ライフサイエンスコーパス: photoperiodic

1 Photoperiodic activation of the bspA promoter was shown

2 we report that SHB1 plays dual roles in both photoperiodic and autonomous flowering.

3 Genetic analyses demonstrated that various photoperiodic and autonomous pathway mutants are epistat

4 nalyses suggest that AA acts upstream of the photoperiodic and autonomous pathways.

5 anching and flowering in side shoots of wild photoperiodic and modern day-neutral accessions.

6 nal means by which plants may integrate both photoperiodic and temperature signals to respond to the

7 EC directly regulates clock outputs, such as photoperiodic and thermoresponsive growth, and provide n

8 No associations were found with photoperiodic and vernalisation response genes known to

9 of Ppd-H1 Our findings demonstrate that the photoperiodic and vernalization pathways interact to con

10 ian rhythms and regulate seasonal rhythms in photoperiodic animals by acting on specific G-protein co

11 ective disorder resemble seasonal changes in photoperiodic animals.

12 encode is important with respect not only to photoperiodic behavior but also to the regulation of oth

13 stry, indicating that FKF1 may function as a photoperiodic blue-light receptor.

14 o the light-dark cycle by retinal input, and photoperiodic changes in melatonin secretion control neu

15 in cortisol production are not required for photoperiodic changes in sickness behaviors to manifest.

16 e responsiveness of the individual animal to photoperiodic changes.

17 same mechanism(s), regardless of the plant's photoperiodic character.

18 ent of the shoot as this trait is delayed by photoperiodic conditions and some mutations that delay f

19 an starlings (Sturnus vulgaris) in different photoperiodic conditions.

20 n tree sparrows were exposed to one of three photoperiodic conditions: (1) Photosensitive birds were

21 n rainforests with low climatic seasonality, photoperiodic control is the only reliable mechanism for

22 ock gene expression in the PT to mediate the photoperiodic control of a summer or winter physiology.

23 ggesting that it plays a central role in the photoperiodic control of both generative and vegetative

24 We use geographic variation in the photoperiodic control of diapause in the pitcher-plant m

25 light inhibition of hypocotyl elongation and photoperiodic control of floral initiation.

26 rbitis nil is a model plant for the study of photoperiodic control of floral initiation.

27 t is thought that the environmental cues for photoperiodic control of flowering are initially perceiv

28 Day-length assessment involves the photoperiodic control of flowering in Arabidopsis thalia

29 lay an important role in light signaling and photoperiodic control of flowering time in plants.

30 es of both red and blue light, and a loss of photoperiodic control of flowering time.

31 transcription factor that is responsible for photoperiodic control of flowering time.

32 as been found to play a critical role in the photoperiodic control of flowering time; and genes have

33 diverse biological processes, including the photoperiodic control of flowering, growth, and abiotic

34 an clock and photoreceptor components, named PHOTOPERIODIC CONTROL OF HYPOCOTYL1 (PCH1).

35 melatonin signal is decoded, we studied the photoperiodic control of prolactin secretion in Soay she

36 provides a rich source of genes involved in photoperiodic control, symbiosis, and defense-related re

37 han did PnCO and was not subject to the same photoperiodic control.

38 GA5, whereas expression of GA4 is not under photoperiodic control.

39 tive (short-day) conditions, indicative of a photoperiodic control.

40 Incorporating a photoperiodic correction of photosynthetic physiology in

41 data reveal a key role for GI in connecting photoperiodic cues and environmental stress independentl

42 Higher plants use photoperiodic cues to regulate many aspects of developme

43 Photoperiodic decoding relies on circadian clocks, but t

44 ian rhythms, photomorphogenic responses, and photoperiodic dependent flowering, most likely by regula

45 esis, photoprotection, stomatal opening, and photoperiodic development, as well as molecular processe

46 tion pharmacologically, largely disrupts the photoperiodic diapause response of the wasps.

47 onia was exacerbated in LD-OBx hamsters; and photoperiodic differences in circulating leukocytes and

48 st that the SCN are not the sole mediator of photoperiodic effects of melatonin on immunity.

49 basal hypothalamus, thus bypassing possible photoperiodic effects on peripheral estradiol availabili

50 f Experiment 2 might have been influenced by photoperiodic effects on peripheral metabolism of estrad

51 he control of body weight and food intake in photoperiodic F344 rats.

52 EARLY FLOWERING3 (ELF3) gene is required for photoperiodic flowering and normal circadian regulation

53 ins positively regulate CO transcription for photoperiodic flowering and that this mechanism may be c

54 Day/night temperature changes modulate photoperiodic flowering by changing FT accumulation patt

55 P2 proteins regulate the circadian clock and photoperiodic flowering by controlling blue-light-depend

56 hed mechanisms that govern light sensing and photoperiodic flowering control.

57 Photoperiodic flowering has been extensively studied in

58 light inhibition of hypocotyl elongation and photoperiodic flowering in Arabidopsis thaliana.

