ライフサイエンスコーパス: teleost

1 ative pathways for DHA biosynthesis exist in teleosts.

2 ance, and somatic growth in both mammals and teleosts.

3 resent, a unique situation compared to other teleosts.

4 r than an exceptional feature of early crown teleosts.

5 latory mechanisms of LC-PUFA biosynthesis in teleosts.

6 ge prior to the divergence of tetrapods from teleosts.

7 eproductive and nonreproductive functions in teleosts.

8 ppose enhanced phenotypic diversification in teleosts.

9 upeocephala which includes all the remaining teleosts.

10 sue distribution distinct from that found in teleosts.

11 tus), a neopterygian fish closely related to teleosts.

12 fish lacking the whole genome duplication of teleosts.

13 s, most of these genes are not restricted to teleosts.

14 erved functions of the melanopsins in marine teleosts.

15 in functions, the only known exception being teleosts.

16 ared with classifications proposed for other teleosts.

17 present in all vertebrate groups, except for teleosts.

18 present in basal fishes, not found in extant teleosts.

19 hed the Sox10 migratory patterns observed in teleosts.

20 retinal specialization is uniquely found in teleosts.

21 the kidney, the main hematopoietic organ in teleosts.

22 on is compared with those proposed for other teleosts.

23 9 shows the highest expression in ovaries of teleosts, a tissue in which both androgen signaling and

24 Many tetrapods and non-teleost actinopterygians have undergone body elongation

25 responsible for the regenerative capacity of teleosts, amphibians, and reptiles have fallen into disu

26 xpression of CARTp has been characterized in teleosts, amphibians, and several mammalian species, but

27 ublished data from lampreys, chondrichthyes, teleosts, amphibians, reptiles, birds, and mammals.

28 frican lineage compared to tilapia and other teleosts, an abundance of non-coding element divergence,

29 omosome rearrangements after speciation from teleost ancestor.

30 d as a membrane androgen receptor in various teleost and mammalian cell models.

31 , a set of lncRNAs are microsyntenic between teleost and vertebrates, which indicates potential regul

32 a shared developmental stage in Aetheretmon, teleosts and all living actinopterygians.

33 Teleosts and amphibians exhibit retinomotor movements, m

34 itional PLIN clade (plin6) that is unique to teleosts and can be traced to the two whole genome dupli

35 fishes (the more extensive clade containing teleosts and holosteans).

36 The Oatp1d subfamily emerged in teleosts and is absent in tetrapods.

37 hat, based on nLV/nI cell responses in other teleosts and isthmic connectivity in A. leptorhynchus, t

38 ellular mechanisms underpinning olfaction in teleosts and mammals are similar despite 430 million yea

39 enteric glia and brain neural stem cells in teleosts and open new possibilities for use of mammalian

40 ghts into the organization of 5-HT nuclei in teleosts and provides neuroanatomical evidence for serot

41 cific DC-like subtype in nonimmune tissue in teleosts and support the hypothesis of a common origin f

42 hway represents an alternative route in some teleosts and we identified the presence of putative Delt

43 ision plays a major role in the life of most teleosts, and is assumingly well adapted to each species

44 In teleosts, and some others, a stunted tail is eclipsed by

45 /urotensin1 (UCN1/UTS1) in primitive fishes, teleosts, and tetrapods.

46 lium, and in the thalamus and cerebellum, of teleosts appear to have evolved following the separation

47 HCs in teleosts are classified into four subtypes (H1-H4), each

48 t those emerging from studies of both extant teleosts as a whole and their sublineages, which general

49 Given the evolutionary position of teleosts as early vertebrates with a fully developed imm

50 The teleost Astyanax mexicanus is one species extant in two

51 tudy examines vestigial eye formation in the teleost Astyanax mexicanus, which consists of a sighted

52 nd evolutionary time scales, we examined the teleost Astyanax mexicanus.

53 steus oculatus), whose lineage diverged from teleosts before teleost genome duplication (TGD).

54 ceed those of stem-, crown-, and total-group teleosts, belying the living fossil reputation of their

55 icated genome, now helps to bridge human and teleost biology.

