ライフサイエンスコーパス: pheromone

1 ble for processing the yeast mating a-factor pheromone.

2 ufficient for the behavioral response to the pheromone.

3 dentified from human semen, is indeed a milt pheromone.

4 ompete to arrive first at a female releasing pheromone.

5 d morphological responses of opaque cells to pheromone.

6 lay increased gene expression in response to pheromone.

7 Prg adhesins and render cells insensitive to pheromone.

8 tested the key compounds in V. velutina sex pheromone.

9 as indicated by a lack of growth response to pheromone.

10 ircuits determine the sexual identity of the pheromone.

11 urons in response to an aggression-promoting pheromone.

12 dentify and quantify the bed bug aggregation pheromone.

13 lected for mutants that export a non-cognate pheromone.

14 d the conditioned behaviours elicited by the pheromone.

15 - disputed - candidate molecules for a male pheromone.

16 as well as a robust access to the target sex pheromone.

17 ic screen to unveil potent/optimized peptide pheromones.

18 s were not attracted by any known cerambycid pheromones.

19 inst insect eggs by responding to insect sex pheromones.

20 and S. carpocapsae IJs without host cadaver pheromones.

21 ting, including appropriate responses to sex pheromones.

22 ights into their mechanism and regulation by pheromones.

23 saltator in detecting cuticular hydrocarbon pheromones.

24 olatile semiochemicals that mimic female sex pheromones.

25 d by the absence or presence of host cadaver pheromones.

26 g molecules including air-borne odorants and pheromones.

27 ptide NLP-24 and dauer formation mediated by pheromones.

28 in semen have been identified as aphrodisiac pheromones.

29 ument that refuted earlier claims of primate pheromones [3,4].

30 , we demonstrate that maternally provisioned pheromone 7,11-heptacosadiene (7,11-HD) in the eggshell'

31 haromyces cerevisiae, the exposure to mating pheromone activates a prototypic mitogen-activated prote

32 We demonstrate that male pheromone acts via this circuit in hermaphrodites to red

33 ify exploratory behavior in response to male pheromone, adult hermaphrodites also require functional

34 educed diving responses to conspecific alarm pheromone after 7 days, but not after 28 days, indicatin

35 Interestingly, pheromones also promote the ingestion of pathogenic bact

36 d for viability during prolonged exposure to pheromone and acts through multiple substrates to down-r

37 h a masculinized nervous system secrete male pheromone and are susceptible to male pheromone killing.

38 ind expression of many genes associated with pheromone and chemical perception.

39 stressors, including exposure to aphid alarm pheromone and crowding, and, in one experiment, we asses

40 ns of a chemoreceptor gene family related to pheromone and kairomone sensing in V. komodoensis and ot

41 ave identified acetic acid as a putative sex pheromone and measured formic acid- and propionic acid-e

42 cted the modifiable selectivity toward their pheromone and operating sequences at the subtle molecula

43 Under short-term starvation (STS, 3 h), both pheromone and opioid signaling were downregulated in gpa

44 p* mutations increased Rgg2Sp sensitivity to pheromone and pheromone variants while displaying decrea

45 fungal ABC transporter that exports a mating pheromone and selected for mutants that export a non-cog

46 ns in males eliminates preference for female pheromones and abrogates mating success, whereas activat

47 with the two component H. halys aggregation pheromone, and pheromone synergist, methyl (2E, 4E, 6Z)-

48 ntification of the male-produced aggregation pheromone, and the recognition that BMSB disperses into

49 lar gland components that act as H. saltator pheromones, and a range of more traditional general odor

50 and related behavioral responses to oxygen, pheromones, and food in Caenorhabditis elegans The molec

51 noate, while CpomOR6a responds to the strong pheromone antagonist codlemone acetate (E,E)-8,10-dodeca

52 d a mechanism by which the signals evoked by pheromones are amplified in the ORNs that selectively pr

53 inding proteins that transport important sex pheromones are colloquially named pheromone binding prot

54 initiated when conserved nematode ascaroside pheromones are sensed, followed by the development of co

55 We now know that pheromones are used by species all across the animal kin

56 In order to implement this sex pheromone as a new environmentally friendly tool to mana

57 Second, hermaphrodites recognize pheromone as male if the concentration of ascr#10 is hig

58 ts of agricultural crops, but the use of sex pheromones as attractants is limited by male multiple ma

59 sulting in the overproduction of known queen pheromones as well as some compounds typically linked to

60 hly sensitive to C. elegans and the nematode pheromone ascarosides, others responded only weakly.

