ライフサイエンスコーパス: endosymbiosis

1 able to develop rhizobial and/or mycorrhizal endosymbiosis.

2 photosynthetic organelles (plastids) through endosymbiosis.

3 he eukaryotic domain through primary plastid endosymbiosis.

4 ar algae with plastids acquired by secondary endosymbiosis.

5 he salamander Ambystoma maculatum forming an endosymbiosis.

6 early progenitor of the Phylum by secondary endosymbiosis.

7 e cellular biology of the coral-Symbiodinium endosymbiosis.

8 by four membranes, deriving from a secondary endosymbiosis.

9 ly variable nature of the coral-Symbiodinium endosymbiosis.

10 important evolutionary pathway toward stable endosymbiosis.

11 functionality of dinoflagellate genomes and endosymbiosis.

12 population genetic theory incompatible with endosymbiosis.

13 ucleus to the other in the context of serial endosymbiosis.

14 related eukaryotes by secondary and tertiary endosymbiosis.

15 erstanding the evolution and function of the endosymbiosis.

16 any role in establishing the primary plastid endosymbiosis.

17 ntegration and favors a host-centric view of endosymbiosis.

18 ymbiont is required for the formation of the endosymbiosis.

19 sm with plastids that derived from secondary endosymbiosis.

20 ed manner and, therefore, forms the heart of endosymbiosis.

21 es and large-scale transfer of genes through endosymbiosis.

22 understanding the biology of this widespread endosymbiosis.

23 re intimate associations of pathogenesis and endosymbiosis.

24 chanisms for plant cell reprogramming during endosymbiosis.

25 a red algal origin via an ancient secondary endosymbiosis.

26 d spread into other eukaryotes via secondary endosymbiosis.

27 cus on understanding early events in plastid endosymbiosis.

28 ltilevel selection on both species encourage endosymbiosis.

29 a unique system to study the cell biology of endosymbiosis.

30 to outstanding questions about mitochondrial endosymbiosis [1, 2].

31 r to the event that led to the mitochondrion endosymbiosis [2,4].

32 have provided fresh evidence that secondary endosymbiosis accounts for this organelle's presence in

33 upy novel environments [1, 2]; consequently, endosymbiosis affects the structure and function of ecos

34 Endosymbiosis allows hosts to acquire new functional tra

35 omplex plastids," which evolved by secondary endosymbiosis and are surrounded by four membranes.

36 sues are key organelles in the regulation of endosymbiosis and exhibit a diel rhythmicity.

37 ions range from weak epibiosis to obligatory endosymbiosis and from restricted commensalism to semi-p

38 ulation genetics sufficiently explanatory of endosymbiosis and its role in evolution?

39 t to the major evolutionary events including endosymbiosis and land colonization.

40 in and LCO perception in innate immunity and endosymbiosis and question how LCOs might modulate the i

41 chloroplasts, multiple origins of bacterial endosymbiosis are known within the cells of diverse anim

42 ular and cellular mechanisms underlying this endosymbiosis are not well understood, in part because o

43 is is an example in which a chemoautotrophic endosymbiosis arose by displacement of an ancestral hete

44 Chromista monophyly and implicates secondary endosymbiosis as an important force in generating eukary

45 evolutionary mechanism for their origin: an endosymbiosis between a clostridium and actinobacterium.

46 The apicoplast is the product of an ancient endosymbiosis between a heterotrophic and a photosynthet

47 The mutualistic endosymbiosis between cnidarians and dinoflagellates is

48 ptome are predicted to support aspects of an endosymbiosis between this microbe and gastric stem cell

49 aeal and bacterial systems via mitochondrial endosymbiosis, but also involved emergence of several ne

50 st it played a crucial role in early plastid endosymbiosis by connecting the endosymbiont and host ca

51 early steps of mitochondrial and chloroplast endosymbiosis by tracing the evolution of dynamins.

52 ole for NAD1 in the maintenance of rhizobial endosymbiosis during nodulation.

53 This may represent a possible serial endosymbiosis event deep in eukaryotic evolutionary hist

54 However, endosymbiosis events and gene duplications provide some

55 l ancestors, but the dating of these primary endosymbiosis events remains very uncertain, despite the

56 Secondary endosymbiosis explains the majority of algal biodiversit

57 During the endosymbiosis formed between plants and arbuscular mycor

58 mycorrhizal (AM) symbiosis is a mutualistic endosymbiosis formed by plant roots and AM fungi.

59 o starch accumulation occurred after plastid endosymbiosis from a preexisting cytosolic host glycogen

60 In this endosymbiosis, fungal hyphae enter the roots, growing th

61 olution, the merging of two lineages through endosymbiosis has also made profound contributions to ev

62 rically, conceptualizations of symbiosis and endosymbiosis have been pitted against Darwinian or neo-

63 The processes accompanying endosymbiosis have led to a complex network of interorga

64 o have originated from a haptophyte tertiary endosymbiosis in an ancestral peridinin-containing dinof

65 larification of the obligatory nature of the endosymbiosis in this nematode is needed.

