ライフサイエンスコーパス: Antirrhinum

1 opsis reflects greater genetic redundancy in Antirrhinum .

2 ter the first described plant PEBP gene from Antirrhinum.

3 space separating two flower color morphs of Antirrhinum.

4 n a downstream target gene RADIALIS (RAD) in Antirrhinum.

5 in Arabidopsis, similar to the situation in Antirrhinum.

6 ene which controls dorsoventral asymmetry in Antirrhinum.

7 transformation in stamen number relative to Antirrhinum, aborting the lateral and adaxial stamens du

8 The fimbriata (fim) gene of Antirrhinum affects both the identity and arrangement of

9 cture is conserved in relation to AG and the Antirrhinum AG orthologue, PLENA (PLE), and low-stringen

10 TEM orthologs were isolated from antirrhinum (AmTEM) and olive (OeTEM) and were expressed

11 rent, reflecting the diverse morphologies of Antirrhinum and Arabidopsis flowers.

12 ion is associated with petal identity, as in Antirrhinum and Arabidopsis, but this is achieved throug

13 In Antirrhinum and Arabidopsis, mutations in the floral mer

14 antly from weak C-function mutant alleles in Antirrhinum and Arabidopsis.

15 t three duplications since the divergence of Antirrhinum and Arabidopsis.

16 rgence among Antirrhinum species and between Antirrhinum and Digitalis is also low.

17 stinct from the expression pattern of RAD in Antirrhinum and from the endogenous RAD-like genes of Ar

18 or establishing petal and stamen identity in Antirrhinum and is expressed in all three layers of the

19 mologous transcription factors FLORICAULA of Antirrhinum and LEAFY of Arabidopsis share conserved rol

20 ibution of Tkn2 KNOX transcripts compared to Antirrhinum and maize suggests either a different spatia

21 f plants sampled from natural populations of Antirrhinum and Misopates species.

22 plains the biosynthesis of 7-epi-iridoids in Antirrhinum and related genera.

23 n protein, closely related to PHANTASTICA in Antirrhinum and ROUGH SHEATH2 in maize, both of which ne

24 a langsdorffii X N. sanderae) homolog of the antirrhinum (Antirrhinum majus) MYB305.

25 e have tested whether the model proposed for Antirrhinum applies to Arabidopsis, by creating transgen

26 red for the ABC functions in Arabidopsis and Antirrhinum are members of the MADS-box gene family, and

27 ogs AG from Arabidopsis and PLENA (PLE) from Antirrhinum are shown to be representatives of separate

28 -evolved with overall leaf shape and size in Antirrhinum because these characters are constrained by

29 ntity is based on studies of Arabidopsis and Antirrhinum, both of which are highly derived eudicots.

30 This feature of the two Antirrhinum C-function-like genes is markedly different

31 We have determined the crystal structure of Antirrhinum CEN to 1.9 A resolution.

32 y a natural variant of the barley homolog of Antirrhinum CENTRORADIALIS (HvCEN) as a contributor to s

33 An allele of the DAG locus of Antirrhinum (dag::Tam3), which is required for chloropla

34 amiana using TRV-VIGS was similar to that of Antirrhinum def and Arabidopsis ap3 mutants and caused t

35 uggest that NbDEF is a functional homolog of Antirrhinum DEF.

36 Dorsoventral asymmetry in flowers of Antirrhinum depends on expression of the cycloidea gene

37 shape--petal asymmetry--in the petal lobe of Antirrhinum depends on the direction of growth rather th

38 The development of reproductive organs in Antirrhinum depends on the expression of an organ identi

39 cterize the phylogenetic orthologue of Ls in Antirrhinum, ERAMOSA (ERA).

40 identity in Arabidopsis; their orthologs in Antirrhinum exhibit similar functions.

41 r the presence of high-fitness ridges in the Antirrhinum floral-color adaptive landscape, their data

42 UPULIFORMIS (CUP) in formation of the ornate Antirrhinum flower shape.

43 lip, and characteristic folds of the closed Antirrhinum flower.

