ライフサイエンスコーパス: Pisum

1 ent speciation, the pea aphid (Acyrthosiphon pisum).

2 tolerance of pea aphid hosts (Acyrthosiphon pisum).

3 a polymorphic state for millions of years in Pisum.

4 trol the proliferation of PDR1 insertions in Pisum.

5 .5 MYA) are mostly found in small subsets of Pisum.

6 tterns, were isolated and characterized from Pisum.

7 r morphs of clonal pea aphids, Acyrthosiphon pisum.

8 ctor protein in the pea aphid, Acyrthosiphon pisum.

9 s carried by 1,104 pea aphids, Acyrthosiphon pisum.

10 onary responses of pea aphids (Acyrthosiphon pisum), a common agricultural pest, to increased frequen

11 YA) tend to be found in small subsets of the Pisum accessions set, "middle-aged" insertions (between

12 ertions has been assessed across 47 selected Pisum accessions, representing the diversity of the genu

13 d to discover putative novel sequences of A. pisum and its symbionts.

14 to parasitism is a general phenomenon in A. pisum and that, at least for the isolates and genotypes

15 s of 50 Spanish wild taxa of Lathyrus, Lens, Pisum and Vicia have been compared.

16 biosis, between the pea aphid (Acyrthosiphon pisum) and its maternally transmitted symbiont, Buchnera

17 ty against both the pea aphid, Acyrthosiphon pisum, and the green peach aphid, Myzus persicae.

18 sly documented for pea aphids (Acyrthosiphon pisum) attacked by the parasitoid wasp Aphidius ervi.

19 In another aphid host, Acyrthosiphon pisum, B. aphidicola has no functional metR and shows no

20 ssed and/or highly enriched in Acyrthosiphon pisum bacteriocyte tissues.

21 enty-nine parthenogenetic clones of three A. pisum biotypes, defined by their capacity to use the leg

22 mbiont isolates underlies variation among A. pisum clones in resistance to A. ervi.

23 idis, Schizaphis graminum, and Acyrthosiphon pisum contain the genes for anthranilate synthase (trpEG

24 rental genotypes of pea aphid (Acyrthosiphon pisum) differing in virulence on a Medicago truncatula h

25 in immunity to the pea aphid (Acyrthosiphon pisum), for which Arabidopsis is normally a nonhost.

26 lla defensa protects the aphid Acyrthosiphon pisum from attack by the parasitoid Aphidius ervi by kil

27 A mutant line of Pisum fulvum was identified that lacked seed lipoxygenas

28 shed five H. defensa isolates in a common A. pisum genetic background.

29 he corresponding retrotransposons within the Pisum genus.

30 one side alone, from a diverse collection of Pisum germ plasm.

31 8, LOC100159667 (named here as Acyrthosiphon pisum glutamine transporter 1, ApGLNT1) functioning as t

32 e performance of the pea aphid Acyrthosiphon pisum Harris, a sap-feeding insect with piercing-sucking

33 Experiments on pea aphids (Acyrthosiphon pisum) have demonstrated that facultative symbionts prot

34 polymorphism in the pea aphid Acyrthosiphon pisum (Hemiptera: Aphididae).

35 n of the essential amino acid arginine in A. pisum hemolymph reduces the transport of the precursor g

36 tent with the transport of glutamine from A. pisum hemolymph to the bacteriocyte cytoplasm.

37 The pea aphid, Acyrthosiphon pisum, maintains extreme variation in resistance to its

38 roposed that the crop-feeding biotypes of A. pisum may have diversified within the last 100 000 years

39 ogaster and four aphid species Acyrthosiphon pisum, Myzus persicae, Toxoptera citricida, and Aphis go

40 stimate of the effective population size for Pisum of approximately 7.5 x 10(5).

41 the survival of the pea aphid (Acyrthosiphon pisum) on fava bean, a host plant.

42 d host races of the pea aphid (Acyrthosiphon pisum pisum; Hemiptera : Aphididae).

43 ant species with behavioural tests on two A. pisum races, to identify metabolites that explain variat

44 e differential acceptability of plants to A. pisum races.

45 ieved following mapping to the Acyrthosiphon pisum reference genome and its mitochondrial and symbion

46 We show that when four aphid pest species-A. pisum, Rhopalosiphum padi, Aphis glycines and Myzus pers

47 ther t-loops exist in the higher order plant Pisum sativum (garden pea).

