ライフサイエンスコーパス: stickleback

1 enriched RAD marker array for the threespine stickleback.

2 condition represented by present-day oceanic stickleback.

3 different gene expression profiles than lake sticklebacks.

4 ng armor plate patterning in wild threespine sticklebacks.

5 e or female sexual development in threespine sticklebacks.

6 ions, characterized by high or low growth in sticklebacks.

7 increase in tooth number in derived benthic sticklebacks.

8 y, the site of spiggin protein production in sticklebacks.

9 ity reference genome assembly for threespine sticklebacks.

10 changes, exemplified by pelvic spine loss in sticklebacks.

11 ect consequences of ecosystem engineering by sticklebacks.

12 ntrol the corresponding traits in threespine sticklebacks.

13 s toward armor-plate reduction in freshwater sticklebacks [10].

14 pe and size evolve and develop in threespine sticklebacks, a model system for understanding vertebrat

15 mune functions, which have likely changed as sticklebacks adapt to contrasting environments.

16 marine populations, we show that freshwater stickleback also act as reservoirs for ancient ancestral

17 es, per2a and per2b, one per1, and one per3; sticklebacks also have per2a, per2b, and one per1 but la

18 naturally occurring variation in three-spine stickleback anatomy.

19 of two natural fish populations (threespine stickleback and Eurasian perch), among-individual diet v

20 ies, including zebrafish, medaka, threespine stickleback and fugu, the amphibian Xenopus tropicalis,

21 t and european hedgehog; the fish genomes of stickleback and medaka and the second example of the gen

22 xperimental diet manipulations in laboratory stickleback and mice confirmed that diet affects microbi

23 prediction within each of two fish species (stickleback and perch), in which individuals vary in the

24 We employed the three-spined stickleback and three ecologically relevant parasite inf

25 l regions that determine male development in sticklebacks and medaka have revealed several features a

26 first genome-wide linkage map for ninespine sticklebacks and used quantitative trait locus mapping t

27 he jaw and pectoral fin joints of zebrafish, stickleback, and gar, with genetic deletion of the zebra

28 evolution of distinct marine and freshwater sticklebacks, and in the maintenance of divergent ecotyp

29 per2a/per2b in madaka, fugu, tetraodon, and stickleback are ancient duplicates.

30 Armor plate changes in sticklebacks are a classic example of repeated adaptive

31 Stickleback Bmp6 is expressed in developing teeth, and n

32 that can be redeployed rapidly when oceanic stickleback colonize freshwater environments.

33 life-history plasticity in female threespine stickleback, considering four traits intimately associat

34 mp6 allele at late, but not early, stages of stickleback development.

35 ed teleosts, but largely missing from marine stickleback due to recent selective sweeps in marine pop

36 udy adaptation of color vision in threespine stickleback during the repeated postglacial colonization

37 A recent study of stickleback 'ecomorphs' generated by independent speciat

38 all five case studies examined: three-spine stickleback, Eurasian perch, Anolis lizards, intertidal

39 support the intriguing hypothesis that most stickleback evolution in fresh water occurs within the f

40 Freshwater sticklebacks exhibit prominent vertical bars that visual

41 basis of pelvic reduction in the threespine stickleback fish (2004).

42 st the hypothesis that dyads of three-spined stickleback fish (Gasterosteus aculeatus) coregulate the

43 ytogenetic studies suggested that threespine stickleback fish (Gasterosteus aculeatus) do not have a

44 glacial adaptive radiation of the threespine stickleback fish (Gasterosteus aculeatus) has been widel

45 he frequency of completely plated threespine stickleback fish (Gasterosteus aculeatus) has increased

46 Stickleback fish (Gasterosteus aculeatus) have undergone

47 logenetic range: house mouse (Mus musculus), stickleback fish (Gasterosteus aculeatus), and honey bee

48 that contribute to speciation in threespine stickleback fish (Gasterosteus aculeatus).

