A diverse repertoire of anti-defense systems is encoded in the leading region of plasmids
暂无分享,去创建一个
[1] Christian Lesterlin,et al. Real-time visualisation of the intracellular dynamics of conjugative plasmid transfer , 2023, Nature Communications.
[2] Gabriele H. Marchler,et al. The conserved domain database in 2023 , 2022, Nucleic Acids Res..
[3] Charles Coluzzi,et al. Origins of transfer establish networks of functional dependencies for plasmid transfer by conjugation , 2022, Nucleic acids research.
[4] N. Li,et al. Functional comparison of anti-restriction and anti-methylation activities of ArdA, KlcA, and KlcAHS from Klebsiella pneumoniae , 2022, Frontiers in Cellular and Infection Microbiology.
[5] K. Palmer,et al. Efficacy of plasmid-encoded CRISPR-Cas antimicrobial is affected by competitive factors found in wild Enterococcus faecalis isolates , 2022, bioRxiv.
[6] E. Rocha,et al. Microbial defenses against mobile genetic elements and viruses: Who defends whom from what? , 2022, PLoS biology.
[7] David A. Baltrus,et al. Introduction: the secret lives of microbial mobile genetic elements , 2021, Philosophical Transactions of the Royal Society B.
[8] Claudia Igler,et al. Conjugative plasmid transfer is limited by prophages but can be overcome by high conjugation rates , 2021, bioRxiv.
[9] P. Christie,et al. Protein Transfer through an F Plasmid-Encoded Type IV Secretion System Suppresses the Mating-Induced SOS Response , 2021, mBio.
[10] P. Bork,et al. Interactive Tree Of Life (iTOL) v5: an online tool for phylogenetic tree display and annotation , 2021, Nucleic Acids Res..
[11] Silvio C. E. Tosatto,et al. Pfam: The protein families database in 2021 , 2020, Nucleic Acids Res..
[12] R. Roberts,et al. Plasmid replication-associated single-strand-specific methyltransferases , 2020, Nucleic acids research.
[13] Chris M. Brown,et al. Discovery of multiple anti-CRISPRs highlights anti-defense gene clustering in mobile genetic elements , 2020, Nature Communications.
[14] Jan Zrimec. Multiple plasmid origin‐of‐transfer regions might aid the spread of antimicrobial resistance to human pathogens , 2020, MicrobiologyOpen.
[15] Christian Lesterlin,et al. Plasmid Transfer by Conjugation in Gram-Negative Bacteria: From the Cellular to the Community Level , 2020, Genes.
[16] S. Gandon,et al. Phage gene expression and host responses lead to infection-dependent costs of CRISPR immunity , 2020, The ISME Journal.
[17] Geneviève Garriss,et al. Lysogeny in Streptococcus pneumoniae , 2020, Microorganisms.
[18] Christian Lesterlin,et al. Bacteria DNA Conjugation: from The Cellular to The Community Level , 2020 .
[19] T. Wood,et al. A Primary Physiological Role of Toxin/Antitoxin Systems Is Phage Inhibition , 2020, Frontiers in Microbiology.
[20] Kira S. Makarova,et al. Machine-learning approach expands the repertoire of anti-CRISPR protein families , 2020, Nature Communications.
[21] Y. Ohtsubo,et al. Transcriptome Analysis of Zygotic Induction During Conjugative Transfer of Plasmid RP4 , 2020, Frontiers in Microbiology.
[22] Frédéric Grenier,et al. IncC conjugative plasmids and SXT/R391 elements repair double-strand breaks caused by CRISPR–Cas during conjugation , 2020, Nucleic acids research.
[23] S. Jergic,et al. Development of a single-stranded DNA-binding protein fluorescent fusion toolbox , 2020, Nucleic acids research.
[24] P. Hardouin,et al. Diversity of molecular mechanisms used by anti-CRISPR proteins: the tip of an iceberg? , 2020, Biochemical Society transactions.
[25] Robert D. Finn,et al. MGnify: the microbiome analysis resource in 2020 , 2019, Nucleic Acids Res..
[26] R. Sorek,et al. The pan-immune system of bacteria: antiviral defence as a community resource , 2019, Nature Reviews Microbiology.
[27] Adair L. Borges,et al. Anti-CRISPR-Associated Proteins Are Crucial Repressors of Anti-CRISPR Transcription , 2019, Cell.
