ライフサイエンスコーパス: Physcomitrella patens

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

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

3 y and structurally characterized in the moss Physcomitrella patens.

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

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

6 , we utilized the genetically tractable moss Physcomitrella patens.

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

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

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

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

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

12 formation during the development of the moss Physcomitrella patens.

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

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

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

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

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

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

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

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

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

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

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

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

25 ultiplanar gametophore bud cells in the moss Physcomitrella patens.

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

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

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

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

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

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

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

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

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

35 Physcomitrella patens, a haploid dominant plant, is fast

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

79 The moss Physcomitrella patens contains the highly conserved DEK1

80 Physcomitrella patens contains two genes that encode Toc

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

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

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

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

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

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

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

88 The model bryophyte Physcomitrella patens exhibits high frequencies of gene

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

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

91 The Physcomitrella patens genome has seven genes apparently

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

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

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

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

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

97 Recently the moss Physcomitrella patens has gained worldwide attention for

98 The moss Physcomitrella patens has recently emerged as a powerful

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

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

101 The moss Physcomitrella patens has six PEX11 isoforms which fall

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

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

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

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

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

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

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

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

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

111 Physcomitrella patens is a bryophyte model plant that is

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

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

114 The moss Physcomitrella patens is an important model organism for

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

130 The moss Physcomitrella patens performs efficient homologous reco

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

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

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

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

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

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

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

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

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

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

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

142 740 unique interactions from 5,695 different Physcomitrella patens proteins.

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

144 The moss Physcomitrella patens provides an ideal system to study

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

168 In the moss Physcomitrella patens, transforming DNA containing homol

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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