ライフサイエンスコーパス: Physcomitrella

1 ] we have generated genetic linkage maps for Physcomitrella.

2 y by which transforming DNA is integrated in Physcomitrella.

3 CE2C was active against acetylated mannan in Physcomitrella.

4 cloned and characterized PpORS from the moss Physcomitrella.

5 we set up methods to investigate meiosis in Physcomitrella and we demonstrate that the RAD51B protei

6 s are not required for import of proteins in Physcomitrella, but may point to involvement in the dete

7 ct on the removal of mannan from tobacco and Physcomitrella cell walls, respectively.

8 abidopsis, tomato, Medicago, rice, maize and Physcomitrella Elevated rates of non-templated nucleotid

9 This will radically enhance the potential of Physcomitrella for determining how gene function has evo

10 We undertook targeted knockout of the Physcomitrella genes encoding components of the principa

11 t of a pipeline for the map-based cloning of Physcomitrella genes.

12 its correspondence with the newly sequenced Physcomitrella genome.

13 Physcomitrella hpat mutants lack cell-wall associated hy

14 Homologous recombination in Physcomitrella is substantially more efficient than in a

15 APR from Physcomitrella is very similar to the well characterized

16 We show that in gametophytic shoots of Physcomitrella, lateral branches arise by re-specificati

17 N-dependent intercellular auxin transport in Physcomitrella mediates crucial developmental transition

18 of spore germination in the model bryophyte Physcomitrella patens (Aphanoregma patens).

19 mber of the Wave/SCAR complex, is deleted in Physcomitrella patens (Deltabrk1), we report a striking

20 and shotgun genomic sequences from the moss Physcomitrella patens (Hedw.) B.S.G. were used to identi

21 ene order between mtDNAs of the hornwort and Physcomitrella patens (moss) differs by only 8 inversion

22 hatase (FBPase), in both cases from the moss Physcomitrella patens (Pp).

23 ohydrolase (NRH) family in two model plants, Physcomitrella patens (PpNRH) and maize (Zea mays; ZmNRH

24 nd characterized the PDK1 gene from the moss Physcomitrella patens (PpPDK1), a nonvascular representa

25 that stomata on the sporophytes of the moss Physcomitrella patens [2] respond to environmental signa

26 idently annotated miRNA families in the moss Physcomitrella patens and 44 in the lycopod Selaginella

27 nogaste, Arabidopsis thaliana, Oryza sativa, Physcomitrella patens and Chlamydomonas reinhardtii, dem

28 ve target genes of PHY signaling in the moss Physcomitrella patens and found light-regulated genes th

29 s-end-directed kinesin-14 motors in the moss Physcomitrella patens and found that none are processive

30 didate genes in auxin-insensitive mutants of Physcomitrella patens and identified mutations in highly

31 gated calcium channel (CNGC) CNGCb gene from Physcomitrella patens and its Arabidopsis thaliana ortho

32 olling caulonema differentiation in the moss Physcomitrella patens and root hair development in the f

33 In the moss Physcomitrella patens and the fern Adiantum capillus-ven

34 erging land plants Marchantia polymorpha and Physcomitrella patens and then experimentally characteri

35 FAMA-like) and PpSCREAM1 (SCRM1) in the moss Physcomitrella patens are orthologous to transcriptional

36 e of POT1 in plants, we established the moss Physcomitrella patens as a new model for telomere biolog

37 Here we examine these principles in Physcomitrella patens as a representative of lower plant

38 nalysis of hcf145 mutants in Arabidopsis and Physcomitrella patens as well as in vivo and in vitro RN

39 in the polarized expansion zone of the moss Physcomitrella patens caulonemal cells through the coale

40 Here we show that the moss Physcomitrella patens Cold-Shock Domain Protein 1 (PpCSP

41 The moss Physcomitrella patens contains the highly conserved DEK1

42 Physcomitrella patens contains two genes that encode Toc

43 rected mutagenesis, we studied the effect on Physcomitrella patens development by deleting the Linker

44 We find that an IRX10 homolog from the moss Physcomitrella patens displays robust activity, and we s

45 erium Synechocystis sp PCC 6803 and the moss Physcomitrella patens does not require PAM68 proteins, a

46 The model bryophyte Physcomitrella patens exhibits high frequencies of gene

47 The moss Physcomitrella patens exhibits strong NPQ by both algal-

48 we have expressed modified-oleosin genes in Physcomitrella patens for transient expression and tobac

49 The Physcomitrella patens genome has seven genes apparently

50 PpLRL1 and PpLRL2, the two LRL genes in the Physcomitrella patens genome.

51 The bryophyte Physcomitrella patens has a single TPS gene, copalyl syn

52 use molecular genetics to show that the moss Physcomitrella patens has conserved homologues of angios

53 Recently the moss Physcomitrella patens has gained worldwide attention for

54 The moss Physcomitrella patens has recently emerged as a powerful

55 nes, and manipulation in the model bryophyte Physcomitrella patens has shown that the bHLH and EPF co

