ライフサイエンスコーパス: japonicus

1 sposase function (except Schizosaccharomyces japonicus).

2 ng isoflavonoid biosynthesis in Lotus (Lotus japonicus).

3 leosome-excluding proteins functioning in S. japonicus.

4 her sequenced legumes, Glycine max and Lotus japonicus.

5 d a decreased rate of nodule formation on L. japonicus.

6 different degrees in Pisum sativum and Lotus japonicus.

7 NA genomes from an Asian congener, Tigriopus japonicus.

8 quercertin 2,3-dioxygenase from Aspergillus japonicus.

9 to elicit nodules on its host legume, Lotus japonicus.

10 determinate symbiosis with the legume Lotus japonicus.

11 sorhizobium loti, the natural symbiont of L. japonicus.

12 ateral root formation and symbiosis in Lotus japonicus.

13 e organogenesis, and nitrogen fixation in L. japonicus.

14 similar to the clv2 mutants of pea and Lotus japonicus.

15 in both infection and organogenesis in Lotus japonicus.

16 ermal cells of Medicago truncatula and Lotus japonicus.

17 osaccharomyces pombe and Schizosaccharomyces japonicus.

18 h LHK1 to mediate nodule organogenesis in L. japonicus.

19 stem in the saprophytic bacterium Cellvibrio japonicus.

20 lso sufficient for nodule formation in Lotus japonicus.

21 (order Poecilostomatoida) than to that of T. japonicus.

22 ndogenous SYMRK in roots of the legume Lotus japonicus.

23 acclimation to tolerate drought stress in L. japonicus.

24 inhibition of LNP blocks nodulation in Lotus japonicus.

25 haromyces octosporus and Schizosaccharomyces japonicus.

26 osaccharomyces pombe and Schizosaccharomyces japonicus [1-3].

27 tified in Medicago truncatula (52) and Lotus japonicus (53), including pseudogenes and non-functional

28 In Lotus japonicus, a LysM receptor kinase, EPR3, distinguishes c

29 cular modelling, and the observation that L. japonicus accessions lacking cyanogenic flowers contain

30 In addition, previously published L. japonicus Affymetrix data are included in the database,

31 e induction of isoflavonoid production in L. japonicus also involves the coordinated down-regulation

32 p records of an ortholog of GmN70 from Lotus japonicus also showed anion currents with a similar sele

33 lase (NahG) in both stably transformed Lotus japonicus and composite Medicago truncatula plants.

34 ensitive ethylene detection system for Lotus japonicus and found that ethylene production increased a

35 milar to MtDHDPS2 and 3 are present in Lotus japonicus and Glycine max, suggesting the existence of a

36 YB14, was constitutively overexpressed in L. japonicus and induced the expression of at least 12 gene

37 for efficient cellodextrin utilization in C. japonicus and is constitutively expressed at high levels

38 Here we show that Lotus japonicus and Medicago truncatula possess very similar L

39 he Medicago truncatula ortholog of the Lotus japonicus and pea (Pisum sativum) NIN gene.

40 he GS52 apyrase can enhance nodulation in L. japonicus and points to an important role for this group

41 accharomyces cryophilus, Schizosaccharomyces japonicus and Schizosaccharomyces octosporus).

42 Here we find in Schizosaccharomyces japonicus and Schizosaccharomyces pombe that, during act

43 na Sea, interspecific comparisons between T. japonicus and T. nanhaiensis indicated possible evolutio

44 two economically important fish (Trichiurus japonicus and T. nanhaiensis) that inhabit the continent

45 o truncatula with those of the diploid Lotus japonicus and the polyploid Glycine max.

46 d that P. palmivora induces disease in Lotus japonicus and used this interaction to identify cellular

47 the previously identified genes HAR1 (Lotus japonicus) and NARK (Glycine max) are orthologs based on

48 unigene sets from Medicago truncatula, Lotus japonicus, and soybean (Glycine max and Glycine soja) to

49 e model legume species, M. truncatula and L. japonicus, and substantially enhanced the knowledgebase

50 ymbiotic and non-symbiotic development of L. japonicus, and suggest that regulatory processes control

51 at has 27% identity to an L-AAO from Scomber japonicus (animal, mackerel) and is a member of the fami

52 pment of root hairs in the angiosperms Lotus japonicus, Arabidopsis thaliana, and rice (Oryza sativa)

53 mackerel (Trachurus symmetricus and Scomber japonicus) are thriving.

