ライフサイエンスコーパス: endosymbiotic

1 al plastid derived from an ancient secondary endosymbiotic acquisition of an alga.

2 Endosymbiotic acquisition of bacteria by a protist, with

3 After their endosymbiotic acquisition, plastids become intimately co

4 The discovery of coral-endosymbiotic algae Chromera velia and Vitrella brassica

5 nce of viral infections in Symbiodinium, the endosymbiotic algae critical for coral survival, and mor

6 hloroviruses and their hosts, zoochlorellae (endosymbiotic algae that live within paramecia), thereby

7 ive tract only partially digested, releasing endosymbiotic algae that still supported viral reproduct

8 evels and trigger death and expulsion of the endosymbiotic algae.

9 t the alphaDP/betaDP/gamma interface and the endosymbiotic alpha-proteobacterial origin of mitochondr

10 We reason that the endosymbiotic ancestors of mitochondria and chloroplasts

11 utS and MutL homologs likely originated from endosymbiotic ancestors of mitochondria or chloroplasts,

12 that the cpn60 gene was transferred from the endosymbiotic ancestors of mitochondria to the nucleus e

13 ied the evolution of chloroplasts from their endosymbiotic ancestors was the host cell recruitment of

14 id proteins are derived from their bacterial endosymbiotic ancestors, but their genes now reside on n

15 acterial and chloroplast DLP that, given the endosymbiotic ancestry of chloroplasts, questions the ev

16 bes experimental approaches towards studying endosymbiotic and horizontal gene transfer processes, di

17 vision machinery contains components of both endosymbiotic and host cell origin, but little is known

18 umber of genes for the anoxic and microoxic, endosymbiotic, and nitrogen-fixing life styles of the al

19 thought to have evolved through the primary endosymbiotic association between a eukaryotic host and

20 believed to have evolved through a secondary endosymbiotic association between a heterotrophic or pos

21 The endosymbiotic association between legumes and soil bacte

22 ysia chlorotica Gould forms an intracellular endosymbiotic association with chloroplasts of the chrom

23 Endosymbiotic associations have played a major role in e

24 in access to these mineral nutrients through endosymbiotic associations with arbuscular mycorrhizal (

25 ecular chaperonins produced by intracellular endosymbiotic bacteria and are the most abundant protein

26 ions, because they are host to a plethora of endosymbiotic bacteria and frequently exhibit multiple i

27 Maternally transmitted associations between endosymbiotic bacteria and insects are diverse and wides

28 Although many highly reduced genomes from endosymbiotic bacteria are stable in gene content and ge

29 verging lineages of terrestrial fungi harbor endosymbiotic bacteria belonging to the Burkholderiaceae

30 Transferring endosymbiotic bacteria between different host species ca

31 In many arthropods, maternally inherited endosymbiotic bacteria can increase infection frequency

32 Endosymbiotic bacteria exist in many animals where they

33 id clams depend entirely on sulfur-oxidizing endosymbiotic bacteria for their nutriment.

34 Wolbachia are common vertically transmitted endosymbiotic bacteria found in < 70% of insect species.

35 from mitochondria, plastids, and mutualistic endosymbiotic bacteria has shown that the stable establi

36 lutionary rate acceleration observed in most endosymbiotic bacteria may be explained by higher mutati

37 s, we recently demonstrated that it is these endosymbiotic bacteria rather than the nematodes per se

38 called root nodules, in which differentiated endosymbiotic bacteria reduce molecular dinitrogen for t

39 The endosymbiotic bacteria reside in polyploid host cells as

40 larvae of Micromalthus are infected with the endosymbiotic bacteria Rickettsia and Wolbachia.

41 vectors, and identifies a panel of core and endosymbiotic bacteria that can be potentially exploited

42 ected with parasitic, maternally transmitted endosymbiotic bacteria that manipulate host reproduction

43 sps, and the pea aphid can carry facultative endosymbiotic bacteria that prevent the development of t

44 Obligate pathogenic and endosymbiotic bacteria typically experience gene loss du

45 Endosymbiotic bacteria were identified by polymerase cha

46 ions between different species or strains of endosymbiotic bacteria within an aphid host influence th

47 ompartment where wood is digested but harbor endosymbiotic bacteria within specialized cells in their

48 ther the bacteriochlorophyll was produced by endosymbiotic bacteria within unusual structures adjacen

49 exception of one cave-dwelling genus, harbor endosymbiotic bacteria, Blattabacterium.