56 The moss Physcomitrella patens has six PEX11 isoforms which fall

57 The moss Physcomitrella patens has three profilin genes, which ar

58 The moss Physcomitrella patens has two AOCs (PpAOC1 and PpAOC2) w

59 Early land plants like moss Physcomitrella patens have developed remarkable drought

60 in nonvascular land plants such as the moss Physcomitrella patens Here, we provide evidence for a si

61 artial purification of His-tagged CesA5 from Physcomitrella patens Immunoblot analysis and mass spect

62 s by fluorescent proteins in the model plant Physcomitrella patens in order to assess evolutionary ch

63 The moss Physcomitrella patens is a model for the study of plant

64 efficient homologous recombination, the moss Physcomitrella patens is a model organism particularly s

65 The moss Physcomitrella patens is an important model organism for

66 Although the moss Physcomitrella patens is known to respond to abscisic ac

67 Interestingly, differentiation of the moss Physcomitrella patens is regulated by as yet unidentifie

68 of diverse organisms revealed that the moss Physcomitrella patens is the most primitive organism pos

69 The moss Physcomitrella patens is unique among plant models for t

70 We found previously that the moss Physcomitrella patens is unique among these organisms in

71 Overexpressing duckweed UAS in the moss Physcomitrella patens led to an increase in the amounts

72 xin regulates gene expression we generated a Physcomitrella patens line that completely lacks Aux/IAA

73 Here, we generated Physcomitrella patens lines expressing histidine-tagged

74 rowth in an array of plant models, including Physcomitrella patens One hypothesis is that diffusion c

75 ven among early land plants such as the moss Physcomitrella patens or the clubmoss Selaginella moelle

76 The moss Physcomitrella patens performs efficient homologous reco

77 The moss Physcomitrella patens possesses a single copy of a Group

78 740 unique interactions from 5,695 different Physcomitrella patens proteins.

79 In planta as in the moss Physcomitrella patens protoplasts, the presence of RY-li

80 The moss Physcomitrella patens provides an ideal system to study

81 and functional characterization of the moss Physcomitrella patens PTEN gene family.

82 trate that ARABIDILLO homologues in the moss Physcomitrella patens regulate a previously undiscovered

83 ors SHORT INTERNODE/STYLISH (SHI/STY) during Physcomitrella patens reproductive development, we have

84 unction in Arabidopsis thaliana and the moss Physcomitrella patens results in a shared defect in game

85 endently, CESA knockout analysis in the moss Physcomitrella patens revealed parallels with Arabidopsi

86 logous recombination in the basal land plant Physcomitrella patens reveals that SMG1 has a conserved

87 Physcomitrella patens RHD SIX-LIKE1 (PpRSL1) and PpRSL2

88 Picea abies, Selaginella moellendorffii and Physcomitrella patens scattered in some clusters.

89 h as Arabidopsis thaliana, Oryza sativa, and Physcomitrella patens to examine the diversity of plant

90 g module has been shown to be conserved from Physcomitrella patens to higher plants.

91 of the gene targeting capability of the moss Physcomitrella patens to investigate the functions of ch

92 e use the highly polarized cells of the moss Physcomitrella patens to show that myosin XI and F-actin

93 ct, we tested their subcellular locations in Physcomitrella patens transformed with the respective al

94 e species were compared bioinformatically to Physcomitrella patens using reciprocal blasts with the I

95 s, we generated knockout mutants in the moss Physcomitrella patens using the moss's ability to perfor

96 on and function of Marchantia polymorpha and Physcomitrella patens UVR8 in experiments with bryophyte

97 still present in nonvascular plants such as Physcomitrella patens We generated P. patens mutants dep

98 rome-mediated phototropism, were observed in Physcomitrella patens when both HY2 and PUBS were disrup

99 hat treating gametophytic shoots of the moss Physcomitrella patens with exogenous auxins and auxin tr

100 universal in plants, including mosses (e.g. Physcomitrella patens) and algae (e.g. Chlamydomomas rei

101 at abscisic acid (ABA) pretreatment of moss (Physcomitrella patens) cells confers desiccation toleran

102 for protein import, we made transgenic moss (Physcomitrella patens) harboring the Km-altering mutatio

103 g many angiosperms, two gymnosperms, a moss (Physcomitrella patens), and a unicellular green alga (Ch

104 Arabidopsis, rice (Oryza sativa), and moss (Physcomitrella patens), and one RUS member, RUS3, is con

105 or induces reporter gene expression in moss (Physcomitrella patens), barley (Hordeum vulgare), and ca

106 of full-length recombinant factor H in moss (Physcomitrella patens).

