ライフサイエンスコーパス: cichlid

1 o discern the phylogenetic history of Malawi cichlids.

2 of southern Africa with ecologically diverse cichlids.

3 portant factor contributing to speciation in cichlids.

4 acrohabitat niche adaptations in Tanganyikan cichlids.

5 ales seem to get the greater share in social cichlids.

6 Here we test this hypothesis in African cichlids.

7 les of adaptive radiations, the East African cichlids.

8 cology, suggesting GRN rewiring in radiating cichlids.

9 ther recent radiations such as Lake Victoria cichlids.

10 does not directly induce male preference in cichlids.

11 ns associated with traits under selection in cichlids.

12 nome assemblies of Lake Malawi haplochromine cichlids.

13 our-bar linkage apparatus--among Lake Malawi cichlids.

14 ty and ecological opportunity in Lake Malawi cichlids.

15 es, blennies, snailfishes, and Afro-American cichlids.

16 ely adaptive color phenotypes in Lake Malawi cichlids.

17 Spexin (SPX, SPX1a in cichlid), an evolutionarily conserved neuropeptide with

18 ion of the Hedgehog and Wingless pathways in cichlid and zebrafish embryos is sufficient to mimic dif

19 protocols for the creation of CRISPR-edited cichlids and create a broadly useful mutant line.

20 genomic sites of piRNA production in African cichlids and find divergence in closely related species,

21 the coral-reef associated fishes as well as cichlids and perches.

22 ationships among closely related Lake Malawi cichlids and provides insights into the pattern of speci

23 some highly species-rich fish clades such as cichlids and wrasses.

24 prey predominantly by motion parallax, while cichlids and zebrafish may mainly use binocular visual c

25 rong conservation of TE silencing factors in cichlids, and an expansion of piwil1 genes in Lake Malaw

26 d rare, but oceanic Howea palms, crater lake cichlids, and parasitic indigobirds provide compelling e

27 rge-bodied snook, mojarra species, nonnative cichlids, and striped mullet, while having little affect

28 freshwater populations (e.g., sticklebacks, cichlids, and whitefishes) recurrently diverge toward sl

29 Neotropical crater lake cichlids are ideal models to study evolutionary processe

30 While most Midas cichlids are of the melanic "dark morph", about 10% of i

31 ical evidence suggesting that these riverine cichlids are products of a recent adaptive radiation in

32 We find that African cichlids are unique among all fishes; they are dominated

33 ceptionally recent dates suggest that Malawi cichlids as a group experience a very active and dynamic

34 oad application of CRISPR/Cas9 to studies of cichlids as well as other non-traditional model aquatic

35 Here we study haplochromine cichlid assemblages in two African Great Lakes to test t

36 ales to fertile females, we used the African cichlid Astatotilapia burtoni and found that adult males

37 eceptor subtypes, ARalpha and ARbeta, in the cichlid Astatotilapia burtoni and show that these subtyp

38 understanding of sex steroid pathways in the cichlid brain and support the important role of nuclear

39 e phenotypic diversification of East African cichlids can be attributed to diverse molecular mechanis

40 rtiheros wesseli is a species of Neotropical cichlid (Cichlidae: Cichlinae) restricted to only a few

41 Aquatic organisms such as cichlids, coelacanths, seals, and cetaceans are active i

42 sual spectrum, in agreement with the African cichlids, despite an order of magnitude difference in th

43 mental manipulation of the Hh pathway during cichlid development recapitulates functionally salient n

44 Wagner et al. analyzed cichlid diversification in 46 African lakes and reported

45 Furthermore, it suggests that the high cichlid diversification rates are not unique.

46 In Lake Malawi cichlids, each tooth is replaced in one-for-one fashion

47 signaling in vivo by treating rock-dwelling cichlid embryos with temporally precise doses of LiCl.

48 merit study to understand their interplay in cichlid evolution.

49 Collectively, our data show that African cichlid evolutionary success has occurred within the con

50 radiations such as the Cameroon crater lake cichlids, existing models have focused on bifurcation in

51 Furthermore, the gonads of African cichlids express a Piwi-interacting RNA (piRNA) pathway

52 g-spot bearing haplochromines, but not other cichlids, feature a transposable element in the cis-regu

53 Here, we examine the cichlid feeding apparatus, an icon of both prodigious ev

54 implicated in the evolutionary divergence of cichlid feeding architecture, is associated with environ

55 pheromone receptor, Or113a, detects fertile cichlid females and thereby promotes male attraction and

56 dark polymorphism that is eponymous of Midas cichlid fish (Amphilophus spp.) adaptive radiations in N