50 Finally, we identified several endosymbiotic bacteria, including Spiroplasma, which hav

51 Originally descended from endosymbiotic bacteria, their genomes have shrunk during

52 mportance, have revealed infections with the endosymbiotic bacteria, Wolbachia and Cardinium.

53 The endosymbiotic bacteria, Wolbachia, induce neutrophilic r

54 identified and characterized snRNAs from the endosymbiotic bacteria, Wolbachia, which are widespread

55 The obligate endosymbiotic bacterium Buchnera aphidicola shows elevat

56 se fly immune system relies on a cue from an endosymbiotic bacterium called Wigglesworthia.

57 tiera aleyrodidarum" is the obligate primary endosymbiotic bacterium of whiteflies, including the swe

58 The endosymbiotic bacterium Rhizobium leguminosarum contains

59 n filarial parasite Brugia malayi harbors an endosymbiotic bacterium Wolbachia (wBm) that is required

60 The introduction of the endosymbiotic bacterium Wolbachia into Aedes aegypti mos

61 The endosymbiotic bacterium Wolbachia spreads rapidly throug

62 er of registered antibiotics that target the endosymbiotic bacterium, Wolbachia, delivering macrofila

63 b(3)-type cytochrome oxidase specifically in endosymbiotic bacteroids of soybean root nodules, which

64 Since its endosymbiotic beginning, the chloroplast has become full

65 Chloroplasts and mitochondria are unique endosymbiotic cellular organelles surrounded by two memb

66 in vitro suggests a potential involvement of endosymbiotic chaperonins in interactions with virions d

67 In organellogenesis of the chloroplast from endosymbiotic cyanobacteria, the establishment of protei

68 A pivotal step in the transformation of an endosymbiotic cyanobacterium to a plastid some 1.5 billi

69 during the evolution of the chloroplast from endosymbiotic cyanobacterium: plastid-encoded and cyanob

70 part, because of the recognition that these endosymbiotic descendants of primordial protobacteria se

71 During bleaching, endosymbiotic dinoflagellate algae (Symbiodinium spp.) e

72 c symbioses between scleractinian corals and endosymbiotic dinoflagellates (Symbiodinium spp.) are th

73 To better understand how corals and their endosymbiotic dinoflagellates (Symbiodinium spp.) respon

74 ir great success is due to interactions with endosymbiotic dinoflagellates (Symbiodinium spp.), with

75 trient-poor tropical waters is attributed to endosymbiotic dinoflagellates.

76 corals and other tropical anthozoans harbor endosymbiotic dinoflagellates.

77 Wide-spread protozoan parasites carry endosymbiotic dsRNA viruses with uncharted implications

78 Many plant-associated fungi host endosymbiotic endobacteria with reduced genomes.

79 roalgae include cells derived from a primary endosymbiotic event (similar to land plants) and cells d

80 hondrion is an organelle originating from an endosymbiotic event and playing a role in several fundam

81 machinery is thought to have arisen with the endosymbiotic event and to be derived, at least in part,

82 iginated in bacteria in conjunction with the endosymbiotic event giving rise to mitochondria, whereas

83 tic mapping analyses indicate that the first endosymbiotic event occurred in low-salinity environment

84 age first evolved, and in what habitats this endosymbiotic event occurred.

85 s have evolved new roles in plants since the endosymbiotic event that gave rise to plastids.

86 oteins from cyanobacteria as a result of the endosymbiotic event that led to chloroplasts.

87 tion has been attributed to a single primary endosymbiotic event that occurred about 1.6 billion year

88 d evolutionary history involving a secondary endosymbiotic event, in which a protist engulfed an exis

89 onary time that has passed since the initial endosymbiotic event, mitochondria have retained many hal

90 he aim of estimating the age for the primary endosymbiotic event, the ages of crown groups for photos

91 After the initial endosymbiotic event, the CR genome was reduced to approx

92 Ilv5p acquired its mtDNA function after the endosymbiotic event.

93 Two consequences of multiple endosymbiotic events include complex targeting mechanism

94 Soon after these endosymbiotic events, thousands of ancestral prokaryotic

95 ed from subsequent secondary and/or tertiary endosymbiotic events.

96 arly eukaryotes via lateral gene transfer or endosymbiotic events.

97 ave been acquired through multiple different endosymbiotic events.

98 c lineage, with acquisition corresponding to endosymbiotic events.

99 to the acquisition of protein import during endosymbiotic evolution of the TOC system in plastids.

100 and mitochondria by eukaryotic cells during endosymbiotic evolution, most of the genes in these orga

101 rkable example of the processes underpinning endosymbiotic evolution.

