ライフサイエンスコーパス: sea anemone

1 desktop and bench-top studies of the starlet sea anemone.

2 inase 1 (PMP1) of jellyfish and in toxins of sea anemone.

3 toxins (a-PFTs) that have been identified in sea anemones.

4 al flaps, the only existing synapomorphy for sea anemones.

5 y simpler relatives-the anthozoan corals and sea anemones.

6 volutionarily related to peptide toxins from sea anemones.

7 Consequently, anemonefishes give their host sea anemones a distinct ecological advantage by enhancin

8 he cnidarian Nematostella vectensis (starlet sea anemone), a close relative to the Bilateria, possess

9 Personality in the beadlet sea anemone Actinia equina is linked to genetically dist

10 natoxin II (EqtII), a protein toxin from the sea anemone Actinia equina, readily creates pores in sph

11 pore-forming protein toxin isolated from the sea anemone Actinia equina.

12 mpetition (e.g. ghost shrimp, Caprella spp.; sea anemones, Actinia equina; cone snails, Conidae; male

13 Unlike sea anemone actinoporins that use sphingomyelin as their

14 LT-1 sharing a high structural similarity to sea anemone actinoporins, the atomic resolution structur

15 d preference of HALTs protein as compared to sea anemone actinoporins, we have determined the first c

16 ive amino acid residues in comparison to the sea anemone actinoporins.

17 e of the highly conserved RGD motif found in sea anemone actinoporins.

18 s oligomerisation interface in comparison to sea anemone actinoporins.

19 toxic polypeptides secreted in the venom of sea anemones, actinoporins are the pore-forming toxins w

20 aposymbiotic (alga-free) populations of the sea anemone Aiptasia (Exaiptasia pallida), suggesting th

21 The planula larvae of the sea anemone Aiptasia have so far not been reported to co

22 s, Symbiodiniaceae cannot proliferate in the sea anemone Aiptasia or jellyfish Cassiopea but can prol

23 nthozoan species, and show that in the model sea anemone Aiptasia pallida the TSR domain promotes col

24 mic changes associated with symbiosis in the sea anemone Aiptasia pallida, an important model system

25 The small sea anemone Aiptasia provides a tractable laboratory mod

26 Using the sea anemone Aiptasia, we show that during symbiosis, the

27 during heat stress in a coral relative, the sea anemone Aiptasia.

28 then applied to identify fatty acids from a sea anemone, Aiptasia pulchella, and dinoflagellate symb

29 f several fungal species than to that of the sea anemone (although the insertion site differs in the

30 g early-branching animals such as amphioxus, sea anemone, amoebas and Trichoplax, and in plants and a

31 ing site conservation identifies new ATLs in sea anemone and ancestral archaea, indicating that ATL i

32 an ever-growing repertoire from jellyfish to sea anemones and corals.

33 proteins found in nematocysts of jellyfish, sea anemones and Hydra, but have lost the most important

34 Cnidaria (e.g. sea anemones and jellyfishes) is the sister group to wel

35 ollow mass extinctions and reef crises, with sea anemones and proteinaceous corals filling empty nich

36 , a bright red colonial anthozoan similar to sea anemones and scleractinian stony corals.

37 l model for evolution of miRNA precursors in sea anemones and their relatives, revealing alternative

38 lour score equal to the controls (unbleached sea anemones and without anemonefish), indicating recove

39 spiders, mites, scorpions), Cnidaria (Hydra, sea anemones), and Mollusca (oysters) but not in most ot

40 Cnidarians (corals, sea anemones, and "jellyfish") diverged from other anima

41 zed the proteomes of cilia from sea urchins, sea anemones, and choanoflagellates.

42 animals, such as snakes, spiders, scorpions, sea anemones, and cone snails, produce a variety of high

43 ocess called 'coral bleaching' where corals, sea anemones, and other cnidarians lose their photosynth

44 The stinging organelles of jellyfish, sea anemones, and other cnidarians, known as nematocysts

45 The sea anemone-anemonefish relationship could, therefore, f

46 Increased growth (abundance and size) of the sea anemone (Anemonia viridis) population was observed a

47 eurin B (ApB) isolated from the venom of the sea anemone Anthopleura xanthogrammica is one of a famil

48 ino acid polypeptide toxins from the Pacific sea anemone Anthopleura xanthogrammica that interfere wi

49 nthopleurin B (ApB), a toxin produced by the sea anemone Anthopleura xanthogrammica, is the most pote

50 Examples include the homology between a sea anemone antihypertensive/antiviral protein and a sea

51 -NF-kappaB alleles in natural populations of sea anemones are discussed.

