The DOI matches its Crossref record; 75 of the 75 references it cites were found in a registry or an index.
Horizontal Transfer, Not Duplication, Drives the Expansion of Protein Families in Prokaryotes
Open accessAbstract
Gene duplication followed by neo- or sub-functionalization deeply impacts the evolution of protein families and is regarded as the main source of adaptive functional novelty in eukaryotes. While there is ample evidence of adaptive gene duplication in prokaryotes, it is not clear whether duplication outweighs the contribution of horizontal gene transfer in the expansion of protein families. We analyzed closely related prokaryote strains or species with small genomes (Helicobacter, Neisseria, Streptococcus, Sulfolobus), average-sized genomes (Bacillus, Enterobacteriaceae), and large genomes (Pseudomonas, Bradyrhizobiaceae) to untangle the effects of duplication and horizontal transfer. After removing the effects of transposable elements and phages, we show that the vast majority of expansions of protein families are due to transfer, even among large genomes. Transferred genes--xenologs--persist longer in prokaryotic lineages possibly due to a higher/longer adaptive role. On the other hand, duplicated genes--paralogs--are expressed more, and, when persistent, they evolve slower. This suggests that gene transfer and gene duplication have very different roles in shaping the evolution of biological systems: transfer allows the acquisition of new functions and duplication leads to higher gene dosage. Accordingly, we show that paralogs share most protein-protein interactions and genetic regulators, whereas xenologs share very few of them. Prokaryotes invented most of life's biochemical diversity. Therefore, the study of the evolution of biology systems should explicitly account for the predominant role of horizontal gene transfer in the diversification of protein families.
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“Recent theoretical, comparative genomic and experimental research on microbial evolution clearly indicates that HGT is the principal factor in microbial adaptation and innovation (46, 65, 66, 80).”
From Origin and Evolution of the Universal Genetic Code (2017) · cites this paper as [80]
Experimental — accuracy not yet measuredIn the citing paper
“Given that HGT, even if limited by both physical and selective barriers, remained a key factor of microbial evolution [36,37,38,39,40], and apparently, a condition for long term survival of microbial populations [41,42]”
From Frozen Accident Pushing 50: Stereochemistry, Expansion, and Chance in the Evolution of the Genetic Code (2017) · cites this paper as [40]
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Cites
Basic local alignment search tool
Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990) · Journal of Molecular Biology · doi:10.1006/jmbi.1990.9999 · Cited by 98,669 · cited 7×
“OrthoMCL defines putative orthologous relationships between a pair of genomes as BLASTP reciprocal better/best hits.”
MethodInfluentialMUSCLE: multiple sequence alignment with high accuracy and high throughput
Edgar, R. C. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh340 · Cited by 44,662 · cited 1×
“Protein alignments were generated using MUSCLE [73] and then back-translated to DNA.”
MethodOrthoMCL: Identification of Ortholog Groups for Eukaryotic Genomes
Li, L., Stoeckert, C. J., & Roos, D. S. (2003) · Genome Research · doi:10.1101/gr.1224503 · Cited by 5,707 · cited 2×
“OrthoMCL defines putative orthologous relationships between a pair of genomes as BLASTP reciprocal better/best hits.”
MethodPAML: a program package for phylogenetic analysis by maximum likelihood
Yang, Z. (1997) · Computer applications in the biosciences · doi:10.1093/bioinformatics/13.5.555 · Cited by 5,377 · cited 1×
“Non-synonymous (dN) and synonymous (dS) substitution rates in paralogs (blue; dashed linear fit) and xenologs (red; solid linear fit) in all clades computed using Codeml from PAML [76] (model = 1, fix_omega = 0).”
MethodSharp, P. M., & Li, W.-H. (1987) · Nucleic Acids Research · doi:10.1093/nar/15.3.1281 · Cited by 3,992 · cited 1×
“We first tested if the two classes of protein families have different gene expression levels using the codon adaptation index (CAI; [44]).”
MethodLateral gene transfer and the nature of bacterial innovation
Ochman, H., Lawrence, J. G., & Groisman, E. A. (2000) · Nature · doi:10.1038/35012500 · Cited by 3,816 · cited 1×
“Horizontal gene transfer (HGT) results in the acquisition of radically new genetic information, liberating genomic evolutionary processes from tinkering exclusively with pre-existing genes”
BackgroundAn efficient algorithm for large-scale detection of protein families
Enright, A. J. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.7.1575 · Cited by 3,536 · cited 4×
“OrthoMCL defines putative orthologous relationships between a pair of genomes as BLASTP reciprocal better/best hits.”