54 The L. japonicus arpc1 mutant showed a distorted trichome pheno

55 egume species, Medicago truncatula and Lotus japonicus, as well as data available for Arabidopsis tha

56 itrogen (N) fixing nodules (Fix(+)) of Lotus japonicus, as well as the link of S-metabolism to symbio

57 a family 35 CBM, derived from the Cellvibrio japonicus beta-1,4-mannanase Man5C.

58 s the light on the metabolic machinery of C. japonicus, but also expands the repertoire of characteri

59 a natural compound isolated from Chloranthus japonicus, can activate AMPK and modulate glucose metabo

60 Although the DMI1 homologs from Lotus japonicus, CASTOR and POLLUX, were recently reported to

61 We have isolated a Lotus japonicus cDNA corresponding to a highly abundant, late

62 arkably however, similar to S. pombe, the S. japonicus cells switch cell/mating type after undergoing

63 and sequenced and their expression in Lotus japonicus characterised.

64 Here, we show that the Lotus japonicus Ckx3 cytokinin oxidase/dehydrogenase gene is i

65 amide genes in the sea cucumber Apostichopus japonicus (class Holothuroidea) and the starfish Patiria

66 us 15 cm, Trachurus trachurus 40 cm, Scomber japonicus colias 60 cm) was carried out using non-conven

67 G. japonicus consumed glucose most quickly and achieved the

68 Flowers and leaves of Lotus japonicus contain alpha-, beta-, and gamma-hydroxynitril

69 erized plant genomes, the TE component of L. japonicus contained several surprises.

70 We show here that L. japonicus contains a small family of four cytokinin rece

71 Gene expression profiling of C. japonicus demonstrated that three of the 12 predicted be

72 DNA sequences of the mating-type loci of S. japonicus differ vastly from those of the S. pombe speci

73 We have identified a gene in Lotus japonicus, Epr3, encoding a receptor-like kinase that co

74 ted in mycorrhizal roots of the legume Lotus japonicus, expression of a unique GRAS protein particula

75 omparison of our data to those for Tigriopus japonicus (family Harpacticidae, order Harpacticoida) re

76 ed specialisation in HNG based defence in L. japonicus flowers is discussed in the context of balanci

77 The nectar of L. japonicus flowers was also found to contain HNGs and add

78 anesulfonate mutagenized population of Lotus japonicus for mutants defective in IT formation and clon

79 tilization in the soil saprophyte Cellvibrio japonicus found that only one of four predicted beta-glu

80 Here we identify a Lotus japonicus gene encoding a predicted ACTIN-RELATED PROTEI

81 me functional genomics, we developed a Lotus japonicus Gene Expression Atlas (LjGEA), which provides

82 mber of a small family of closely related L. japonicus genes.

83 Finally, the L. japonicus genome contains many hundreds, perhaps thousan

84 Database studies of the Lotus japonicus genome have revealed the presence of 24 sequen

85 vailability of a significant amount of Lotus japonicus genome sequence has permitted for the first ti

86 No other AS genes were detected in the L. japonicus genome.

87 light of previous studies on the Cellvibrio japonicus GH26 mannanases CjMan26A and CjMan26C reveals

88 tic steps form nitrogen-fixing nodules on L. japonicus Gifu after a delay, whereas mutants affected i

89 ween Mesorhizobium loti strain R7A and Lotus japonicus Gifu, rhizobial exopolysaccharide (EPS) plays

90 nscript data from Medicago truncatula, Lotus japonicus, Glycine max and Arabidopsis thaliana.

91 eated the physiological roles of the four C. japonicus glycoside hydrolase family 3 (GH3) members on

92 The bacterium Cellvibrio japonicus has a robust capacity for plant polysaccharide

93 Lotus japonicus has been used for decades as a model legume to

94 e conducted a detailed analysis of the Lotus japonicus hypernodulating mutants, har1-1, 2 and 3 that

95 japonicus in North America and a continued rapid expansi

96 expression of the GS52 ecto-apyrase in Lotus japonicus increased the level of rhizobial infection and

97 Lotus japonicus is a model species for legume genomics.

98 cteroides thetaiotaomicron, the genome of C. japonicus is predicted to encode a large number of GH43

99 Most importantly, the genome of C. japonicus is remarkably similar to that of the gram-nega

100 e III sucrose transporter homolog from Lotus japonicus, is expressed in nodules and its transport act

101 esponses to waterlogging of the legume Lotus japonicus, it was previously suggested that, during hypo

102 Aedes japonicus japonicus (Theobald) (Diptera: Culicidae) has

103 escribed cDNA, LjNOD16, which encodes the L. japonicus late nodulin Nlj16.