61 ucidate a mechanism whereby a seminal plasma pheromone attracts ready-to-mate females and implicates

62 Taken together, these data suggest that pheromone-based technology will be of global utility for

63 The reality of invisible chemical signals, pheromones, between members of the same species was reco

64 ortant sex pheromones are colloquially named pheromone binding proteins (PBPs).

65 are allosterically regulated through direct pheromone binding to control transcriptional activity; h

66 one receptors sharing a structurally similar pheromone-binding domain that functions allosterically t

67 NPR-17 opioid receptor signaling suppressed pheromone biosynthesis and the overexpression of opioid

68 nhanced by or reliant upon presentation of a pheromone blend.

69 nsor aequorin have shown that in response to pheromone, budding yeast cells undergo a rise of cytosol

70 de ant colonies is orchestrated with diverse pheromones, but it is not clear how ants perceive these

71 rmites produce a multi-component aggregation pheromone by combining a volatile hydrocarbon and non-vo

72 The pheromone can be exploited as a cost-effective and envir

73 Although trace amounts of pheromones can be detected by many insects, context-depe

74 t large, hydrophobic molecules comparable to pheromones can be transferred from one fly to the wing m

75 In Caenorhabditis elegans, ascaroside pheromones can dictate local population density; high le

76 Pheromones can induce both "releaser" (behavioral) and "

77 Upon sensing of the peptide pheromone cCF10, Enterococcus faecalis cells carrying pC

78 Host searching, pheromone communication, and microclimatic preferences a

79 e been used to selectively capture the major pheromone component, 1,7-dioxaspiro[5,5]undecane.

80 -5-hydroxy-4-decanolide (RR) as an extra sex pheromone component.

81 y to gamergate extract and a candidate queen pheromone component.

82 Both compounds are known pheromone components for species in the same subfamily.

83 They are also sex pheromone components of the female Zeleboria.

84 owed us to propose models for the binding of pheromone components to EposPBP3.

85 Pheromone concentration modulates burst frequency in a m

86 The pheromone consists of an aromatic compound (2-phenylunde

87 Here, we report that diapause-inducing pheromones correct heterochronic developmental cell line

88 Manipulating such pheromones could increase the efficacy of malaria-vector

89 A new study reveals that additional pheromone cues released only by younger females may prom

90 absent in C. elegans daf-22 larvae which are pheromone deficient.

91 he food-leaving behaviour is conspecific and pheromone dependent: C. elegans adults respond more stro

92 urons and the germline are required for male pheromone-dependent male death.

93 on to the larval cue while tracking the male pheromone despite each containing attractive 3-keto petr

94 merge as strong candidates for divergence in pheromone detection and host plant discrimination, respe

95 We evaluated the role of pheromone detection by receptors expressed in the apical

96 Pheromone detection by the vomeronasal organ (VNO) media

97 Our results reveal a direct influence of pheromone detection on territorial dominance, indicating

98 y in ants, through their functional roles in pheromone detection that characterizes reproductive stat

99 responses [1] or 'stereotyped behavior' [2], pheromones differ from mammalian scent signatures that c

100 Males contaminated with female pheromone displayed lower courtship, because residual fe

101 Exposure to pheromones does not significantly affect the pine needle

102 Whereas a high pheromone dose induces growth arrest and formation of a

103 shmoo-like morphology in yeast cells, lower pheromone doses elicit elongated cell growth.

104 Females conceivably benefit from the mimetic pheromone during mate search but must discriminate again

105 Here, Helms et al. identify the insect pheromone E,S-conophthorin produced by the goldenrod gal

106 In the fungus Ustilago maydis, sexual pheromones elicit mating resulting in an infective filam

107 male German cockroaches detect a contact sex pheromone embedded in the female's cuticular lipids.

