ライフサイエンスコーパス: Lotus japonicus

1 gulating isoflavonoid biosynthesis in Lotus (Lotus japonicus).

2 ociated with Nod factor receptor 5 (NFR5) in Lotus japonicus.

3 subcellular localizations in Arabidopsis and Lotus japonicus.

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

5 olved in both infection and organogenesis in Lotus japonicus.

6 t epidermal cells of Medicago truncatula and Lotus japonicus.

7 and also sufficient for nodule formation in Lotus japonicus.

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

9 sense inhibition of LNP blocks nodulation in Lotus japonicus.

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

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

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

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

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

15 n of many genes required for AM formation in Lotus japonicus.

16 development of nodules in the model legume, Lotus japonicus.

17 n AM colonisation and rhizobial infection in Lotus japonicus.

18 bial suppression of plant innate immunity in Lotus japonicus.

19 ntial for infection thread (IT) formation in Lotus japonicus.

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

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

22 his by exploring the phenotypic diversity of Lotus japonicus accessions that uncouple nodule organoge

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

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

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

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

27 s, and compare these results to the AM model Lotus japonicus and its ipd3 knockout mutant cyclops-4.

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

29 Studies in the model legumes Lotus japonicus and Medicago truncatula showed that rhiz

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

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

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

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

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

35 odel legume species, Medicago truncatula and Lotus japonicus, and two crop species, Glycine max (soyb

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

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

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

39 1 (CERK1), in rice, Medicago truncatula, and Lotus japonicus, as well as the non-host of AM fungi, Ar

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

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

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

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

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

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

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

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

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

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

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

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

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

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

54 e applied this methodology to mutants of the Lotus japonicus GRAS transcription factor RAM1 and the O

55 tion as well as target promoter induction in Lotus japonicus hairy roots depends on MYCS (MYCORRHIZA

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

57 action is unclear and the function of VPY in Lotus japonicus has not been studied.

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

59 ssing is observed in Medicago truncatula and Lotus japonicus, implying a conserved mechanism of cell

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

61 tin and nodulation (Nod) factor receptors of Lotus japonicus initiate differential signaling of immun

62 Here we show that CASTOR from Lotus japonicus is a highly selective Ca(2+) channel who

63 Lotus japonicus is a model species for legume genomics.

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

65 that VTL8, the closest homologue of SEN1 in Lotus japonicus, is the main route for delivering iron t

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

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

68 ognition, we determined the structure of the Lotus japonicus (Lotus) exopolysaccharide receptor 3 (EP

69 lycan, as might be inferred from work on the Lotus japonicus MtLYK10 ortholog, LjEPR3.

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

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

72 crystal structure of the signaling-competent Lotus japonicus NFR5 intracellular domain, comprising th

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

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

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

76 inate (Medicago truncatula) and determinate (Lotus japonicus) nodulation.

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

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

79 (Nicotiana benthamiana, Medicago truncatula, Lotus japonicus, Oryza sativa) and captured the altered

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

81 Transgenic Lotus japonicus plants were constructed constitutively e

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

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

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

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

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

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

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

89 elix (bHLH) transcription factors encoded by LOTUS JAPONICUS ROOTHAIRLESS1-LIKE (LRL) genes positivel

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

91 ar iron transporter family and homologous to Lotus japonicus SEN1 (LjSEN1), which is essential for ni

92 Here we show that Lotus japonicus SMAX1 is specifically degraded in the pr

93 While the kinase domain of NF receptors in Lotus japonicus suffices for nodule organogenesis, their

94 ds in high-turgor cells in the phloem cap of Lotus japonicus, suggesting that storage of defensive co

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

96 mbrane-associated protein interactomes using Lotus japonicus symbiotically active receptor kinases as

97 The Lotus japonicus T-DNA insertion line T90, carrying a pro

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

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

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

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

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

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

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

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

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

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