review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1146/ANNUREV.BIOCHEM.66.1.437 |
P698 | PubMed publication ID | 9242914 |
P2093 | author name string | Craig NL | |
P1104 | number of pages | 38 | |
P304 | page(s) | 437-474 | |
P577 | publication date | 1997-01-01 | |
P1433 | published in | Annual Review of Biochemistry | Q567356 |
P1476 | title | Target site selection in transposition | |
P478 | volume | 66 |
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Q33789770 | A new IS4 family insertion sequence, IS4Bsu1, responsible for genetic instability of poly-gamma-glutamic acid production in Bacillus subtilis |
Q42628361 | A new set of Mu DNA transposition intermediates: alternate pathways of target capture preceding strand transfer |
Q31063275 | A novel family of mobile genetic elements is limited to the germline genome in Tetrahymena thermophila |
Q34723856 | A piggyBac transposon-based mutagenesis system for the fission yeast Schizosaccharomyces pombe |
Q39647805 | A target specificity switch in IS911 transposition: the role of the OrfA protein |
Q39482837 | Abr1, a transposon-like element in the genome of the cultivated mushroom Agaricus bisporus (Lange) Imbach |
Q52669038 | Abundance and chromosomal distribution of six Drosophila buzzatii transposons: BuT1, BuT2, BuT3, BuT4, BuT5, and BuT6. |
Q52682425 | Abundant, diverse, and consequential P elements segregate in promoters of small heat-shock genes in Drosophila populations. |
Q41784854 | Accurate localization of the integration sites of two genomic islands at single-nucleotide resolution in the genome of Bacillus cereus ATCC 10987. |
Q36758423 | Active recombinant Tol2 transposase for gene transfer and gene discovery applications |
Q81471641 | Agrobacterium T-DNA integration in Arabidopsis is correlated with DNA sequence compositions that occur frequently in gene promoter regions |
Q37367632 | Alternative interactions between the Tn7 transposase and the Tn7 target DNA binding protein regulate target immunity and transposition |
Q33889534 | An ATP-ADP switch in MuB controls progression of the Mu transposition pathway |
Q34612754 | An ancient retrovirus-like element contains hot spots for SINE insertion |
Q37017245 | Analysis of phage Mu DNA transposition by whole-genome Escherichia coli tiling arrays reveals a complex relationship to distribution of target selection protein B, transcription and chromosome architectural elements. |
Q90062826 | Bacterial group II intron genomic neighborhoods reflect survival strategies: hiding and hijacking |
Q33237569 | Bacterial repetitive extragenic palindromic sequences are DNA targets for Insertion Sequence elements |
Q24672697 | Barrier-to-autointegration factor (BAF) bridges DNA in a discrete, higher-order nucleoprotein complex |
Q33692244 | Chance favors the prepared genome |
Q42654974 | Characterization of a retrotransposon-like element from Entamoeba histolytica |
Q45855517 | Common physical properties of DNA affecting target site selection of sleeping beauty and other Tc1/mariner transposable elements. |
Q38664185 | Complex chromosomal neighborhood effects determine the adaptive potential of a gene under selection. |
Q36862999 | Congruence of in vivo and in vitro insertion patterns in hot E. coli gene targets of transposable element Mu: opposing roles of MuB in target capture and integration |
Q31110538 | Construction and characterization of transposon insertion mutations in Corynebacterium diphtheriae that affect expression of the diphtheria toxin repressor (DtxR). |
Q84077280 | Contrasting evolutionary patterns and target specificities among three Tourist-like MITE families in the maize genome |
Q38544467 | Control of Transposon-Mediated Directed Mutation by the Escherichia coli Phosphoenolpyruvate:Sugar Phosphotransferase System |
Q35022347 | Controlling integration specificity of a yeast retrotransposon |
Q47750695 | DNA transposition by the RAG1 and RAG2 proteins: a possible source of oncogenic translocations |
Q97520440 | Deep sequencing reveals new roles for MuB in transposition immunity and target-capture, and redefines the insular Ter region of E. coli |
Q27496626 | Demonstration of IS711 transposition in Brucella ovis and Brucella pinnipedialis |
Q28728492 | Development of an efficient in vivo system (Pjunc-TpaseIS1223) for random transposon mutagenesis of Lactobacillus casei |
Q44017740 | Direct observation of single MuB polymers: evidence for a DNA-dependent conformational change for generating an active target complex |
Q49789963 | Diverse genetic error modes constrain large-scale bio-based production. |
Q52626819 | Double insertion of transposable elements provides a substrate for the evolution of satellite DNA. |
Q34086159 | Dynamics of a protein polymer: the assembly and disassembly pathways of the MuB transposition target complex |
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Q36417225 | Enhanced production of recombinant proteins with Corynebacterium glutamicum by deletion of insertion sequences (IS elements). |
Q33741044 | Escherichia coli DNA topoisomerase I and suppression of killing by Tn5 transposase overproduction: topoisomerase I modulates Tn5 transposition |
Q33992047 | Escherichia coli DNA topoisomerase I copurifies with Tn5 transposase, and Tn5 transposase inhibits topoisomerase I |