44 In Antirrhinum, flower asymmetry depends on activation of R

45 The Antirrhinum gene CENTRORADIALIS (CEN) and the Arabidopsi

46 revealed that Stp is the pea homolog of the Antirrhinum gene Fimbriata (Fim) and of UNUSUAL FLORAL O

47 that cyc and fil1 are among the least biased Antirrhinum genes, so that their low diversity is not du

48 gest either that these gene families (or the Antirrhinum genome) are unusually constrained or that th

49 Antirrhinum has two genes corresponding to AP2, termed L

50 e controlling floral asymmetry, cycloidea in Antirrhinum, has been isolated.

51 e used primers designed from three published Antirrhinum hispanicum S-allele sequences in PCR reactio

52 hese phenotypes resemble the Arabidopsis and Antirrhinum homeotic B-function mutants apetala3/deficie

53 ra (desert ghost flower), which differs from Antirrhinum in corolla (petal) symmetry and pollination

54 in Senecio versus dorsal petal elongation in Antirrhinum In S vulgaris, diversification of CYC genes

55 lower 1 in Arabidopsis and centroradialis in Antirrhinum, inflorescences that are normally indetermin

56 Introduction of a RAD genomic clone from Antirrhinum into Arabidopsis leads to a novel expression

57 ablishment and maintenance and, in maize and Antirrhinum, it has been proposed that PHAN acts as an e

58 Dorsoventral asymmetry of Antirrhinum leaves requires activity of the Phantastica

59 umulation of knox gene products in maize and Antirrhinum leaves, respectively.

60 the coupling of RAD to CYC regulation in the Antirrhinum lineage and hence the co-option of RAD had a

61 of RAD may have occurred specifically in the Antirrhinum lineage.

62 etic replicas of petal surfaces and isogenic Antirrhinum lines differing only in petal epidermal cell

63 Compared with Antirrhinum, little divergence is again observed.

64 We report the discovery of an Antirrhinum MADS-box gene, FARINELLI (FAR), and the isol

65 ble for model organisms such as Arabidopsis, Antirrhinum, maize, rice and wheat, a phylogenetic persp

66 lly symmetrical flowers of the model species Antirrhinum majus (Plantaginaceae) are highly specialize

67 unctional genomic approach, we identified an Antirrhinum majus (snapdragon) BALDH, which exhibits 40%

68 In the model developmental system Antirrhinum majus (snapdragon), the closely related gene

69 The model species Antirrhinum majus (the garden snapdragon) has over 20 cl

70 Tam3 from Antirrhinum majus belongs to the Ac/Ds family of transpo

71 An Antirrhinum majus dihydroflavonol reductase (DFR) cDNA w

72 Here we report the isolation of a gene from Antirrhinum majus encoding a protein from an entirely no

73 ne responsible for conferring dorsal fate in Antirrhinum majus flowers.

74 Ectopic expression of the MIXTA gene from Antirrhinum majus in S. dulcamara results in the formati

75 w that the growth and asymmetry of leaves in Antirrhinum majus involves the related YABBY transcripti

76 MIXTA, which in Antirrhinum majus is reported to regulate certain aspect

77 n the distantly related core eudicot species Antirrhinum majus L., paralogous SBP-box proteins SBP1 a

78 The identification of Antirrhinum majus mutants with ectopic petal spurs sugge

79 he reporter system is based on expression of Antirrhinum majus MYB-related Rosea1 (Ros1) transcriptio

80 In four Antirrhinum majus populations with different mating syst

81 ve identified a mutation at the DAG locus of Antirrhinum majus which blocks the development of chloro

82 Here, snapdragon (Antirrhinum majus) GPPS-SSU was over-expressed in tomato

83 Here, we show that expression of snapdragon (Antirrhinum majus) GPPS.SSU in tobacco (Nicotiana tabacu

84 le) and Dicotyledonae (Nicotiana tabacum and Antirrhinum majus) indicating that LINEs are a universal

85 i X N. sanderae) homolog of the antirrhinum (Antirrhinum majus) MYB305.

