ライフサイエンスコーパス: Lotus

1 Lotus japonicus has been used for decades as a model leg

2 Lotus japonicus is a model species for legume genomics.

3 Lotus SYMRK is required for a symbiotic signal transduct

4 e legume functional genomics, we developed a Lotus japonicus Gene Expression Atlas (LjGEA), which pro

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

6 Here we identify a Lotus japonicus nodulation pectate lyase gene (LjNPL), w

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

8 s identified in Medicago truncatula (52) and Lotus japonicus (53), including pseudogenes and non-func

9 egumes, Medicago truncatula, Glycine max and Lotus japonicus plus two reference plant species, A. tha

10 two other sequenced legumes, Glycine max and Lotus japonicus.

11 receptor5 (nfr5), Nodule inception (nin) and Lotus histidine kinase1 (lhk1) genes identified a previo

12 type, similar to the clv2 mutants of pea and Lotus japonicus.

13 ed between Mesorhizobium loti strain R7A and Lotus japonicus Gifu, rhizobial exopolysaccharide (EPS)

14 nt (396 and 273 mg kg(-1), respectively) and Lotus creticus, the lowest (20 mg kg(-1)).

15 ty to different degrees in Pisum sativum and Lotus japonicus.

16 gume species, namely pea (Pisum sativum) and Lotus japonicus, we show that this motor organ identity

17 odel legume species, Medicago truncatula and Lotus japonicus, as well as data available for Arabidops

18 e two model legumes, Medicago truncatula and Lotus japonicus, provide a unique opportunity to address

19 f the model legumes, Medicago truncatula and Lotus japonicus, provides an opportunity for large-scale

20 t epidermal cells of Medicago truncatula and Lotus japonicus.

21 development of root hairs in the angiosperms Lotus japonicus, Arabidopsis thaliana, and rice (Oryza s

22 a SAPIEN-type valve (n=20,40.0%) or a Boston Lotus valve (n=1, 2.0%).

23 t a subset of these epithelial tubules bound Lotus tetragonolobus and expressed alpha(1) Na(+)/K(+) A

24 %; P=0.62), or major vascular complications (Lotus, 2.9%; ES3, 2.4%; P=0.69).

25 edicago truncatula with those of the diploid Lotus japonicus and the polyploid Glycine max.

26 ed a sensitive ethylene detection system for Lotus japonicus and found that ethylene production incre

27 formed from fucose-specific isolectin A from Lotus tetragonolobus cross-linked with difucosyllacto-N-

28 Boeing 787 Dreamliner; lightweight cars from Lotus, Ferrari and TVR; and high-speed trains, speedboat

29 e the characterization of a gene family from Lotus japonicus that encodes a novel class of plant PITP

30 'symbiosis receptor-like kinase') genes from Lotus and pea, which are required for both fungal and ba

31 e clamp records of an ortholog of GmN70 from Lotus japonicus also showed anion currents with a simila

32 a type III sucrose transporter homolog from Lotus japonicus, is expressed in nodules and its transpo

33 Although the DMI1 homologs from Lotus japonicus, CASTOR and POLLUX, were recently report

34 Gene order in Glycine, Lotus, and Medicago differs from the usual gene order fo

35 Comparisons of Glycine, Lotus and Medicago confirm the organization of legume ch

36 NN and the previously identified genes HAR1 (Lotus japonicus) and NARK (Glycine max) are orthologs ba

37 ra: Arabidopsis, Brassica, Glycine, Hordeum, Lotus, Lycopersicon, Medicago, Oryza, Solanum, Sorghum,

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

39 In Lotus japonicus, a LysM receptor kinase, EPR3, distingui

40 In Lotus japonicus, two symbiotic cation channels, CASTOR a

41 Overexpression of the GS52 ecto-apyrase in Lotus japonicus increased the level of rhizobial infecti

42 d in regulating isoflavonoid biosynthesis in Lotus (Lotus japonicus).

43 ve gain-of-function CNGC mutation (brush) in Lotus japonicus resulting in a leaky tetrameric channel.

44 e found that P. palmivora induces disease in Lotus japonicus and used this interaction to identify ce

45 tified and sequenced and their expression in Lotus japonicus characterised.

46 and also sufficient for nodule formation in Lotus japonicus.

47 We have identified a gene in Lotus japonicus, Epr3, encoding a receptor-like kinase t

48 TOR and POLLUX, the twin homologous genes in Lotus japonicus that encode putative ion channel protein

49 sense inhibition of LNP blocks nodulation in Lotus japonicus.

50 olved in both infection and organogenesis in Lotus japonicus.

51 ces similar to MtDHDPS2 and 3 are present in Lotus japonicus and Glycine max, suggesting the existenc

52 ene, LjNOD70, associated with late stages in Lotus japonicus nodule development and/or functioning wa

53 s in lateral root formation and symbiosis in Lotus japonicus.

54 f 16S rRNA gene amplicons, we reveal that in Lotus, distinctive nodule- and root-inhabiting communiti

55 e cauliflower mosaic virus 35S promoter into Lotus corniculatus, which is nodulated by R. loti.

56 (LjNPP2C1 and LjPP2C2) from the model legume Lotus japonicus that encode protein phosphatase type 2C

57 the symbiosome membrane of the model legume Lotus japonicus were analyzed by patch-clamp recording.

58 utamine (Gln) synthetase in the model legume Lotus japonicus were investigated.

