ライフサイエンスコーパス: coronatine

1 p-regulated by ABA, bacterial infection, and coronatine.

2 uced sensitivity to the bacterial phytotoxin coronatine.

3 educed sensitivity to the bacterial effector coronatine.

4 rB in DC3000, suggesting that AvrB may mimic coronatine.

5 ds, 12-oxo-phytodienoic acid, and phytotoxin coronatine.

6 e functional analog of jasmonoyl-isoleucine, coronatine.

7 ae pv. tomato DC3000 produces the phytotoxin coronatine, a major determinant of the leaf chlorosis as

8 Pseudomonas syringae produces coronatine, a toxin that mimics the plant hormone jasmon

9 s the polyketide component of the phytotoxin coronatine, a virulence factor of the plant pathogen Pse

10 gest that P. syringae type III effectors and coronatine act by augmenting a COI1-dependent pathway to

11 coronatine-mediated virulence and show that coronatine activates three homologous NAC transcription

12 e hypotheses that the P. syringae phytotoxin coronatine acts to promote virulence by inhibiting host

13 s essential for production of the phytotoxin coronatine and for expression of the structural genes en

14 These results not only suggest that coronatine and JA-Ile target the physical interaction be

15 a combination of the bacterial JA-Ile mimic coronatine and type III virulence-associated effectors.

16 with PtCOI1 in the presence of the JA mimic coronatine, and PtJAZ6 is degraded in plant tissues afte

17 type III secretion system and the phytotoxin coronatine are required for RAP2.6 induction.

18 all other sequenced P. syringae strains with coronatine biosynthesis genes.

19 restore coronatine production, showing that coronatine biosynthesis requires factors other than hrpL

20 f Cfa1, suggesting that FabD plays a role in coronatine biosynthesis.

21 virulence genes, including hrp/hrc, avr and coronatine biosynthetic genes.

22 Here we show that coronatine, but not its two biosynthetic precursors, als

23 Thus, a signaling cascade by which coronatine confers its multiple virulence activities has

24 to the plant host cell, while the phytotoxin coronatine (COR) contributes to virulence and disease sy

25 Coronatine (COR) facilitates entry of bacteria into the

26 Coronatine (COR) is a phytotoxin produced by several pat

27 Coronatine (COR) is a plasmid-encoded phytotoxin synthes

28 The phytotoxin coronatine (COR) promotes various aspects of Pseudomonas

29 solution was achieved through treatment with coronatine (COR), a high-affinity agonist of the JA rece

30 udomonas syringae pv. tomato DC3000 produces coronatine (COR), a jasmonic acid (JA) mimic.

31 Arabidopsis (Arabidopsis thaliana), produces coronatine (COR), a non-host-specific phytotoxin.

32 -elicited SIS is caused by the production of coronatine (COR), a pathogen-derived functional and stru

33 ic acid (CFA) is the polyketide component of coronatine (COR), a phytotoxin produced by the plant pat

34 ic acid (CFA) is the polyketide component of coronatine (COR), a phytotoxin produced by the plant pat

35 ic acid (CFA) is the polyketide component of coronatine (COR), a phytotoxin produced by the plant-pat

36 t tvrR mutant strains are able to synthesize coronatine (COR), a phytotoxin required for virulence of

37 phytohormone mimics, such as the phytotoxin coronatine (COR), have not been directly quantified in p

38 (flg22), and a pathogen-derived phytotoxin, coronatine (COR), induced a shoot-to-root signal regulat

39 effectors, as well as a JA-mimicking toxin, coronatine (COR), to activate JA signaling as a mechanis

40 smonate, JA-Ile, and its functional homolog, coronatine (COR), we demonstrate that (1) JA-Ile/COR-bas

41 Pseudomonas syringae produce the phytotoxin coronatine (COR), which contains an unusual amino acid,

42 The virulence factor coronatine (COR), which is produced by plant pathogenic

43 proteins into host cells and the phytotoxin coronatine (COR), which is thought to mimic the action o

44 Jas domain were identified as essential for coronatine-dependent COI1-JAZ interactions.

45 main of JAZ proteins, is critical for JA-Ile/coronatine-dependent interaction with COI1.

46 ds in the Jas domain in mediating the JA-Ile/coronatine-dependent JAZ interaction with COI1.

47 ic acid, and the bacterial virulence factor, coronatine, during progression of P. syringae infection

48 The main genetic and metabolic targets of coronatine in Arabidopsis (Arabidopsis thaliana) remain

49 Interestingly, the role of coronatine in RAP2.6 induction can be partially substitu

50 mutants demonstrates that these TFs mediate coronatine-induced stomatal reopening and bacterial prop

51 re, analysis of bacterial supernatants under coronatine-inducing conditions revealed that mutants lac

52 C. roseus JA signaling components, including CORONATINE INSENSITIVE 1 (COI1) and JASMONATE ZIM domain

53 The F-box protein CORONATINE INSENSITIVE 1 (COI1) mediates jasmonate signa

54 ene response factor (ERF) gene, RAP2.6, in a coronatine insensitive 1 (COI1)-dependent manner.

