ライフサイエンスコーパス: lateral organ

1 e stem cell population and initiation of the lateral organs.

2 ernode and pedicels, as well as the shape of lateral organs.

3 hich is restricted to the growing regions of lateral organs.

4 the KANADI genes cause an adaxialization of lateral organs.

5 ZIP gene family, result in adaxialization of lateral organs.

6 is specific to meristems and does not affect lateral organs.

7 identified which interact to polarize plant lateral organs.

8 elaboration of cotyledons and post-embryonic lateral organs.

9 f abaxial cell types by adaxial ones in most lateral organs.

10 for the normal initiation and development of lateral organs.

11 loss of polar differentiation of tissues in lateral organs.

12 he development of ectopic abaxial tissues in lateral organs.

13 is a boundary similar to that at the base of lateral organs.

14 al cell identity within leaves and leaf-like lateral organs.

15 rotein, and AS1 to suppress BP expression in lateral organs.

16 ads to loss of the shoot apical meristem and lateral organs.

17 trol the enlargement and patterning of plant lateral organs.

18 ribed positive regulator of cell division in lateral organs.

19 cell types often develop radially symmetric lateral organs.

20 ty and must be repressed to form determinate lateral organs.

21 s that are overexpressed in the meristem and lateral organs.

22 ines new roles for ANT in the development of lateral organs.

23 y regulator of shape that promotes growth in lateral organs.

24 nts also exhibit aberrant shoot phyllotaxis, lateral organ abnormalities, and altered meristem morpho

25 ot cap contributes to the regular spacing of lateral organs along the primary root axis.

26 ene family, are characterized by adaxialized lateral organs and alterations in the radial patterning

27 Such meristems form lateral organs and develop into a side shoot or a flower

28 -like genes, LeT6 is expressed in developing lateral organs and developing ovaries in flowers.

29 all cases studied are expressed primarily in lateral organs and in a polar manner.

30 n, CUP is expressed at the boundaries of all lateral organs and meristems.

31 n plays a critical role in the initiation of lateral organs and meristems.

32 in polarity determination and patterning in lateral organs and primary vascular tissues and in the i

33 kn1 mutants form fewer lateral organs and td1 inflorescences are fasciated with

34 cells whilst providing cells for developing lateral organs and the stem.

35 y with Phantastica to promote dorsal fate in lateral organs and to maintain activity of stem cells wi

36 -Zip and KANADI genes function in patterning lateral organs and vascular bundles produced from the sh

37 In angiosperms, individual lateral organs and whole flowers may develop asymmetrica

38 pattern of organ initiation is disturbed and lateral organs are initiated more frequently.

39 Lateral organs are patterned along proximodistal, dorsov

40 he specification of founder cells from which lateral organs arise.

41 a wide range of morphological defects in all lateral organs as well as the shoot apical meristem (SAM

42 The LATERAL ORGAN BOUNDARIES (LOB) DOMAIN (LBD) gene family

43 We show that the LATERAL ORGAN BOUNDARIES (LOB) domain genes ASYMMETRIC L

44 CsLOB1 is a member of the Lateral Organ Boundaries (LOB) gene family of transcript

45 The LATERAL ORGAN BOUNDARIES (LOB) gene in Arabidopsis defin

46 he Arabidopsis thaliana transcription factor lateral organ boundaries (LOB) negatively regulates accu

47 oss-section of LBD proteins, and showed that LATERAL ORGAN BOUNDARIES (LOB), the founding member of t

48 r of the recently identified, plant-specific LATERAL ORGAN BOUNDARIES (LOB)-domain gene family.

49 AT2, and positively regulates the novel gene LATERAL ORGAN BOUNDARIES (LOB).

50 ized gene that encodes a novel member of the LATERAL ORGAN BOUNDARIES DOMAIN (LBD) family of transcri

51 ASYMMETRIC LEAVES2 (AS2)/LATERAL ORGAN BOUNDARIES DOMAIN (LBD) family proteins ar

52 ially expressed genes contained at least one LATERAL ORGAN BOUNDARIES domain (LBD) motif within 1 kb

53 ig1 encodes a LATERAL ORGAN BOUNDARIES domain protein with high simila

54 ral genes, such as those encoding members of LATERAL ORGAN BOUNDARIES domain proteins and AUXIN-REGUL

55 The paralogous maize (Zea mays) LBD (Lateral Organ Boundaries Domain) genes rtcs (rootless co

56 al meristem, including cup-shaped cotyledon, lateral organ boundaries, blade-on-petiole, asymmetric l

57 R production by regulating the expression of LATERAL ORGAN BOUNDARIES-DOMAIN29 and EXPANSIN17 genes.

58 ssion patterns of bHLH048 and LOB overlap at lateral organ boundaries.

59 slationally regulates the function of LOB at lateral organ boundaries.

60 rmal and peridermal cells as well as in stem lateral organ boundary cells.