86 proteins, initially described in snapdragon (Antirrhinum majus) petals, are known regulators of epide

87 unds detected in the majority of snapdragon (Antirrhinum majus) varieties.

88 ms such as Arabidopsis thaliana, snapdragon (Antirrhinum majus), and petunia (Petunia hybrida).

89 transcription factor genes from snapdragon (Antirrhinum majus), paying particular attention to chang

90 rved in Arabidopsis thaliana and snapdragon (Antirrhinum majus).

91 This observation extends previous reports in Antirrhinum majus, Epilobium hirsutum, Nicotiana tabacum

92 In Antirrhinum majus, floral zygomorphy is established by t

93 In Antirrhinum majus, one proposed role of the gene fimbria

94 ridoids in the ornamental flower snapdragon (Antirrhinum majus, Plantaginaceae family) are derived fr

95 ng bZIP proteins are expressed in flowers of Antirrhinum majus, predominantly in vascular tissues, ca

96 ing mechanisms used by four such proteins in Antirrhinum majus, SQUA, PLE, DEF and GLO.

97 In Antirrhinum majus, the MIXTA protein directs the formati

98 variation in 3000 leaves from 400 plants of Antirrhinum majus.

99 ment of conical epidermal cells in petals of Antirrhinum majus.

100 to the development of dorsal petal lobes of Antirrhinum majus.

101 ptide-encoding sequence from the oli gene of Antirrhinum majus.

102 class in Arabidopsis (TCP1) and snapdragon (Antirrhinum majus; CYCLOIDEA) have been shown to be asym

103 e show that the previous inability to obtain Antirrhinum mutants corresponding to the A class gene AP

104 Snapdragon (Antirrhinum) mutants lacking conical cells have been sho

105 Unlike the situation in Antirrhinum, none of the Arabidopsis RAD-like genes are

106 is expressed only in the inner epidermis of Antirrhinum petals.

107 gene sequence was found to be similar to the Antirrhinum PHANTASTICA (PHAN) gene sequence, which enco

108 ily conserved sequences in the intron of the Antirrhinum PLENA (PLE) gene to establish whether they r

109 ences, and one to a very similar unpublished Antirrhinum S-like RNase sequence.

110 red in Arabidopsis are therefore separate in Antirrhinum, showing that the genetic basis of some aspe

111 fied visually, to observe the development of Antirrhinum (snapdragon) petals.

112 antify differences in leaf allometry between Antirrhinum (snapdragon) species, including variation in

113 Divergence among Antirrhinum species and between Antirrhinum and Digitali

114 mined the evolutionary relationships between Antirrhinum species and how these relate to geography an

115 Hybrids between Antirrhinum species have been used successfully to ident

116 Antirrhinum species with diverse floral phenotypes forme

117 s, euAP1 (including Arabidopsis APETALA1 and Antirrhinum SQUAMOSA) and euFUL (including Arabidopsis F

118 It has previously been proposed for Antirrhinum that another gene, FIMBRIATA (FIM), mediates

119 A transcription factor couple from Antirrhinum that is known to control anthocyanin biosynt

120 In Antirrhinum, the inflorescence can be distinguished by i

121 ved role in petal growth in both Senecio and Antirrhinum, the regulatory relationships and expression

122 the normally indeterminate inflorescence of Antirrhinum to terminate in a flower.

123 ed an Impatiens homologue of the FIM gene of Antirrhinum (UFO in Arabidopsis), Imp-FIM, and analysed

124 zfl2, the maize homolog of FLORICAULA of Antirrhinum, was associated with plant height.

125 and FT were observed in both Arabidopsis and antirrhinum, which correlated with the length of the JVP

126 rsity studies revealed that the fil1 gene of Antirrhinum, which has been reported to be single copy,

127 We have studied the cin mutant of Antirrhinum, which has crinkly rather than flat leaves.