48 ave isolated a DESD-box containing cDNA from Pisum sativum (Pea) and named it as PDH45.

49 The complex was purified from Pisum sativum (pea) chloroplast envelopes by native gel

50 us analysis of the MAP kinase homologue from Pisum sativum (PsMAPK) revealed a potential MAP kinase m

51 and characterization of recombinant p68 from Pisum sativum (Psp68) is presented.

52 e required for plant life in that a UGT from Pisum sativum (PsUGT1) controls plant development by opp

53 lectins Galanthus nivalis agglutinin (GNA), Pisum sativum agglutinin (PSA), and Lens culinaris agglu

54 ously selected for resistance to pea lectin (Pisum sativum agglutinin) and shown to behave dominantly

55 ectin, Griffonia simplicifolia lectin I, and Pisum sativum agglutinin.

56 against equine plasma amine oxidase (EPAO), Pisum sativum amine oxidase (PSAO), Pichia pastoris lysy

57 n of leaf complexity to different degrees in Pisum sativum and Lotus japonicus.

58 ein fusions, and import assays with purified Pisum sativum chloroplasts, indicated chloroplastic loca

59 of aggregated proteins from tobacco and pea (Pisum sativum cv "Little Marvel") chloroplasts showed th

60 is localized to developing vacuoles in pea (Pisum sativum cv Extra Early Alaska).

61 romoter fragment of the Blec4 gene from pea (Pisum sativum cv. Alaska) and demonstrate that it is cap

62 t phenotype was introgressed into a standard Pisum sativum cv. Birte to provide near-isogenic lines w

63 full-length CPCT cDNA (designated PCT2) from Pisum sativum cv. Feltham First using an Arabidopsis pro

64 olymorphic PDR1 retrotransposon insertion in Pisum sativum have been developed.

65 Pisum sativum is of great economic and nutritional inter

66 solated a class 1 knox cDNA from pea, Pskn1 (Pisum sativum knotted1) and examined its expression patt

67 ravitropic curvature response of intact pea (Pisum sativum L. cv Alaska) epicotyls was examined by ge

68 were extracted from 7 day old etiolated pea (Pisum sativum L. cv Alaska) epicotyls with 3 molar LiCl.

69 Pea (Pisum sativum L. cv Alcan) endocarp tissue challenged wi

70 cDNA has been cloned and sequenced from pea (Pisum sativum L. cv. Birte).

71 was imported and processed by isolated pea (Pisum sativum L. Laxton's Progress No. 9) chloroplasts a

72 was investigated in etiolated pea seedlings (Pisum sativum L. var Alaska) by excising the cotyledons.

73 ation zone of the epicotyl of etiolated pea (Pisum sativum L. var Alaska) seedlings, there is little

74 When pea (Pisum sativum L. var Onward) seedlings are treated with

75 GalAT activity in homogenates from pea (Pisum sativum L. var. Alaska) stem internodes co-localiz

76 5% of the SMM was extrachloroplastic in pea (Pisum sativum L.) and spinach (Spinacia oleracea L.), wh

77 A cDNA fragment coding for the pea (Pisum sativum L.) chloroplastic glyceraldehyde-3-P dehyd

78 phatase was purified from the stroma of Pea (Pisum sativum L.) chloroplasts that is capable of dephos

79 t across the inner-envelope membrane of pea (Pisum sativum L.) chloroplasts was directly measured by

80 We show for pea (Pisum sativum L.) epicotyl sections that this hypothesis

81 The lip1 mutant of pea (Pisum sativum L.) exhibits a de-etiolated phenotype.

82 tely 80% identical with Arabidopsis and pea (Pisum sativum L.) homologs.

83 lin (GA) controlling stem elongation in pea (Pisum sativum L.) is GA1, which is formed from GA20 by 3

84 Stem elongation in peas (Pisum sativum L.) is under partial control by gibberelli

85 P21 complex purified from heat-stressed pea (Pisum sativum L.) leaves contained no proteins other tha

86 ase (ACCase) have been characterized in pea (Pisum sativum L.) leaves; a heteromeric chloroplast enzy

87 A pea (Pisum sativum L.) nuclear enzyme with protein tyrosine p

88 op genetics and processing in two pea lines (Pisum sativum L.) on starch digestion kinetics.

