ライフサイエンスコーパス: cambial

1 cated ERF-1 as a potential key checkpoint of cambial activities, explaining how cambium-driven growth

2 ent to which carbon assimilation (source) or cambial activity (sink) mediate wood production are fund

3 wn about the genetic mechanisms that control cambial activity and the differentiation of secondary xy

4 n, our findings suggest that reinitiation of cambial activity and transdifferentiation of xylem paren

5 tCLE47 gene is a major positive regulator of cambial activity in hybrid aspen, mainly promoting the p

6 otosynthesis, despite mounting evidence that cambial activity is rather directly constrained by limit

7 Peaks of cambial activity occur substantially earlier compared to

8 ulatory network underlying ethylene-mediated cambial activity remains to be elucidated.

9 t cytokinins function as major regulators of cambial activity, these trees displayed stimulated cambi

10 pecies can be linked to a distinct period of cambial activity, we applied a bi-weekly pinning to six

11 is also essential to establish and maintain cambial activity.

12 ite warmer temperatures being favourable for cambial activity.

13 biosynthesis and auxin transport to maintain cambial activity.

14 he cambium adjacent to the xylem to maintain cambial activity.

15 one finger (DOF) transcription factors, HIGH CAMBIAL ACTIVITY2 (HCA2), TARGET OF MONOPTEROS6 (TMO6),

16 e found that phylloxera exploits preexisting cambial and leaf meristems and promotes callus formation

17 induce cell divisions and the expression of cambial and phloem markers in the adjacent cells, which

18 nal activity of the gene is highest in root, cambial and shoot meristems and immature tissues of the

19 involving a polyphagan wood-borer consuming cambial and wood tissues of the conifer Ningxiaites spec

20 tected in developing embryos and procambial, cambial, and vascular cells of cotyledons, leaves, roots

21 l cytokinin content and signaling level, the cambial auxin concentration and auxin-responsive gene ex

22 ibution that influences the amplitude of the cambial auxin gradient.

23 l activity, these trees displayed stimulated cambial cell division activity resulting in dramatically

24 onal pathway that regulates both the rate of cambial cell division and woody tissue organization.

25 and CLE41 and a receptor kinase PXY controls cambial cell divisions; however, the pathway regulating

26 ype also correlated with a reduced number of cambial cell layers.

27 uring vascular development, the meristematic cambial cells divide down their long axis in a highly or

28 th a xylem identity direct adjacent vascular cambial cells to divide and function as stem cells.

29 ghest concentration in the actively dividing cambial cells, cytokinins peak in the developing phloem

30 ort due to damage to the tree crown and stem cambial cells, respectively, can cause tree mortality.

31 estingly, in addition to showing an elevated cambial cytokinin content and signaling level, the cambi

32 width of the cambial zone and inhibition of cambial daughter cell differentiation.

33 in VC activity and prolonged maintenance of cambial-derived cells in a meristematic state was crucia

34 birch (Betula pubescens) trees, we show that cambial development is modulated systemically along the

35 onal significance of cytokinin signaling for cambial development, we engineered transgenic Populus tr

36 scriptome analyses reveal modules related to cambial growth and development, photosynthesis, and defe

37 t regulation of the transcriptome underlying cambial growth and wood formation comprises numerous mod

38 ng of the transcriptional network underlying cambial growth and wood formation.

39 Approaching vascular cambial growth as a complex developmental process, we re

40 ints to identify developmental components of cambial growth based on fossil anatomy.

41 duced in the superficial tissues by vascular cambial growth from within.

42 Temperature is an important factor for the cambial growth in temperate trees.

43 t modes of secondary growth demonstrate that cambial growth is an assemblage of regulatory modules wh

44 We show that the orientation of cambial growth is regulated by microRNA (miRNA)-directed

45 We investigate cambial growth periodicity in Brachystegia spiciformis,

46 atively short (three to four months maximum) cambial growth season corresponded to the core of the ra

47 ainfall event occurring after the end of the cambial growth season did not induce xylem initiation or

48 rapid tissue differentiation is critical for cambial growth under mechanical stress.

49 Our results show that the onset and end of cambial growth was synchronous between trees, but was no

50 utative constituent developmental modules of cambial growth, for which we review developmental anatom

51 of regulatory mechanisms (modules) acting in cambial growth, representing four distinct modes of seco

52 rise from divisions of stem cells within the cambial meristem.

53 ase, the symmetry of the defects implies (1) cambial orientation is controlled by a vector quantity a

54 nificant constraints on proposed theories of cambial orientation.

55 and consequently for normal stem elongation, cambial proliferation, and xylem fiber differentiation.

56 tures of 2013 and 2014 shifted the timing of cambial reactivation and had different effects on cambia

57 inter to early spring affected the timing of cambial reactivation and xylem differentiation in stems

58 formula for calculation of CRI predicted the cambial reactivation in 2015.

59 al reactivation and had different effects on cambial reactivation in the two consecutive years becaus

60 critical factor in determining the timing of cambial reactivation in trees.

61 accumulated temperature above the threshold (cambial reactivation index; CRI) of 13 degrees C in 11 d

62 se earlier from late winter to early spring, cambial reactivation occurred earlier.

63 hat the mRNA is present predominantly in the cambial region in stems, leaves, and roots and in the va

64 auxin- and cytokinin-regulated induction and cambial region localization, encourage us to suggest tha

65 tration of indole-3-acetic acid (IAA) in the cambial region of a tree branch and the radial expansion

66 In addition, the gene expression in the bark/cambial region was up-regulated in spring and fall when

67 RpALN gene was highly expressed in the bark/cambial region, but had no detectable expression in the

68 ons of XTH4 and XTH9 abundantly expressed in cambial regions during secondary growth of Arabidopsis (

69 nt with these results, expression of several cambial regulator genes was downregulated in the stems o

70 Our results indicate that the cambial sink is affected by carbon supply, but within-tr

71 nd a cle41 mutant with altered regulation of cambial stem cell maintenance and differentiation, that

72 onal to the mass of IAA per unit area on the cambial surface, and (3) IAA is transported basipetally

73 ary growth, ARK2 is expressed broadly in the cambial zone and in terminally differentiating cell type

74 iming of cambium formation, the width of the cambial zone and inhibition of cambial daughter cell dif

75 h WT, along with a more mechanically elastic cambial zone and radial compression of xylem cell size,

76 in both the shoot apical meristem and in the cambial zone and secondary vascular tissues.

77 bundant in ray parenchyma cells, followed by cambial zone cells and resin duct epithelia.

78 reid lignification, and reprogramming of the cambial zone to form traumatic resin ducts in Pseudotsug

79 The cambial zone xylem mother cells are reprogrammed to diff

80 n unprecedentedly high resolution across the cambial zone.

81 was most highly expressed in the phloem and cambial zone.