52 Since sea anemones are opportunistic suspension feeders, they

53 Sea anemones are seemingly primitive animals that, along

54 mic approaches, we demonstrate that the host sea anemones are the drivers of convergent evolution in

55 dinium and its cnidarian hosts (e.g. corals, sea anemones) are the foundation of coral-reef ecosystem

56 Feeney and Brooker introduce sea-anemone associated fish.

57 lves and polychaetes in the upper layers and sea anemones at the base.

58 using a double-digest RADseq dataset for the sea anemone Bartholomea annulata.

59 neae) was first described in 2006 as a giant sea anemone based on morphology.

60 Cnidarians, including jellyfish and sea anemones, both detect and capture prey using stingin

61 To test this, bleached and unbleached sea anemones, both with and without anemonefish, were mo

62 cells, which are common in other species of sea anemone but appear to have been silenced in N. vecte

63 e detected in the COI and ND5 genes of other sea anemones, but not in the COI and ND5 genes of other

64 rphological evolution in anthozoans (corals, sea anemones) by examining skeletal traits in the contex

65 Several polypeptide toxins from sea anemones caused delayed inactivation of mammalian vo

66 aria - controls hair cell development in the sea anemone cnidarian Nematostella vectensis.

67 -type diversity of mechanosensory neurons in sea-anemone cnidarian Nematostella vectensis.

68 mination, PM(1) was detected in 21 of the 22 sea anemones collected from Taiwan and Southeast China,

69 ionships (five species of Symbiodiniaceae in sea anemone, coral, and jellyfish hosts) revealed that i

70 The phylum Cnidaria (sea anemones, corals, hydras and jellyfish) is the likel

71 cterized in basal phyla, including Cnidaria (sea anemones, corals, hydras, and jellyfish), Porifera (

72 eria and includes familiar animals including sea anemones, corals, hydroids, and jellyfish.

73 However, the coral and sea anemone cox1 group I introns differed in several asp

74 suggested based on the existence of PM(1) in sea anemone eggs and in brooding and released juveniles.

75 the molecular and genetic approaches in this sea anemone, endogenous protein tagging is still challen

76 ild-type red fluorescent progenitor eqFP578 (sea anemone Entacmaea quadricolor), is monomeric and cha

77 In sea anemones, epithelia emerge both during embryonic dev

78 mparisons we reveal that toxin expression in sea anemones evolves rapidly and that in each species di

79 munohistochemistry and immunoblotting in the sea anemone Exaiptasia diaphana ('Aiptasia'): Prostaglan

80 rns from O. arbuscula with prior work in the sea anemone Exaiptasia pallida (Aiptasia) and the salama

81 Symbiont-free individuals of the sea anemone Exaiptasia pallida (commonly referred to as

82 s (both ITS2-type A4) were isolated from the sea anemone Exaiptasia pallida and placed into unialgal

83 y scale we have characterized NF-kappaB in a sea anemone (Exaiptasia pallida; called Aiptasia herein)

84 The larvae of the sea anemone, Exaiptasia pallida (commonly referred to as

85 Jellyfish and sea anemones fire single-use, venom-covered barbs to imm

86 The sea anemone genome is complex, with a gene repertoire, e

87 Their association with sea anemones has been proposed to be a key innovation th

88 tacles, column, and mesenterial filaments of sea anemone Heteractis crispa, revealing the diversity a

89 vide a major revision of the known clownfish-sea anemone host associations, accounting for the biolog

90 lgae as they reach high-densities within the sea anemone host Exaiptasia pallida.

91 Our findings reveal that the sea anemone host plays a crucial role in driving clownfi

92 standing mystery by testing the influence of sea anemone host use on phenotypic divergence.

93 Cnidarians (corals, sea anemones, hydroids, and jellyfish) are a basal taxon

94 nel gene families are highly expanded in the sea anemone, including three subfamilies of the Shaker K

95 ium) and their cnidarian hosts (e.g. corals, sea anemones) is the foundation of coral reef ecosystems

96 ), including 14 874 predicted genes from the sea anemone itself.

97 th cnidarians, a group that includes corals, sea anemones, jellyfish, and hydroids, is supported by s

98 Hox and TALE proteins interact in a sea anemone, just as they do in flies and mice, indicati

99 nd NADH dehydrogenase subunit 5 (ND5) of the sea anemone Metridium senile (phylum Cnidaria) each cont

100 reported for the cox1 group I intron in the sea anemone Metridium senile.

101 ents of TRPA1 was isolated from the venom of sea anemone Metridium senile.

