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1 e, provides evidence for several examples of lateral gene transfer.
2 ce cell-type specialization were acquired by lateral gene transfer.
3 somal islands that may have been acquired by lateral gene transfer.
4 y of AP2 domains supports the possibility of lateral gene transfer.
5 , as well as the entire cassette, evolved by lateral gene transfer.
6  of distinct virulence elements acquired via lateral gene transfer.
7 c respiration may have been acquired through lateral gene transfer.
8 maripaludis may have acquired cysS by a late lateral gene transfer.
9 able mutational rates, site variability, and lateral gene transfer.
10 ved from a combination of common descent and lateral gene transfer.
11 otAB stator, the latter possibly acquired by lateral gene transfer.
12 inary fission and lacks all natural means of lateral gene transfer.
13 halophilic archaea and bacteria may indicate lateral gene transfer.
14 -like minimal system Fe/S cluster pathway by lateral gene transfer.
15 quired the capacity for homoacetogenesis via lateral gene transfer.
16 change, mating pair formation and widespread lateral gene transfer.
17  occurrences in eukaryotes are the result of lateral gene transfer.
18 acteria community organization and mediating lateral gene transfer.
19 , one protozoan, and cyanophages, suggesting lateral gene transfer.
20 stical support for acquisition as islands by lateral gene transfer.
21 en in this small subset of diatoms through a lateral gene transfer.
22 om other bacteria and are likely acquired by lateral gene transfer.
23 ze, almost 20% of the genome is derived from lateral gene transfer.
24 revious niche with greater opportunities for lateral gene transfer.
25 0 sequence was recently acquired by means of lateral gene transfer.
26 cus I were acquired by independent events of lateral gene transfer.
27 SBS/NAAAR appear to have been transmitted by lateral gene transfer.
28 onstraints are there on gene duplication and lateral gene transfer?
29         Plasmids often serve as mediators of lateral gene transfer, a process considered to be a stro
30         Commonly dismissed as an artefact of lateral gene transfer after oxygenic photosynthesis evol
31 rotransposition, duplication-divergence, and lateral gene transfer, all of which involve recruitment
32 with evolution dominated by link turnover or lateral gene transfer alone.
33 s; and (3) that continuous, lineage-specific lateral gene transfer, although it sometimes occurs, doe
34 ications of transposition as a mechanism for lateral gene transfer among Archaea are discussed.
35                     Despite apparent rampant lateral gene transfer among microorganisms, these result
36              fsr could also have arisen from lateral gene transfer and gene fusion events.
37 domains must have included several events of lateral gene transfer and gene loss as well as lineage-s
38 but it is possible that the combined rate of lateral gene transfer and gene loss is higher than that
39 ds are all consistent with the hypothesis of lateral gene transfer and not ancient gene duplication.
40               In many bacteria expression of lateral gene transfer and of virulence factors is contro
41 from complete genome sequencing results that lateral gene transfer and recombination are essential co
42                                              Lateral gene transfer and recombination play important r
43 uire and eliminate blocks of DNA sequence by lateral gene transfer and spontaneous deletion, respecti
44 coding sequences might have been acquired by lateral gene transfer and the number of hemerythrin-like
45 converting the uninitiated to their cause by lateral gene transfer, and enforcing cooperative behavio
46 have been acquired in part by phage-mediated lateral gene transfer, and some are differentially expre
47 pproximately 7 to 15 represent genes where a lateral gene transfer appears to have generated homoplas
48 s instances of tandem duplication as well as lateral gene transfer are evident in the genome.
49 hat evolutionary forces underlie the rate of lateral gene transfer are not well understood.
50 estor analysis indicates gene divergence and lateral gene transfer as equally important origins of th
51 terial species, which rules out interspecies lateral gene transfer as the origin of lux-rib2 in P. le
52 ferences revealed nine potential examples of lateral gene transfer associated with metal efflux prote
53 l "crystallized," i.e., became refractory to lateral gene transfer, at different stages of "cooling,"
54 impact host-cell phage immunity and defense, lateral gene transfer, bacteriophage-induced cell mortal
55  this method is resilient to some effects of lateral gene transfer because transfers of genes are mas
56 oson and represents a possible mechanism for lateral gene transfer between Archaea or possibly betwee
57 yotes, supplemented by possible instances of lateral gene transfer between bacteria and eukaryotes.