56 Although TRH is abundantly expressed in teleost brain and believed to mediate neuronal communica

57 RGCs) are the most abundant macroglia in the teleost brain and have established roles in neurogenesis

58 Enrichment of gene sets indicative of teleost brain-pituitary-gonadal-hepatic (BPGH) axis func

59 NF involvement in the aging processes of the teleost brain.

60 supporting conserved roles for both genes in teleost brains.

61 e sequence of spotted gar, a fish related to teleosts but lacking a duplicated genome, now helps to b

62 are highly conserved among distantly related teleosts, but largely missing from marine stickleback du

63 ted in the brain of mammals, amphibians, and teleosts, but the relevant information in avian brain is

64 ferent Ca(2+)-binding properties between the teleost cardiac (cTnC or TnC1a) and slow-skeletal (ssTnC

65 tinize the development and specialization of teleost CD4(+) leukocytes in vivo.

66 by the imaging of intimate contacts between teleost CD4(+) T cells and mononuclear phagocytes.

67 we reveal the conserved subspecialization of teleost CD4(+) T cells in vivo.

68 activity, thus establishing a novel role for teleost chemokines in antimicrobial immunity that suppor

69 ctional insights into how POA populations in teleosts compare to the POA and anterior hypothalamus of

70 cis regulatory) undetectable in direct human-teleost comparisons become apparent using gar: functiona

71 As the first marine teleost demonstrated to have the ability to biosynthesiz

72 We find that early teleosts do not show enhanced phenotypic evolution relat

73 iological and evolutionary links between non-teleost electroreceptors and hair cells.

74 beta subtypes are critically involved in the teleost estrogenic response, with the ERalpha:ERbeta rat

75 likely resulting from a duplication event in teleost evolution.

76 Although stem teleosts excel at discovering new body shapes, early cro

77 finned fishes (Actinopterygii), relatives of teleosts, exhibited ancestral scale-covered tails curved

78 might not directly drive diversification of teleost Fads2 as initially hypothesised, and other facto

79 nderstanding of phenotypic plasticity in the teleost feeding apparatus and in doing so contribute key

80 The symmetrical, flexible teleost fish 'tail' has been a prime example of recapitu

81 ab, great spider crab, and edible crab); and teleost fish (Atlantic cod, European place, and Lemon so

82 m a biomineral called otolith extracted from Teleost fish (Plagioscion Squamosissimus) and multiwalle

83 family, we characterized a novel GHR from a teleost fish (rainbow trout).

84 , we demonstrate that eggs from amphibia and teleost fish also release zinc.

85 are the largest neurons in the hindbrain of teleost fish and most amphibians.

86 s from zebrafish are extending older work on teleost fish and reptiles to reveal rich color circuitry

87 is seen in some homoiotherm species such as teleost fish and urodelian amphibians leading to the hyp

88 Teleost fish are among the most ancient vertebrates poss

89 Teleost fish are capable of complex behaviors, including

90 Teleost fish are exceptional in retaining a rhombomeric

91 Marine teleost fish are important carbonate producers in neriti

92 taglandin F2alpha (PGF2alpha) levels rise in teleost fish around the time of ovulation [10, 14, 15].

93 functional implications of jaw protrusion in teleost fish assemblages from shallow coastal seas since

94 vity in a hippocampal (CA3)-like region of a teleost fish brain and connects it to active sensing of

95 mokine receptors have rapidly diversified in teleost fish but their immune functions remain unclear.

96 Teleost fish contain two 17A P450s; zebrafish P450 17A1

97 Even though teleost fish do not have either of these secondary lymph

98 Teleost fish express at least three estrogen receptor (E

99 By contrast, teleost fish functionally regenerate their retina follow

100 The lymphatic system in teleost fish has genetic and developmental origins simil

101 on nutrient-poor squid and invertebrates as teleost fish have declined in availability.

102 s a consequence of whole genome duplication, teleost fish have two ridA paralogs, while other extant

103 utionary conservation of trained immunity in teleost fish is lacking.

