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 bule overlap in the phragmoplast of the moss Physcomitrella patens.

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

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

5 , we utilized the genetically tractable moss Physcomitrella patens.

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

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

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

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

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

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

12 formation during the development of the moss Physcomitrella patens.

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

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

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

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

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

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

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

20 ultiplanar gametophore bud cells in the moss Physcomitrella patens.

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

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

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

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

25 y and structurally characterized in the moss Physcomitrella patens.

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

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

28 Physcomitrella patens, a haploid dominant plant, is fast

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

63 The moss Physcomitrella patens contains the highly conserved DEK1

64 Physcomitrella patens contains two genes that encode Toc

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

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

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

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

69 The model bryophyte Physcomitrella patens exhibits high frequencies of gene

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

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

72 The Physcomitrella patens genome has seven genes apparently

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

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

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

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

77 Recently the moss Physcomitrella patens has gained worldwide attention for

78 The moss Physcomitrella patens has recently emerged as a powerful

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

80 The moss Physcomitrella patens has six PEX11 isoforms which fall

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

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

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

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

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

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

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

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

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

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

91 The moss Physcomitrella patens is an important model organism for

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

107 The moss Physcomitrella patens performs efficient homologous reco

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

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

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

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

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

113 740 unique interactions from 5,695 different Physcomitrella patens proteins.

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

115 The moss Physcomitrella patens provides an ideal system to study

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

131 In the moss Physcomitrella patens, transforming DNA containing homol

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

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

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

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

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

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

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

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

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

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

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

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

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