58                     The results suggest that lateral gene transfer between eubacteria subsequent to t
59  the DnaK trees suggested the possibility of lateral gene transfer between Firmicutes and Methanosarc
60 rsification at the species level by allowing lateral gene transfer between strains that are too dista
61                                   Widespread lateral gene transfer between viruses and their hosts pl
62                  These data indicate ongoing lateral gene transfers between species, including mixing
63 e sequences, however, increasingly implicate lateral gene transfer, both from prokaryotes to eukaryot
64  the ability and/or opportunity to engage in lateral gene transfer, but despite this it has retained
65 e complex signaling network used to regulate lateral gene transfer can be resolved as individual sign
66                 Our results demonstrate that lateral gene transfers, detected by probabilistic models
67                                 Duplication, lateral gene transfer, domain fusion/fission and de novo
68 tive pathways have been subject to extensive lateral gene transfers during their evolution.
69 ired from diverse biological sources through lateral gene transfer early in the evolution of Nucleo-C
70  PKS gene family in Stramenopiles suggests a lateral gene transfer event from an actinobacterium.
71 e, which we hypothesize may be a result of a lateral gene transfer event, and an unidentified 456 ami
72 n mammoth may be acquired through an ancient lateral gene transfer event.
73                                              Lateral gene transfer events between bacteria and animal
74 ermotoga maritima MSB8 presents evidence for lateral gene transfer events between bacterial and archa
75                                              Lateral gene transfer events brought unique genomic regi
76  the Bcep781 group phages can also engage in lateral gene transfer events with otherwise unrelated ph
77 uplication and secondary losses, interdomain lateral gene transfer events, alteration of cellular loc
78 st in identifying mobile genetic elements or lateral gene transfer events.
79 e document the presence of multiple putative lateral gene transfer events.
80 d their corresponding host genomes confirmed lateral gene transfer events.
81 ated genes could also arise from small-scale lateral gene transfer events.
82 ng secreted phospholipase A2 enzymes through lateral gene transfer events.
83 nd a type II membrane protein has evolved by lateral gene transfer for the esterification of many bac
84 . brevicollis was believed to have arisen by lateral gene transfer from a prokaryote, and is a fusion
85 omplexa, is likely to have been obtained via lateral gene transfer from a prokaryote.
86 on the emergence of spontaneous mutations or lateral gene transfer from a reservoir of pre-existing v
87 ion, we conclude that chy1 probably arose by lateral gene transfer from an actinomycete bacterium.
88                        This is attributed to lateral gene transfer from an ancestral cryptomonad to a
89 h various means, including gene duplication, lateral gene transfer from bacteria that are not their c
90 olic pathways that likely transpired through lateral gene transfer from bacteria, and amplification o
91 the latter two groups could be the result of lateral gene transfer from Bacteria.
92                                              Lateral gene transfer from bacterial and archaeal donors
93 uster assembly, one of which was acquired by lateral gene transfer from Chlamydiae.
94 om separate and different sources, involving lateral gene transfer from eubacteria, than did all othe
95  the canonical glutaminyl-tRNA synthetase by lateral gene transfer from eukaryotes.
96 t in either bacteria or spiders, followed by lateral gene transfer from one lineage to the other.
97 ed that all three genes had been acquired by lateral gene transfer from the low-moles-percent G+C gra
98 omes are usually ascribed to gene loss or to lateral gene transfer from unrelated cellular organisms.
99 tin operon, which was primarily acquired via lateral gene transfer from unrelated intracellular bacte
100 e acquired via a minimum of four independent lateral gene transfers from C(4) taxa that diverged from
101 g from non-coding DNA, chimeric fusions, and lateral gene transfers from other organisms [3-7].
102        The presence of IS6110 indicates that lateral gene transfer has occurred among mycobacterial s
103                                 We find that lateral gene transfer has played a fundamental role in t
104                                              Lateral gene transfer has played a prominent role in bac
105                        Numerous instances of lateral gene transfer have contributed to the complex an
106 ernative gene losses in different groups and lateral gene transfer have ramified CoqF across the euka
107                                Horizontal or Lateral Gene Transfer (HGT or LGT) is the transmission o
108 the mutation rate and the scope and level of lateral gene transfer, i.e., evolutionary temperature, d
109 ights into eukaryotic evolution, the role of lateral gene transfer in amebic biology and the adaptati
110                 Herein, we report functional lateral gene transfer in animal parasitic nematodes.
111 the first direct evidence of a mechanism for lateral gene transfer in B. burgdorferi.
112                          A main mechanism of lateral gene transfer in bacteria is transformation, whe
113 gens, and have established the importance of lateral gene transfer in generating structural diversity
114         Despite the recognized importance of lateral gene transfer in shaping the genomes of marine c
115  of selfish genetic elements in facilitating lateral gene transfer in the deep-sea biosphere.