102 -pair mitochondrial (mt) DNA molecule of the sea anemone, Metridium senile (class Anthozoa, phylum Cn

103 ing metazoans, we present 15 newly-sequenced sea anemone mitochondrial genomes and a mitogenome-based

104 This suggests that the sea anemone mitochondrial introns may have been acquired

105 We used both the sea anemone model system Aiptasia and several species of

106 Based in part on experiments in a sea-anemone model system, we targeted the gene encoding

107 s, including entamoeba, soybean rust, hydra, sea anemone, nematodes, fruit flies, beetle, sea urchin,

108 The sea anemone Nematostella is a non-bilaterian animal, a m

109 The sea anemone Nematostella vectensis (Anthozoa, Cnidaria)

110 The sea anemone Nematostella vectensis (Nv) is a leading mod

111 Among the basal animals, the starlet sea anemone Nematostella vectensis (phylum Cnidaria) has

112 We searched for neuropeptides in the sea anemone Nematostella vectensis and created a library

113 d transcriptomes of the apical tissue in the sea anemone Nematostella vectensis and showed that it ha

114 Here we utilize the tentacles of the sea anemone Nematostella vectensis as an experimental pa

115 teins and associated factors for the starlet sea anemone Nematostella vectensis based on in silico pr

116 Among marine invertebrates, the starlet sea anemone Nematostella vectensis has emerged as an imp

117 tic analysis of the Talpid3 homolog from the sea anemone Nematostella vectensis identified a highly c

118 Interestingly, STING from the sea anemone Nematostella vectensis induces autophagy but

119 The sea anemone Nematostella vectensis is a useful cnidarian

120 The sea anemone Nematostella vectensis is the leading develo

121 e functions of two Argonaute paralogs in the sea anemone Nematostella vectensis of the phylum Cnidari

122 The starlet sea anemone Nematostella vectensis serves as a cnidarian

123 Here, we probe the capacity of the starlet sea anemone Nematostella vectensis to form associative m

124 Here, we use the embryos of the sea anemone Nematostella vectensis to investigate the ev

125 Here, we used the sea anemone Nematostella vectensis to test the impact of

126 n-bilaterian phylum Cnidaria, embryos of the sea anemone Nematostella vectensis undergo rapid synchro

127 a model cnidarian invertebrate, the starlet sea anemone Nematostella vectensis Using RNA sequencing,

128 ration gene regulatory networks (GRN) in the sea anemone Nematostella vectensis using transcriptomic

129 A simple NF-kappaB pathway is present in the sea anemone Nematostella vectensis, an important model o

130 Bilateria, some representatives, such as the sea anemone Nematostella vectensis, exhibit bilateral sy

131 s, is expressed in the nervous system in the sea anemone Nematostella vectensis, similar to its mamma

132 approaches in embryos of the early-branching sea anemone Nematostella vectensis, we identified the Ne

133 g CRISPR/Cas9-mediated genome editing in the sea anemone Nematostella vectensis, we show that a singl

134 Here, we use the sea anemone Nematostella vectensis, which has evolved th

135 of an emerging cnidarian model, the starlet sea anemone Nematostella vectensis.

136 t the onset of gastrulation in the anthozoan sea anemone Nematostella vectensis.

137 ole adults and gastrula-stage embryos of the sea anemone Nematostella vectensis.

138 equence of nematocyst operation in the model sea anemone Nematostella vectensis.

139 ent polarization in developing larvae of the sea anemone Nematostella vectensis.

140 s recombination-mediated transgenesis in the sea anemone Nematostella vectensis.

141 nd characterized Erg channel paralogs in the sea anemone Nematostella vectensis.

142 cular composition of the apical organ of the sea anemone Nematostella vectensis.

143 velopment of a basal metazoan, the cnidarian sea anemone Nematostella vectensis.

144 me assemblies of two related anthozoans, the sea anemones Nematostella vectensis and Scolanthus calli

145 proteins derived from human and the starlet sea anemone (Nematostella vectensis) in 1) a high-throug

146 ined how the axial properties of the starlet sea anemone, Nematostella vectensis (Anthozoa, Cnidaria)

147 Over the past 20 years, the starlet sea anemone, Nematostella vectensis, a small estuarine a

148 The starlet sea anemone, Nematostella vectensis, is a basal metazoan

149 In-depth analysis of the sea anemone, Nematostella vectensis, revealed striking v

150 Using functional genomics in the sea anemone, Nematostella vectensis, we show that cnidoc

151 lly during bilaterian embryogenesis from the sea anemone, Nematostella vectensis.

152 for an emerging model system, the cnidarian sea anemone, Nematostella vectensis.

153 onents of the circadian clock in the starlet sea anemone, Nematostella vectensis: a model cnidarian w

154 Anthopleurin B (ApB) is a high-affinity sea anemone neurotoxin that interacts with voltage-sensi

155 one antihypertensive/antiviral protein and a sea anemone neurotoxin, and the homology between tick an

156 For sea anemones, nutritional benefits derived from hosting

157 ite of APETx1, a peptide toxin purified from sea anemone, on the human ether-a-go-go-related gene (hE

158 Cnidarians such as sea anemones or jellyfish possess a nerve net, which lac

159 or, alternatively, large cnidarians such as sea anemones or sea pens.