57 A gravid female cichlid fish (Astatotilapia burtoni) chose between two s

58 tionary radiations, as inferred from work in cichlid fish [9], white-eye birds [10], new world lupins

59 chnique to amplify RNA from two tissues of a cichlid fish and compared expression levels of unamplifi

60 We evaluate these hypotheses using cichlid fish as model animals, and although differences

61 during the ontogeny of the direct-developing cichlid fish Astatotilapia burtoni Distinct transcriptio

62 The African cichlid fish Astatotilapia burtoni has become an importa

63 The African cichlid fish Astatotilapia burtoni is a powerful model s

64 The African cichlid fish Astatotilapia burtoni is an ideal study spe

65 The cichlid fish Astatotilapia burtoni is ideal for studying

66 The African cichlid fish Astatotilapia burtoni presents an attractiv

67 linergic neurons in the brain of the African cichlid fish Astatotilapia burtoni using in situ hybridi

68 on between dominance and influence using the cichlid fish Astatotilapia burtoni, comparing the influe

69 r examining the AVT system in female African cichlid fish Astatotilapia burtoni, including immunohist

70 ntified two tac3 genes in the social African cichlid fish Astatotilapia burtoni, only one of which pr

71 ricular surfaces in the brain of the African cichlid fish Astatotilapia burtoni.

72 y reared juveniles of cooperatively breeding cichlid fish by varying the social environment and simul

73 on of early-stage adaptive divergence of two cichlid fish ecomorphs in a small (700 meters in diamete

74 ase is Perissodus microlepis, a scale-eating cichlid fish endemic to Lake Tanganyika.

75 The cichlid fish family provides a notable example of such v

76 Five neighbouring populations of a cichlid fish from Lake Malawi differ in male courtship c

77 Astatotilapia burtoni, a cichlid fish from the rivers and shoreline around Lake T

78 Many species of cichlid fish in Lake Malawi carry a haploid, female-rest

79 The spectacular adaptive radiation of cichlid fish in Lake Tanganyika encompasses extensive mo

80 results imply that the rate of speciation of cichlid fish in this tropical lake has been extremely ra

81 ke Malawi, Africa, there are >200 species of cichlid fish in which the males form leks and spend seve

82 evolution of a courtship behavior in Malawi cichlid fish is associated with rapid, extensive, and sp

83 D on secondary sexual characteristics in the cichlid fish Metriaclima mbenjii, where one female (W) a

84 transcriptomics and CRISPR gene editing in a cichlid fish model to identify and test the roles of key

85 Here, we show that offspring of the cichlid fish Neolamprologus pulcher developed faster C-s

86 e Magadi tilapia, Alcolapia grahami, a small cichlid fish of Lake Magadi, Kenya lives in one of the m

87 under sexually antagonistic selection in the cichlid fish of Lake Malawi, East Africa.

88 The haplochromine cichlid fish of the East African Great Lakes represent s

89 ying 1375 genomes of the species-rich Malawi cichlid fish radiation, we discovered five large inversi

90 ion over a similar time period to the recent cichlid fish radiations, which are an order of magnitude

91 Our targeted genome modification in a cichlid fish shows that dissection of gene function can

92 rofound influence on the Lake Malawi endemic cichlid fish species flock; the geographically extensive

93 dently for the lake's extraordinary array of cichlid fish species, suggesting a direct link between e

94 ly distinct ecomorphs of the Lake Tanganyika cichlid fish Telmatochromis temporalis.

95 e Malawi contains a flock of >500 species of cichlid fish that have evolved from a common ancestor wi

96 The cichlid fish, Astatotilapia burtoni, can switch between

97 In an African cichlid fish, Astatotilapia burtoni, fertile females sel

98 localized two known GnRH receptor types in a cichlid fish, Astatotilapia burtoni, in which GnRH1 is s

99 e used females of the mouth brooding African cichlid fish, Astatotilapia burtoni, to test for reprodu

100 uption of the habitat of a colony of African cichlid fish, Haplochromis burtoni (Gunther) caused male

101 We have shown previously in the African cichlid fish, Haplochromis burtoni, that changes in soci

102 oth fossils of Lake Victoria's haplochromine cichlid fish, the most rapid and youngest of the classic

103 hologically similar species of haplochromine cichlid fish.

104 re than 300 endemic species of haplochromine cichlid fish.

105 ed in many species including any Neotropical cichlid fish.

106 neurons in adult male Astatotilapia burtoni cichlid fish.

107 both within and among genera of Lake Malawi cichlid fish.

108 ithin a young species complex of neotropical cichlid fishes (Amphilophus spp.), we analysed genomic d

109 d one each in salamanders (Desmognathus) and cichlid fishes (Pseudotropheus).

110 nization on visual acuity in closely related cichlid fishes (the Ectodini clade).

