ライフサイエンスコーパス: pericycle

1 roteins remain restricted to the phloem-pole pericycle.

2 ter developmental stage, additionally in the pericycle.

3 tion from proliferative cell division in the pericycle.

4 in mature Frankia-infected cells and in the pericycle.

5 rent after the first set of divisions of the pericycle.

6 d proteins are diverted into the phloem-pole pericycle, a tissue connected to the protophloem by a un

7 is required for meristematic activity in the pericycle analogous to its requirement in the shoot apic

8 in genes expressed in the meristematic zone, pericycle and endodermis of the Arabidopsis thaliana (Ar

9 tips, and accumulates to lower levels in the pericycle and lateral root primordia.

10 AtABCG14 is expressed primarily in the pericycle and stelar cells of roots.

11 ons reveal differences in gene expression in pericycle and surrounding cells even before infection.

12 ein revealed that WRKY75 is expressed in the pericycle and vascular tissue and that the WRKY75 RNA or

13 Both pericycle and xylem parenchyma cells are involved in ene

14 ed the concentrations of K, Na and Cl in the pericycle and xylem parenchyma cells at the subapical re

15 irect role for SHR in gene regulation in the pericycle and xylem.

16 ding triggered a Ca(2+) transient within the pericycle, and blocking this change in Ca(2+) also block

17 ots, with localized expression in root tips, pericycle, and cortex cells at the base of lateral roots

18 formation of a multi-layered xylem-adjacent pericycle, but did not rescue the primordium formation.

19 The estimated duration of a pericycle cell cycle in the root apical meristem was sim

20 he differential contribution of primary root pericycle cell files to developing lateral root primordi

21 These effects are correlated with decreased pericycle cell length and increased lateral root primord

22 The pericycle cell length was less dramatically reduced than

23 l length, suggesting that a reduction in the pericycle cell number relative to the cortex could occur

24 y, and elaborating on the three key steps of pericycle cell priming, founder cell establishment and a

25 by the root apical meristem in Arabidopsis, pericycle cells adjacent to the protoxylem poles of the

26 primary and lateral roots, only the walls of pericycle cells and the outer walls of epidermal cells a

27 However, only some of the dividing pericycle cells are committed to the asymmetric, formati

28 before lateral root initiation in quiescent, pericycle cells arrested in the G2 phase of the cell cyc

29 Enhanced cytokinin responses in pericycle cells between existing LRP might restrict LRI

30 The observation that pericycle cells divide and lateral root primordia form w

31 Conditioning small groups of root pericycle cells for future lateral root formation has a

32 Files of shortened pericycle cells found in dgt1-1 roots were unrelated to

33 Localized AtNCED2 and AtNCED3 expression in pericycle cells is an early marker of lateral initiation

34 mmetric cell division of a limited number of pericycle cells located at the xylem pole.

35 lateral root primordia (LRPs) originate from pericycle cells located deep within the parental root an

36 Lateral roots are initiated from the pericycle cells of other types of roots and remain in co

37 tion in the nucleus was observed in dividing pericycle cells of the lateral root meristem.

38 The model also revealed that pericycle cells on opposite xylem poles compete for auxi

39 ugh some unknown mechanism, in most eudicots pericycle cells positioned against the protoxylem change

40 uter cell layer of the root, and also in the pericycle cells surrounding the central vascular tissue.

41 oses of ACC strongly inhibits the ability of pericycle cells to initiate new lateral root primordia,

42 in plants involves the stimulation of mature pericycle cells to proliferate and redifferentiate to cr

43 Auxin stimulates pericycle cells within elongating primary roots to enter

44 to accumulate specifically in the xylem-pole pericycle cells, an important early step in lateral root

45 cy in roots, predominantly expressed in root pericycle cells, and their overexpression repressed the

46 last biogenesis in hypocotyl cortex and root pericycle cells, based on increases in the number and si

47 s of some xylem parenchyma cells and in some pericycle cells, particularly in the wild-type mature ro

48 effect of the IYO/RIMA pathway on xylem pole pericycle cells, we provide compelling evidence reinforc

49 In Arabidopsis, lateral roots originate from pericycle cells, which undergo a program of morphogenesi

50 s PYE and BTS were specifically activated in pericycle cells.

51 s, peripheral root cap cells, and xylem pole pericycle cells.

52 ression and auxin-dependent induction in the pericycle cells.

53 l analysis of a cyclin-GUS fusion protein in pericycle cells.

54 l cells from the elongation zone, and mature pericycle cells.

55 nded, whereas the xylem and xylem-associated pericycle diminished.

56 osmotic and salt stress, the endodermis and pericycle displayed prolonged oscillations in cytosolic

57 m the root protophloem was restricted to the pericycle-endodermis boundary, identifying plasmodesmata

58 in shr, the phloem and the phloem-associated pericycle expanded, whereas the xylem and xylem-associat

59 In plants, lateral roots originate from pericycle founder cells that are specified at regular in

60 t primordium derive from the central file of pericycle founder cells while off-centre founder cells c

61 demonstrate a major role for the phloem-pole pericycle in regulating phloem unloading in roots.

62 proliferative capacity of the xylem-adjacent pericycle in the differentiated root portion.

63 ing and instead functions in maintaining the pericycle in the mitotically competent state needed for

64 olonged stress, Na(+) accumulated inside the pericycle in thsos1-4, while sodium was confined in vacu

65 is expressed in the vascular tissue, in the pericycle, in stamen, and in the chalazal seed coat of o

66 Arsenate reduction by HAC1 in the pericycle may play a role in limiting arsenic loading in

67 n could not induce any cell divisions in the pericycle of the most distal dgt1-1 root-tip portion.

68 s showed that ENOD40 mRNA accumulated in the pericycle of the vascular bundle at 24 h after root inoc

69 ots showed the expression of MtNPF6.8 in the pericycle region of primary roots and lateral roots, and

70 ur results provide genetic evidence that the pericycle shares properties with meristems and that this

71 c transcriptional profiling, we identified a pericycle-specific iron deficiency response and a bHLH t

72 Lateral root primordia (LRP) originate from pericycle stem cells located deep within parental root t

73 p to a greater extent with cells of the root pericycle than any other cell type.

74 y expressed in the root cap and in a ring of pericycle tissues during lateral root initiation and ear

75 with at least one baroresponsive cell, joint pericycle-triggered histograms detected synchrony indica

76 sponsive assemblies were detected with joint pericycle-triggered histograms, the gravitational repres

77 Db-LNP is also present in the root pericycle where its level decreases upon initiation of n