[28] Karthik Hullahalli,et al. Conjugative Delivery of CRISPR-Cas9 for the Selective Depletion of Antibiotic-Resistant Enterococci , 2019, Antimicrobial Agents and Chemotherapy.
[29] Franklin L. Nobrega,et al. Keeping crispr in check: diverse mechanisms of phage-encoded anti-crisprs , 2019, FEMS microbiology letters.
[30] R. Hall,et al. pBuzz: A cryptic rolling-circle plasmid from a commensal Escherichia coli has two inversely oriented oriTs and is mobilised by a B/O plasmid. , 2019, Plasmid.
[31] I. Manukhov,et al. Antirestriction activities of KlcA (RP4) and ArdB (R64) proteins , 2018, FEMS microbiology letters.
[32] Cui Tai,et al. oriTfinder: a web-based tool for the identification of origin of transfers in DNA sequences of bacterial mobile genetic elements , 2018, Nucleic Acids Res..
[33] A. Wong,et al. Plasmid persistence: costs, benefits, and the plasmid paradox. , 2018, Canadian journal of microbiology.
[34] Rotem Sorek,et al. Systematic discovery of antiphage defense systems in the microbial pangenome , 2018, Science.
[35] N. Leblond-Bourget,et al. The Obscure World of Integrative and Mobilizable Elements, Highly Widespread Elements that Pirate Bacterial Conjugative Systems , 2017, Genes.
[36] Johannes Söding,et al. MMseqs2: sensitive protein sequence searching for the analysis of massive data sets , 2017, bioRxiv.
[37] Alan R Davidson,et al. The Discovery, Mechanisms, and Evolutionary Impact of Anti-CRISPRs. , 2017, Annual review of virology.
[38] R. MacLean,et al. Fitness Costs of Plasmids: a Limit to Plasmid Transmission , 2017, Microbiology spectrum.
[39] J. Kiss,et al. Identification of oriT and a recombination hot spot in the IncA/C plasmid backbone , 2017, Scientific Reports.
[40] N. Firth,et al. Diverse mobilization strategies facilitate transfer of non-conjugative mobile genetic elements. , 2017, Current opinion in microbiology.
[41] Xiaofei Jiang,et al. Anti-Restriction Protein, KlcAHS, Promotes Dissemination of Carbapenem Resistance , 2017, Front. Cell. Infect. Microbiol..
[42] C. Fraser,et al. Horizontal DNA Transfer Mechanisms of Bacteria as Weapons of Intragenomic Conflict , 2016, PLoS biology.
[43] Petra F. G. Wolffs,et al. Dissemination of Antimicrobial Resistance in Microbial Ecosystems through Horizontal Gene Transfer , 2016, Front. Microbiol..
[44] D. Qi,et al. An ADP‐ribosyltransferase Alt of bacteriophage T4 negatively regulates the Escherichia coli MazF toxin of a toxin–antitoxin module , 2016, Molecular microbiology.
[45] Y. Chemla,et al. Structural dynamics of E. coli single-stranded DNA binding protein reveal DNA wrapping and unwrapping pathways , 2015, eLife.
[46] G. Waksman,et al. Structural biology of the Gram-negative bacterial conjugation systems. , 2015, Trends in microbiology.
[47] Eugene V Koonin,et al. No evidence of inhibition of horizontal gene transfer by CRISPR–Cas on evolutionary timescales , 2015, The ISME Journal.
[48] Timothy K Lu,et al. Sequence-specific antimicrobials using efficiently delivered RNA-guided nucleases , 2014, Nature Biotechnology.
[49] Torsten Seemann,et al. Prokka: rapid prokaryotic genome annotation , 2014, Bioinform..
[50] Ian T. Paulsen,et al. Sequences of Two Related Multiple Antibiotic Resistance Virulence Plasmids Sharing a Unique IS26-Related Molecular Signature Isolated from Different Escherichia coli Pathotypes from Different Hosts , 2013, PloS one.
[51] D. van Sinderen,et al. Bacteriophage Orphan DNA Methyltransferases: Insights from Their Bacterial Origin, Function, and Occurrence , 2013, Applied and Environmental Microbiology.
[52] Alessandra Carattoli,et al. Plasmids and the spread of resistance. , 2013, International journal of medical microbiology : IJMM.