66 nated via a putative single, ancient primary endosymbiosis in which a heterotrophic protist engulfed

67 The arbuscular mycorrhiza is an endosymbiosis in which the fungus inhabits the root cort

68 rent knowledge suggests that plastid primary endosymbiosis, in which a single-celled protist engulfs

69 oximately 1,260 million years ago) secondary endosymbiosis involving a red alga.

70 Obligate endosymbiosis is operationally defined when loss or remo

71 In summary, although bacterial endosymbiosis is widely detected in clinical isolates of

72 stead be asking how explanatory of evolution endosymbiosis is, and exactly which features of evolutio

73 ) from prokaryotes to eukaryotes, outside of endosymbiosis, is still rather limited.

74 the plastid, suggesting that the process of endosymbiosis likely is accompanied by an intimate coevo

75 asking whether population genetics explains endosymbiosis may have the question the wrong way around

76 end utilization paths in a constructed quasi-endosymbiosis model.

77 e-living bacteria that were acquired through endosymbiosis more than a billion years ago.

78 rred approximately 900 Mya and mitochondrial endosymbiosis occurred approximately 1,200 Mya.

79 Our results suggest that primary plastid endosymbiosis occurred approximately 900 Mya and mitocho

80 Today, this endosymbiosis occurs broadly in the plant kingdom where

81 Stable endosymbiosis of a bacterium into a host cell promotes c

82 assembly machinery from prokaryotes via the endosymbiosis of a bacterium that led to formation of mi

83 anelles, originated >1 billion y ago via the endosymbiosis of a cyanobacterium.

84 t appears to have been acquired by secondary endosymbiosis of a green alga.

85 yotic stem lineage gained organelles through endosymbiosis of already diversified bacterial lineages.

86 apicoplast, a plastid acquired by secondary endosymbiosis of an alga.

87 An ancient endosymbiosis of an alpha-proteobacterium produced a div

88 The chloroplast originated from the endosymbiosis of an ancient photosynthetic bacterium by

89 her alveolates, may have been acquired by an endosymbiosis of an early ochrophyte.

90 Endosymbiosis of bacteria by eukaryotes is a defining fe

91 source organisms in a process termed "serial endosymbiosis of chloroplasts." However, it is not known

92 The endosymbiosis of proto-mitochondrial prokaryotes (PMP) i

93 lastid genes and to understand the impact of endosymbiosis on genome evolution.

94 ether M. rubrum is the result of a permanent endosymbiosis or a transient association between a cilia

95 a few species and is usually associated with endosymbiosis or parasitism.

96 The phenomenon of endosymbiosis, or one organism living within another, ha

97 Following endosymbiosis, plastids have evolved to optimize their f

98 Apicomplexa acquired a plastid by secondary endosymbiosis, probably from a green alga.

99 The aphid-Buchnera endosymbiosis provides a powerful system to elucidate ho

100 tic host ancestral participants of secondary endosymbiosis, respectively, a mechanistic model of olea

101 lulose synthases acquired before the primary endosymbiosis showing the polyphyly of cellulose synthes

102 It is widely accepted that the endosymbiosis that established the chloroplast lineage i

103 It is very likely that the primary endosymbiosis that explains plastid origin relied initia

104 The endosymbiosis that gave rise to mitochondria restructure

105 have been acquired by the Eucarya during the endosymbiosis that gave rise to the mitochondrion and ch

106 A single cyanobacterial primary endosymbiosis that occurred approximately 1.5 billion ye

107 llates originated from a haptophyte tertiary endosymbiosis that occurred before the split of these li

108 Derived from secondary endosymbiosis, the apicoplast depends on novel, but larg

109 These results suggest that prior to plastid endosymbiosis, the dinoflagellate ancestor possessed com

110 This organelle is the product of secondary endosymbiosis, the marriage of an alga and an auxotrophi

111 Maintenance of the endosymbiosis then depends on reciprocal nutrient exchan

112 Overwhelming evidence supports the endosymbiosis theory that mitochondria originated once f

113 According to classical endosymbiosis theory, insertion of a host-nuclear-encode

114 pproach, which is derived from the wisdom of endosymbiosis theory, to fill gaps by finding the most e

115 nuclear spliceosome evolved after bacterial endosymbiosis through fragmentation of self-splicing gro

116 s plastid lineage, acquired through tertiary endosymbiosis, utilises transcript processing pathways t

117 Endosymbiosis was essential to the success of chromalveo

118 ry of a recent proposal that primary plastid endosymbiosis was facilitated by the secretion into the

119 his question by showing that primary plastid endosymbiosis was likely to have been primed by the secr

120 er-Smith, 1981) plastids evolved via primary endosymbiosis whereby a heterotrophic protist enslaved a

121 eukaryotes diverged before the mitochondrial endosymbiosis, which would make them one of the earliest

122 e plastids have been replaced through serial endosymbiosis with plastids derived from a different phy