104 ure of the full-length CR4/5 domain from the teleost fish medaka (Oryzias latipes).

105 s by a unique fauna that includes a group of teleost fish of the sub-order Cottoidei.

106 regulation and antimicrobial response, many teleost fish present multiple copies of hepcidin, most l

107 Marine teleost fish produce CaCO3 in their intestine as part of

108 haracters in other sonic and weakly electric teleost fish provide a striking example of convergent ev

109 Teleost fish rely heavily on their innate immunity for a

110 Teleost fish represent the most ancient bony vertebrates

111 SC) and comparisons with a 1.7A structure of teleost fish SC (tSC), an early pIgR ancestor.

112 ng for nocturnal vertebrates, including many teleost fish species that are also highly vocal during p

113 c position at the base of the ~30,000 modern teleost fish species.

114 calis and Anolis lizard and three members in teleost fish such as stickleback and medaka.

115 on, we demonstrate in a nocturnally breeding teleost fish that (1) courtship vocalization exhibits an

116 Astyanax mexicanus is a teleost fish that is in the process of allopatric specia

117 In conclusion, teleost fish that present two hepcidin types show a degr

118 re for the vertebrate t/PK is conserved from teleost fish to human.

119 ng and single-cell sequencing of two related teleost fish uncovered species-specific and evolutionari

120 In contrast, teleost fish v2r genes are intermingled with all other o

121 es including passeriform birds, reptiles and teleost fish whose egg yolk contain phosvitin.

122 er cell (M-cell) is a command-like neuron in teleost fish whose firing in response to aversive stimul

123 The brain of zebrafish, a teleost fish widely used as vertebrate model, also posse

124 shipman (Porichthys notatus), a highly vocal teleost fish with two male morphs that follow alternativ

125 As in mammals, teleost fish, and amphibians, CARTp-ir terminals and cel

126 etween the representative mammal, amphibian, teleost fish, and basal vertebrate indicate that all of

127 Phylogenetic analysis revealed six Mates in teleost fish, annotated as Mate3-8, which form a distinc

128 cells, called eurydendroid neurons (ENs) in teleost fish, are inhibited by Purkinje cells and excite

129 ere we analyze the genetic divergence of the teleost fish, Fundulus heteroclitus, among microhabitats

130 In teleost fish, gill slits arise through opening of endode

131 Zebrafish, as a model for teleost fish, have two paralogous troponin C (TnC) genes

132 mutations that arose in an ancestor of most teleost fish, implying that most fish lack effective RNA

133 In teleost fish, increased galanin expression is associated

134 esence of two Cx36 homologs is restricted to teleost fish, it might also be based on differences in p

135 The three-spined stickleback is a small teleost fish, native to coastal regions of the Northern

136 The present survey was conducted in a teleost fish, Nothobranchius furzeri, because it is an e

137 o maintain O-MALT structures in adulthood of teleost fish, sarcopterygian fish, or birds.

138 In teleost fish, the immune functions of mannan-binding lec

139 c behavior in the nocturnal and highly vocal teleost fish, the plainfin midshipman (Porichthys notatu

140 Even though adaptive immunity is present in teleost fish, these species lack lymph nodes and GCs.

141 In teleost fish, two distinct IGF-IR duplicates are conserv

142 By studying teleost fish, we find that gene duplication followed by

143 , although P2a.1 is not predicted to form in teleost fish, we find that it forms in the full-length p

144 To study the roles of hepcidin in teleost fish, we have isolated and characterized several

145 uals feeding mainly on small crustaceans and teleost fish, whereas the diet of larger fish included m

146 from primates to early vertebrates, such as teleost fish.

147 amide (LPXRFa) motif have been identified in teleost fish.

148 g of T cell function and immune responses in teleost fish.

149 of Tnfalpha production in trout, a primitive teleost fish.

150 rtant for maintaining calcium homeostasis in teleost fish.

151 types (named I and II) of TNF-alpha exist in teleost fish.

152 iderably less comparative data available for teleost fish.