107 In the kaurene synthase from the moss Physcomitrella patens, 16-alpha-hydroxy-ent-kaurane as w

108 Physcomitrella patens, a haploid dominant plant, is fast

109 The moss Physcomitrella patens, a model for early terrestrial pla

110 In the evolutionary intermediate Physcomitrella patens, a moss, both gene products are ac

111 In the moss Physcomitrella patens, ADF is encoded by a single, intro

112 The mechanism of quenching was studied in Physcomitrella patens, an early divergent streptophyta (

113 Here, we demonstrate that the moss Physcomitrella patens, an extant relative of the earlies

114 y analysis of the walls of P. margaritaceum, Physcomitrella patens, and Arabidopsis (Arabidopsis thal

115 s of full-length AAH cDNAs from Pinus taeda, Physcomitrella patens, and Chlamydomonas reinhardtii ind

116 omain first emerged in the early land plant, Physcomitrella patens, and it likely originated de novo

117 cophyte Selaginella moellendorffii, the moss Physcomitrella patens, and the representative angiosperm

118 nd plant lineage, as exemplified by the moss Physcomitrella patens, auxin transport by PIN transporte

119 A is conserved in plants, including the moss Physcomitrella patens, but is absent in the algae and ou

120 we show that an early diverging land plant, Physcomitrella patens, can be continuously cultured with

121 show that disruption of PpTEL1 from the moss Physcomitrella patens, causes reduced protonema growth a

122 ses in the life cycle of the model bryophyte Physcomitrella patens, including detailed sporophyte dev

123 The moss Physcomitrella patens, like seed plants, shows alternati

124 Here we show that in the basal land plant Physcomitrella patens, mutation of the GLR genes GLR1 an

125 In charophytes and Physcomitrella patens, one or more gene family members c

126 rotonemata to leafy gametophores in the moss Physcomitrella patens, opposite to its role as an inhibi

127 vestigate the insertion of two proteins from Physcomitrella patens, PpOEP64-1 and PpOEP64-2 (formerly

128 geting ability of a variety of proteins from Physcomitrella patens, rice (Oryza sativa), and Arabidop

129 l members of MET1 and CMT families, the moss Physcomitrella patens, serving as a model for early dive

130 In the moss Physcomitrella patens, transforming DNA containing homol

131 miR535, which occurs in the moss Physcomitrella patens, was also detected in California p

132 However, in the moss Physcomitrella patens, we found a second FDBR that catal

133 for photosynthetic performances in the moss Physcomitrella patens, we generated a pgrl1 knockout mut

134 g small RNA-sequencing (RNA-seq) of the moss Physcomitrella patens, we identified 1090 loci that prod

135 t in chloronemal and caulonemal filaments of Physcomitrella patens, where they are prevalent at cell

136 terized PS functions in the early land plant Physcomitrella patens, which lacks Notch, ErbB4, and APP

137 ologs from Arabidopsis thaliana and the moss Physcomitrella patens, which represent a distinct clade

138 bule overlap in the phragmoplast of the moss Physcomitrella patens.

139 y and structurally characterized in the moss Physcomitrella patens.

140 in the cloning of sRNAs from the model moss Physcomitrella patens.

141 that AIP1 is a single-copy gene in the moss Physcomitrella patens.

142 , we utilized the genetically tractable moss Physcomitrella patens.

143 pid 1-week complementation assay in the moss Physcomitrella patens.

144 omplemented by the PpMKN2 gene from the moss Physcomitrella patens.

145 nction of all 9 formin genes within the moss Physcomitrella patens.

146 tions between growth forms occur in the moss Physcomitrella patens.

147 ent in the gametophytes (n) of the bryophyte Physcomitrella patens.

148 ip cells of protonemal filaments of the moss Physcomitrella patens.

149 formation during the development of the moss Physcomitrella patens.

150 -proteins from a nonvascular plant, the moss Physcomitrella patens.

151 explore the role of the pathway in the moss Physcomitrella patens.

152 xillary hairs on the gametophyte of the moss Physcomitrella patens.

153 ified 11,976 Khib sites in 3,001 proteins in Physcomitrella patens.

154 tion of the TAS3 tasiRNA pathway in the moss Physcomitrella patens.

155 sites in histone and non-histone proteins in Physcomitrella patens.

156 nt in Arabidopsis thaliana) in the bryophyte Physcomitrella patens.

157 ultiplanar gametophore bud cells in the moss Physcomitrella patens.

158 ntal regulation of DEK1 activity in the moss Physcomitrella patens.

159 ed the role of RAD51B in the model bryophyte Physcomitrella patens.

160 f all known prenylation subunits in the moss Physcomitrella patens.

161 cing to obtain HS transcriptomes in the moss Physcomitrella patens.

162 me-mediated tropic responses are impaired in Physcomitrella phot(-) mutants.

163 the phytochrome steering growth direction in Physcomitrella protonemata binds several phototropins sp

164 promoter activity by transient expression in Physcomitrella protoplasts shows the PpLEA-1 promoter to

165 Knocking out the two HPAT genes of Physcomitrella results in larger multicellular filamento

166 Microscopy examination of Physcomitrella revealed that oil bodies (OBs) were abund

167 7 to CjCE2C potentiated its activity against Physcomitrella walls, whereas a xylan binding CBM reduce

168 terns in flowering plants, this is not so in Physcomitrella, where bi-directional transport is requir