108 t our hypothesis that plant responses to sex pheromones emitted by an herbivorous insect can boost pl

109 This pheromone enables rapid, long-lasting aggregation of ter

110 Thus, our study adds to the understanding of pheromone evolution by showing that subtle mutations in

111 one synaptic connection following early-life pheromone exposure are sufficient to permanently enhance

112 Pheromone exposure inhibits learning by disrupting this

113 Upon pheromone exposure, these cells overproduce the Prg adhe

114 ifically causes "mating-induced death" after pheromone exposure.

115 e quiescent period was overcome by dispersal pheromone extracts of their own, other Steinernema spp.

116 Sex pheromones facilitate reproduction by attracting potenti

117 of a volatile, male-produced aggregation-sex pheromone for this species.

118 ot expected to use chemical signals or queen pheromones for this purpose.

119 antennal grooming effectively removed female pheromone from males' antennae and maintained their chem

120 We sought to identify a pheromone from the milt (fish semen) of sea lamprey (Pet

121 High resolution structure of synthetic alpha-pheromone from the plant pathogenic ascomycete Fusarium

122 ors does not accurately reflect the external pheromone gradient.

123 However, pheromone-gradient sensing must override the Rsr1-depend

124 Third, internal cues remain active during pheromone-gradient tracking and can interfere with this

125 example, yeast have been reported to detect pheromone gradients as shallow as 0.1 nM/mum.

126 r than wild type with artificially generated pheromone gradients.

127 l and metabolomic analysis of dauer-inducing pheromone has identified a family of small molecules, as

128 However, the chemical components of this pheromone have never been determined.

129 However, no bona fide primate pheromones have been identified.

130 These identified aggregation pheromones have great potential for exploitation against

131 how males maintain their sensitivity to sex pheromone in aggregations.

132 mating, suggesting that MMB might mimic sex pheromone in Caenorhabditis species.

133 d the first chemical identification of a sex pheromone in the eusocial hornets.

134 nes (reproductive females) produced this sex pheromone in the sixth intersegmental sternal glands of

135 antagonistic interaction between opioids and pheromones in a cell-specific manner.

136 the 2 species: Trichoid sensilla respond to pheromones in Drosophila but respond to a wide diversity

137 ty of C. pomonella to exploit kairomones and pheromones in locating both host plants and mates.

138 2] claimed to have identified "the first sex pheromones in primates." However, reliance on one male i

139 gical contexts, from trail, alarm, and queen pheromones in social insects to the mammary pheromone pr

140 th caste-specific biosynthesis of fatty acid pheromones in the MG, including members of cytochrome P4

141 s for the biosynthesis of fatty acid-derived pheromones in the MGs.

142 f the specific biological functions of these pheromones in the worm.

143 bVSNs compromises dendritic knob formation, pheromone induced activation, correct glomeruli formatio

144 ast fusion through interaction with Fus2p, a pheromone-induced amphiphysin-like protein.

145 ts, we show that Dia2 is required to sustain pheromone-induced vacuolar targeting.

146 d trans-vaccenic acid), and cholesterol; the pheromone induces long-term aggregation at new nesting a

147 ate local population density; high levels of pheromones inhibit the reproductive maturation of indivi

148 The non-covalent capture of olive pheromones inside the beta-cyclodextrin cavity leads to

149 o expand their nesting areas; an aggregation pheromone is presumed to regulate this process.

150 One class of small signaling pheromones is the cyclic autoinducing peptides (AIPs), w

151 onochoristic species are susceptible to male pheromone killing.

152 e male pheromone and are susceptible to male pheromone killing.

153 rhabditis elegans produces a broad family of pheromones, known as the ascarosides, that are modified

154 tron microscopy, we demonstrate how maternal pheromones leak-proof the egg, consequently concealing i

155 s bind and stabilize the release of volatile pheromone ligands, and some MUPs exhibit pheromonal prop

156 ons to conducting anode via the redox active pheromone lipoproteins localized at the cell membrane.