153 reported to have a miRNome larger than most teleost fish.

154 vertebrates and to the regenerating heart of teleost fish.

155 otelomer sulfonate (6:2 FTS) was detected in teleost fish.

156 TrkA receptor with the viral glycoprotein in teleost fish.

157 gs for future studies on trained immunity in teleost fish.

158 s, which has not been previously observed in teleost fish.

159 paralogues (IL-4/13 A and IL-4/13B) exist in teleost fish.

160 usly identified in the optic tectum of other teleost fish: the tectal pyramidal neuron (PyrN).

161 how widespread this dependence is across all teleost fishery target species and within atolls is uncl

162 the face and braincase modules of a clade of teleost fishes (Gymnotiformes) and a clade of mammals (C

163 CRH2 was subsequently lost in both teleost fishes and eutherian mammals but retained in oth

164 ichthyans in addition to previously reported teleost fishes and reptiles.

165 The gills of most teleost fishes are covered by plate-like structures, the

166 Antifreeze proteins (AFPs) of polar marine teleost fishes are widely recognized as an evolutionary

167 Crown teleost fishes diversified relatively recently, during t

168 A new study reveals teleost fishes evolved their solid vertebrae following g

169 with depth, going from 40 to 261 mmol/kg in teleost fishes from 0 to 4,850 m.

170 Previous work in teleost fishes has focused on hypothalamic tac3 expressi

171 In teleost fishes, 17alpha,20beta-dihydroxy-4-pregnen-3-one

172 with 40-42 genes in birds to 66-74 genes in teleost fishes, all NRs had clear homologs in human and

173 m groups as diverse as sharks, rays and stem teleost fishes, and in mysticete whales.

174 In teleost fishes, details of the organization of this syst

175 Percomorpha, comprising about 60% of modern teleost fishes, has been described as the "(unresolved)

176 een struck by the extraordinary diversity of teleost fishes, particularly in contrast to their closes

177 In teleost fishes, the most species-rich vertebrate group,

178 In teleost fishes, there is considerable mixing between cel

179 By examining extant teleost fishes, we identified a robust morphological pre

180 ntially remains unexplored, especially among teleost fishes, which comprise nearly one-half of living

181 ne cell type described for the first time in teleost fishes.

182 sensory functions and alters the behavior of teleost fishes.

183 t critical life-history transitions for most teleost fishes.

184 the diversity gill morphologies observed in teleost fishes.

185 role in the adaptive evolution of vision in teleost fishes.

186 domains and expression levels for duplicated teleost genes often approximate the patterns and levels

187 cry2 and cry3; and following the third-round teleost genome duplication (TGD) and subsequent gene los

188 whose lineage diverged from teleosts before teleost genome duplication (TGD).

189 vergence of gene paralogues generated in the teleost genome duplication.

190 cavefish, contrast repeat elements to other teleost genomes, identify candidate genes underlying qua

191 hat these regulatory regions, active in both teleost genomes, represent key constrained nodes of the

192 nt, the presence of dendritic cells (DCs) in teleosts has been addressed only briefly, and the identi

193 reveals that the hypothalamus in mammals and teleosts has evolved in a divergent manner: placental ma

194 y of the nonvisual photoreception systems in teleosts has just started to be appreciated, with coloca

195 However, the presence of TEPs in teleosts has only been speculated.

196 ne knockout in animal cells, particularly in teleosts, has proven to be very efficient with regards t

197 Teleosts have emerged as important model organisms, yet

198 Teleosts have gone to the other extreme; losing tail out

199 ve lost the monoaminergic CSF-c cells, while teleosts have increased their relative number.