59 xpression and activity is a key mechanism in photoperiodic flowering in Arabidopsis.

60 Photoperiodic flowering in plants is regulated by photos

61 The photoperiodic flowering involves two key components, CON

62 Mutations that impair the photoperiodic flowering pathway prevent this downregulat

63 In facultative photoperiodic flowering plants, noninductive photoperiod

64 t FT2c may have underpinned the evolution of photoperiodic flowering regulation in soybean domesticat

65 We also show that TOC1 controls photoperiodic flowering response through clock function.

66 Finally, we found that the photoperiodic flowering response, which is influenced by

67 Finally, we found that the photoperiodic flowering response, which is regulated by

68 e also active locally in leaves to fine-tune photoperiodic flowering responses.

69 plays an essential role in the regulation of photoperiodic flowering under long-day conditions.

70 le for specific 14-3-3 isoforms in affecting photoperiodic flowering via interaction with CONSTANS, p

71 ort that TZP acts as a positive regulator of photoperiodic flowering via physical interactions with t

72 y) regulate seedling deetiolation responses, photoperiodic flowering, and circadian rhythm.

73 dopsis thaliana GIGANTEA (GI) contributes to photoperiodic flowering, circadian clock control, and ph

74 n of COL2 increases its expression, inducing photoperiodic flowering, which could have contributed to

75 endent repression is a critical mechanism in photoperiodic flowering.

76 nce of light with circadian timing regulates photoperiodic flowering.

77 necessary for day-length discrimination for photoperiodic flowering.

78 utputs that control the expression of CO and photoperiodic flowering.

79 light regulation of seedling development and photoperiodic flowering.

80 ow developmental signals are associated with photoperiodic flowering.

81 iate the FLOWERING LOCUS T (FT)-FD module in photoperiodic flowering.

82 iption factor which plays a critical role in photoperiodic flowering.

83 ular knob that links developmental aging and photoperiodic flowering.

84 hyon, PHYTOCHROME C (PHYC), is necessary for photoperiodic flowering.

85 nt for regulation of the circadian clock and photoperiodic flowering.

86 hanisms for proper day-length measurement in photoperiodic flowering.

87 w floral delay and reduced expression of the photoperiodic genes CO and FLOWERING LOCUS T.

88 Photoperiodic growth of the song-control system during t

89 t the RER proteins functionally interconnect photoperiodic growth, amino acid homeostasis, and reacti

90 s known about how long it takes to establish photoperiodic histories or how long they endure.

91 long summer day lengths acquired a long-day photoperiodic history that determined subsequent reprodu

92 e outcomes transpires depends on an animal's photoperiodic history, suggesting that hamsters must enc

93 gests a role for inrpk1 in some aspect of SD photoperiodic-induced flowering in morning glory.

94 y monitoring tracer movement under different photoperiodic induction conditions and in a number of ge

95 balance between FLC-mediated repression and photoperiodic induction of flowering to favor the latter

96 elopment, including hypocotyl elongation and photoperiodic induction of flowering.

97 s of the brain of fifth-instar larvae on the photoperiodic induction of pupal diapause.

98 in leaves is not maintained after transient photoperiodic induction, the molecular basis for stable

99 and mPOA of SP females, suggesting that the photoperiodic influences on PR induction observed in Exp

100 owth and reproduction despite the absence of photoperiodic information for most of the year.

101 otoreceptors can be involved in signaling of photoperiodic information through multiple pathways, inv

102 mammals, the pineal hormone melatonin relays photoperiodic information to the hypothalamus to control

103 p-brain photoreceptors directly transmitting photoperiodic information to the hypothalamus-pituitary

104 cells and acts as a neuromodulator imparting photoperiodic information to the retina.

105 Recent studies have defined the photoperiodic input to this rhythm, wherein melatonin ac

106 Photoperiodic manipulations alter hypothalamic TH availa

107 ed to other aspects of the seasonal cycle or photoperiodic manipulations.

108 These data suggest that photoperiodic mechanisms can alter the density of V(1a)R

109 as molecular calendars, carrying a form of "photoperiodic memory."

110 ineal gland has been co-opted to provide the photoperiodic message.

111 -activated gene in sheep, revealing a common photoperiodic molecular response in birds and mammals.

112 lowering without a significant effect on the photoperiodic or vernalization responses.

113 In Arabidopsis (Arabidopsis thaliana), the photoperiodic pathway acts through FLOWERING LOCUS T (FT

114 ith lower mRNA levels of circadian clock and photoperiodic pathway genes compared with plants treated

115 For example, circadian clock and photoperiodic pathway genes were significantly higher in

116 rs of the FLC/MAF gene family, including the photoperiodic pathway regulator MAF1/FLM.

117 In the photoperiodic pathway, a mobile signal, florigen, encode

118 ects expression of genes associated with the photoperiodic pathway.

119 CONSTANS and promoting flowering through the photoperiodic pathway.

120 -Plus3), as a signal integrator of light and photoperiodic pathways in transcriptional nuclear foci.