[53] Sarah Neumann,et al. CRISPR-Cas systems preferentially target the leading regions of MOBF conjugative plasmids , 2013, RNA biology.
[54] A. Khanna,et al. Serratia marcescens- a rare opportunistic nosocomial pathogen and measures to limit its spread in hospitalized patients. , 2013, Journal of clinical and diagnostic research : JCDR.
[55] Gonzalo Riadi,et al. TnpPred: A Web Service for the Robust Prediction of Prokaryotic Transposases , 2012, Comparative and functional genomics.
[56] T. Yonesaki,et al. Dmd of bacteriophage T4 functions as an antitoxin against Escherichia coli LsoA and RnlA toxins , 2012, Molecular microbiology.
[57] Peter F. Stadler,et al. ViennaRNA Package 2.0 , 2011, Algorithms for Molecular Biology.
[58] Sean R. Eddy,et al. Accelerated Profile HMM Searches , 2011, PLoS Comput. Biol..
[59] Fernando de la Cruz,et al. Identification of bacterial plasmids based on mobility and plasmid population biology. , 2011, FEMS microbiology reviews.
[60] T. Komano,et al. The genome sequence of the incompatibility group Iγ plasmid R621a: evolution of IncI plasmids. , 2011, Plasmid.
[61] V. Kotova,et al. Antimodification activity of the ArdA and Ocr proteins , 2011, Russian Journal of Genetics.
[62] Z. Baharoglu,et al. Conjugative DNA Transfer Induces the Bacterial SOS Response and Promotes Antibiotic Resistance Development through Integron Activation , 2010, PLoS genetics.
[63] Fernando de la Cruz,et al. Conjugative DNA metabolism in Gram-negative bacteria. , 2010, FEMS microbiology reviews.
[64] Miriam L. Land,et al. Trace: Tennessee Research and Creative Exchange Prodigal: Prokaryotic Gene Recognition and Translation Initiation Site Identification Recommended Citation Prodigal: Prokaryotic Gene Recognition and Translation Initiation Site Identification , 2022 .
[65] Ning Ma,et al. BLAST+: architecture and applications , 2009, BMC Bioinformatics.
[66] M. Cox,et al. An SOS inhibitor that binds to free RecA protein: the PsiB protein. , 2009, Molecular cell.
[67] Søren J. Sørensen,et al. Conjugative plasmids: vessels of the communal gene pool , 2009, Philosophical Transactions of the Royal Society B: Biological Sciences.
[68] G. Fichant,et al. SpxA1, a novel transcriptional regulator involved in X‐state (competence) development in Streptococcus pneumoniae , 2009, Molecular microbiology.
[69] Kathryn S. Lilley,et al. The phage abortive infection system, ToxIN, functions as a protein–RNA toxin–antitoxin pair , 2009, Proceedings of the National Academy of Sciences.
[70] J. Keck,et al. Structural basis of Escherichia coli single-stranded DNA-binding protein stimulation of exonuclease I , 2008, Proceedings of the National Academy of Sciences.
[71] Ronny Lorenz,et al. The Vienna RNA Websuite , 2008, Nucleic Acids Res..
[72] A. Kozlov,et al. SSB as an Organizer/Mobilizer of Genome Maintenance Complexes , 2008, Critical reviews in biochemistry and molecular biology.
[73] Adam Godzik,et al. Cd-hit: a fast program for clustering and comparing large sets of protein or nucleotide sequences , 2006, Bioinform..
[74] Johannes Söding,et al. The HHpred interactive server for protein homology detection and structure prediction , 2005, Nucleic Acids Res..
[75] K. Gerdes,et al. Prokaryotic toxin–antitoxin stress response loci , 2005, Nature Reviews Microbiology.
[76] D. Krüger,et al. Active protection by bacteriophages T3 and T7 againstE. coli B-and K-specific restriction of their DNA , 1977, Molecular and General Genetics MGG.
[77] R. de Groot,et al. Streptococcus pneumoniae colonisation: the key to pneumococcal disease. , 2004, The Lancet. Infectious diseases.
[78] M. Lucas,et al. Recognition and processing of the origin of transfer DNA by conjugative relaxase TrwC , 2003, Nature Structural Biology.
[79] I. Kobayashi,et al. A DNA Methyltransferase Can Protect the Genome from Postdisturbance Attack by a Restriction-Modification Gene Complex , 2002, Journal of bacteriology.
