ライフサイエンスコーパス: L. japonicus

1 is duplicated in L. japonicus We obtained a L. japonicus Ljein2a Ljein2b double mutant that exhibits

2 Symbiosis between M. loti and L. japonicus requires bacterial synthesis of secreted an

3 d us to establish putative M. truncatula and L. japonicus orthologues.

4 the model legume species, M. truncatula and L. japonicus, and substantially enhanced the knowledgeba

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

6 Together with previously described L. japonicus Nck-associated protein1 and 121F-specific p

7 Spot inoculations of NahG-expressing L. japonicus plants confirmed increased nodulation in th

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

9 elopment: arbuscule branching is arrested in L. japonicus ram1 mutants, and ectopic expression of RAM

10 s not a factor controlling N-assimilation in L. japonicus roots during stable growth in N-sufficient

11 transcripts and metabolites that changed in L. japonicus plants during the transfer from photorespir

12 erved specialisation in HNG based defence in L. japonicus flowers is discussed in the context of bala

13 s controlled by EIN2, which is duplicated in L. japonicus We obtained a L. japonicus Ljein2a Ljein2b

14 l cells before spreading to the epidermis in L. japonicus While mutant analysis identified redundancy

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

16 dule organogenesis, and nitrogen fixation in L. japonicus.

17 f the GS52 apyrase can enhance nodulation in L. japonicus and points to an important role for this gr

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

19 LjMYB14, was constitutively overexpressed in L. japonicus and induced the expression of at least 12 g

20 The induction of isoflavonoid production in L. japonicus also involves the coordinated down-regulati

21 ene was found to be enhanced specifically in L. japonicus nodules, whereas the LjPP2C2 gene was expre

22 in acclimation to tolerate drought stress in L. japonicus.

23 characterization carried out in independent L. japonicus LORE1 insertion lines indicates a positive

24 ormed phenotypic analysis of two independent L. japonicus mutant alleles and investigated the regulat

25 o be expressed only in the infected cells of L. japonicus nodules.

26 acterized plant genomes, the TE component of L. japonicus contained several surprises.

27 h symbiotic and non-symbiotic development of L. japonicus, and suggest that regulatory processes cont

28 pollux, and castor pollux double mutants of L. japonicus were rescued by DMI1 alone, while both Lj-C

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

30 induced during late developmental stages of L. japonicus nodule organogenesis and provide important,

31 Mesorhizobium loti, the natural symbiont of L. japonicus.

32 and a decreased rate of nodule formation on L. japonicus.

33 thetic steps form nitrogen-fixing nodules on L. japonicus Gifu after a delay, whereas mutants affecte

34 In addition, previously published L. japonicus Affymetrix data are included in the databas

35 member of a small family of closely related L. japonicus genes.

36 found to be drastically altered in specific L. japonicus lines carrying monogenic-recessive mutation

37 We show here that L. japonicus contains a small family of four cytokinin r

38 olecular modelling, and the observation that L. japonicus accessions lacking cyanogenic flowers conta

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

40 The L. japonicus arpc1 mutant showed a distorted trichome ph

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

42 y described cDNA, LjNOD16, which encodes the L. japonicus late nodulin Nlj16.

43 Finally, the L. japonicus genome contains many hundreds, perhaps thou

44 mble the expression pattern observed for the L. japonicus leghemoglobin gene.

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

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

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

48 As in M. truncatula, the L. japonicus ram1 mutant lines show compromised AM colon

49 subgroups of proteins that were specific to L. japonicus or closely related to known regulators of t