ライフサイエンスコーパス: sieve element

1 as associated with entry into, or exit from, sieve elements.

2 c movement of mRNA from companion cells into sieve elements.

3 plasmodesmata from mesophyll cells into the sieve elements.

4 be involved in the rapid sealing of injured sieve elements.

5 cell border interfaces between mesophyll and sieve elements.

6 movement between phloem companion cells and sieve elements.

7 s detected RBP50 in both companion cells and sieve elements.

8 ry little time in contact with phloem sap in sieve elements.

9 e companion cells associated with metaphloem sieve elements.

10 , in particular companion cells and immature sieve elements.

11 alline patches in xylem parenchyma cells and sieve elements.

12 ethod allows high-resolution measurements of sieve element and sieve plate geometries.

13 R plants, GFP was unable to traffic into the sieve element and was restricted solely to the companion

14 ells plasmolyzed in 600 mM sorbitol, whereas sieve elements and companion cells did not plasmolyze ev

15 the vRNA-dependent RNA polymerase in phloem sieve elements and in xylem vessels.

16 e phloem; it moved from companion cells into sieve elements and into a previously undiscovered sympla

17 GPAs had difficulty feeding from sieve elements and tapping into the xylem of lipoxygenas

18 hat allows the virus to rapidly move through sieve elements and unload at the growing parts of the pl

19 Phloem sieve elements and xylem vessels from Potato virus X-inf

20 riate data on the geometry of pores, plates, sieve elements, and flow parameters are lacking.

21 ters were expressed specifically in immature sieve elements, and GFP-SEO fusion proteins formed parie

22 on was detected in the root cap, protophloem sieve elements, and the companion cells associated with

23 lls, guard cells, phloem companion cells and sieve elements are clearly described, this is not the ca

24 Given that phloem sieve elements are enucleate and lack translation machin

25 Sieve elements are one of the least understood cell type

26 o be able to travel between plant organs via sieve elements as a putative long-distance signaling mol

27 teins formed parietal agglomerates in intact sieve elements as well as sieve plate plugs after woundi

28 ted specifically with the plasma membrane of sieve elements, but not companion cells, and accumulates

29 Small amounts of dilute, mobile sap from sieve elements can be obtained, although there is eviden

30 tomic force microscopy indicates that phloem sieve element cell walls have a lower indentation modulu

31 a glycan epitope that is specific to phloem sieve element cell walls in several systems.

32 uch as sugars are transported through phloem sieve element cells in plants.

33 ffuse through plasmodesmata up to the phloem sieve element companion cell complex (SECCC).

34 One well-documented symplasmic domain is the sieve element-companion cell (SE-CC) complex in the phlo

35 Membrane proteins within the sieve element-companion cell complex have essential role

36 sucrose transfer from the apoplast into the sieve element-companion cell complex, so-called apoplast

37 a cells feeding H(+)-coupled import into the sieve element-companion cell complex.

38 AVP1 localized at the plasma membrane of the sieve element-companion cell complexes functions as a sy

39 ssion of the transporter was targeted to the sieve element-companion cell complexes of the leaf phloe

40 ensions of plasmodesmal channels involved in sieve element/companion cell (SE/CC) unloading and post-

41 r subsequent active uptake into cells of the sieve element/companion cell complex.

42 n of wall ingrowths adjacent to cells of the sieve element/companion cell complex.

43 scular cambium, and in the phloem, including sieve-element/companion cell complexes, parenchyma, and

44 presence of CmNACP RNA in the companion cell-sieve element complex of leaf, stem and root phloem.

45 ting complex of the phloem (i.e., the C cell/sieve element complex).

46 er cell walls adjacent to the companion cell/sieve element complex.

47 s spectrometry-based proteomics of exudates, sieve element contents and microdissected stem tissues e

48 proteins (about 10%) were shared between the sieve element contents of FP and EFP, and enriched Gene

49 Adapted for effective transport, sieve elements develop as enucleated living cells.

50 Thus, sieve elements differentiate through a specialized autol

51 We show that sieve element differentiation involves enucleation, in w

52 s, and accumulates at the earliest stages of sieve element differentiation.