89 Pea (Pisum sativum L.) ornithine transcarbamylase (OTC) antis

90 A cDNA of pea (Pisum sativum L.) RbcS 3A, encoding a small subunit prot

91 lene biosynthesis in stems of etiolated pea (Pisum sativum L.) seedlings by rapidly increasing the ex

92 Treatment of 5- to 6-day-old etiolated pea (Pisum sativum L.) seedlings with indole-3-acetic acid (I

93 In pea (Pisum sativum L.) seeds, GA 2-oxidation is controlled by

94 on on pods of specific genetic lines of pea (Pisum sativum L.) stimulates cell division at the sites

95 Among a set of genes in pea (Pisum sativum L.) that were induced under drought-stress

96 An artificial gene encoding PBGS of pea (Pisum sativum L.) was designed to overcome previous prob

97 In pea (Pisum sativum L.), source to sink partitioning of amino

98 ox and GA 3beta-hy transcript levels in pea (Pisum sativum L.).

99 Herein, we show that Pisum sativum LecRLK (PsLecRLK) localized in plasma memb

100 rmation of individual transcription units in Pisum sativum plant nucleoli using a novel labelling tec

101 Thermal profiles of viable, aged, and dead Pisum sativum seeds were recorded, and image analysis of

102 dopsis thaliana, Lycopersicon esculentum and Pisum sativum tissues.

103 opersicon lycopersicum), and sugar snap pea (Pisum sativum var. macrocarpon) from an industrially imp

104 um meliloti, required for nodulation of pea (Pisum sativum) and alfalfa (Medicago sativum), respectiv

105 ng of endogenous Toc75 POTRA domains in pea (Pisum sativum) and Arabidopsis (Arabidopsis thaliana) co

106 Pea (Pisum sativum) and Arabidopsis contain similar, if not i

107 We characterized the class II smHSPs of pea (Pisum sativum) and compared them with class I smHSPs.

108 ologs from other legume species, namely pea (Pisum sativum) and Lotus japonicus, we show that this mo

109 rminal in some legume species, such as peas (Pisum sativum) and peanuts (Arachis hypogaea), likely du

110 ke cells." Whereas root border cells of pea (Pisum sativum) are clearly involved in defense against f

111 The Tic20 protein was identified in pea (Pisum sativum) as a component of the chloroplast protein

112 hese complexes by the embryo, using the pea (Pisum sativum) as a model species.

113 nd alpha-CT were imported into isolated pea (Pisum sativum) chloroplasts and became integrated into A

114 Dual import assays with purified pea (Pisum sativum) chloroplasts and mitochondria, and subcel

115 d AtBCCP2 was competent for import into pea (Pisum sativum) chloroplasts and processed to a 25-kD pol

116 Import assays with pea (Pisum sativum) chloroplasts showed that PyrR and PyrD ar

117 An in vitro assay with pea (Pisum sativum) chloroplasts was developed to conduct mut

118 vement across the thylakoid membrane of pea (Pisum sativum) chloroplasts was directly measured by sto

119 t across the inner envelope membrane of pea (Pisum sativum) chloroplasts was directly measured by sto

120 Upon incubation of the precursor with pea (Pisum sativum) chloroplasts, it was imported and process

121 been studied extensively using isolated pea (Pisum sativum) chloroplasts.

122 I integral membrane protein abundant in pea (Pisum sativum) clathrin-coated vesicles (CCVs) that bind

123 uncatula nodule root (noot) mutants and pea (Pisum sativum) cochleata (coch) mutants, which are chara

124 An apyrase from pea (Pisum sativum) complements a yeast (Saccharomyces cerevi

125 A protein of 80 kD from developing pea (Pisum sativum) cotyledons has previously been shown to e

126 r chaperones, Escherichia coli DnaK and pea (Pisum sativum) CSS1, was investigated in detail.

127 ansport chain, we overexpressed a minor pea (Pisum sativum) Fd isoform (PsFd1) in tobacco (Nicotiana

128 sgenic tobacco (Nicotiana tabacum), the pea (Pisum sativum) Ferredoxin 1 (Fed-1) mRNA dissociates fro

129 -1,4-D-glucanase (EGase, EC 3.2.1.4) of pea (Pisum sativum) has been cloned and characterized.

