ライフサイエンスコーパス: lateral organ

1 cell containing meristem and differentiating lateral organ.

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

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

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

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

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

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

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

9 the KANADI genes cause an adaxialization of lateral organs.

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

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

12 identified which interact to polarize plant lateral organs.

13 elaboration of cotyledons and post-embryonic lateral organs.

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

15 for the normal initiation and development of lateral organs.

16 loss of polar differentiation of tissues in lateral organs.

17 he development of ectopic abaxial tissues in lateral organs.

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

19 mmetric patterns (phyllotaxis) are formed by lateral organs.

20 he trade-off between growth of apical versus lateral organs.

21 vents can result in new stem cell niches and lateral organs.

22 ophyte axes with nonphotosynthetic scalelike lateral organs.

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

24 hanisms control the development of analogous lateral organs.

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

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

27 trol the enlargement and patterning of plant lateral organs.

28 ribed positive regulator of cell division in lateral organs.

29 cell types often develop radially symmetric lateral organs.

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

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

32 sis, the root clock regulates the spacing of lateral organs along the primary root through oscillatin

33 onvergent evolution of independently evolved lateral organs among highly divergent plant lineages, co

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

35 23) and JACKDAW (JKD), promotes formation of lateral organs and controls shoot meristem size.

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

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

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

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

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

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

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

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

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

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

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

47 y responsible for the formation of branches, lateral organs, and stems, and thus directly affect plan

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

49 Plant lateral organs are often elaborated through repetitive f

50 Lateral organs are patterned along proximodistal, dorsov

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

52 tations to the terrestrial environment, with lateral organs arising independently in different lineag

53 However, it remains unclear what lateral organ arrangements were present in early leafy p

54 lant shoot structures evolved a diversity of lateral organs as morphological adaptations to the terre

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

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

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

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

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

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

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

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

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

64 ion between the pulvinus and internode where LATERAL ORGAN BOUNDARIES (SbLOB), a boundary layer gene,

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

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

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

68 cotyledon 69 (NAC069), binds the promoter of lateral organ boundaries domain 31 (LBD31), and regulate

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

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

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

72 Overexpression of LATERAL ORGAN BOUNDARIES DOMAIN29 (LBD29) is responsible

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 ganic nitrogen (N) allocation from apical to lateral organs, coinciding with strong lateral organ out

89 Understanding the mechanisms of lateral organ development among divergent plant lineages

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

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

92 (MpLOS1), regulates meristem maintenance and lateral organ development in Marchantia.

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

94 Plant lateral organ development is a complex process involving

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

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

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

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

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

100 nsights into the complex regulation of plant lateral organ development.

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

102 However, our current knowledge of lateral organ differentiation mechanisms comes almost en

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

104 Lateral organ distribution at the shoot apical meristem

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

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

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

108 Lateral organ emergence in plant embryos and meristems d

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

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

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

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

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

114 rgans and tune systemic N supply to restrict lateral organ formation by C/N depletion.

115 ime importance of sugar signaling to unleash lateral organ formation has just recently emerged.

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

117 duletaxis'; this decreased the length of the lateral organ formation zone on roots.

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

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

120 uch as long-distance molecular transport and lateral organ formation.

121 Lateral organs formed by the shoot apical meristem (SAM)

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

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

124 ytes (basally diverging land plants) develop lateral organs from meristems of sporophytes and gametop

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

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

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

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

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

130 we identified several genes associated with lateral organ growth that may mediate the role of ANT in

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

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

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

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

135 that ALOG genes regulate the development of lateral organs in both gametophyte and sporophyte shoots

136 Lateral organs in flowering plants display polarity alon

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

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

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

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

141 , the regular arrangement of leaves or other lateral organs in plants including pineapples, sunflower

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

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

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

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

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

147 ation in MpLOS1, preferentially expressed in lateral organs, induces lateral organs with misspecified

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

149 involved in mediolateral patterning of plant lateral organs, inform a model for the fusion of coleopt

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

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

152 tion of meristem identity and maturation and lateral organ initiation via positive and negative regul

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

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

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

156 The proper initiation of lateral organs is crucial for plant growth and crop yiel

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

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

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

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

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

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

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

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

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

166 Lateral organs of plants display asymmetry with abaxial

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

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

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

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

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

172 ormation of auxin maxima, which develop into lateral organs or leaf serrations.

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

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

175 al to lateral organs, coinciding with strong lateral organ outgrowth.

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

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

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

179 Lateral organ polarity in Arabidopsis is regulated by an

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

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

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

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

184 SAM growth and development, and how sites of lateral organ primordia are determined in the peripheral

185 , where their mitotic activity increases and lateral organ primordia are formed.

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

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

188 ripheral zone, auxin accumulates at sites of lateral organ primordia initiation and activates SHR exp

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

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

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

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

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

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

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

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

197 Lateral organs produced by shoot apical and flower meris

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

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

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

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

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

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

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

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

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

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

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

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

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

211 lels with other evolutionarily related plant lateral organs such as leaves to argue that hormones lik

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

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

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

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

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

217 1 (ALOG) family protein, named M. polymorpha LATERAL ORGAN SUPRESSOR 1 (MpLOS1), regulates meristem m

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

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

220 the identity, number and arrangement of the lateral organs they form.

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

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

223 Plants tightly control growth of their lateral organs, which led to the concept of apical domin

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

225 ntially expressed in lateral organs, induces lateral organs with misspecified identity and increased