157 subunit of the G-protein complex (STE4), the pheromone MAPK scaffold (CST5), and the two terminal MAP

158 Milt pheromones may also have management implications for sea

159 g behavioural data indicate that aggregation pheromones may mediate the formation and maintenance of

160 Male pheromone-mediated killing is unique to androdioecious C

161 unts of fly odors, including the aggregation pheromones methyl laurate, methyl myristate, and methyl

162 Here, we report that a pheromone mixture that signals overcrowding inhibits C.

163 As in other species [1], male sex pheromones modulate several behaviors and physiological

164 th a model of mass transfer showed that most pheromone molecules are deflected around the microstruct

165 and hermaphrodites secrete similar blends of pheromone molecules, two of which are present in differe

166 excretion of particular MUPs, including the pheromone MUP20 (darcin), and a volatile pheromone that

167 an affect accumulation of the AinS-generated pheromone N-octanoyl homoserine lactone, which may accou

168 ide (RS) and 4-methylquinazoline (MQ) as sex pheromones, Nasonia vitripennis evolved (4R,5R)-5-hydrox

169 ynthesize, and field test the sex attractant pheromone of adults of Melanotus communis, commonly call

170 electively detect the presence of female sex pheromone of olive fruit fly before the onset of pest in

171 ective and sensitive detection of female sex pheromone of olive fruit pest, Bactocera oleae.

172 Here, we show that identification of pheromones of invasive pest species can be expedited by

173 Pheromones of many gram-positive bacteria, such as Bacil

174 ily Cerambycinae, and that identification of pheromones of novel species can be expedited by knowledg

175 vel species can be expedited by knowledge of pheromones of related species.

176 iors, including appropriate responses to the pheromones of the opposite sex.

177 A as strongly as they did to their own alarm pheromone on natural inflorescences.

178 yed lower courtship, because residual female pheromone on their antennae adapted their peripheral sen

179 Our results show how pheromone or endocrine signaling pathways can coordinate

180 females were less responsive to the male sex pheromone or unable to use it as a cue at all.

181 man or animal odorants, CO(2), sex and alarm pheromones, or other odorants known to attract or repel

182 demonstrate how integration of MAPK from the pheromone pathway allows one to tune the competition of

183 It has been proposed that pheromone perception in ants evolved via expansions in t

184 ically dissected, from the enzymes producing pheromones, perception by chemosensory receptors, throug

185 Stimulation of the QS system using synthetic pheromones prior to inoculation did not significantly in

186 We analysed the volatile alarm pheromone produced by attacked workers of the most abund

187 pheromones in social insects to the mammary pheromone produced by mother rabbits.

188 ary activation, ovulation, and modulation of pheromone production) and transcriptional changes after

189 tinue response (which is influenced by queen pheromone production), and transcriptional changes in qu

190 Second, the Rax1-Rax2 complex functions as a pheromone-promoted polarity cue in the distal pole of th

191 y described "olfactory lens," an increase in pheromone reception at the proximal end of the sensors.

192 has maintained the recent variation in this pheromone receptor gene.

193 of-function deletions that impair duplicated pheromone receptor genes (srg-36 and srg-37), which were

194 we show that a niche-associated variation in pheromone receptor genes contributes to natural differen

195 Likewise, DAF-37 pheromone receptor signaling negatively modulated nlp-24

196 a class D GPCR, the Saccharomyces cerevisiae pheromone receptor Ste2, in an active state coupled to t

197 The pathway comprises a pheromone receptor, a heterotrimeric G protein, and intr

198 his behavioral plasticity requires the Or47b pheromone receptor.

199 These proteins are cytoplasmic pheromone receptors sharing a structurally similar phero

200 oughs in the deorphanization of codling moth pheromone receptors, as well as more broadly into insect

201 imaging the behavior of polarity factors and pheromone receptors, we quantified the accuracy of initi

202 h as cell cycle arrest is initiated upon the pheromone recognition in each mating partner, and sustai

203 osure of Pinus sylvestris to pine sawfly sex pheromones reduces the survival rate of subsequently lai

204 with pathogenic bacteria leads to increased pheromone release, which attracts healthy flies.

