan D. J., Ostrowski M., Mazard S., et al. (2009). Ecological genomics of marine picocyanobacteria. Microbiol. Mol. Biol. Rev. 73:249−299. DOI:10.1128/MMBR.00035-08

    View in Article CrossRef Google Scholar

    [128] Becker E. A., Seitzer P. M., Tritt A., et al. (2014). Phylogenetically driven sequencing of extremely halophilic archaea reveals strategies for static and dynamic osmo-response. PLOS Genet. 10:e1004784. DOI:10.1371/journal.pgen.1004784

    View in Article CrossRef Google Scholar

    [129] Ionescu D., Zoccarato L., Cabello-Yeves P. J., et al. (2023). Extreme fluctuations in ambient salinity select for bacteria with a hybrid "salt-in"/"salt-out" osmoregulation strategy. Front. Microbiomes 2:1329925. DOI:10.3389/frmbi.2023.1329925

    View in Article CrossRef Google Scholar

    [130] Ghai R., Pasic L., Fernandez A. B., et al. (2011). New abundant microbial groups in aquatic hypersaline environments. Sci. Rep. 1:135. DOI:10.1038/srep00135

    View in Article CrossRef Google Scholar

    [131] Narasingarao P., Podell S., Ugalde J. A., et al. (2012). De novo metagenomic assembly reveals abundant novel major lineage of archaea in hypersaline microbial communities. ISME J. 6:81−93. DOI:10.1038/ismej.2011.78

    View in Article CrossRef Google Scholar

    [132] Zhao D., Zhang S., Kumar S., et al. (2022). Comparative genomic insights into the evolution of Halobacteria-associated "Candidatus Nanohaloarchaeota". mSystems 7:e0066922. DOI:10.1128/msystems.00669-22

    View in Article CrossRef Google Scholar

    [133] Sorokin D. Y., Makarova K. S., Abbas B., et al. (2017). Discovery of extremely halophilic, methyl-reducing euryarchaea provides insights into the evolutionary origin of methanogenesis. Nat. Microbiol. 2:17081. DOI:10.1038/nmicrobiol.2017.81

    View in Article CrossRef Google Scholar

    [134] Zhou H., Zhao D., Zhang S., et al. (2022). Metagenomic insights into the environmental adaptation and metabolism of Candidatus Haloplasmatales, one archaeal order thriving in saline lakes. Environ. Microbiol. 24:2239−2258. DOI:10.1111/1462-2920.15899

    View in Article CrossRef Google Scholar

    [135] Michoud G., Ngugi D. K., Barozzi A., et al. (2021). Fine-scale metabolic discontinuity in a stratified prokaryote microbiome of a Red Sea deep halocline. ISME J. 15:2351−2365. DOI:10.1038/s41396-021-00931-z

    View in Article CrossRef Google Scholar

    [136] Roesser M. and Muller V. (2001). Osmoadaptation in bacteria and archaea: Common principles and differences. Environ. Microbiol. 3:743−754. DOI:10.1046/j.1462-2920.2001.00252.x

    View in Article CrossRef Google Scholar

    [137] Protasov E., Nonoh J. O., Kastle Silva J. M., et al. (2023). Diversity and taxonomic revision of methanogens and other archaea in the intestinal tract of terrestrial arthropods. Front. Microbiol. 14:1281628. DOI:10.3389/fmicb.2023.1281628

    View in Article CrossRef Google Scholar

    [138] Mazurie A., Bonchev D., Schwikowski B., et al. (2010). Evolution of metabolic network organization. BMC Syst. Biol. 4:59. DOI:10.1186/1752-0509-4-59

    View in Article CrossRef Google Scholar

    [139] Raymond J. and Segre D. (2006). The effect of oxygen on biochemical networks and the evolution of complex life. Science 311:1764−1767. DOI:10.1126/science.1118439

    View in Article CrossRef Google Scholar

    [140] Takemoto K. and Yoshitake I. (2013). Limited influence of oxygen on the evolution of chemical diversity in metabolic networks. Metabolites 3:979−992. DOI:10.3390/metabo3040979