59 In the model legume Lotus japonicus, one of these LegCYC genes has been show

60 ts during nodule organogenesis in the legume Lotus japonicus were identified using mRNA differential

61 regulated in mycorrhizal roots of the legume Lotus japonicus, expression of a unique GRAS protein par

62 olic responses to waterlogging of the legume Lotus japonicus, it was previously suggested that, durin

63 with endogenous SYMRK in roots of the legume Lotus japonicus.

64 s in a determinate symbiosis with the legume Lotus japonicus.

65 bility to elicit nodules on its host legume, Lotus japonicus.

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

67 t to the other completely sequenced legumes, Lotus and Medicago.

68 mporal changes in the cytoskeleton of living Lotus japonicus root hairs, which precede root-hair defo

69 gulating isoflavonoid biosynthesis in Lotus (Lotus japonicus).

70 Medicago-Lotus comparisons also indicate similar and largely homo

71 e in the primary end point within 12 months (Lotus, 15.5%; ES3, 18.6%; P=0.69) and 24 months (Lotus,

72 s, 15.5%; ES3, 18.6%; P=0.69) and 24 months (Lotus, 21.9%; ES3, 26.4%; P=0.49).

73 s with no difference in all-cause mortality (Lotus, 1.9%; ES3, 1.8%; P=0.87), rate of disabling strok

74 m japonicum, which nodulates soybean and not Lotus spp.

75 rtion line, we identify two novel alleles of Lotus japonicus REDUCED ARBUSCULAR MYCORRHIZA1 (RAM1) en

76 The availability of a significant amount of Lotus japonicus genome sequence has permitted for the fi

77 ed tannins (CTs) in 'hairy root' cultures of Lotus corniculatus (bird's foot trefoil) using genetic m

78 m in nitrogen (N) fixing nodules (Fix(+)) of Lotus japonicus, as well as the link of S-metabolism to

79 Three clonal genotypes of Lotus corniculatus L.

80 tenotic Aortic Valve Through Implantation of Lotus Valve System: Evaluation of Safety and Performance

81 Flowers and leaves of Lotus japonicus contain alpha-, beta-, and gamma-hydroxy

82 l methanesulfonate mutagenized population of Lotus japonicus for mutants defective in IT formation an

83 -based expression studies and a selection of Lotus japonicus mutants uncoupling different symbiosis s

84 way genes in a sliding developmental zone of Lotus japonicus roots.

85 ale genome duplication in either Medicago or Lotus but instead a duplication predating speciation.

86 led at our center, and 202 patients received Lotus and 335 ES3.

87 significantly higher with the repositionable Lotus device.

88 ower with the repositionable and retrievable Lotus valve compared with the ES3.

89 d 24-month outcomes of the Boston Scientific Lotus valve (Lotus) and the balloon-expandable Edwards S

90 Medicago truncatula, Glycine max (soybean), Lotus japonicus, Phaseolus vulgaris (common bean), Cicer

91 diversification of the streptophyte-specific Lotus japonicus ROOTHAIRLESS LIKE (LRL) transcription fa

92 S3, 1.8%; P=0.87), rate of disabling stroke (Lotus, 1.5%; ES3, 2.1%; P=0.62), or major vascular compl

93 Here we show that Lotus japonicus and Medicago truncatula possess very sim

94 The Lotus and Medicago genomes share a minimum of 10 large-s

95 The Lotus japonicus SYMBIOSIS RECEPTOR-LIKE KINASE (SYMRK) i

96 The Lotus valve, designed to improve upon earlier devices, i

97 rough light-induced photodegradation and the Lotus effect are presented.

98 ortic valve replacement with the ES3 and the Lotus were associated with similar 30-day, 12-month, and

99 Previous analysis of the Lotus histidine kinase1 (Lhk1) cytokinin receptor gene h

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

101 Database studies of the Lotus japonicus genome have revealed the presence of 24

102 cess we conducted a detailed analysis of the Lotus japonicus hypernodulating mutants, har1-1, 2 and 3

103 here the characterization of a member of the Lotus japonicus nitrate transporter1/peptide transporter

104 nstrates the safety and effectiveness of the Lotus valve in patients with severe aortic stenosis who

105 Here, we show that the Lotus japonicus Ckx3 cytokinin oxidase/dehydrogenase gen

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

107 for aberrant nodulation phenotypes using the Lotus japonicus LORE1 insertion mutant collection.

108 plantation was significantly higher with the Lotus valve compared with the ES3 valve (36.1% versus 14

109 ydroxylase (NahG) in both stably transformed Lotus japonicus and composite Medicago truncatula plants

110 Transgenic Lotus japonicus plants were constructed constitutively e

111 ssion in the nodule parenchyma of transgenic Lotus corniculatus plants.

112 he pattern observed in nodules of transgenic Lotus corniculatus plants.

113 ifolium pratense L.), and birdsfoot trefoil (Lotus corniculatus L.).

114 mpare unigene sets from Medicago truncatula, Lotus japonicus, and soybean (Glycine max and Glycine so

115 of transcript data from Medicago truncatula, Lotus japonicus, Glycine max and Arabidopsis thaliana.

116 forward genetic approach, we identified two Lotus japonicus mutants defective in AM-specific paralog

117 tcomes of the Boston Scientific Lotus valve (Lotus) and the balloon-expandable Edwards Sapien 3 (ES3)

118 ass were determined in sections stained with Lotus tetragonolobus lectin.