49 ight pigmentation in animals as divergent as stickleback fish and humans.

50 on in a sympatric species pair of threespine stickleback fish by mapping the environment-dependent ef

51 leverage natural variation in the threespine stickleback fish Gasterosteus aculeatus to investigate t

52 ing the adaptive radiation of the threespine stickleback fish Gasterosteus aculeatus.

53 different natural populations of threespine stickleback fish has occurred through regulatory mutatio

54 Marine stickleback fish have colonized and adapted to thousands

55 es suggest that recently diverged species of stickleback fish have different sex chromosome complemen

56 phenotypes of resident freshwater threespine stickleback fish on at least three of these islands have

57 In previous work, we found that pairs of stickleback fish prefer to synchronize their trips out o

58 ius) and threespine (Gasterosteus aculeatus) stickleback fish provide many examples of convergent evo

59 rried out genetic crosses between threespine stickleback fish with complete or missing pelvic structu

60 d large size variation in mtDNA of the brook stickleback fish, Culaea inconstans, and characterized f

61 s that visually break up the body shape, but sticklebacks from marine populations do not.

62 arker for pelvic fin position in three-spine stickleback Gasterosteus aculeatus.

63 n the evolution of body size in three-spined sticklebacks Gasterosteus aculeatus on the island of Nor

64 dus persistently infects 0-80% of threespine stickleback (Gasterosteus aculeatus) in lakes on Vancouv

65 Male three-spined stickleback (Gasterosteus aculeatus) kidneys produce spi

66 ects of adaptive radiation in the threespine stickleback (Gasterosteus aculeatus) over the past 10,00

67 The red coloration of male stickleback (Gasterosteus aculeatus) possesses signal va

68 g of known behavioral types in free-swimming stickleback (Gasterosteus aculeatus) shoals.

69 ions of the androgen responsive three-spined stickleback (Gasterosteus aculeatus) spiggin genes in si

70 postglacial adaptation of marine threespine stickleback (Gasterosteus aculeatus) to freshwater.

71 genome-wide linkage map for the three-spined stickleback (Gasterosteus aculeatus), an extensively stu

72 underlie sex determination in the threespine stickleback (Gasterosteus aculeatus).

73 nce data from a fish species: the threespine stickleback (Gasterosteus aculeatus).

74 n: sympatric benthic and limnetic threespine stickleback (Gasterosteus aculeatus).

75 distributed lacustrine fish, the three-spine stickleback (Gasterosteus aculeatus).

76 k by using an experiment on the three-spined stickleback (Gasterosteus aculeatus, Linnaeus) in which

77 chooling marine and weakly schooling benthic sticklebacks (Gasterosteus aculeatus) and found that dis

78 ic pigment pattern among juvenile threespine sticklebacks (Gasterosteus aculeatus) from different env

79 We used three-spined sticklebacks (Gasterosteus aculeatus) to test whether th

80 s of argentine ants (Linepithema humile) and sticklebacks (Gasterosteus aculeatus), showing that a un

81 freshwater populations of Alaskan threespine stickleback, Gasterosteus aculeatus, that evolved from f

82 2 hybrids of benthic and limnetic threespine sticklebacks, Gasterosteus aculeatus Linnaeus, 1758, to

83 Here, we show that in pairs of sticklebacks, Gasterosteus aculeatus, leadership arises

84 ams Pisidium sp.), 131 +/- 105 (three-spined sticklebacks: Gasterosteus aculeatus), 41 +/- 38 (char),

85 We identify 6664 regions of the stickleback genome, totaling 1.7 Mbp, which show consist

86 ions of known pigment candidate genes in the stickleback genome.