200 cyl desaturase 2 (Fads2) enzymes, since many teleosts have lost the gene encoding a Delta5 desaturase

201 Most teleosts have two kiss genes, kiss1 and kiss2, but their

202 We demonstrate that the effects of teleost IL-6 on naive spleen B cells include proliferati

203 firming this hypothesis, we show that IgT, a teleost immunoglobulin specialized in gut immunity, play

204 Comparison with other teleosts indicates similar expression of Sox2 and Sox19

205 mammals, T cell development in the thymus of teleosts is driven by a degenerate multicomponent networ

206 significant difference between tetrapods and teleosts is that teleosts possess an additional CSF-c ce

207 upper and lower jaw identity in mammals and teleosts--is a primitive feature of the mandibular, hyoi

208 is arrangement was thought to be retained in teleost larva and overgrown, mirroring an ancestral tran

209 d some evidence for heterogeneity within the teleost lineage.

210 ed enteric glia might have evolved after the teleost lineage.This article has an associated 'The peop

211 1 fish genomes, we found that three deep-sea teleost lineages have independently expanded their RH1 g

212 e results indicate for the first time that a teleost MAP acts one hand as a regulator that promotes t

213 we speculate on how patterns in more distant teleosts may have evolved to produce a stunningly divers

214 nd retinal pigmented epithelium (RPE) of the teleost medaka (Oryzias latipes) coordinate their growth

215 ark psmb13, and tap2t and psmb10 outside the teleost MHC), implying distinct immune functions and con

216 esn't represent a miRNAome larger than other teleost miRNomes.

217 Evidence suggests that teleost MSTN plays a role in the regulation of muscle gr

218 in rainbow trout and that it resembles other teleost mucosa-associated lymphoid tissues.

219 developed immune system, we hypothesize that teleost myeloid cells show features of trained immunity

220 This is particularly important in teleost nutrition, because fish do not possess some of t

221 study aimed to characterise Fads2 from four teleosts occupying different trophic levels, namely Sarp

222 In other teleosts, OE inhibits octavolateral hair cells during lo

223 ucker Catostomus commersonii is a freshwater teleost often utilized as a resident sentinel.

224 For teleosts, olfactory stimuli are key elements of mating a

225 ificantly contribute to the understanding of teleost ontogenesis but might also shed light on paralog

226 Catfish represent 12% of teleost or 6.3% of all vertebrate species, and are of en

227 ell pathologies have been reported from five teleost orders: Pleuronectiformes (flatfish), Perciforme

228 e strong support for the hypothesis that the teleost PAG is centrally involved in auditory-vocal inte

229 Thus, the teleost PAG may have functional subdivisions playing dif

230 In contrast, the teleost pallium is not well understood and its relation

231 rence between tetrapods and teleosts is that teleosts possess an additional CSF-c cell population aro

232 Alternatively, some teleosts possess fatty acyl desaturases 2 (Fads2) that e

233 ggesting this feature is likely conserved in teleosts regardless of the type of germ cell development

234 ntogenetic data for the 350-million-year-old teleost relative Aetheretmon overturns this long-held hy

235 eflects low rates of shape evolution in stem teleosts relative to all other neopterygian taxa, rather

236 he identification of a specific DC subset in teleosts remained elusive because of the lack of specifi

237 Although teleosts represent about half of all living vertebrates,

238 ublished data from lampreys, chondrichthyes, teleosts, reptiles, birds, and mammals.

239 ion are unclear even in the well-established teleost research model, the zebrafish.

240 ive trajectory observed in some urodeles and teleosts, resulting in the formation of a structurally d

241 physiological environment and establish the teleost retina as an ideal model for studying adult stem

242 uced at different rates and locations in the teleost retina.

243 Thus, we hypothesized that, because teleost SALT and gut-associated lymphoid tissue have pro

244 Interestingly, teleost SALT structurally resembles that of the gut-asso

245 brafish (Danio rerio), two distantly related teleosts separated by an evolutionary distance of 115-20

246 have described 5-HT distribution in various teleosts, serotonergic raphe subgroups in fish are not w

247 hat the non-neuronal ENS cell compartment of teleosts shares molecular and morphological characterist

248 Strikingly, we found that the teleost skin mucosa showed key features of mammalian muc

249 Due to its lack of keratinization, teleost skin possesses living epithelial cells in direct

250 Furthermore, we assessed regeneration in 4 teleost species and show that, with the exception of the

251 he ponli and crb2b genes are conserved among teleost species and that they share sequence motifs that

252 In some teleost species another protein kinase, Z-DNA-dependent

253 ds possess all four subgroups, whereas other teleost species have one or more but not all groups.