111 x chromosome evolution in a group of African cichlid fishes (tribe Tropheini) which began to diverge

112 tial methylome divergence in closely-related cichlid fishes and represents a resource to study the ro

113 vidence that the modified pharyngeal jaws of cichlid fishes and several marine fish lineages, a class

114 d that the conclusions reached regarding the cichlid fishes apply also to other examples of adaptive

115 Cichlid fishes are famous for large, diverse and replica

116 assive evolutionary radiation of Lake Malawi cichlid fishes displaying extensive phenotypic diversity

117 Lake Malawi cichlid fishes exhibit extensive divergence in form and

118 Furthermore, while cichlid fishes exhibit extensive parental care, for most

119 e brain development in ecologically distinct cichlid fishes from Lake Malawi and demonstrate that bra

120 Here, using rock- and sand-dwelling cichlid fishes from Lake Malawi, we demonstrate that dif

121 East African cichlid fishes have diversified in an explosive fashion,

122 African cichlid fishes have repeatedly evolved highly specialize

123 mpatric homoploid hybrid speciation in Midas cichlid fishes in Crater Lake Xiloa, Nicaragua.

124 unrecognized role in the mass extinction of cichlid fishes in Lake Victoria after Nile perch invasio

125 Haplochromine cichlid fishes of Africa's Lake Victoria region encompas

126 The cichlid fishes of Lake Malawi are famously diverse.

127 he largest adaptive radiations on Earth, the cichlid fishes of Lake Tanganyika.

128 On the example of the cichlid fishes of Lake Victoria, we demonstrate how the

129 The cichlid fishes of the East African Rift Lakes represent

130 East African cichlid fishes represent one of the most striking exampl

131 cologically diverse radiation of Neotropical cichlid fishes that spans North, Central and South Ameri

132 exploit the dental diversity of Lake Malawi cichlid fishes to ask how vertebrates generally replace

133 utterflies, Darwin's finches, sunflowers and cichlid fishes, and the implications of introgression fo

134 bower construction behaviors in Lake Malawi cichlid fishes, in which males use their mouths to sculp

135 t least 12 of 22 chromosomes in East African cichlid fishes, indicating a high rate of sex chromosome

136 by highly diverse groups such as wrasses and cichlid fishes, is hypothesized to increase foraging cap

137 In previous studies of African cichlid fishes, we found evidence for positive selection

138 Using genetic mapping in cichlid fishes, we identified shared loci controlling a

139 rds, whereas social signals regulate GnRH in cichlid fishes, with crucial consequences for reproducti

140 ng of single loci and quantitative traits in cichlid fishes.

141 oidance of paternal care among haplochromine cichlid fishes.

142 al role for these nORFs in speciation of the cichlid fishes.

143 lding, a recently-evolved social behavior in cichlid fishes.

144 endrobatid frogs, and Xenotilapia species of cichlid fishes.

145 ically diverging species pair of crater lake cichlid fishes.

146 solated radiations of Nicaraguan crater lake cichlid fishes.

147 es the species-area relationship for African cichlid fishes.

148 anisms of sex determination and evolution in cichlid fishes.

149 Cichlids fishes exhibit extensive phenotypic diversifica

150 a system that rivals other groups, including cichlids, for understanding rapid species diversificatio

151 y relevant differences in the elaboration of cichlid forebrain compartments.

152 in the same direction exhibited in a native cichlid-free population, suggesting rapid adaptive evolu

153 adapted to living with cichlid predators to cichlid-free streams, and tested for evolutionary diverg

154 Outgroup sequences from a cichlid from Lake Tanganyika permit model parameter esti

155 These findings underscore that the cichlid genome is shaped both by small-nucleotide mutati

156 titative genetics to identify regions of the cichlid genome responsible for functionally important sh

157 which is 33.1% longer than that of a single cichlid genome.

158 Assembly of 100 cichlid genomes within the most rapidly speciating cichl

159 of molecular mechanisms shaped East African cichlid genomes, and that amassing of standing variation

160 ate regulators and regulatory regions across cichlid genomes, including some novel and some previousl

161 se that this co-evolution has contributed to cichlid genomic diversity.

162 dynamic patterns of TE expression in African cichlid gonads and during early development.

163 Overall, the Midas cichlid has one of the most diverse repertoires of MHC c

164 Cichlids have undergone extensive evolutionary modificat

165 The African cichlid hepadnavirus (ACHBV) and the Tibetan frog hepadn

166 stand the interactions between TEs and their cichlid hosts.

167 r of Julidochromis ornatus, a common endemic cichlid in Lake Tanganyika.