MethodInfluentialISfinder: the reference centre for bacterial insertion sequences
Siguier, P. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkj014 · Cited by 2,767 · cited 2×
“coli our databank contained all IS present in IS Finder [67].”
BackgroundTREE-PUZZLE: maximum likelihood phylogenetic analysis using quartets and parallel computing
Schmidt, H. A., Strimmer, K., Vingron, M., & von Haeseler, A. (2002) · Bioinformatics · doi:10.1093/bioinformatics/18.3.502 · Cited by 2,512 · cited 1×
“Tree-Puzzle [74] was used to generate the matrix of distances by maximum likelihood with the HKY+C model and exact parameter estimates.”
MethodBIONJ: an improved version of the NJ algorithm based on a simple model of sequence data
Gascuel, O. (1997) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a025808 · Cited by 1,850 · cited 2×
“The trees were then computed from these distance matrices using BIONJ [75].”
MethodInfluential
Flagged first, then by citations
Research works printed but not linked: 1
- G Vernikos, 2007, Genetic flux over time in the Salmonella lineage., Genome Biology, 8, R100, 10.1186/gb-2007-8-6-r100 · DOI
Cited by
Sorted by citations
Items 401–500 of 514
Pereira, I. S., da Cunha, M., Leal, I. P., Luís, M. P., Gonçalves, P. M., Gonçalves, C., & Mota, L. J. (2024) · Medical Microbiology and Immunology · doi:10.1007/s00430-024-00798-9 · Cited by 1
“Scale bars, 5 μm 1 3 Gene duplication is a major mechanism in the evolu - tion of eukaryotes [56], but it is thought to be less common in prokaryotes, where horizontal gene transfer has a more important role in driving protein diversification [ 57–59].”
BackgroundEc W: A Novel Narrow-Spectrum Class IIb Microcin from Escherichia coli
Bhattarai, S. K., Bucci, V., & Mortzfeld, B. M. (2025) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-025-10549-8 · Cited by 2
“Maintaining two homologous copies of a gene cluster acquired through gene cluster duplication or horizontal gene transfer can have numerous advantages for an organism, including increased product output, here mature class IIb microcin production, or expansion of protein families [33, 34].”
Zúñiga-Chaves, I., Flores-Dı́az, M., & Alape‐Girón, A. (2016) · Toxinology · doi:10.1007/978-94-007-6725-6_33-1 · Cited by 1
Avni, E., & Snir, S. (2018) · Journal of Computational Biology · doi:10.1089/cmb.2018.0129 · Cited by 1
“…events, duplications and losses in gene families, incomplete lineage sorting (ILS), and horizontal genetic transfer (HGT) (Maddison, 1997; Doolittle, 1999; Ochman et al., 2000), the latter often regarded as the most prominent one, especially in the prokaryotic world (Treangen and Rocha, 2011).”
González-Siso, M.-I. (2019) · MDPI eBooks · doi:10.3390/books978-3-03897-817-6 · Cited by 1
Genetic Variation in Holobionts
ROSENBERG, E. B. (2021) · The microbiomes of humans, animals, plants, and the environment · doi:10.1007/978-3-030-65317-0_8 · Cited by 1
Edward, K., Ibekwe, V. I., Amadi, E. S., & Umeh, S. I. (2021) · Bacterial Empire · doi:10.36547/be.262 · Cited by 1
How should we think about evolution in the age of genomics?
Shapiro, J. A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-90752-1.00010-9 · Cited by 1
1. All creatures great and small
Seshasayee, A. S. N. (2025) · Open Book Publishers · doi:10.11647/obp.0446.01 · Cited by 1
Rangel, L. T. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.95.2017.tde-06122017-114559 · Cited by 1
Fast Methods for Solving the Cluster Containment Problem for Phylogenetic NetworksPreprint
Gunawan, A. D. M., Lu, B., & Zhang, L. (2018) · arXiv (Cornell University) · doi:10.48550/arxiv.1801.04498 · Cited by 1
“Genome evolution is shaped not only by random mutations over generations but also horizontal genetic transfers between individuals of different species [3], [5], [25].”