53 onsible for callose deposition in developing sieve elements during phloem formation and in mature phl

54 ehavior indicates that the GPA stylets found sieve elements faster when feeding on the adf3 mutant co

55 iant, interferes not only with commitment to sieve element fate but also with the formative sieve ele

56 etermines cellular commitment to protophloem sieve element fate, with OPS acting as a positive, quant

57 rs to be a secondary effect of discontinuous sieve element files and subsequent systemically reduced

58 US5 and SUS6) known to be confined to phloem sieve elements in Arabidopsis (Arabidopsis thaliana).

59 Suc unloading from de-energized protophloem sieve elements in meristematic zones may be mediated by

60 e RTM system may function within phloem, and sieve elements in particular, to restrict TEV long-dista

61 , we were able to locate the same FP-labeled sieve elements in semithin and ultrathin sections.

62 nated LM26, binds to the cell wall of phloem sieve elements in stems of Arabidopsis (Arabidopsis thal

63 ys of sucrose movement from endosperm to the sieve elements in the cotyledons.

64 Sieve elements in the phloem of most angiosperms contain

65 r than turgor reported in the literature for sieve elements in the stems of willow.

66 cell fractions and the contents of enucleate sieve elements, in the form of phloem sap, were used to

67 factor(s) functions at or beyond the C cell/sieve element interface with other cells to allow effici

68 RS6, selected from hybridomas raised against sieve elements isolated from California shield leaf (Str

69 In angiosperms, functional, mature sieve elements lack nuclei, vacuoles, ribosomes, and mos

70 ons, we identified the small heat shock-like SIEVE ELEMENT-LINING CHAPERONE1 (SLI1).

71 fic loss of proteins from companion cells to sieve elements may explain the plethora of macromolecule

72 d three-dimensional reconstruction to follow sieve element morphogenesis in Arabidopsis.

73 The sieve element occlusion (SEO) gene family originally was

74 Both types are encoded by members of the sieve element occlusion (SEO) gene family, which compris

75 sgenic lines expressing Arabidopsis thaliana Sieve-Element-Occlusion-Related1 (SEOR1)-yellow fluoresc

76 monstrate that gai RNA entry into functional sieve elements occurs via a selective process.

77 the GPA fed for a more prolonged period from sieve elements of adf3 compared to the wild-type plant.

78 lutionary origin for P-proteins found in the sieve elements of all dicotyledonous plants and demonstr

79 A spends more time actively feeding from the sieve elements of pad4 mutants than from wild-type plant

80 morphine detected corresponding antigens in sieve elements of the phloem, as described previously fo

81 s to exist between companion cells (CCs) and sieve elements of the phloem, which suggests that small

82 lized in slime plugs and P-protein bodies in sieve elements of the phloem.

83 ranscript distribution between meristems and sieve elements of the protophloem, suggesting CmNACP mRN

84 approximately 15 kD that is attached to the sieve element plasma membrane via a carboxy-terminal gly

85 eve element fate but also with the formative sieve element precursor cell division that creates proto

86 In the absence of the formative sieve element precursor cell division, metaphloem identi

87 tophloem in Arabidopsis roots by locking the sieve element precursor cell in its preceding developmen

88 Ultrastructural analysis of developing sieve elements revealed that callose failed to accumulat

89 is study dealt with the visualization of the sieve element (SE) cytoskeleton and its involvement in e

90 ed by its abbreviation SUmCR, yielded stable sieve element (SE) plasma membrane fluorescence labeling

91 tissue, whereas protein appears confined to sieve elements (SE).

92 In the sieve elements (SEs) of the phloem, carbohydrates are tr

93 and carboxy-terminal domains of the 21.5-kD sieve element-specific ENOD are posttranslationally clea

94 s in both floral and vegetative tissues, the sieve element-specific ENOD is expressed only within the

95 sely with plant height because of a shift in sieve element structure along the length of individual t

96 arenchyma or companion cells adjacent to the sieve elements, suggesting that the block in long-distan

97 In addition, once they found the sieve elements, the GPA fed for a more prolonged period

98 CmeIF5A was not necessary for entry into the sieve elements, this unique post-translational modificat

99 ly function in Suc retrieval into metaphloem sieve elements to maintain a high turgor to drive sympla

100 Entry of CmCPK1 into sieve elements via plasmodesmata and the potential roles

101 deposition in the phloem, especially in the sieve elements, was greatly reduced in cs7 mutants.

102 escent protein and RTM1 or RTM2 localized to sieve elements when expressed from their native regulato

103 owed that SLI1 is confined to the margins of sieve elements where it lines the parietal layer and col

104 ridine biosynthesis appears to occur only in sieve elements, whereas conversion of thebaine to morphi

105 , other than SbSUT4, were immunolocalized to sieve elements, while for elongating and recently elonga