Q34030990 | Evaluation of a transposase protocol for rapid generation of shotgun high-throughput sequencing libraries from nanogram quantities of DNA |
Q33344328 | Expanded molecular diversity generation during directed evolution by trinucleotide exchange (TriNEx). |
Q28476065 | Fast growth increases the selective advantage of a mutation arising recurrently during evolution under metal limitation |
Q39607366 | Fission yeast retrotransposon Tf1 integration is targeted to 5' ends of open reading frames |
Q37976151 | Fitness effects of mutations in bacteria. |
Q39585663 | Functional organization and insertion specificity of IS607, a chimeric element of Helicobacter pylori |
Q33820587 | Genetic variation: molecular mechanisms and impact on microbial evolution |
Q52700351 | Genomic distribution of retrotransposons 297, 1731, copia, mdg1 and roo in the Drosophila melanogaster species subgroup. |
Q34050694 | HIV-1 integrase inhibitors: past, present, and future |
Q28655848 | Harnessing mobile genetic elements to explore gene regulation |
Q40409230 | Heat shock treatment increases the frequency of loss of an erythromycin resistance-encoding transposable element from the chromosome of Lactobacillus crispatus CHCC3692. |
Q33259824 | Heat-shock promoters: targets for evolution by P transposable elements in Drosophila |
Q48286997 | High-throughput retroviral tagging to identify components of specific signaling pathways in cancer |
Q40987278 | Hopping into a hot seat: Role of DNA structural features on IS5-mediated gene activation and inactivation under stress |
Q33889652 | Host proteins can stimulate Tn7 transposition: a novel role for the ribosomal protein L29 and the acyl carrier protein |
Q33836581 | IS elements as constituents of bacterial genomes |
Q39497925 | IS1397 is active for transposition into the chromosome of Escherichia coli K-12 and inserts specifically into palindromic units of bacterial interspersed mosaic elements. |
Q39585875 | IS1675, a novel lactococcal insertion element, forms a transposon-like structure including the lacticin 481 lantibiotic operon |
Q39504228 | Identification and distribution of new insertion sequences in the genome of alkaliphilic Bacillus halodurans C-125. |
Q36026134 | Identification of Bari Transposons in 23 Sequenced Drosophila Genomes Reveals Novel Structural Variants, MITEs and Horizontal Transfer |
Q33756830 | Identification of Corynebacterium diphtheriae gene involved in adherence to epithelial cells |
Q30913384 | Identification of essential genes in the human fungal pathogen Aspergillus fumigatus by transposon mutagenesis |
Q37720822 | Identifying Distal cis-acting Gene-Regulatory Sequences by Expressing BACs Functionalized with loxP-Tn10 Transposons in Zebrafish. |
Q34960198 | Identifying essential genes in fungal pathogens of humans. |
Q33724108 | Immunity of replicating Mu to self-integration: a novel mechanism employing MuB protein. |
Q33235511 | In vivo Himar1-based transposon mutagenesis of Francisella tularensis |
Q43410216 | In vivo random mutagenesis of streptomycetes using mariner-based transposon Himar1. |
Q35007757 | In vivo transposition of mariner-based elements in enteric bacteria and mycobacteria. |
Q35800281 | Insertion of group II intron retroelements after intrinsic transcriptional terminators |
Q37228914 | Insertion sequence-caused large-scale rearrangements in the genome of Escherichia coli |
Q29617579 | Insertion sequences |
Q30736255 | Insertional mutagenesis: transposon-insertion libraries as mutagens in yeast |
Q39678456 | IntI2 integron integrase in Tn7. |
Q58599272 | Intensive targeting of regulatory competence genes by transposable elements in streptococci |
Q47954762 | Interspersed DNA element restricted to a specific group of telomeres in the dipteran Chironomus pallidivittatus |
Q80508455 | Inversions and inverted transpositions as the basis for an almost universal "format" of genome sequences |
Q33990189 | Isolation of an insertion sequence from Ralstonia solanacearum race 1 and its potential use for strain characterization and detection |
Q48188848 | Magic Pools: Parallel Assessment of Transposon Delivery Vectors in Bacteria |
Q38483310 | Mapped Ds/T-DNA launch pads for functional genomics in barley. |
Q54942206 | Mapping Transposon Insertions in Bacterial Genomes by Arbitrarily Primed PCR. |
Q36448960 | Microarray analysis of transposition targets in Escherichia coli: the impact of transcription |
Q34589640 | Minos as a genetic and genomic tool in Drosophila melanogaster |
Q35280826 | Mobile elements and chromosomal evolution in the virilis group of Drosophila |
Q33996827 | Molecular evidence for independent occurrence of IS6110 insertions at the same sites of the genome of Mycobacterium tuberculosis in different clinical isolates |
Q73168277 | Molecular systematics: Perfect SINEs of evolutionary history? |
Q37488189 | MuB gives a new twist to target DNA selection. |
Q27678672 | MuB is an AAA+ ATPase that forms helical filaments to control target selection for DNA transposition |
Q33287807 | Multiple homoplasious insertions and deletions of a Triticeae (Poaceae) DNA transposon: a phylogenetic perspective |
Q35038542 | Natural history of transposition in the green alga Chlamydomonas reinhardtii: use of the AMT4 locus as an experimental system |