102 actions that includes amoeboid predation and endosymbiotic existence.

103 ics, ruling out sex-linked, cytoplasmic, and endosymbiotic factors.

104 GT) from algal prey or symbionts, or through endosymbiotic gene transfer (EGT) during a putative phot

105 Endosymbiotic gene transfer (EGT) from the intracellular

106 re genome to the host nuclear genome through endosymbiotic gene transfer (EGT).

107 ndosymbiont genes to the host nucleus (i.e., endosymbiotic gene transfer [EGT]).

108 Horizontal and endosymbiotic gene transfer events have diversified oomy

109 mes has made it possible to reconstruct this endosymbiotic gene transfer in laboratory experiments an

110 e and potential impact of nucleus-to-nucleus endosymbiotic gene transfer in the evolution of complex

111 statistical approaches to assess impacts of endosymbiotic gene transfer on three principal chromist

112 ree, sampling prokaryotic pangenomes through endosymbiotic gene transfer would lead to inherited chim

113 symbiont genes to the "host" nuclear genome (endosymbiotic gene transfer), and plastid spread through

114 relinquished to the chromosomes of the host (endosymbiotic gene transfer).

115 In addition to endosymbiotic gene transfer, horizontal gene transfer ev

116 the cyanobacterial ancestors of plastids via endosymbiotic gene transfer.

117 find staining for lipid A in free-living and endosymbiotic green algae and in the chloroplasts of vas

118 omes precludes such comparisons, leaving the endosymbiotic history of this organelle unclear.

119 d sequence tag contigs that show evidence of endosymbiotic/horizontal gene transfer involving stramen

120 id origins as well as genes of the secondary endosymbiotic host (the exosymbiont), yet little is know

121 ple the endomembrane system, evolved without endosymbiotic input remains poorly understood.

122 Chloroplasts originate through the endosymbiotic integration of a host and a photosynthetic

123 Endosymbiotic interactions are characterized by the form

124 nformation for understanding host-controlled endosymbiotic life in eukaryotic cells.

125 robial genome revealed strong evidence of an endosymbiotic lifestyle and extreme genome reduction.

126 FLE-Am transitioned recently to its current endosymbiotic lifestyle and likely replaced an ancient e

127 To understand how the endosymbiotic lifestyle has affected the organellar geno

128 rm a monophyletic group, indicating that the endosymbiotic lifestyle has evolved multiple times in Ch

129 arge and are not streamlined for an obligate endosymbiotic lifestyle, implying that they have free-li

130 g bacterium transitions to a host-beneficial endosymbiotic lifestyle, it almost invariably loses a la

131 These endosymbiotic lineages show distinctive population struc

132 l enemies, while insect herbivores may carry endosymbiotic microorganisms that directly improve herbi

133 Because of their obligate endosymbiotic nature, Wolbachia strains by necessity are

134 ivated plants for their ability to carry out endosymbiotic nitrogen fixation with rhizobial bacteria,

135 and thereby contributed to the evolution of endosymbiotic nitrogen fixation.

136 idae, which includes most species capable of endosymbiotic nitrogen fixation.

137 Similar to other endosymbiotic organelles (mitochondria, chloroplasts), t

138 ome species of mesophilic archaea and in the endosymbiotic organelles of eukaryotes.

139 shape of plastids, which are plant-specific endosymbiotic organelles responsible for photosynthesis,

140 distinct types of secretory vesicles and two endosymbiotic organelles.

141 estigation of protein targeting to secondary endosymbiotic organelles.

142 o-chemical GTPases--to drive the division of endosymbiotic organelles.

143 division proteins identified to date are of endosymbiotic origin and are localized inside the organe

144 stids, which suggest that there was a single endosymbiotic origin for these organelles in a common an

145 mes indicate that mitochondria have a single endosymbiotic origin from an alpha-proteobacterial-type

146 elated to bacterial ACADs is consistent with endosymbiotic origin of ACADs in eukaryotes and further

147 tify an ancient mechanism dating back to the endosymbiotic origin of chloroplasts as a key element of

148 DeltapH pathway has been conserved since the endosymbiotic origin of chloroplasts.

149 Following the endosymbiotic origin of eukaryotic cells, increased cell

150 r article, not only did Margulis champion an endosymbiotic origin of mitochondria and plastids from b

151 branching eukaryote that evolved before the endosymbiotic origin of mitochondria, there is also evid

152 The endosymbiotic origin of plastids from cyanobacteria was

153 The idea of an endosymbiotic origin of plastids has become incontrovert

154 The primary endosymbiotic origin of the plastid in eukaryotes more t

155 Therefore, an endosymbiotic origin of Toc75 has been postulated.

156 Mitochondria are essential organelles of endosymbiotic origin that are responsible for oxidative

157 otein translocases in different membranes of endosymbiotic origin.