61 JAGGED LATERAL ORGANS (JLO), a member of the LATERAL ORGAN BOUNDARY DOMAIN (LBD) gene family, is requ

62 ion of ELONGATED PETIOLULE1, which encodes a lateral organ boundary domain protein, and that the dist

63 by chromosome walking and shown to encode a LATERAL ORGAN BOUNDARY domain transcription factor.

64 d in stems at the floral transition, and the lateral organ boundary genes BLADE-ON-PETIOLE1 (BOP1) an

65 We show here that pny pnf apices misexpress lateral organ boundary genes BLADE-ON-PETIOLE1/2 (BOP1/2

66 a potential mechanism by which repression of lateral organ boundary genes by PNY-PNF is essential for

67 t BOP1 and BOP2 act in cells adjacent to the lateral organ boundary to repress genes that confer meri

68 rossly perturbed cell geometry in developing lateral organs by interfering independently with growth

69 and BOP2 in regulating Arabidopsis thaliana lateral organ cell fate and polarity, through the analys

70 -type plants, BOP1 and BOP2 are expressed in lateral organs close to boundaries of the SAM, whereas i

71 (PRS1) performs a conserved function during lateral organ development in Arabidopsis (Arabidopsis th

72 d2) is a novel, recessive mutation affecting lateral organ development in maize.

73 llels between early patterning events during lateral organ development in plants and animals are disc

74 Differential growth of tissues during lateral organ development is essential for producing var

75 udy, a GmCLV1A mutant (F-S562L) with altered lateral organ development, and two mutants of GmNARK, is

76 organs suggests a potential role for LOB in lateral organ development.

77 cell maintenance, embryonic patterning, and lateral organ development.

78 le in meristem maintenance, determinacy, and lateral organ development.

79 1) and BOP2 are known to control Arabidopsis lateral organ differentiation by regulating gene express

80 show its role in balancing meristem growth, lateral organ differentiation, and determinacy.

81 Lateral organ distribution at the shoot apical meristem

82 in the initiation of axillary meristems and lateral organs during vegetative and inflorescence devel

83 rlapping role with bif2 in the initiation of lateral organs during vegetative development.

84 enance in maize; analyses of the first three lateral organs elaborated from maize embryos provides in

85 Lateral organ emergence in plant embryos and meristems d

86 As and CUC2 in a regulatory module governing lateral organ enlargement and patterning.

87 stem cell fate and induce genes that promote lateral organ fate and polarity, thereby restricting the

88 An early marker of lateral organ fate is the AP2/ERF-type transcription fac

89 In the angiosperm flower, specification of lateral organ fate relies on the spatial regulation of t

90 Lateral organs form on the shoot of an adult plant from

91 intervening mitotic quiescence suggests that lateral organ formation in roots and shoots might not be

92 ical meristem activity, delayed and abnormal lateral organ formation, and arrested root growth.

93 ce, particularly as it affects branching and lateral organ formation.

94 n a band of cells at the adaxial base of all lateral organs formed from the shoot apical meristem and

95 lso suggest that meristematic stem cells and lateral organ founder cells are intrinsically similar an

96 o cotyledon and floral organ fusions, severe lateral organ fusion is found in leaves and inflorescenc

97 es, blade-on-petiole, asymmetric leaves, and lateral organ fusion.

98 n factor related to the Arabidopsis thaliana LATERAL ORGAN FUSION1 (LOF1) and LOF2 proteins.

99 Arabidopsis thaliana LATERAL ORGAN FUSION1 (LOF1) encodes a MYB-domain transc

100 Mutations in the closely related LATERAL ORGAN FUSION2 (LOF2) gene enhance the lof1 pheno

101 control of both vegetative and reproductive lateral organ identity and provides molecular support fo

102 boundaries between the apical meristems and lateral organs in Arabidopsis embryos, seedlings, and ma

103 domain, in controlling the morphogenesis of lateral organs in Arabidopsis thaliana.

104 proteins redundantly regulate development of lateral organs in Arabidopsis thaliana.

105 Lateral organs in flowering plants display polarity alon

106 ormation of boundaries and the separation of lateral organs in M. truncatula.

107 late the formation of axillary meristems and lateral organs in maize.

108 Lateral organs in plants arise from the meristem in a st

109 The formation of leaves and other lateral organs in plants depends on the proper specifica

110 GED, a key gene involved in the sculpting of lateral organs in several model species, we identified i

111 The meristem produces lateral organs in specific patterns, referred to as phyl

112 xiality was observed in leaves as well as in lateral organs in the flower, and the number of leaflets

113 t, lateral root initiation, morphogenesis of lateral organs in the shoot, shoot apical dominance and

114 in Arabidopsis plants with abnormally shaped lateral organs including serrated leaves, narrow floral

115 Here, we show that the periodicity of lateral organ induction is driven by recurrent programme

116 Asymmetric development of plant lateral organs initiates by partitioning of organ primor

117 addition, we show that CUL1 is required for lateral organ initiation in the shoot apical meristem an

118 processes, including cell-fate acquisition, lateral organ initiation, and maintenance of shoot apica

119 redirects meristem fate from maintenance to lateral organ initiation, through the regulation of the

120 Communication between the meristem and lateral organs is crucial for meristem maintenance and o

121 Asymmetric development of plant lateral organs is initiated by a partitioning of organ p

122 The development of plant lateral organs is interesting because, although many of

123 ts suggest that adaxial/abaxial asymmetry of lateral organs is specified in the shoot apical meristem

124 re, we show that Arabidopsis thaliana JAGGED LATERAL ORGANS (JLO), a member of the LATERAL ORGAN BOUN

125 rning as well as floral organ abscission and lateral organ lamina outgrowth.