130 The inheritance of flower color in pea (Pisum sativum) has been studied for more than a century,

131 Pea (Pisum sativum) has served as a model for development of

132 eral ramosus (rms) branching mutants in pea (Pisum sativum) have SL defects, perturbed xylem CK level

133 The function of PsBRC1, the pea (Pisum sativum) homolog of the maize (Zea mays) TEOSINTE

134 tured firefly luciferase (Luc) bound to pea (Pisum sativum) Hsp18.1 as a model to define the minimum

135 t Aux/IAA proteins from Arabidopsis and pea (Pisum sativum) interact in vitro with recombinant phytoc

136 Here, we show that this dwarfism in pea (Pisum sativum) is not attributable to the strong branchi

137 eversibly glycosylated polypeptide from pea (Pisum sativum) is thought to have a role in the biosynth

138 Subcellular fractionation of pea (Pisum sativum) leaf protoplasts indicated that 30% of ly

139 The vacuoles of pea (Pisum sativum) leaves and red beet (Beta vulgaris) stora

140 Three pea (Pisum sativum) loci controlling photoperiod sensitivity,

141 Dual-import assays with purified pea (Pisum sativum) mitochondria and chloroplasts, and subcel

142 hread formation, as a null SL-deficient pea (Pisum sativum) mutant forms significantly fewer infectio

143 ula ortholog of the Lotus japonicus and pea (Pisum sativum) NIN gene.

144 rries a nonsense mutation in the single pea (Pisum sativum) ortholog of the ethylene signaling gene E

145 Two pea (Pisum sativum) P450 cDNAs (CYP73A9v1, encoding trans-cin

146 ify the role of GA3ox expression during pea (Pisum sativum) plant growth and development, we generate

147 In this study, pea (Pisum sativum) plants overexpressing AMINO ACID PERMEASE

148 ortant for the metabolism and growth of pea (Pisum sativum) plants.

149 Our data indicate that moss and pea (Pisum sativum) plastid transport systems are functionall

150 a nucleolar protein was selected from a pea (Pisum sativum) plumule library, cloned, and sequenced.

151 t) DC3000 hrcC(-) and to the nonadapted pea (Pisum sativum) powdery mildew Erysiphe pisi However, PLC

152 r a pea seed nuclear DNA-binding protein (of Pisum sativum) present at the cell expansion phase.

153 d IV of the AUX/IAA protein PsIAA4 from pea (Pisum sativum) revealed a globular ubiquitin-like beta-g

154 iptomic and metabolomic analyses of the pea (Pisum sativum) rhizosphere, a suite of bioreporters has

155 took a systematic, detailed analysis of pea (Pisum sativum) root tip cell walls.

156 Pea (Pisum sativum) root tips incubated with [(32)P]dCTP duri

157 the production of root border cells by pea (Pisum sativum) root tips.

158 Yet, when pea (Pisum sativum) roots are inoculated with the pea pathoge

159 rrying genes encoding soybean lectin or pea (Pisum sativum) seed lectin (PSL) were inoculated with Br

160 c activity found within the germinating pea (Pisum sativum) seed, 4 days from the initiation of imbib

161 eolin mRNA using plumules of dark-grown pea (Pisum sativum) seedlings.

162 complex (mt-PDC) by using intact green pea (Pisum sativum) seedlings.

163 Here, we show that in pea (Pisum sativum) seeds, 4-chloroindole-3-acetic acid is sy

164 However, in maturing pea (Pisum sativum) seeds, the level of the chlorinated auxin

165 from endoplasmic reticula of developing pea (Pisum sativum) seeds.

166 ids, Percoll-isolated chloroplasts from pea (Pisum sativum) synthesized FAD from imported riboflavin.

167 n nodulation in Medicago truncatula and pea (Pisum sativum) that form indeterminate nodules.

168 t at the LATE BLOOMER2 (LATE2) locus in pea (Pisum sativum) that is late-flowering with a reduced res

169 m of 45Ca2+ transport into the lumen of pea (Pisum sativum) thylakoid membranes using silicone-oil ce

170 We purified from pea (Pisum sativum) tissue an approximately 40 kDa reversibly

171 s trend is found in the Fabaceae, where pea (Pisum sativum) uses UNIFOLIATA, an ortholog of the flora

172 n the Toc159 GTPase domain (Toc159G) of pea (Pisum sativum) using cleavage by bound preproteins conju

173 profile from the oil of harvested field pea (Pisum sativum) varieties as part of a research project t

174 The STERILE NODES (SN) locus in pea (Pisum sativum) was one of the first photoperiod response

175 Nectria haematococca infection of pea (Pisum sativum) was used as a model to explore possible m

176 nt steps of ABA biosynthesis as well as pea (Pisum sativum) wilty and tomato (Solanum lycopersicum) f

177 istatic isoflavonoid produced by garden pea (Pisum sativum), a host for this fungus.