254 As in other teleost species, ERbeta1 and ERbeta2 were robustly expre

255 LPXRFa and LPXRFa-R has not been studied in teleost species, partially because of the lack of fish-s

256 rts of differential gene expression in other teleost species.

257 this migrating placode, in this cypriniform teleost species.

258 into two clades bearing the hallmarks of the teleost-specific genome duplication (referred to as 3R).

259 proteome is uncharacterized, and whether the teleost-specific genome duplication (TSGD) influenced co

260 ther analysis of the mutation implicated the teleost-specific notochord protein, Calymmin, as a key r

261 Teleost-specific TnC paralogs have not yet been function

262 ression pattern of paralogs generated by the teleost-specific whole genome duplication is overlapping

263 Actinopterygii, and N increased to 2 by the teleost-specific whole genome duplication, but then decr

264 llowed us to infer that they originated from teleost-specific whole genome duplication.

265 s that were retained as duplicates after the teleost-specific whole-genome duplication 320 million ye

266 Due to a teleost-specific whole-genome duplication, A. burtoni po

267 ce, highlighting specific transitions during teleost spine evolution.

268 analysis revealed that Antarctic fish of the teleost suborder Notothenioidei, including icefishes, di

269 Hypothesized drivers of teleost success include innovations in jaw mechanics, re

270 , we selected a spectrally-diverse set of 11 teleost Sws2 photopigments for which both amino acid seq

271 ether with the generalized advantages of the teleost system, makes this model readily adaptable to hi

272 Here, we report that teleost TAARs evolved a new way to recognize amines in a

273 In contrast to other teleosts, tac3 expression was absent from the pituitary.

274 The teleost telencephalon has subpallial and pallial compone

275 ng jawed vertebrates, and review evidence in teleosts that the notochord plays an instructive role in

276 wever, this ability is not shared by another teleost, the medaka.

277 Compared to many other teleosts, the degree of polymorphism in A. gigas was low

278 In both mammals and teleosts, the differentiation of postmeiotic spermatids

279 While both lineages exist already in teleosts, the primordial contributions of FHF and SHF to

280 In contrast to other teleosts, the sea bass LPXRFa precursor contains only tw

281 It represents an ancient lineage of teleosts: the Osteoglossomorpha.

282 eover, KANK genes were further duplicated in teleosts through the bony-fish specific WGD, while only

283 Teleost thyroid follicles produce the same thyroid hormo

284 enomic organization is highly conserved from teleosts to humans.

285 Gar bridges teleosts to tetrapods by illuminating the evolution of i

286 referred to as the "bush at the top" of the teleost tree, and indicates acanthomorphs originated in

287 Retinal damage in teleosts, unlike mammals, induces robust Muller glia-med

288 The teleost v1r-related ora genes are a small, highly conser

289 a of an osteoblast-independent mechanism for teleost vertebral centra formation.

290 alization of CNGA3 protein to stereocilia of teleost vestibular and mammalian cochlear hair cells.

291 ctory type of CNGA3 transcript in a purified teleost vestibular hair cell preparation with immunoloca

292 To examine the biological role of il7 in teleosts, we generated an il7 allele lacking most of its

293 cidate the prevalence of both pathways among teleosts, we investigated the Delta6 ability towards C24

294 syntenies between seabass LG2 and five other teleosts were identified.

295 howed distribution patterns similar to other teleosts, which included localization to the lateral tub

296 Zebrafish (Danio rerio), a distantly related teleost with a well-known miRNome, served as comparator.

297 Teleosts with alternative reproductive tactics exhibit s

298 Sunfish fed mainly on crustaceans and teleosts, with cnidarians comprising only 16% of the con

299 ntage of a repositioning strategy, the small teleost zebrafish (Danio rerio) is a particularly appeal

300 me) map of pallium construction in the adult teleost zebrafish.