BackgroundUsefulness of a Concept Called Autonomous SelectionPreprint
Solon, I. S. (2019) · Preprints.org · doi:10.20944/preprints201907.0285.v1
Rabelo, D. B., Nkomo, N. P., Shyntum, D. Y., & Moleleki, L. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/776476 · Cited by 1
“For instance, it has been estimated that in representatives of both 368 Escherichia and Salmonella genera, more than 98% of protein family expansions arise from HGT (37).”
BackgroundA non-adaptive demographic mechanism for genome expansion in StreptomycesPreprint
Choudoir, M. J., Järvenpää, M. J., Marttinen, P., & Buckley, D. H. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.09.426074 · Cited by 2
Illuminating the first bacteria
Katz, L. A. (2021) · Science · doi:10.1126/science.abh2814 · Cited by 1
Fiamenghi, M. B., Prodonoff, J. S., Borelli, G., Carazzolle, M. F., Pereira, G. A. G., & José, J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.08.531619 · Cited by 1
“Gene duplication is an important phenomenon in eukaryotes as a source of novelty and adaptation [70], 288 however in prokaryotes it is rarely seen, as arisen duplications are costly to maintain [1].”
BackgroundFortuitous events in the evolution of Light-dependent Protochlorophyllide OxidoreductasePreprint
Vedalankar, P., & Tripathy, B. C. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.16.537069 · Cited by 1
“Pseudogenes are non-functional but still beneficial in evolution as it helps the organism to counter or survive the changed environmental conditions (Treangen and Rocha, 2011).”
BackgroundGene protein sequence evolution can predict the rapid divergence of ovariole numbers in DrosophilaPreprint
Whittle, C. A., & Extavour, C. G. M. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.03.556080 · Cited by 1
Cyanobacterial genome evolution subsequent to domestication by a plant (Azolla)
Larsson, J. (2011) · DiVA (Stockholm University) · Cited by 1
The path of the blind watchmaker: a model of evolution
Patterson, D. A., & Poggio, A. A. (2011)
Naushad, S. (2015) · MacSphere (McMaster University) · doi:10.71548/23167
M. Pilar Francino (ed): Horizontal gene transfer in microorganisms
Knapp, C. W. (2013) · Ecotoxicology · doi:10.1007/s10646-013-1119-0
Influence of Feed Supplements on the Porcine Intestinal Escherichia coli Microbiota
Bednorz, C. (2015) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-6968
Influence of homology and node age on the growth of protein-protein interaction networks
Bottinelli, A., Bassetti, B., Lagomarsino, M. C., & Gherardi, M. (2012) · Physical Review E · doi:10.1103/physreve.86.041919
López, C. E., & Carrascal, L. (2011)
Computational Problems in Modeling Evolution and Inferring Gene Families.
Khan, M. A. (2016) · KTH Publication Database DiVA (KTH Royal Institute of Technology)
Structural and functional advances in the evolutionary studies of cells and viruses
Nasir, A. (2015) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign)
Horizontal Gene Transfer in Microbial Evolution
Gogarten, J. P., & Papke, R. T. (2018) · CRC Press eBooks · doi:10.1201/b22230-36
The ecology and evolution of horizontal gene transfer in bacteria
Stevenson, C. (2019) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)
Kumar, P. M., & Manoharan, P. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/505230
Slightly beneficial genes are retained by evolving Horizontal Gene Transfer despite selfish elementsPreprint
van Dijk, B., Hogeweg, P., Doekes, H. M., & Takeuchi, N. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.13.947077
Dynamics of Phytoplasma Effector Interactions with Plant TCP Transcription Factor (sub)classes
Capdevielle, S. (2019) · UEA Digital Repository (University of East Anglia)
KOMB: Graph-Based Characterization of Genome Dynamics in Microbial CommunitiesPreprint
Balaji, A., Sapoval, N., Seto, C., Elworth, R. A. L., Nute, M., Savidge, T., Segarra, S., & Treangen, T. J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.21.109587
“Communities in metagenomes consist of individual organisms whose genomes are dynamic because of processes such as # Contact: treangen@rice.edu † These authors share senior authorship 1 gene duplication, gene loss/gain, horizontal gene transfer, and gene rearrangements [4, 5, 6, 7].”
