ライフサイエンスコーパス: Lotus japonicus

1 gulating isoflavonoid biosynthesis in Lotus (Lotus japonicus).

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

3 olved in both infection and organogenesis in Lotus japonicus.

4 t epidermal cells of Medicago truncatula and Lotus japonicus.

5 and also sufficient for nodule formation in Lotus japonicus.

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

7 sense inhibition of LNP blocks nodulation in Lotus japonicus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

45 Lotus japonicus is a model species for legume genomics.

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

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

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

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

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

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

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

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

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

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

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

57 Transgenic Lotus japonicus plants were constructed constitutively e

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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