160 The sea anemone peptide APETx2 is a potent and selective blo

161 The structurally defined sea anemone peptide toxins ShK and BgK potently block th

162 1) according to a structure similar to other sea anemone peptides belonging to structural group 9a.

163 s, with a primary structure similar to other sea anemone peptides belonging to structural group 9a.

164 e2 but not ShK-like1 is conserved throughout sea anemone phylogeny, we conclude that the two paralogs

165 Studies of the starlet sea anemone provide important insights into the early ev

166 he cnidarian Nematostella vectensis (starlet sea anemone) provides a molecular genetic view into the

167 ucturally defined polypeptide, ShK, from the sea anemone Stichodactyla helianthus inhibited Kv1.3 pot

168 ShK toxin from the sea anemone Stichodactyla helianthus is a 35-residue pro

169 ) T(EM) cells, and the potent Kv1.3-blocking sea anemone Stichodactyla helianthus peptide (ShK) suppr

170 y analoging to ShK, a peptide toxin from the sea anemone Stichodactyla helianthus that inhibits the v

171 versatile serine protease inhibitor from the sea anemone Stichodactyla helianthus with high biomedica

172 toxin, a potassium channel blocker from the sea anemone Stichodactyla helianthus, is a 35 residue po

173 cholysins I and II (StnI and StnII) from the sea anemone Stichodactyla helianthus, it is shown that a

174 I, a pore-forming protein from the Caribbean Sea anemone Stichodactyla helianthus, was encapsulated w

175 disulfide-linked polypeptide produced by the sea anemone Stichodactyla helianthus, which blocks the p

176 protein ion-channel ligand isolated from the sea anemone Stichodactyla helianthus.

177 natoxin II (EqtII) is a model alpha-PFT from sea anemone that oligomerizes and forms pores in sphingo

178 d a Kv1.3 blocker peptide (ShK) derived from sea anemone to generate a subtype-selective Kv1.3 blocke

179 In the presence of sea anemone toxin (ATX-II; 20 nmol/L), an increase in pa

180 The sea anemone toxin anthopleurin B, which impairs open-cha

181 ashion at the transcriptional level, and the sea anemone toxin BDS-I is shown to protect against Abet

182 loop participate in alpha-scorpion toxin and sea anemone toxin binding to overlapping sites and that

183 I(Kr) (mimicking long QT syndrome 2) or with sea anemone toxin II to impair Na(+) channel inactivatio

184 mined the ability of anthopleurin B (ApB), a sea anemone toxin that selectively modifies inactivation

185 ssion electron microscopy in a drug-induced (sea anemone toxin, ATXII) Na(+) channel GOF isolated hea

186 Anthopleurin B (ApB) is a type 1 sea anemone toxin, which binds to voltage-sensitive sodi

187 ffects on binding of alpha-scorpion toxin or sea anemone toxin.

188 xD) shows close structural similarity to the sea anemone toxins BgK and ShK.

189 alpha-Scorpion toxins and sea anemone toxins bind to a common extracellular site o

190 a, revealing the diversity and complexity of sea anemone toxins in different tissues.

191 fold lower affinities for alpha-scorpion and sea anemone toxins, respectively.

192 mol), a residue that is conserved among many sea anemone toxins.

193 of proteins that contain domains related to sea anemone toxins.

194 We report here that AETX-K, a sea anemone type I (SAK1) peptide toxin we isolated from

195 fabricated on the scaffold present in ShK, a sea anemone type I (SAK1) toxin stabilized by three disu

196 d that oxybenzone caused high mortality of a sea anemone under simulated sunlight including ultraviol

197 peptides were isolated from the venom of the sea anemone Urticina grebelnyi.

198 Peptide toxins found in sea anemones venom have diverse properties that make the

199 Scorpion and sea anemone venoms contain several polypeptides that del

200 The bioaccumulation factor of PM(1) in sea anemones was approximately 5-7 orders of magnitude.

201 e were lower in the bleached than unbleached sea anemones, whereas total chlorophyll remained similar

202 f functions for FPs in a clade of intertidal sea anemones whose FPs control a genetic color polymorph

203 Unbleached sea anemones with anemonefish also showed positive chang

204 After 106 days, bleached sea anemones with anemonefish had an algal symbiont dens

205 l chlorophyll was 66% higher in the bleached sea anemones with anemonefish than the controls.

206 ast, recovery did not occur for the bleached sea anemones without anemonefish as they had 78% fewer a