BackgroundSelf-citationProbabilistic Models for Species Tree Inference and Orthology Analysis
Ullah, I. (2015) · KTH Publication Database DiVA (KTH Royal Institute of Technology)
(2020) · Wiley eBooks · doi:10.1002/9781119309697.ref
A graph-based approach for the visualisation and analysis of bacterial pangenomesPreprint
Harling-Lee, J. D., Gorzynski, J., Yebra, G., Angus, T., Fitzgerald, J. R., & Freeman, T. C. (2022) · Research Square · doi:10.21203/rs.3.rs-1406006/v1
СОВРЕМЕННЫЕ ВЗГЛЯДЫ НА ЭВОЛЮЦИЮ: О РОЛИ ГОРИЗОНТАЛЬНОГО ПЕРЕНОСА ГЕНОВ
(2013) · Izvestiya VUZ Applied Nonlinear Dynamics · doi:10.18500/0869-6632-2013-21-4-34-51
“Из результатов исследований последних лет по теме молекулярных механизмов эволюции обращает на себя вни-мание работа [40].”
(2011) · Nature · doi:10.1038/471269f
(2020) · PeerJ · doi:10.7287/peerj.10312v0.1/reviews/2
“According to previous studies ( Treangen & Rocha, 2011 ; Mohanta et al., 2019 ), it is likely that the deficiency of these tRNAs is compensated for by the transfer of corresponding tRNAs from the nucleus or mitochondria.”
Rodrigues, T. C. V., Jaiswal, A. K., Aburjaile, F. F., Almeida, C. A., Carvalho, R. D. D. O., de Paula, J. A., Santos, R. P. S., Dominici, F. V., Felice, A. G., Marques, P. H., et al. (2023) · Springer eBooks · doi:10.1007/978-981-19-9342-8_3
Promoter capture drives the emergence of proto-genes in Escherichia coliPreprint
uz‐Zaman, M. H., D’Alton, S., Barrick, J. E., & Ochman, H. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.15.567300
Functional Diversification of Gene Duplicates under the Constraint of Protein StructurePreprint
Guo, K., Yang, Y., You, T., & Zhu, K. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.06.583810
“Although gene family expansion in prokaryotes is often considered to be driven by horizontal gene transfer 19 , our study ruled out the possibility of the four agarases.”
BackgroundShchyogolev, S. Y., Dykman, L. A., Sokolov, A. O., Соколов, О. И., & Matora, L. Y. (2024) · Archives of Microbiology · doi:10.1007/s00203-024-03896-7
“The numbers near the nodes are branch significance estimates made with REQ (2023) Micrococcaceae members, of “noncongruent” species with a small (almost zero) MF, may be associated with HGT (Medlar et al. 2018; Treangen and Rocha 2011).”
Manzano-Morales, S., Liu, Y., González-Bodí, S., Huerta‐Cepas, J., & Iranzo, J. (2023) · Figshare · doi:10.6084/m9.figshare.24465142
Liu, Y., Brinkhoff, T., Berger, M., Poehlein, A., Voget, S., Paoli, L., Sunagawa, S., Amann, R., & Simon, M. (2023) · Figshare · doi:10.6084/m9.figshare.24634512
Investigating the nature of prokaryotic genomic island locations within a genome
Aldaihani, R., & Heath, L. S. (2024) · PLoS ONE · doi:10.1371/journal.pone.0301172
Concepts and definitions in microbiology and nanotechnology in plant sciences
Kumar, N., Vishwakarma, K., & Lateef, A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-18822-0.00001-3
A Review of the Archaea First Hypothesis for the Origin of Life
Gordon, R. (2024) · Wiley eBooks · doi:10.1002/9781119901228.ch9
Pangenome biology and evolution in harmful algal-bloom-forming pelagophyte algaePreprint
Sibbald, S. J., Lawton, M., Maclean, C., Roger, A. J., & Archibald, J. M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.30.620910
Computational Methods for Disentangling Host-Pathogen Interaction Landscapes
Abdullah‐Zawawi, M., Rozano, L., Jalal, M. I. A., Mokhtar, M. F. M., Ang, M. Y., & Jamal, R. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95502-7.00257-8
Wang, X., Xu, P., Lu, M., Li, X., Luo, M., Yu, S., Zhang, C., Li, H., & Zheng, C. (2024) · ACS ES&T Water · doi:10.1021/acsestwater.4c00790
