ライフサイエンスコーパス: Physcomitrella

1 CE2C was active against acetylated mannan in Physcomitrella.

2 cloned and characterized PpORS from the moss Physcomitrella.

3 ] we have generated genetic linkage maps for Physcomitrella.

4 y by which transforming DNA is integrated in Physcomitrella.

5 ugh for recovery of cells from DNA damage in Physcomitrella.

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

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

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

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

10 e introduce an interactive expression atlas, Physcomitrella Expression Atlas Tool (PEATmoss), that un

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

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

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

14 its correspondence with the newly sequenced Physcomitrella genome.

15 genetically tractable as Nannochloropsis and Physcomitrella, hence rapidly advancing functional diato

16 Physcomitrella hpat mutants lack cell-wall associated hy

17 ctionally conserved in Physcomitrium patens (Physcomitrella), in the moss lineage of bryophytes.

18 further aspects of the CRISPR methodology in Physcomitrella, including the significance of spacing be

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

20 APR from Physcomitrella is very similar to the well characterized

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

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

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

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

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

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

27 inct eukaryotic kingdoms, including the moss Physcomitrella patens (Plantae), the brown alga Ectocarp

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

29 dentified nine orthologs of FAAH in the moss Physcomitrella patens (PpFAAH1 to PpFAAH9) with amidase

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

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

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

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

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

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

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

37 o ALDH12 family members from the lower plant Physcomitrella patens and higher plant Zea mays.

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

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

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

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

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

43 te that sporophytes of some wild isolates of Physcomitrella patens are associated with AHL-producing

44 y of CRISPR/Cas12a in the non-vascular plant Physcomitrella patens are largely unknown.

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

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

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

48 Here, we present Physcomitrella patens as the second plant system, beside

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

50 re efficiently integrated into the genome of Physcomitrella patens by homologous recombination, this

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

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

53 The moss Physcomitrella patens contains the highly conserved DEK1

54 Physcomitrella patens contains two genes that encode Toc

55 , where represents a hydrophobic residue) in Physcomitrella patens dehydrin (PpDHNA), a poikilohydric

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

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

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

59 lyses also show that phy mutants of the moss Physcomitrella patens exhibit abnormal cuticle compositi

60 The model bryophyte Physcomitrella patens exhibits high frequencies of gene

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

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

63 The Physcomitrella patens genome has seven genes apparently

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

65 c relationships within the S. caninervis and Physcomitrella patens genomes indicate the S. caninervis

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

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

68 Recently the moss Physcomitrella patens has gained worldwide attention for

69 The moss Physcomitrella patens has recently emerged as a powerful

70 The moss Physcomitrella patens has rosette CSCs and seven CESAs,

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

72 The moss Physcomitrella patens has six PEX11 isoforms which fall

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

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

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

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

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

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

79 Physcomitrella patens is a bryophyte model plant that is

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

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

82 The moss Physcomitrella patens is an important model organism for

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

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

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

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

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

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

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

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

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

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

93 The moss Physcomitrella patens performs efficient homologous reco

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

95 740 unique interactions from 5,695 different Physcomitrella patens proteins.

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

97 The moss Physcomitrella patens provides an ideal system to study

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

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

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

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

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

103 otein X-ray crystal structure of a CHIL from Physcomitrella patens reveals key amino acid differences

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

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

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

107 ferase (APT)-based RNAi technology (APTi) in Physcomitrella patens that improves upon the multiple li

108 We aimed to localize DEK1 in the moss Physcomitrella patens to decipher its function during th

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

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

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

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

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

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

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

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

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

118 However, expression data from Physcomitrella patens were so far generated using differ

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

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

121 e bryophyte Physcomitrium patens (previously Physcomitrella patens) against the important plant patho

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

123 he model moss Physcomitrium patens (formerly Physcomitrella patens) and regulate its development, in

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

125 male fertility difference between two moss (Physcomitrella patens) ecotypes to explore spermatozoid

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

127 Two moss (Physcomitrella patens) PPR proteins containing DYW-deami

128 rabidopsis (Arabidopsis thaliana), and moss (Physcomitrella patens) were examined through grazing inc

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

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

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

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

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

134 However, in the early divergent moss Physcomitrella patens, 3D growth is preceded by an exten

135 In the moss, Physcomitrella patens, a 3D leafy gametophore originates

136 Physcomitrella patens, a haploid dominant plant, is fast

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

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

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

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

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

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

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

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

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

146 hylakoid protein phosphorylation in the moss Physcomitrella patens, assessing the thylakoid phospho-p

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

148 Mass spectrometry analysis of the moss Physcomitrella patens, both the wild type and the cerk m

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

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

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

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

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

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

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

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

157 on analysis, we demonstrate that in the moss Physcomitrella patens, phytochrome4 physically interacts

158 sts that this macro2 domain gene in the moss Physcomitrella patens, PpMACRO2, is important in epigene

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

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

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

162 ROS production in the protonema of the moss Physcomitrella patens, suggesting the possibility of rec

163 from within Physcomitrium Thus, rather than Physcomitrella patens, the species should be named Physc

164 Here we use genetic screening in Physcomitrella patens, to identify a locus GTRC, that wh

165 In the moss Physcomitrella patens, transforming DNA containing homol

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

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

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

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

170 In the moss Physcomitrella patens, we show that phytochrome 4 (PpPHY

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

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

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

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

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

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

177 y and structurally characterized in the moss Physcomitrella patens.

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

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

180 , we utilized the genetically tractable moss Physcomitrella patens.

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

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

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

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

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

186 formation during the development of the moss Physcomitrella patens.

187 spects different from that of the model moss Physcomitrella patens.

188 earliest plants on land, the Bryophyte moss Physcomitrella patens.

189 RAD51 and its antagonist, RTEL1, in the moss Physcomitrella patens.

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

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

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

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

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

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

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

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

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

199 ultiplanar gametophore bud cells in the moss Physcomitrella patens.

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

201 We mutated all seven Physcomitrium (Physcomitrella) patens phytochrome genes using highly-ef

202 of DELLA proteins in the moss Physcomitrium (Physcomitrella) patens, in the sister group of vascular

203 In the moss Physcomitrium (Physcomitrella) patens, the Sec23/24 gene families are e

204 family in the model bryophyte Physcomitrium (Physcomitrella) patens.

205 alidated target for miR171 in Physcomitrium (Physcomitrella) patens.

206 generated a fluorescent moss (Physcomitrium [Physcomitrella] patens) ROP4 fusion protein by inserting

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

208 Here we show that in the moss, Physcomitrella (Physcomitrium patens), CLAVATA affects s

209 In the moss Physcomitrella (Physcomitrium patens), SMC6 and NSE4 are

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

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

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

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

214 7 to CjCE2C potentiated its activity against Physcomitrella walls, whereas a xylan binding CBM reduce

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