87 Thus parallel evolution of low-plated sticklebacks has occurred through a shared DNA regulator

88 Although freshwater stickleback have repeatedly evolved from marine populati

89 n together, our data suggest that threespine sticklebacks have a simple chromosomal mechanism for sex

90 As a consequence, sticklebacks have been extensively used as model hosts i

91 ions that have arisen from studies involving stickleback hosts, highlight areas of current research a

92 phenotypic traits reduces the growth of some stickleback hybrids beyond that expected from an interme

93 We tested groups of sticklebacks in patchy foraging environments that differ

94 anted lake and stream ecotypes of threespine stickleback into lake and stream habitats, while manipul

95 The three-spined stickleback is a small teleost fish, native to coastal r

96 Phylogenetic analysis shows that the stickleback is most closely related to the large yellow

97 The Eda gene in three-spined stickleback is one of the best studied major adaptation

98 Morphology in stickleback is primarily reset only in that developmenta

99 e of how we think plasticity may play out in stickleback life history given what we know of plasticit

100 Recent work on stickleback life history, community ecology and speciati

101 tly in black- and clearwater habitats, while sticklebacks lost one paralog.

102 l populations and that parallel evolution of stickleback low-plated phenotypes at most freshwater loc

103 polymorphism in the bony armor of threespine stickleback maintained with a deficit of heterozygotes a

104 Armor bone-size differences in sticklebacks map to a major effect locus overlapping BMP

105 stinal epithelial cells (IECs) in zebrafish, stickleback, mouse, and human species to determine if co

106 tial infection led to contrasting effects of sticklebacks on a broad range of ecosystem properties, i

107 Three-spined sticklebacks on North Uist show almost unprecedented int

108 ay to study patterns of genetic variation in sticklebacks over a wide geographic range, and to scan t

109 re we show that a derived benthic freshwater stickleback population has evolved an approximate twofol

110 us, rapid and repeated armor loss in Alaskan stickleback populations appears to be occurring through

111 build-up of mating incompatibilities between stickleback populations can be largely accounted for by

112 We find that two derived freshwater stickleback populations have both convergently evolved m

113 e of body size on reproductive isolation for stickleback populations spread across the Northern Hemis

114 ntly in two independently derived freshwater stickleback populations using largely distinct developme

115 Sticklebacks possess a well-documented and experimentall

116 for threespine sticklebacks; thus, ninespine sticklebacks provide a unique opportunity to critically

117 Comparative genetics in sticklebacks provides an exciting opportunity to study t

118 smaller competitor species, the nine-spined stickleback Pungitius pungitius, and with low pH indicat

119 Our results show that stickleback recently evolved heritable variation in thei

120 Instead, pelvic-reduced sticklebacks show site-specific regulatory changes in Pi

121 ferent from the mechanism for pelvic loss in stickleback, showing that different taxa can evolve simi

122 iming and frequency of breeding; three-spine stickleback spawned earlier and more often in response t

123 orphologies seen in the benthic and limnetic stickleback species from Priest Lake, British Columbia.

124 Further analysis of the stickleback system will provide an exciting window into

125 Male sticklebacks that had experienced a more benign environm

126 In ninespine sticklebacks, these traits mapped to chromosome regions

127 The Lake Washington stickleback thus provides a novel example of reverse evo

128 important traits is now known for threespine sticklebacks; thus, ninespine sticklebacks provide a uni

129 Here we use genetic crosses in sticklebacks to investigate the parallel origin of pigme

130 We exposed adult female sticklebacks to LNG at 5.5, 40, and 358 ng L(-1) for 21

131 ow that rapid evolutionary change in Miocene stickleback was associated with shifts in feeding, provi

132 ations) pair of lake and stream three-spined sticklebacks, we tested how experimental exposure to a c

133 ations, and a selection experiment, in which stickleback were transplanted from a blackwater lake int

134 In both environments, we found that stream sticklebacks were more resistant to Gyrodactylus and had

135 We experimentally infected three-spined sticklebacks with a large tapeworm (Schistocephalus soli

136 zation (FISH), we report that the threespine stickleback Y chromosome is heteromorphic and has suffer

137 the current physical state of the threespine stickleback Y chromosome.