Phylogenetic Placement of Aligned Genomes and Metagenomes With Non-Tree-Like Evolutionary Histories
Alamin, M., & Liu, K. J. (2025) · IEEE Transactions on Computational Biology and Bioinformatics · doi:10.1109/tcbbio.2024.3519311
Seshasayee, A. S. N. (2025) · Open Book Publishers · doi:10.11647/obp.0446.00
4. The ebb and flow of bacterial genomes
Seshasayee, A. S. N. (2025) · Open Book Publishers · doi:10.11647/obp.0446.04
Seshasayee, A. S. N. (2025) · Open Book Publishers · doi:10.11647/obp.0446.03
5. Reading and organising the genome
Seshasayee, A. S. N. (2025) · Open Book Publishers · doi:10.11647/obp.0446.05
2. The molecules of bacteria and of life
Seshasayee, A. S. N. (2025) · Open Book Publishers · doi:10.11647/obp.0446.02
Untying Rates of Gene Gain and Loss Leads to a New Phylogenetic Approach
Dvir, Y., & Snir, S. (2025) · Lecture notes in computer science · doi:10.1007/978-3-031-90252-9_51
Host range and ARG dissemination are shaped by distinct survival strategies of conjugative plasmidsPreprint
Ono, R., Konno, N., Nishimura, Y., & Furusawa, C. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.22.655438
“Horizontal gene transfer (HGT) plays a pivotal role in the remarkable adaptability and rapid evolution of prokaryotes (1, 2).”
Evolution of Bacterial Genome Size, Structure and Organization
uz‐Zaman, M. H., & Ochman, H. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-15750-9.00157-9
Polyacrylamide bead split-pool method for microbial community analysisPreprint
Smolander, N., Talvitie, J., & Tamminen, M. V. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.26.661670
Parameterized Algorithms for the Tree Containment Problem on Multifurcating Phylogenetic Network
Shi, F., Lin, Z., Zeng, X., & Liu, J. (2025) · Lecture notes in computer science · doi:10.1007/978-981-95-0695-8_32
Metabolic ecology, microbial community structure, and gene-centric metagenomicsPreprint
Arroyo, J. I., Dı́ez, B., & Marquet, P. A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.05.668563
Zhou, Q., Li, N., Jiao, L., & Sun, D. (2025) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2025.152668
Koech, N., Muoma, J. V. O., Banerjee, A., OKOTH, P. K., & Wekesa, C. (2025) · Archives of Microbiology · doi:10.1007/s00203-025-04535-5
“Anchors were classified as solo (operon size = 1) or polycistronic (operon size ≥ 2) genes in accessory genomes (Treangen and Rocha 2011; Lercher and Pál 2008).”
Lécuyer, E. (2012) · OpenGrey (Institut de l'Information Scientifique et Technique)
Manzano-Morales, S., Liu, Y., González-Bodí, S., Huerta‐Cepas, J., & Iranzo, J. (2024) · Figshare · doi:10.6084/m9.figshare.24465318
Manzano-Morales, S., Liu, Y., González-Bodí, S., Huerta‐Cepas, J., & Iranzo, J. (2024) · Figshare · doi:10.6084/m9.figshare.26634015
Manzano-Morales, S., Liu, Y., González-Bodí, S., Huerta‐Cepas, J., & Iranzo, J. (2024) · Figshare · doi:10.6084/m9.figshare.26634021
Manzano-Morales, S., Liu, Y., González-Bodí, S., Huerta‐Cepas, J., & Iranzo, J. (2024) · Figshare · doi:10.6084/m9.figshare.26634018
Harling-Lee, J. D., Gorzynski, J., Yebra, G., Angus, T., Fitzgerald, J. R., & Freeman, T. C. (2022) · Figshare · doi:10.6084/m9.figshare.21303499
Additional file 1 of Multiple genome alignment in the telomere-to-telomere assembly era
Kille, B., Balaji, A., Sedlazeck, F. J., Nute, M., & Treangen, T. J. (2022) · Figshare · doi:10.6084/m9.figshare.20727632
Self-citationSun, Y., Wang, M., Cao, L., Seim, I., Zhou, L., Chen, J., Wang, H., Zhong, Z., Chen, H., Fu, L., et al. (2024) · Figshare · doi:10.6084/m9.figshare.24580498