    View in Article CrossRef Google Scholar

    [141] Martemucci G., Costagliola C., Mariano M., et al. (2022). Free radical properties, source and targets, antioxidant consumption and health. Oxygen 2:48−78. DOI:10.3390/oxygen2020006

    View in Article CrossRef Google Scholar

    [142] Davies M. J. (2005). The oxidative environment and protein damage. Biochim. Biophys. Acta 1703:93−109. DOI:10.1016/j.bbapap.2004.08.007

    View in Article CrossRef Google Scholar

    [143] Carlton J. D., Langwig M. V., Gong X., et al. (2023). Expansion of Armatimonadota through marine sediment sequencing describes two classes with unique ecological roles. ISME Commun. 3:64. DOI:10.1038/s43705-023-00269-x

    View in Article CrossRef Google Scholar

    [144] Liang C., Yang B., Cao Y. C., et al. (2024). Salinization mechanism of lakes and controls on organic matter enrichment: From present to deep-time records. Earth-Sci. Rev. 251:104720. DOI:10.1016/j.earscirev.2024.104720

    View in Article CrossRef Google Scholar

    [145] Swan B. K., Tupper B., Sczyrba A., et al. (2013). Prevalent genome streamlining and latitudinal divergence of planktonic bacteria in the surface ocean. Proc. Natl. Acad. Sci. USA 110:11463−11468. DOI:10.1073/pnas.1304246110

    View in Article CrossRef Google Scholar

    [146] Giovannoni S. J., Tripp H. J., Givan S., et al. (2005). Genome streamlining in a cosmopolitan oceanic bacterium. Science 309:1242−1245. DOI:10.1126/science.1114057

    View in Article CrossRef Google Scholar

    [147] Brixi G., Durrant M. G., Ku J., et al. (2025). Genome modeling and design across all domains of life with Evo 2. bioRxiv:2025.2002.2018.638918. DOI:10.1101/2025.02.18.638918

    View in Article Google Scholar

    [148] Hamamsy T., Morton J. T., Blackwell R., et al. (2024). Protein remote homology detection and structural alignment using deep learning. Nat. Biotechnol. 42:975−985. DOI:10.1038/s41587-023-01917-2

    View in Article CrossRef Google Scholar

    [149] Varadi M., Bertoni D., Magana P., et al. (2024). AlphaFold Protein Structure Database in 2024: Providing structure coverage for over 214 million protein sequences. Nucleic Acids Res. 52:D368−D375. DOI:10.1093/nar/gkad1011

    View in Article CrossRef Google Scholar

    [150] Jumper J., Evans R., Pritzel A., et al. (2021). Highly accurate protein structure prediction with AlphaFold. Nature 596:583−589. DOI:10.1038/s41586-021-03819-2

    View in Article CrossRef Google Scholar

    [151] van Kempen M., Kim S. S., Tumescheit C., et al. (2024). Fast and accurate protein structure search with Foldseek. Nat. Biotechnol. 42:243−246. DOI:10.1038/s41587-023-01773-0

    View in Article CrossRef Google Scholar

    [152] Ramoneda J., Hoffert M., Stallard-Olivera E., et al. (2024). Leveraging genomic information to predict environmental preferences of bacteria. ISME J. 18:wrae195. DOI:10.1093/ismejo/wrae195

    View in Article CrossRef Google Scholar

  • Cite this article:

    Lv Z., Wang F. and Wang Y. (2026). Radiating pattern revealed by a deep learning model traces the evolutionary dynamics of the Archaea domain. The Innovation Life 4:100235. https://doi.org/10.59717/j.xinn-life.2026.100235
    Lv Z., Wang F. and Wang Y. (2026). Radiating pattern revealed by a deep learning model traces the evolutionary dynamics of the Archaea domain. The Innovation Life 4:100235. https://doi.org/10.59717/j.xinn-life.2026.100235

Welcome!

To request copyright permission to republish or share portions of our works, please visit Copyright Clearance Center's (CCC) Marketplace website at marketplace.copyright.com.

Figures(7)    

Supplementary Information

Share

  • Share the QR code with wechat scanning code to friends and circle of friends.

Article Metrics

Article views(524) PDF downloads(128)

Relative Articles

Cited by

Catalog

    /

    DownLoad:  Full-Size Img  PowerPoint