55 biquitin ligase complex containing the F-box CORONATINE INSENSITIVE 1 (COI1).

56 A) promotes AAL toxin induced PCD in a COI1 (coronatine insensitive 1, JA receptor)-dependent manner

57 Blocked JA signaling in coronatine-insensitive (coi1) and enhanced expression of

58 le), stimulates binding of the F-box protein coronatine-insensitive 1 (COI1) to, and subsequent ubiqu

59 A new allele of the coronatine-insensitive locus (COI1) was isolated in a sc

60 f LBD20 expression in roots was abolished in coronatine insensitive1 (coi1) and myc2 (allelic to jasm

61 stablished pathway requiring the JA receptor CORONATINE INSENSITIVE1 (COI1) and the JA-regulated tran

62 eption of bioactive JAs by the F-box protein CORONATINE INSENSITIVE1 (COI1) causes degradation of JAZ

63 monoyl-L-isoleucine (JA-Ile) to the F-box of CORONATINE INSENSITIVE1 (COI1) is required for many JA-d

64 ated by constitutive expression of ERF1 in a coronatine insensitive1 (coi1) mutant background (35S::E

65 cells of wild-type (Col-0) Arabidopsis, the CORONATINE INSENSITIVE1 (COI1) mutant coi1-1 and the PM

66 gatively regulated by the jasmonate receptor Coronatine Insensitive1 (COI1), as loss of functional CO

67 AZ repressor proteins with the F-box protein CORONATINE INSENSITIVE1 (COI1), part of an S-phase kinas

68 main (JAZ) repressors with the F-box protein CORONATINE INSENSITIVE1 (COI1), which results in JAZ deg

69 that JA rapidly induces RGL3 expression in a CORONATINE INSENSITIVE1 (COI1)- and JASMONATE INSENSITIV

70 he plant defense hormone jasmonic acid (JA), CORONATINE INSENSITIVE1 (COI1).

71 ontrolling the transcriptional repression of CORONATINE INSENSITIVE1 in an evening-phase-specific man

72 the tomato ortholog of the ubiquitin ligase CORONATINE INSENSITIVE1 in Arabidopsis (Arabidopsis thal

73 that are deficient in jasmonate perception (coronatine insensitive1) or in the biogenesis of small i

74 ion, allene oxide synthase and coi1-16B (for coronatine insensitive1), respectively.

75 Double mutants of ago1 and coronatine insensitive1, the jasmonate receptor, showed

76 inding to the F-box-containing JA coreceptor CORONATINE INSENSITIVE1.

77 tionally high JA levels and was dependent on CORONATINE INSENSITIVE1.

78 Moreover, elp2 is as susceptible as coronatine-insensitive1 (coi1) and ethylene-insensitive2

79 he loss of function of the tomato homolog of CORONATINE-INSENSITIVE1 (COI1), an F-box protein that is

80 Wound-induced expression of JAZ and other CORONATINE-INSENSITIVE1 (COI1)-dependent genes was not i

81 sis-like phenotype upon COR application in a Coronatine-Insensitive1 (COI1)-dependent manner.

82 acid fragment of the pseudomonal phytotoxin coronatine involves construction of the cyclopropane rin

83 Coronatine is an important virulence factor produced by

84 Coronatine is produced by the ligation of two moieties,

85 The structure of coronatine is similar to that of a class of plant hormon

86 We examined the mechanisms underlying coronatine-mediated virulence and show that coronatine a

87 onsive to pathogen virulence factors such as coronatine (phytotoxin produced by the bacterium Pseudom

88 The bacterial toxin, coronatine, produced by several pathogenic strains of Ps

89 showed the same virulence toward nrt2 as the coronatine-producing strain.

90 CmaL identifies a critical missing factor in coronatine production and provides a foundation for furt

91 idenced by the fact that wild-type levels of coronatine production are restored to a DeltacmaL mutant

92 f hrpL in ES4326 rpoN::Km(r) did not restore coronatine production, showing that coronatine biosynthe

93 (IaaL), and a subsidiary regulon controlling coronatine production.

94 ma operon or cmaL accumulate CFA rather than coronatine, supporting a role for CmaL in the regulation

95 addition, a P. syringae strain defective in coronatine synthesis showed the same virulence toward nr

96 clopropane), a constituent of the phytotoxin coronatine synthesized by the phytopathogenic bacterium

97 ants can be triggered by the bacterial toxin coronatine through a light-dependent process.

98 pv. tomato DC3000 uses the virulence factor coronatine to actively open stomata.

99 Coronatine-triggered and spontaneous lesion spreading in

100 0) responds by secreting a virulence factor, coronatine, which blocks the functioning of guard cells

101 nse was mediated by the bacterial phytotoxin coronatine, which exerts its virulence effects by co-opt

102 on system and a polyketide phytotoxin called coronatine, which structurally mimics the plant hormone