104 e the expression pattern observed for the L. japonicus leghemoglobin gene.

105 und to be drastically altered in specific L. japonicus lines carrying monogenic-recessive mutations i

106 The single- and double-copy sense gs52 L. japonicus lines had enhanced nodulation that correlated

107 phenotypically normal divisions with the S. japonicus lipin acquiring an S. pombe-like mitotic phosp

108 duplicated in L. japonicus We obtained a L. japonicus Ljein2a Ljein2b double mutant that exhibits co

109 Therefore, we postulate that the L. japonicus LjNOD70 gene family encodes nodule-specific tr

110 aracterization carried out in independent L. japonicus LORE1 insertion lines indicates a positive rol

111 errant nodulation phenotypes using the Lotus japonicus LORE1 insertion mutant collection.

112 Therefore the S. pombe and S. japonicus mating systems provide the first two examples

113 ed crystal structures of Schizosaccharomyces japonicus Mis16 alone and in complex with the helix 1 of

114 noted, this feature is also conserved in T. japonicus mtDNAs; whether this sequence is processed int

115 ed phenotypic analysis of two independent L. japonicus mutant alleles and investigated the regulation

116 The L. japonicus mutant carrying the loss-of-function lhk1-1 al

117 rd genetic approach, we identified two Lotus japonicus mutants defective in AM-specific paralogs of l

118 expression studies and a selection of Lotus japonicus mutants uncoupling different symbiosis stages

119 Together with previously described L. japonicus Nck-associated protein1 and 121F-specific p53

120 he characterization of a member of the Lotus japonicus nitrate transporter1/peptide transporter famil

121 Here, we show that the Lotus japonicus Nod factor receptor 5 (NFR5) and Nod factor re

122 Here we identify a Lotus japonicus nodulation pectate lyase gene (LjNPL), which i

123 jNOD70, associated with late stages in Lotus japonicus nodule development and/or functioning was char

124 duced during late developmental stages of L. japonicus nodule organogenesis and provide important, no

125 was found to be enhanced specifically in L. japonicus nodules, whereas the LjPP2C2 gene was expresse

126 e expressed only in the infected cells of L. japonicus nodules.

127 pombe, S. octosporus, S. cryophilus, and S. japonicus--occupies the basal branch of Ascomycete fungi

128 ition from the Japanese white-eye (Zosterops japonicus) on native Hawaiian passerine birds.

129 acid bacteria species (one of Gluconobacter japonicus, one of Gluconobacter oxydans and one of Aceto

130 In the model legume Lotus japonicus, one of these LegCYC genes has been shown, lik

131 bgroups of proteins that were specific to L. japonicus or closely related to known regulators of the

132 s to establish putative M. truncatula and L. japonicus orthologues.

133 ago truncatula, Glycine max (soybean), Lotus japonicus, Phaseolus vulgaris (common bean), Cicer ariet

134 discovered in the sea cucumber Apostichopus japonicus (Phylum Echinodermata; Class Holothuroidea).

135 Approximately 50% of the predicted C. japonicus plant-degradative apparatus appears to be shar

136 Spot inoculations of NahG-expressing L. japonicus plants confirmed increased nodulation in these

137 anscripts and metabolites that changed in L. japonicus plants during the transfer from photorespirati

138 Transgenic Lotus japonicus plants were constructed constitutively express

139 , Medicago truncatula, Glycine max and Lotus japonicus plus two reference plant species, A. thaliana

140 comparison of the demographic history of T. japonicus populations from the East China and South Chin

141 The findings suggest that L. japonicus possesses a voltage-dependent cation efflux ch

142 The results presented here predict that C. japonicus possesses an extensive range of glycoside hydr

143 model legumes, Medicago truncatula and Lotus japonicus, provide a unique opportunity to address biolo