158 Mitochondria and chloroplasts are of endosymbiotic origin.

159 s mitochondria and chloroplasts, that are of endosymbiotic origin.

160 lasts are essential eukaryotic organelles of endosymbiotic origin.

161 ukaryotic circadian clocks and organelles of endosymbiotic origin.

162 Consistent with their endosymbiotic origins, mitochondria in protists and chlo

163 Wolbachia bacteria are endosymbiotic partners of many animal species, in which

164 chondrion-containing eukaryotic cell from an endosymbiotic partnership is analyzed as a series of tra

165 However, the endosymbiotic phase within Symbiodinium life history is

166 hat form close mutualistic associations with endosymbiotic photosynthetic algae of the genus Symbiodi

167 ical significance for this pattern: becoming endosymbiotic predictably results in decreased stability

168 o groups once harbored mitochondria or their endosymbiotic progenitors.

169 nd interactions between an ancient, obligate endosymbiotic prokaryote with its obligate plant-symbiot

170 nd plastids of eukaryotic cells evolved from endosymbiotic prokaryotes.

171 le (the apicoplast) that was derived from an endosymbiotic relationship between the alveolate ancesto

172 Today, the sheer abundance of endosymbiotic relationships across diverse host lineages

173 Endosymbiotic relationships between eukaryotic and proka

174 Ancient endosymbiotic relationships have led to extreme genomic

175 conduct symbiotic nitrogen fixation through endosymbiotic relationships with bacteria in root nodule

176 Certain bacteria and fungi form root endosymbiotic relationships with plants enabling them to

177 ns observed from biological control systems, endosymbiotic relationships, diseases of cultivated mush

178 hat each matriline was subject to a distinct endosymbiotic reproductive manipulation.

179 nodules mediates metabolite exchange between endosymbiotic rhizobia bacteria and the legume host.

180 ge) and mitotic apparatus originated from an endosymbiotic, spirochete-like organism.

181 xtremophile taxa, including those containing endosymbiotic sulfur-oxidizing bacteria (Lucinoma aequiz

182 he arrangement of hosts and symbionts across endosymbiotic systems suggest that substrate feedback in

183 volutionary theory, in particular the serial endosymbiotic theory and Muller's ratchet.

184 A central component of the endosymbiotic theory for the bacterial origin of the mit

185 Endosymbiotic theory in eukaryotic-cell evolution rests

186 al host and are discussed in relation to the endosymbiotic theory of eukaryote origins.

187 Endosymbiotic theory posits that bacterial genes in euka

188 ew theories that stand to eventually replace endosymbiotic theory with descriptive, gene tree-based v

189 According to the endosymbiotic theory, mitochondrial genomes evolved from

190 trees, once used to test the predictions of endosymbiotic theory, now spawn new theories that stand

191 Viewed from the perspective of endosymbiotic theory, the critical transition at the euk

192 acterial and chloroplast 16s rRNAs, implying endosymbiotic transfer of CesA from cyanobacteria to pla

193 These results suggest that endosymbiotic transfer of recA genes occurred from mitoc

194 During the endosymbiotic transformation of a cyanobacterium into th

195 but little is known about the effects of the endosymbiotic transition on the organellar genomes of eu

196 We show that endosymbiotic Trichomonasvirus, highly prevalent in T. v

197 Endosymbiotic Wolbachia bacteria are abundant in the fil

198 Endosymbiotic Wolbachia bacteria are potential transgene

199 river blindness and elephantiasis, depend on endosymbiotic Wolbachia bacteria for growth, development

200 onema viteae, which is not infected with the endosymbiotic Wolbachia bacteria found in the majority o

201 s studies demonstrated an essential role for endosymbiotic Wolbachia bacteria in corneal disease, whi

202 The discovery that endosymbiotic Wolbachia bacteria play an important role

203 Endosymbiotic Wolbachia bacteria that infect the filaria

204 nematode Onchocerca volvulus, which harbors endosymbiotic Wolbachia bacteria.

205 response in the cornea was due to species of endosymbiotic Wolbachia bacteria.

206 he innate inflammatory pathways activated by endosymbiotic Wolbachia in B. malayi and O. volvulus fil

207 worldwide, a result of the loss of obligate endosymbiotic zooxanthellae.