205 Antheridiogens are pheromones released by sexually mature female fern gamet

206 response of the oogenic germline to the male pheromone requires serotonin signal from NSM and HSN neu

207 Particularly, recent studies in the yeast pheromone response have shown how positive feedback gene

208 analysis has shown that heterogeneity in the pheromone response is prevalent.

209 suggested a potential crosstalk between the pheromone response pathway and the target of rapamycin (

210 In the yeast pheromone response pathway, the MAPK Fus3 triggers negat

211 we investigated the mechanism that restricts pheromone response to adult hermaphrodites.

212 The specifically pheromone response-defective mutants are severely impair

213 rgoes nuclear localization bursts during the pheromone response.

214 ore, understanding the mechanisms underlying pheromone responses could reveal how reproduction-relate

215 ut how natural genetic diversity affects the pheromone responses of individuals from diverse habitats

216 genes contributes to natural differences in pheromone responses.

217 Enterococcal pheromone responsive conjugative plasmids like pCF10 pro

218 All pheromone-responsive lcPNs appeared to exhibit "basket-l

219 l and morphological properties of a group of pheromone-responsive olfactory projection neurons with c

220 Previous reports have demonstrated that pheromone-responsive projection neurons with cell bodies

221 or O2 experience has opposite effects on the pheromone responsiveness of these neurons.

222 ty of the hermaphrodite response to the male pheromone, restricting it to situations in which the pre

223 Here we show that the ascaroside ascr#18, a pheromone secreted by plant-parasitic nematodes, is meta

224 al compound isolated from perianal glandular pheromone secretion of the African civet cat.

225 wding to change feeding behavior by coupling pheromone sensing to signaling via insulin-like peptides

226 ude in another male's territory unless their pheromone-sensing is disabled.

227 -16 and INS-4, which act respectively in the pheromone-sensing neuron ADL and the bacteria-sensing ne

228 ge of mapping receptor-ligand pairings among pheromone-sensing neurons in mice.

229 t the world; this deletion underlies reduced pheromone sensitivity across the global C. elegans popul

230 he polyglutamine domain of Whi3 restored the pheromone sensitivity of old cells.

231 which social context can directly influence pheromone sensitivity, thereby modulating social behavio

232 raised questions concerning the mechanism of pheromone-sensor recognition and coevolution.

233 sults suggest that plant-editing of nematode pheromones serves as a defense mechanism that acts in pa

234 Thus, the pheromone should find immediate use in worldwide quarant

235 We provide evidence for a pheromone signal produced by C. elegans larvae that modi

236 r cell fusion to take place, the increase on pheromone signaling promotes Cdc25 degradation, which se

237 ms of dominance, acute and chronic, and that pheromone signaling through V1R receptors is involved in

238 In yeast, multiple stress signals regulate pheromone signaling to prevent mating under unfavorable

239 ess-triggered crosstalk mechanism modulating pheromone signaling, polarized growth, and cell-cell fus

240 rylates and positively regulates Rga2 during pheromone signaling.

241 h multiple substrates to down-regulate yeast pheromone signaling.

242 ciation and function of Ste50 mutants in the pheromone-signaling complex.

243 xistence of a new and distinct branch of the pheromone-signaling pathway, one that likely leads to va

244 From quorum sensing in bacteria to pheromone signalling in social insects, chemical communi

245 Because opioid and pheromone signals both originate in ASI chemosensory neu

246 interaction between foraging strategies and pheromone signals will help uncover molecular mechanisms

247 iosynthetic pathways leading to the sand fly pheromone sobralene and taxadiene have been made.

248 partner by determining the direction of the pheromone source and polarizing their growth toward it.

249 nabling redistribution of the GTM toward the pheromone source.