144 model legumes, Medicago truncatula and Lotus japonicus, provides an opportunity for large-scale seque

145 As in M. truncatula, the L. japonicus ram1 mutant lines show compromised AM coloniza

146 pment: arbuscule branching is arrested in L. japonicus ram1 mutants, and ectopic expression of RAM1 a

147 line, we identify two novel alleles of Lotus japonicus REDUCED ARBUSCULAR MYCORRHIZA1 (RAM1) encoding

148 ssembly of the actomyosin ring in mitotic S. japonicus relies on the cortical anchor protein Cdc15 re

149 Symbiosis between M. loti and L. japonicus requires bacterial synthesis of secreted and c

150 NahG expression in L. japonicus resulted in a marked reduction of SA levels.

151 n-of-function CNGC mutation (brush) in Lotus japonicus resulting in a leaky tetrameric channel.

152 changes in the cytoskeleton of living Lotus japonicus root hairs, which precede root-hair deformatio

153 ification of the streptophyte-specific Lotus japonicus ROOTHAIRLESS LIKE (LRL) transcription factor (

154 bHLH) transcription factors encoded by LOTUS JAPONICUS ROOTHAIRLESS1-LIKE (LRL) genes positively regu

155 ot a factor controlling N-assimilation in L. japonicus roots during stable growth in N-sufficient con

156 nes in a sliding developmental zone of Lotus japonicus roots.

157 The A. japonicus SALMFamide precursor comprises eight putative

158 eport that the Japanese sea catfish Plotosus japonicus senses local pH-associated increases in H(+)/C

159 The diving beetle Cybister japonicus Sharp shows a remarkable sexual dimorphism.

160 Significantly, several of the L. japonicus Sireviruses have recently amplified and may st

161 The Lotus japonicus SYMBIOSIS RECEPTOR-LIKE KINASE (SYMRK) is requ

162 2C1 and LjPP2C2) from the model legume Lotus japonicus that encode protein phosphatase type 2C (PP2C)

163 d POLLUX, the twin homologous genes in Lotus japonicus that encode putative ion channel proteins.

164 characterization of a gene family from Lotus japonicus that encodes a novel class of plant PITP-like

165 In Schizosaccharomyces japonicus, the conserved LEM-domain nuclear envelope pro

166 In Papilionoideae legume, Lotus japonicus, the development of dorsal-ventral (DV) asymme

167 Ned1 is not regulated during division in S. japonicus, thus limiting membrane availability and neces

168 Interestingly, analysis of the A. japonicus transcriptome reveals that the only protein co

169 In Lotus japonicus, two symbiotic cation channels, CASTOR and POL

170 ing in the fission yeast Schizosaccharomyces japonicus, unlike its role in S. pombe.

171 n cellulose utilization and suggests that C. japonicus utilizes a combination of hydrolytic and oxida

172 ontrolled by EIN2, which is duplicated in L. japonicus We obtained a L. japonicus Ljein2a Ljein2b dou

173 by the saprophytic soil bacterium Cellvibrio japonicus, we sequenced and analyzed its genome, which p

174 pecies, namely pea (Pisum sativum) and Lotus japonicus, we show that this motor organ identity is reg

175 ymbiosome membrane of the model legume Lotus japonicus were analyzed by patch-clamp recording.

176 ing nodule organogenesis in the legume Lotus japonicus were identified using mRNA differential displa

177 e (Gln) synthetase in the model legume Lotus japonicus were investigated.

178 llux, and castor pollux double mutants of L. japonicus were rescued by DMI1 alone, while both Lj-CAST

179 between the genomes of M. truncatula and L. japonicus, whereas lower levels of conservation were evi

180 n the GH10 xylanase CjXyn10A from Cellvibrio japonicus, which contains an extended calcium binding lo

181 into a symbiosis with the legume host, Lotus japonicus, which results in the formation of novel plant

182 ells before spreading to the epidermis in L. japonicus While mutant analysis identified redundancy in

183 ble connective tissue in the body wall of A. japonicus, whilst holokinins (PLGYMFR and derivative pep

184 in the recently sequenced fission yeast, S. japonicus (with 36% GC content), which is highly diverge

185 o-mannobiohydrolase CjMan26C from Cellvibrio japonicus, with a conserved glycone region (-1 and -2 su