121 e, degeneration of vision and progression of photoperiodic perception, tolerance to hypercapnia and h

122 ossypium hirsutum) converted it from a lanky photoperiodic perennial to a day-neutral annual row-crop

123 ation, pupillary aperture, and circadian and photoperiodic physiology.

124 radient; it was least in the two qualitative photoperiodic plants studied, the long-day plant Nicotia

125 psis thaliana cryptochrome 2 (CRY2) mediates photoperiodic promotion of floral initiation and blue li

126 light inhibition of hypocotyl elongation and photoperiodic promotion of floral initiation in the nucl

127 veal a molecular machinery that controls the photoperiodic regulation of flowering and growth and off

128 trast, CONSTANS (CO) plays a key role in the photoperiodic regulation of flowering in Arabidopsis (Ar

129 ht into an external coincidence mechanism of photoperiodic regulation of flowering time mediated by P

130 rnode elongation, anthocyanin synthesis, and photoperiodic regulation of flowering, were altered in a

131 modulates light-dependent processes such as photoperiodic regulation of flowering.

132 is well defined, the molecular basis for the photoperiodic regulation of seasonal activities is large

133 set, sexual differentiation of the brain and photoperiodic regulation of seasonal reproduction.

134 ur findings provide a novel insight into the photoperiodic regulation of the vernalization pathway in

135 that a change in a single gene reverses the photoperiodic requirements for flowering.

136 istatic effects to the genetic divergence of photoperiodic response along latitudinal, altitudinal, a

137 nta that is required to coordinate a correct photoperiodic response in Arabidopsis.

138 r reports that UV radiation can regulate the photoperiodic response in this animal.

139 We selected on divergent photoperiodic response in three separate lines from a na

140 This photoperiodic response mechanism differs from those desc

141 demonstrates that the suppression is a true photoperiodic response mediated by the inactivation of t

142 he last 30 years, the genetically controlled photoperiodic response of the pitcher-plant mosquito, Wy

143 Regardless of the photoperiodic response of the source plants, the respons

144 duration of the night is critical for wheat photoperiodic response.

145 of type-II cells did not interfere with the photoperiodic response.

146 the hypothalamus have been implicated in the photoperiodic response.

147 to the facultative nature of the Arabidopsis photoperiodic response.

148 ly implicate VA opsin in mediating the avian photoperiodic response.

149 erging model organism that exhibits a strong photoperiodic response: Short autumnal days experienced

150 In mammals and birds, photoperiodic responses depend crucially on expression o

151 ory system has a modulatory role in seasonal photoperiodic responses in certain species, we hypothesi

152 Seasonal photoperiodic responses in mammals depend on the pineal

153 located within the hypothalamus and regulate photoperiodic responses to day length.

154 Photoperiodic responses, such as the daylength-dependent

155 ay length and to mediate a diverse number of photoperiodic responses.

156 s, and the eyes are not involved in seasonal photoperiodic responses.

157 es and cryptochromes work together to confer photoperiodic responsiveness in Arabidopsis.

158 ased on these results and a finding that the photoperiodic responsiveness of plants depends on light

159 oth the pattern of circadian entrainment and photoperiodic responsiveness of Siberian hamsters to an

160 ty to TEF, reflecting species variability in photoperiodic responsiveness.

161 in functional phytochrome B exhibits reduced photoperiodic sensitivity and constitutively expresses a

162 3 gene is one of six genes that regulate the photoperiodic sensitivity of flowering in sorghum (Sorgh

163 d-instar larvae programmed for diapause by a photoperiodic (short-day) signal were assayed as they tr

164 each of which occurs in response to a daily photoperiodic signal, but only in the presence of estrad

165 d acclimation, and termination by cold or by photoperiodic signal.

166 In rodents, E2 and photoperiodic signals converge in the anteroventral peri

167 how temperature signals are coordinated with photoperiodic signals in the timing of seasonal flowerin

168 long days, suggesting that it is the central photoperiodic state rather than the peripheral adiposity

169 nce of increased adiposity or of the central photoperiodic state.

170 ple floral induction pathways, including the photoperiodic, the autonomous, the vernalization, and th

171 y was to determine whether genes involved in photoperiodic time measurement (TSHbeta and Dio2) and ce

172 t within populations or for the evolution of photoperiodic time measurement among populations over a

173 causal basis for the adaptive divergence of photoperiodic time measurement within populations or for

174 hypothalamus is reversible and critical for photoperiodic time measurement.

175 Here we propose a new mechanism of photoperiodic timekeeping based on the perception of var

176 n the daily circadian clock and the seasonal photoperiodic timer remains a subject of intense controv

177 ical photoperiod (an overt expression of the photoperiodic timer) evolves independently of the rhythm

178 However, the molecular mechanisms underlying photoperiodic timing are largely unknown.

179 Photoperiodic timing mechanisms in plants appear to use

180 Circadian and photoperiodic timing mechanisms were first described in

181 mple for a role of DNA methylation in insect photoperiodic timing.