250 Ascaroside pheromones stimulate dispersal, a key nematode behavior

251 When pheromone-stimulated cells are unable to sense a gradien

252 The female pheromone stimulates courtship behavior in males, notabl

253 reporter assays, we demonstrate that mating pheromone stimulates vacuolar targeting of a cytoplasmic

254 olomics measurements in yeast under salt and pheromone stimulation and developed a machine learning a

255 ng to qualitative and temporal facets of the pheromone stimulus to a more expansive number of protoce

256 omponent H. halys aggregation pheromone, and pheromone synergist, methyl (2E, 4E, 6Z)-decatrienoate w

257 however, they were less sensitive to mating pheromone than were young cells because of age-dependent

258 Female pheromone that contaminated the male's antennae also eli

259 avoidance responses to osas#9, an ascaroside pheromone that incorporates the neurotransmitter, octopa

260 the pheromone MUP20 (darcin), and a volatile pheromone that influences female reproductive physiology

261 reams; once sexually mature, males release a pheromone that mimics the larval cue and attracts female

262 d the chemical properties of the aggregation pheromone that signals nestmate presence and induces arr

263 y complex NDMMs, some of which act as primer pheromones that are capable of triggering irreversible d

264 um-sensing systems use extracellular peptide pheromones that are detected by cytoplasmic receptors to

265 to 7% O2 are aroused by CO2 and repelled by pheromones that attract animals acclimated to 21% O2 Thi

266 An. gambiae produce and release aggregation pheromones that attract individuals to the swarm and enh

267 The two yeast mating types secrete peptide pheromones that bind to GPCRs on cells of the opposite t

268 transient period of competence, triggered by pheromones that they produce, secrete and sense under co

269 teria process and release small peptides, or pheromones, that act as signals for the induction of ada

270 ander scale [ Aspidiotus nerii (Bouche)] sex pheromone, the unique sesquiterpenoid containing a cyclo

271 When exposed to a high dose of mating pheromone, the yeast cell undergoes growth arrest and fo

272 ior: The advection and diffusion of heat and pheromones through a porous medium are modified by the m

273 ndicated that R. speratus worker release the pheromone to their nesting site.

274 use blends of chiral hydroxylactones as sex pheromones to attract conspecific females.

275 Many species use pheromones to communicate information about the location

276 discriminate relevant signals in a myriad of pheromones to execute appropriate responses.

277 e reliably decode gradients of extracellular pheromones to find their mates.

278 a use diffusible chemical messengers, termed pheromones, to coordinate gene expression and behavior a

279 ress activates Pkc1, which prevents lysis of pheromone-treated cells by inhibiting polarized growth.

280 indicators, we show that both vegetative and pheromone-treated yeast cells exhibit discrete and async

281 lication of a single, well-timed aggregation pheromone treatment per generation increased the efficac

282 or the perception of trisporic acids, mating pheromones unique to Mucoromycotina.

283 f the prothoracic gland trait for predicting pheromone use in cerambycid species in the subfamily Cer

284 An aggregation pheromone used by D. carinulata to locate conspecifics i

285 production of male-produced aggregation-sex pheromones, usually characterized by 2,3-alkanediol/hydr

286 provide a physiological correlate of altered pheromone valence.

287 ncreased Rgg2Sp sensitivity to pheromone and pheromone variants while displaying decreased sensitivit

288 d for controlled release of this aggregation pheromone was developed as a lure to manipulate adult de

289 tivity of the MEMS devices towards the olive pheromone was found to be directly correlated with the i

290 owth inhibitory effect of F. oxysporum alpha-pheromone was independent of the cognate G protein-coupl

291 olfactory responses to a food odorant and a pheromone were reduced to a similar degree by OSPW, agai

292 Animal CCDs (mostly insect pheromones) were usually more integrated than those of p

293 to a value as low as 0.297 ppq of the olive pheromone when the devices were functionalized with one

294 Harpegnathos saltator, the queen produces a pheromone which suppresses the development of workers' o

295 for farnesylated peptides, like the a-factor pheromone, which could potentially also transport farnes

296 The pheromone will also be a crucial tool in ongoing efforts

297 synthetic sequence afforded the A. nerii sex pheromone with minimum intermediate purification and goo

298 reversed selectivity toward the heterologous pheromone with only five point mutations, as well as oth

299 ius and pyogenic groups of streptococci, the pheromone XIP is sensed by the intra-cellular regulator

300 signaling, a system based on the mature ComS pheromone (XIP), which is internalized to activate the (