Additional file 1 of Assessment of assumptions underlying models of prokaryotic pangenome evolution
Sela, I., Wolf, Y. I., & Koonin, E. V. (2021) · Figshare · doi:10.6084/m9.figshare.13844032
Sun, Y., Wang, M., Cao, L., Seim, I., Zhou, L., Chen, J., Wang, H., Zhong, Z., Chen, H., Fu, L., et al. (2023) · Figshare · doi:10.6084/m9.figshare.24580374
Forni, G., Martelossi, J., Morel, B., Pistone, D., Bandi, C., & Montagna, M. (2026) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2026.108532 · Cited by 1
Insights into Biocides and Bacterial Resistance
Yeptho, H. A., Ghodasara, S. N., Javia, B. B., & Barad, D. B. (2025) · Indian Journal of Comparative Microbiology Immunology and Infectious Diseases · doi:10.5958/0974-0147.2025.00004.7
Sapoval, N., Treangen, T. J., & Nakhleh, L. K. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.10.710879
“Given the prevalence of HGT in bacteria and its role as a driver of bacterial adaptation and response [Treangen and Rocha, 2011, Brito, 2021, Arnold et al., 2022, Bhaya et al., 2025], the insensitivity of diversity measures to this factor is problematic.”
Self-citationModeling Metabolic Networks and their Environment Interaction
Budinich, M. (2017) · theses.fr (ABES) · doi:10.70675/97895b25zdfe7z4432z8766z801bf0b81cd6
Oñate, F. P. (2018) · doi:10.70675/88df14a5z15aaz45aezac37z2a096f79eef8
“Le fait que les gènes cloud soient les plus nombreux suggère que les espèces acquièrent en permanence de nouveaux gènes par transfert horizontal et dans une moindre mesure par duplication [31] mais que seule une petite proportion d’entre eux apportent un avantage sélectif suffisant pour être fixés dans la population.”
BackgroundComparative genomic analysis in taxonomy : classification and reclassification of bacterial species
Zgheib, R. (2021) · theses.fr (ABES) · doi:10.70675/43888f17z8ddfz4c18za819zc86b2288b819
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Perrin, A. (2022) · theses.fr (ABES) · doi:10.70675/a061aa00z774bz40c5zb870zba9af4cac64b
Metadata
- Authors
- Treangen, T. J., & Rocha, E. P. C.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Corresponding author
- Treangen, Todd J.
- Venue
- PLoS Genetics
- Publisher
- Public Library of Science (PLoS)
- Published
- 2011-01-27
- Volume
- 7
- Issue
- 1
- Pages
- e1001284
- ISSN
- 1553-7390 (ISSN-L)
- 1553-7404
- PMC
- PMC3029252
- OpenAlex
- W2022927779
- Cited by
- 509
- References
- 75
- Citations by year
- 2026: 18 · 2025: 34 · 2024: 36 · 2023: 26 · 2022: 29 · 2021: 32 · 2020: 52 · 2019: 27 · 2018: 33 · 2017: 31 · 2016: 38 · 2015: 29 · 2014: 34 · 2013: 33 · 2012: 28
- FWCI
- 15.99
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS Genetics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, other-oa)
- PubMed (publishedVersion)
- HAL (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- Centre National de la Recherche Scientifique
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Keywords
- horizontal gene transfer, gene duplication, protein family expansion, prokaryotes, paralogs, functional novelty, gene dosage, protein-protein interaction, regulatory genes, genome size, Helicobacter, Neisseria, Streptococcus, Sulfolobus, Bacillus, Enterobacteriaceae, Pseudomonas, Bradyrhizobiaceae
- MeSH terms
- Bacillus, Bacteria, Enterobacteriaceae, Multigene Family, Neisseria, Phylogeny, Pseudomonas, Streptococcus, Genome, Bacterial, Sulfolobus, Helicobacter, Evolution, Molecular, Computational Biology, Gene Duplication, Gene Transfer, Horizontal, Bradyrhizobiaceae
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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