[80] K. Katoh,et al. MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform. , 2002, Nucleic acids research.
[81] M. Gelfand,et al. Damage-repair error-prone polymerases of eubacteria: association with mobile genome elements. , 2002, Gene.
[82] A. Pantosti,et al. Macrolide Efflux Genes mef(A) and mef(E) Are Carried by Different Genetic Elements in Streptococcus pneumoniae , 2002, Journal of Clinical Microbiology.
[83] Fan Yang,et al. TIGRFAMs: a protein family resource for the functional identification of proteins , 2001, Nucleic Acids Res..
[84] Z. Livneh,et al. Plasmid-encoded MucB protein is a DNA polymerase (pol RI) specialized for lesion bypass in the presence of MucA', RecA, and SSB. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[85] H. Ochman,et al. Lateral gene transfer and the nature of bacterial innovation , 2000, Nature.
[86] T. N. Bhat,et al. The Protein Data Bank , 2000, Nucleic Acids Res..
[87] R. Woodgate,et al. The Bacteriophage P1 HumD Protein Is a Functional Homolog of the Prokaryotic UmuD′-Like Proteins and Facilitates SOS Mutagenesis in Escherichia coli , 1999, Journal of bacteriology.
[88] W. J. Brammar,et al. Expression of leading region genes on IncI1 plasmid ColIb-P9: genetic evidence for single-stranded DNA transcription. , 1999, Microbiology.
[89] J. Lawrence. Gene transfer, speciation, and the evolution of bacterial genomes. , 1999, Current opinion in microbiology.
[90] M. N. Vijayakumar,et al. An Operon That Confers UV Resistance by Evoking the SOS Mutagenic Response in Streptococcal Conjugative Transposon Tn5252 , 1999, Journal of bacteriology.
[91] W. J. Brammar,et al. Transient transcriptional activation of the IncI1 plasmid anti‐restriction gene (ardA) and SOS inhibition gene (psiB) early in conjugating recipient bacteria , 1999, Molecular microbiology.
[92] Hiroyuki Ogata,et al. KEGG: Kyoto Encyclopedia of Genes and Genomes , 1999, Nucleic Acids Res..
[93] K. Arai,et al. F rpo : A Novel Single-Stranded DNA Promoter for Transcription and for Primer RNA Synthesis of DNA Replication , 1997, Cell.
[94] T. Read,et al. Evasion of type I and type II DNA restriction systems by Incl1 plasmid Collb‐P9 during transfer by bacterial conjugation , 1992, Molecular microbiology.
[95] J. Angulo,et al. PsiB, an anti‐SOS protein, is transiently expressed by the F sex factor during its transmission to an Escherichia coli K‐12 recipient , 1992, Molecular microbiology.
[96] B. Wilkins,et al. Zygotic induction of plasmid ssb and psiB genes following conjugative transfer of Incl1 plasmid Collb‐P9 , 1992, Molecular microbiology.
[97] T. Sofuni,et al. Salmonella typhimurium has two homologous but different umuDC operons: cloning of a new umuDC-like operon (samAB) present in a 60-megadalton cryptic plasmid of S. typhimurium , 1991, Journal of bacteriology.
[98] K. Arai,et al. Identification of eleven single-strand initiation sequences (ssi) for priming of DNA replication in the F, R6K, R100 and ColE2 plasmids. , 1991, Gene.
[99] D. Owen,et al. DNA sequence analysis of the imp UV protection and mutation operon of the plasmid TP110: identification of a third gene. , 1990, Nucleic acids research.
[100] E. Golub,et al. A gene encoding an SOS inhibitor is present in different conjugative plasmids , 1988, Journal of bacteriology.
[101] U. Günthert,et al. Bacillus subtilis phage SPR codes for a DNA methyltransferase with triple sequence specificity. , 1987, Nucleic acids research.
[102] N. Willetts. Structure and function of the F factor and mechanism of conjugation , 1987 .
[103] K. Timmis,et al. An inhibitor of SOS induction, specified by a plasmid locus in Escherichia coli. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[104] F. Studier. Gene 0.3 of bacteriophage T7 acts to overcome the DNA restriction system of the host. , 1975, Journal of molecular biology.
[105] Supplemental Information 2: Kyoto Encyclopedia of genes and genomes. , 2022 .