168 inferiority shaped the adaptive radiation of cichlids in Lake Tanganyika and played a pivotal and pre

169 that the repertoire of hunting movements of cichlids is broader than that of zebrafish, but shares b

170 These data demonstrate the utility of the cichlid jaw as a model for studying the genetic and deve

171 view this body of work, which shows that the cichlid jaw is regulated by a few genes of major additiv

172 patterns of morphological integration of the cichlid jaw reflect a balance among conflicting function

173 Adaptive variation in cichlid jaw shape is evident early in development and is

174 rafish model reproduces natural variation in cichlid jaw shape, supporting a role for bmp4 in craniof

175 ividual quantitative trait loci suggest that cichlid jaws and teeth evolved in response to strong, di

176 ifferences in jaw shape are obvious early in cichlid larval development and are correlated with patte

177 In the cichlids, latent-trait axes incorporate male-coloration

178 an expansion of piwil1 genes in Lake Malawi cichlids, likely driven by PiggyBac TEs.

179 In Africa's Lake Victoria region, one cichlid lineage radiated in every lake, with the largest

180 been associated with phenotypic variation in cichlids, little is known about their transcriptional ac

181 opening and closing lever mechanisms of the cichlid lower jaw, which have traditionally been used to

182 a cooperatively breeding fish, the daffodil cichlid (Neolamprologus pulcher), we conducted the first

183 The cichlids of Lake Malawi are a similar model for visual e

184 evolutionary relationships among the endemic cichlids of Lake Malawi.

185 This includes the cichlids of Lake Victoria where sequence variation has b

186 such as Anolis lizards on Caribbean islands, cichlids of the East African Great Lakes, finches on the

187 Hedgehog (Hh) pathways suggest that a common cichlid oral lamina is competent to form teeth or taste

188 derstand the molecular mechanisms underlying cichlid phenotypic diversity, we sequenced the genomes a

189 (Poecilia reticulata) adapted to living with cichlid predators to cichlid-free streams, and tested fo

190 cation of an HBV-like sequence in an African cichlid provide evidence that a novel genus of the famil

191 A recent study of Tanganykan cichlids provides compelling evidence that sperm competi

192 icient to explain this striking diversity of cichlid radiation because other taxa coexistent with the

193 exual selection have strongly influenced the cichlid radiation, which indicates the existence of unkn

194 d genomes within the most rapidly speciating cichlid radiation, which is found in Lake Victoria, reve

195 s and host silencing pathways in the African cichlid radiations.

196 grating quantitative behavioral data from 57 cichlid species (702 wild-caught individuals) with high-

197 he genes of MHC class IIB chain of the Midas cichlid species complex (Amphilophus cf. citrinellus) in

198 signed compound loci to develop portraits of cichlid species divergence.

199 contributed to the origin and maintenance of cichlid species diversity.

200 We compared the behavior of four cichlid species from Lake Tanganyika endemic to deep ben

201 niche compared to the other sympatric Midas cichlid species in Crater Lake Xiloa.

202 naling, were differentially expressed across cichlid species with divergent tooth and taste bud densi

203 lasticity are distinct among closely related cichlid species, underscoring the evolutionary potential

204 a large phylogeny of all currently described cichlid species, we show that explosive speciation is so

205 d muscle tissues in phenotypically divergent cichlid species.

206 proteomic signatures from two tissues of two cichlids species, identified nORFs and performed evoluti

207 itation of novel resources among Neotropical cichlids such that pharyngeal specialization has increas

208 as interspecies structural variation between cichlids, suggesting substantial genomic diversity under

209 chart organogenesis of continually replacing cichlid teeth and discovered an epithelial down-growth t

210 Comparison with modern cichlid teeth suggests that large-scale diversification

211 l contribute to the study of closely related cichlids that have undergone explosive adaptive radiatio

212 ake Victoria hybrid lineage of haplochromine cichlids that seeded the radiation and the unusual speed

213 innovation of the most species-rich group of cichlids, the haplochromines, where these conspicuous ma

214 d transcriptomes of five lineages of African cichlids: the Nile tilapia (Oreochromis niloticus), an a

215 t al. linked exploratory behavior in African cichlids to a SNP in the promoter of a gene, the homolog

216 lencephalon of dominant and subordinate male cichlids to test the hypothesis that response properties

217 s to characterize the sex chromosomes of the cichlid tribe Cyprichromini from Lake Tanganyika.

218 contributed to the origin and maintenance of cichlid trophic diversity.

219 ply that the rapid and replicative nature of cichlid trophic evolution is the result of directional s

220 Here we show that in cooperatively breeding cichlids, unrelated subordinate females provide more all

221 al tuning is important at the margins of the cichlid visual spectrum.

222 ants, and investigate their association with cichlid visual system evolution.