Q42565115 | Natural transposon mutagenesis of clinical isolates of Mycobacterium tuberculosis: how many genes does a pathogen need? |
Q41813880 | New transposon delivery plasmids for insertional mutagenesis in Bacillus anthracis |
Q48000332 | Novel sequence organization and insertion specificity of IS605 and IS606: chimaeric transposable elements of Helicobacter pylori |
Q42673139 | Optional mitochondrial introns and evidence for a homing-endonuclease gene in the mtDNA rnl gene in Ophiostoma ulmi s. lat. |
Q47769461 | Overview of mechanisms of antibiotic resistance in Pseudomonas aeruginosa: an ocular perspective. |
Q39568272 | Oxygen-insensitive nitroreductases: analysis of the roles of nfsA and nfsB in development of resistance to 5-nitrofuran derivatives in Escherichia coli. |
Q33947891 | P instability factor: an active maize transposon system associated with the amplification of Tourist-like MITEs and a new superfamily of transposases |
Q52601168 | Patterns of insertion and deletion in contrasting chromatin domains. |
Q22121986 | Plasmid encoded antibiotic resistance: acquisition and transfer of antibiotic resistance genes in bacteria |
Q34697885 | Plasticity of the P junc promoter of ISEc11, a new insertion sequence of the IS1111 family |
Q33968578 | RAG transposase can capture and commit to target DNA before or after donor cleavage |
Q28486329 | Random mutagenesis in Corynebacterium glutamicum ATCC 13032 using an IS6100-based transposon vector identified the last unknown gene in the histidine biosynthesis pathway |
Q35666658 | Recognition of triple-helical DNA structures by transposon Tn7. |
Q36846414 | Resetting the site: redirecting integration of an insertion sequence in a predictable way. |
Q36483417 | Retrotransposon target site selection by imitation of a cellular protein |
Q36318150 | Retroviral insertional mutagenesis: past, present and future |
Q33594313 | Revising the selfish DNA hypothesis: new evidence on accumulation of transposable elements in heterochromatin |
Q52561905 | Site preferences of insertional mutagenesis agents in Arabidopsis. |
Q34294570 | Sleeping beauty transposition: biology and applications for molecular therapy |
Q34442366 | Sleeping beauty transposon-mediated gene therapy for prolonged expression |
Q48252221 | Somatic mobility of the maize element Ac and its utility for gene tagging in aspen |
Q77317122 | Specific expression of the Fusarium transposon Fot1 and effects on target gene transcription |
Q42105719 | Structure-based prediction of insertion-site preferences of transposons into chromosomes |
Q28652378 | Survey of chimeric IStron elements in bacterial genomes: multiple molecular symbioses between group I intron ribozymes and DNA transposons |
Q73567993 | Target DNA bending is an important specificity determinant in target site selection in Tn10 transposition |
Q34582667 | Target DNA structure plays a critical role in Tn7 transposition |
Q33745196 | Target choice and orientation preference of the insertion sequence IS903 |
Q38498177 | Target sites for SINE integration in Brassica genomes display nuclear matrix binding activity |
Q38336070 | Target specificity of insertion element IS30. |
Q52326193 | Targeting IS608 transposon integration to highly specific sequences by structure-based transposon engineering. |
Q36677297 | Targeting of P-Element Reporters to Heterochromatic Domains by Transposable Element 1360 in Drosophila melanogaster |
Q24338330 | The DDN catalytic motif is required for Metnase functions in non-homologous end joining (NHEJ) repair and replication restart |
Q36581635 | The Mu story: how a maverick phage moved the field forward |
Q34261119 | The abundant polyadenylated transcript 2 DNA sequence of the pathogenic protozoan parasite Entamoeba histolytica represents a nonautonomous non-long-terminal-repeat retrotransposon-like element which is absent in the closely related nonpathogenic sp |
Q33264073 | The genome and transcriptomes of the anti-tumor agent Clostridium novyi-NT. |
Q39240966 | The impact of insertion sequences on bacterial genome plasticity and adaptability. |
Q47931334 | Tn5053 family transposons are res site hunters sensing plasmidal res sites occupied by cognate resolvases |
Q40423760 | Tn7 recognizes transposition target structures associated with DNA replication using the DNA-binding protein TnsE. |
Q64388355 | Tn7 transposes proximal to DNA double-strand breaks and into regions where chromosomal DNA replication terminates |
Q34443592 | Tn7: smarter than we thought |
Q34041294 | Transgene silencing by the host genome defense: implications for the evolution of epigenetic control mechanisms in plants and vertebrates |
Q35801161 | Transposable Phage Mu |
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Q33888644 | Transposase makes critical contacts with, and is stimulated by, single-stranded DNA at the P element termini in vitro |
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Q41011364 | Transposition mediated by RAG1 and RAG2 and its implications for the evolution of the immune system |
Q54037989 | Transposon Tn7 gene insertion into an evolutionarily conserved human homolog of Escherichia coli attTn7. |
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