116                                              Lateral gene transfer is considered the primary explanat
117                                 We find that lateral gene transfer is far more extensive than previou
118                   While the role of LCTRs in lateral gene transfer is not known, the Mal I cluster in
119                                              Lateral gene transfer is of fundamental importance to th
120            Initially, both mutation rate and lateral gene transfer levels were elevated.
121 idered to be obstructed by the potential for lateral gene transfer (LGT) among lineages at virtually
122 ratchet, while limiting the effectiveness of lateral gene transfer (LGT) at purging deleterious mutat
123 this anomaly had originally been ascribed to lateral gene transfer (LGT) from eukaryotes.
124                                              Lateral gene transfer (LGT) from microbial symbionts to
125 ledge of the extent and functional impact of lateral gene transfer (LGT) from prokaryotes to eukaryot
126           Evidence of eukaryote-to-eukaryote lateral gene transfer (LGT) has accumulated in recent ye
127      Genetic recombinants that resulted from lateral gene transfer (LGT) have been detected in sexual
128 sequences has demonstrated the importance of lateral gene transfer (LGT) in prokaryotic evolution.
129 picocyanobacteria (cyanophages), to evaluate lateral gene transfer (LGT) in this group.
130 is genome, we detect a substantial number of lateral gene transfer (LGT) instances from bacteria (15%
131 exually transmitted infections suggests that lateral gene transfer (LGT) is an important means by whi
132                                              Lateral gene transfer (LGT) is essential for generating
133                                              Lateral gene transfer (LGT) is now accepted as an import
134                                              Lateral gene transfer (LGT) is the movement of DNA betwe
135                                              Lateral gene transfer (LGT) occurs in a broad range of p
136                                              Lateral gene transfer (LGT) plays a key role in shaping
137                                              Lateral gene transfer (LGT), also known as horizontal ge
138 trososphaerales to investigate the impact of lateral gene transfer (LGT), gene duplication and loss a
139 aeal genomes are known to have acquired, via lateral gene transfer (LGT), several genes from eubacter
140                                              Lateral gene transfer (LGT), the acquisition of genes fr
141 yotes acquire genes from the environment via lateral gene transfer (LGT).
142 ulfur mobilization (SUF) system acquired via lateral gene transfer (LGT).
143 st 322 genes appear to have been obtained by lateral gene transfer (LGT).
144 ryotic genomes can acquire bacterial DNA via lateral gene transfer (LGT).(1) A prominent source of LG
145                                 We find that lateral gene transfer, likely occurring intracellularly
146 quivalog' families, where both orthology and lateral gene transfer may be part of the evolutionary hi
147  many of the clustered regions suggests that lateral gene transfer may have occurred between thermoph
148                                              Lateral gene transfer may play a critical role in shapin
149               P. woesei may have acquired by lateral gene transfer more than 100 ORFs from other orga
150     Phylogenetic analyses suggested that two lateral gene transfers occurred in the DapL genes, one f
151                         Therefore, heritable lateral gene transfer occurs into eukaryotic hosts from
152 hylogenomic analysis identifies evidence for lateral gene transfer of bacterial genes into the E. his
153                  Evidence of intersubspecies lateral gene transfer of the housekeeping gene recA, whi
154 of alleles between hosts, indicating limited lateral gene transfer of these alleles despite host prox
155               The last stage encompassed the lateral gene transfers of some members of the three glob
156          This tree requires few instances of lateral gene transfer or convergence, and instead sugges
157 ed between bacteria and early eukaryotes via lateral gene transfer or endosymbiotic events.
158 lastp hits in Methanocaldococcus jannaschii, lateral gene transfer or gene loss has apparently result
159 se of their ability to pick up new traits by lateral gene transfer, our gut microbes also enable adap
160 1950s-era prototype and vaccine strains by a lateral gene transfer, substituting the coding region fo
161                                However, with lateral gene transfer, the first histone fold could alte
162              Although common among bacteria, lateral gene transfer-the movement of genes between dist
163 ruginous fields, unlocking the impact of the lateral gene transfer to adjust the genome for extreme e
164              The transition from prokaryotic lateral gene transfer to eukaryotic meiotic sex is poorl
165                                              Lateral gene transfer, which may have a significant infl
166 the phylum Thermotogota have shown extensive lateral gene transfer with distantly related organisms,
167            We also detected two instances of lateral gene transfer within the internalins, but the es

 
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