126 G expression extends into all cell layers of lateral organs, NUB is restricted to the interior adaxia

127 that the establishment of polarity in plant lateral organs occurs via mutual repression interactions

128 or the specification of abaxial cell fate in lateral organs of Arabidopsis.

129 in determining abaxial/adaxial cell fate in lateral organs of eudicots, and repressing meristematic

130 Lateral organs of plants display asymmetry with abaxial

131 ntial part of the morphological variation in lateral organs of seed plants.

132 Leaf-like lateral organs of the inflorescences and flowers show si

133 The normal development of lateral organs of the shoot requires the simultaneous re

134 ition to reducing the size of both roots and lateral organs of the shoot, hst mutations affect the si

135 ke MADS-box transcription factors within the lateral organs of the spikelet, similar to the function

136 pical dominance and growth, phyllotaxis, and lateral organ orientation.

137 ns suggest that maize yabby genes may direct lateral organ outgrowth rather than determine cell fate.

138 regulatory module that acts as a governor of lateral organ patterning and expansion.

139 This and lateral organ patterning phenotypes in cuc2-1D suggest t

140 lecular event that is functionally linked to lateral organ placement in these species.

141 Lateral organ polarity in Arabidopsis is regulated by an

142 -basal and radial polarity in the embryo and lateral organ polarity in the shoot.

143 which direct both SAM development and shoot lateral organ polarity.

144 anisms may control dorsoventral asymmetry in lateral organ primordia and in floral meristems.

145 ncodes a Myb-domain protein, is expressed in lateral organ primordia and their initials.

146 daughter cells that become incorporated into lateral organ primordia around the meristem periphery.

147 ession of ids1 was detected in many types of lateral organ primordia as well as spikelet meristems.

148 genes is expressed in a polar manner in all lateral organ primordia produced from the apical and flo

149 JAG mRNA is localized to lateral organ primordia throughout the plant but is not

150 or ASYMMETRIC LEAVES1, which is expressed in lateral organ primordia, and homeobox transcription fact

151 gene that promotes initiation and growth of lateral organ primordia, and polarity genes.

152 l meristem, and the adaxial (upper) sides of lateral organ primordia.

153 diated meristem-born signaling that patterns lateral organ primordia.

154 istems, and (with notable exceptions) not in lateral organ primordia.

155 al meristems, lateral root primordia and all lateral organ primordia.

156 Lateral organs produced by shoot apical and flower meris

157 em that patterns abaxial-adaxial polarity in lateral organs produced from the apical meristem.

158 nts had enlarged vegetative and reproductive lateral organs relative to wild-type plants.

159 ation of normal adaxial-abaxial asymmetry in lateral organs, resulting in the replacement of abaxial

160 ssion of PNH on the abaxial (lower) sides of lateral organs results in upward curling of leaf blades.

161 M shares the role of CUC/NAM family genes in lateral organ separation and compound leaf development,

162 ly regulate both leaf margin development and lateral organ separation, and the regulation is partiall

163 mily of genes control boundary formation and lateral organ separation, which is critical for proper l

164 Thus, JAG is necessary for proper lateral organ shape and is sufficient to induce the prol

165 reduced plant size with striking, distorted lateral organ shape.

166 esses such as axial patterning and growth of lateral organs, shoot apical meristem activity, and infl

167 mily genes led to striking dwarfism, reduced lateral organ size and abnormal flower development, incl

168 Meristem maintenance and lateral organ specification are regulated in part by neg

169 In seed plants, lateral organs such as leaves and floral organs are form

170 o prevent KNOX gene expression in developing lateral organs such as leaves.

171 derivatives, which include founder cells for lateral organs such as leaves.

172 Plant lateral organs, such as leaves, are derived from the sho

173 is lobed leaf margins and more widely spaced lateral organs, suggesting that the trans-acting siRNA3

174 The expression of LOB at the base of lateral organs suggests a potential role for LOB in late

175 legume plants can form nodules, specialized lateral organs that form on roots, and house nitrogen-fi

176 functions to promote cell proliferation in a lateral organ, the pulvinus, and influences inflorescenc

177 is sufficient to induce the proliferation of lateral organ tissue.

178 ular, the transition from forming vegetative lateral organs to producing flowers often occurs in resp

179 cell layers to allow for development of new lateral organs while maintaining its barrier functions.