ライフサイエンスコーパス: phototropic

1 Cones may be phototropic, actively orientating themselves towards lig

2 Young rhizoids are negatively phototropic, and NPA also inhibits rhizoid phototropism.

3 acterized in the purple nonsulfur anoxygenic phototropic bacterium Rhodopseudomonas palustris.

4 displayed elongated hypocotyls but retained phototropic behavior and the ability to fully deetiolate

5 utant, in which phyA remains in the cytosol, phototropic bending is slower than in the wild type.

6 ocotyl growth rate, apical hook opening, and phototropic bending with high spatiotemporal resolution.

7 ropins are flavoprotein kinases that control phototropic bending, light-induced chloroplast movement,

8 ich encodes phototropin, a photoreceptor for phototropic bending.

9 optical performance is further optimized by phototropic chromatophores that regulate the dose of ill

10 Modulatory increases in the magnitude of phototropic curvature have been termed "enhancement." He

11 The development of phototropic curvature of etiolated seedlings of Arabidop

12 c responsiveness, accounting for the greater phototropic curvature of the nph2 and nph4 mutants to UV

13 The amplitude of phototropic curvature to blue light is enhanced by a pri

14 owth rates were equal for both genotypes and phototropic curvature was only slightly inhibited in NS

15 d required for phot1-directed first-positive phototropic curvature.

16 ts overexpressing CRY1 or CRY2 show enhanced phototropic curvature.

17 dephosphorylation of NPH3 and development of phototropic curvatures by protein phosphatase inhibitors

18 een termed "enhancement." Here, we show that phototropic enhancement is primarily a phytochrome A (ph

19 ultimate target(s) of phyA action during the phototropic enhancement response is a rate-limiting ARF-

20 Consistent with its lack of phototropic function in Arabidopsis, Otphot does not ass

21 l evolution of the lamellar structures under phototropic growth conditions.

22 ateral auxin gradient, ultimately leading to phototropic growth in shoots.

23 These inorganic nanostructures exhibited phototropic growth in which lamellar stripes grew toward

24 iments and simulations are consistent with a phototropic growth mechanism in which the optical near-f

25 Genes implicated in control of phototropic growth, but not clock genes, are differentia

26 -A/blue-light activated kinases that trigger phototropic growth.

27 family of proteins and is homologous to NON-PHOTOTROPIC HYPOCOTYL 3 (NPH3), a BTB/POZ protein that r

28 onjunction with the signalling component Non-Phototropic Hypocotyl 3 (NPH3).

29 of the phototropic signalling component Non-Phototropic Hypocotyl 3 (NPH3).

30 eins identified to date, only one, NPH3 (non-phototropic hypocotyl 3), is essential for all phot1-dep

31 Phototropic hypocotyl bending in response to blue light

32 In Arabidopsis thaliana, phototropic hypocotyl bending is initiated by the blue l

33 Here, we show that phototropic hypocotyl bending is strongly dependent on t

34 hromes and phytochromes are not required for phototropic induction, these photoreceptors do modulate

35 hese stromatolites were probably accreted by phototropic microbes that, from their habitat in shallow

36 A phototropic mutant of P. blakesleeanus with a heterozygo

37 ese loci, NPH1, encodes the apoprotein for a phototropic photoreceptor.

38 In etiolated seedlings, the phototropic response is enhanced by the red/far-red (R/F

39 The phototropic response of Arabidopsis (Arabidopsis thalian

40 pin is a blue-light receptor involved in the phototropic response of higher plants.

41 ant were essentially agravitropic, but their phototropic response was robust.

42 ss to direct sunlight becomes important, the phototropic response was strong.

43 A, we show that nuclear phyA accelerates the phototropic response, whereas in the fhy1 fhl mutant, in

44 ue-light photoreceptors are deficient in the phototropic response.

45 L 3 (NPH3), a BTB/POZ protein that regulates phototropic responses along with the protein kinase PHOT

46 Phototropic responses also require auxin transport and w

47 Despite their altered phototropic responses in blue and green light as etiolat

48 phoric flavoprotein photoreceptor regulating phototropic responses in higher plants.

49 ylating flavoprotein photoreceptor mediating phototropic responses in higher plants.

50 1-5 mutant exhibited enhanced phot2-mediated phototropic responses like those of the phot1-5 rcn1-1 d

51 Examination of the phototropic responses of a mutant deficient in biologica

52 Thus, the phototropic responses of fungi through madA and plants t

53 ngly, both auxin-regulated organogenesis and phototropic responses require an auxin response factor (

54 cells, and mutant hypocotyls display strong phototropic responses to lateral light stimulation.

55 iated signaling pathways have been linked to phototropic responses under various conditions.

56 utants are all altered with respect to their phototropic responses, only the nph4 mutants are also al

57 tyl 3), is essential for all phot1-dependent phototropic responses, yet little is known about how pho

58 dules into a single gene, thereby optimizing phototropic responses.

59 ner that is physiologically similar to plant phototropic responses.

60 her, our results support the hypothesis that phototropic responsiveness is modulated by inputs that i

61 mation by UV-A light mediates an increase in phototropic responsiveness, accounting for the greater p

62 g pathways have also been shown to influence phototropic responsiveness, and these pathways are influ

63 kinase domain, which is tightly coupled with phototropic responsiveness.

64 regulation of this E3 is required for normal phototropic responsiveness.

65 rassinosteroids and auxin signaling modulate phototropic responsiveness.

66 nd PP2A activity is reduced, showed enhanced phototropic sensitivity and enhanced blue light-induced

67 Though several components of the phototropic signal response pathway have been identified

68 significance of the A'alpha helix region in phototropic signaling of tomato.

69 ate with or trigger dephosphorylation of the phototropic signalling component Non-Phototropic Hypocot