178 In leguminous plants such as pea (Pisum sativum), alfalfa (Medicago sativa), barrel medic

179 fected region of soybean (Glycine max), pea (Pisum sativum), clover (Trifolium pratense), and common

180 bi5 mutants in a second legume species, pea (Pisum sativum), confirmed a role for ABI5 in the regulat

181 sponds to a native protein of 159 kD in pea (Pisum sativum), designated Toc159.

182 ha and beta subunits of the ch-cpn60 of pea (Pisum sativum), expressed them individually in Escherich

183 ariations were then cross-compared with pea (Pisum sativum), leading to the identification of candida

184 to Arabidopsis (Arabidopsis thaliana), pea (Pisum sativum), or tomato (Lycopersicon esculentum) tiss

185 phenylpropanoid biosynthetic pathway of pea (Pisum sativum), partial cDNAs representing four distinct

186 eat (Triticum aestivum); but the dicots pea (Pisum sativum), soybean (Glycine max Merr.), and spinach

187 In pea (Pisum sativum), the protein-lysine methyltransferase (Ps

188 In pea (Pisum sativum), the reverse reaction, phenylpyruvate to

189 In contrast to peas (Pisum sativum), where mitochondrial lipoamide dehydrogen

190 We describe here the FRO1 gene from pea (Pisum sativum), which encodes an Fe(III)-chelate reducta

191 mutants at the Crispoid (Crd) locus in pea (Pisum sativum), which have altered auxin homeostasis and

192 ll wall of the root cap in two species: pea (Pisum sativum), which makes border cells, and Brassica n

193 ed or regulated during bud outgrowth in pea (Pisum sativum).

194 nd Tha4 and disulfide bond formation in pea (Pisum sativum).

195 s for their hormonal activity in garden pea (Pisum sativum).

196 coordinately regulate bud outgrowth in pea (Pisum sativum).

197 Arabidopsis (Arabidopsis thaliana) and pea (Pisum sativum).

198 d in the supernodulating nod3 mutant of pea (Pisum sativum).

199 tematic cells exist within root tips of pea (Pisum sativum): the root apical meristem, which gives ri

200 cotyledon phenotypes, has been identified in Pisum sativum, Arabidopsis thaliana, and Festuca pratens

201 ivity in nuclei purified from etiolated pea (Pisum sativum, L.) plumules is present in a single enzym

202 bacteriophages were isolated from leaves of Pisum sativum, Phaseolus vulgaris, Lycopersicon esculent

203 Rhizobium leguminosarum 3841, a symbiont of Pisum sativum, using chemical methods, mass spectrometry

204 ith legumes belonging to the galegoid clade (Pisum sativum, Vicia faba and Vicia hirsuta).

205 part of the chloroplast import machinery in Pisum sativum.

206 lar, is phytotoxic to etiolated seedlings of Pisum sativum.

207 syltransferase, was cloned from root tips of Pisum sativum.

208 s type of learning occurs in the garden pea, Pisum sativum.

209 -hydroxymaackiain 3-O-methyltransferase from Pisum sativum.

210 curonosyltransferase-encoding gene from pea (Pisum sativum; PsUGT1).

211 een used to precipitate PCNA from crude pea (Pisum savitum) extracts.

212 In pea aphids (Acyrthosiphon pisum), several inherited endosymbiont species protect t

213 ia and Lens, respectively, whereas the genus Pisum showed the lowest protein-digestibility corrected

214 ucts coming from other Lathyrus or Vicia and Pisum species.

215 these facultative symbioses in Acyrthosiphon pisum (the pea aphid) for vulnerability of the aphid hos

216 tative symbionts of pea aphid (Acyrthosiphon pisum), the bacterium Regiella insecticola, has a major

217 We use the pea aphid (Acyrthosiphon pisum) to address this problem.

218 of their host, the pea aphid (Acyrthosiphon pisum), under natural conditions.

219 ) in the gut of the pea aphid, Acyrthosiphon pisum, using a far-Western blot method.

220 tic diversity in the pea aphid Acyrthosiphon pisum was investigated by a restriction fragment length

221 on dodder vines by pea aphids (Acyrthosiphon pisum) were reduced significantly when dodder parasitize

222 to the hemocoel of pea aphids, Acyrthosiphon pisum, without virion assembly.