ライフサイエンスコーパス: mesophyll cell

1 es but not in the most common cell type, the mesophyll cell.

2 ereas beta-glucans were more abundant in the mesophyll cells.

3 ates repression of rbcS-m3 reporter genes in mesophyll cells.

4 d to chloroplasts, in both bundle sheath and mesophyll cells.

5 ified Ins(3,4,5,6) P(4) 1-kinase activity in mesophyll cells.

6 4,5) P(3) and D- and/or L-Ins(3,5,6) P(3) in mesophyll cells.

7 onally there was necrosis of one or two host mesophyll cells.

8 in their chloroplast development compared to mesophyll cells.

9 the leaves or H2O2 challenge in the cultured mesophyll cells.

10 the vacuoles of bundle-sheath and paraveinal mesophyll cells.

11 fewer starch granules compared with control mesophyll cells.

12 l was 80-fold greater in guard cells than in mesophyll cells.

13 e interactions between the bundle sheath and mesophyll cells.

14 itrogen metabolism between bundle sheath and mesophyll cells.

15 esistant membranes from Arabidopsis thaliana mesophyll cells.

16 gene was expressed in both bundle sheath and mesophyll cells.

17 s, higher ploidy levels, and larger palisade mesophyll cells.

18 tal gradient and in mature bundle sheath and mesophyll cells.

19 while chloroplastic PPDK also accumulates in mesophyll cells.

20 ntially expressed in guard cells compared to mesophyll cells.

21 atterning with the development of underlying mesophyll cells.

22 K proteins operate cell-autonomously in leaf mesophyll cells.

23 mary acceptor for fixation of bicarbonate in mesophyll cells.

24 development, but is also sugar-inducible in mesophyll cells.

25 ulated Se in their leaf vascular tissues and mesophyll cells.

26 of a subset of auxin response genes in leaf mesophyll cells.

27 n phloem have abundant plasmodesmata between mesophyll cells.

28 as detected in xylem parenchyma, phloem, and mesophyll cells.

29 3 are required for suppressing expression in mesophyll cells.

30 enger for the activation of defense genes in mesophyll cells.

31 last cell or transported in from surrounding mesophyll cells.

32 requires different rbcS-m3 sequences than in mesophyll cells [31].

33 rmediate temperature reveal abnormally large mesophyll cells, a disorganized mesophyll layer, and col

34 inoculation with E. cichoracearum, and dead mesophyll cells accumulated in edr1 leaves starting 5 da

35 es, are located in the cytosol of paraveinal mesophyll cells and are active at pH values typically fo

36 tiation of cotyledon bundle sheath cells and mesophyll cells and for cell-type-specific expression of

37 These findings indicate that mesophyll cells and guard cells use distinct and differe

38 edominantly as sucrose, which is produced in mesophyll cells and imported into phloem cells for trans

39 ard cells, and low or undetectable levels in mesophyll cells and in roots.

40 eath in these plants was limited to palisade mesophyll cells and required light for induction.

41 nnels, linking it with Na(+) accumulation in mesophyll cells and salt bladders as well as leaf photos

42 luding the route of sucrose efflux from leaf mesophyll cells and transport across vacuolar membranes.

43 minantly in the intracellular compartment of mesophyll cells and was enriched in chloroplasts where i

44 leaves have dramatically elongated palisade mesophyll cells and, in some cases, increased leaf ploid

45 culent-like, have a second layer of palisade mesophyll cells, and are frequently shed during extreme

46 sma membrane region of leaf epidermal cells, mesophyll cells, and guard cells, where its distribution

47 otein indicated tonoplast location in spongy mesophyll cells, and high signal intensity in palisade m

48 ty was highest in vascular elements, in leaf mesophyll cells, and in root tips.

49 ng cells such as guard cells, trichomes, and mesophyll cells, and in vascular tissue.

50 The coordinated positioning of veins, mesophyll cells, and stomata across a leaf is crucial fo

51 altered leaf structure, a reduced number of mesophyll cells, and ultrastructural changes of the chlo

52 distinguished in tobacco (Nicotiana tabacum) mesophyll cells; and (c) shown that interaction between

53 normal chloroplasts, whereas chloroplasts in mesophyll cells are abnormal, reduced in number per cell

54 of photosynthesis in C4 plants, whereas the mesophyll cells are only involved in CO2 fixation.

55 ls were found to originate primarily in leaf mesophyll cells, as detected by aniline blue staining.

56 ls, whereas BAM3 is the dominant activity in mesophyll cells at night.

57 the conidium, and there was necrosis of host mesophyll cells at the sites of infection.

58 These two genes are not expressed in mesophyll cells but are in adjacent bundle-sheath cells

59 nals in the leaf vasculature and surrounding mesophyll cells but low-intensity signals are also detec

60 ecifically in leaf photosynthetically active mesophyll cells but not in other nonphotosynthetic tissu

61 re of barley plants to nitrate were large in mesophyll cells but small in epidermal cells.

62 in Nicotiana benthamiana leaf epidermal and mesophyll cells, but did not possess AO activity, as sho

63 uced ZNT1 transcript abundance in the spongy mesophyll cells, but less in the other cell types.

64 ts, photosynthesis occurs in both the BS and mesophyll cells, but the BS cells are the major sites of

65 ences was unable to move out of the injected mesophyll cells, but when PSTVd was fused to this transc

66 late biosynthetic steps occur in specialized mesophyll cells called idioblasts.

67 nthesized from guard cell RNA to that from a mesophyll cell cDNA probe.

68 ifferential development of bundle sheath and mesophyll cell chloroplasts, a screen of reticulate leaf

69 defective in plastid division, and its leaf mesophyll cells contain only one or two grossly enlarged

70 Furthermore, rapidly after transfer to Suc, mesophyll cells contained fewer and smaller plastids, wh

71 Adjacent bundle sheath and mesophyll cells cooperate for carbon fixation in the lea

72 (LLL) were used in a zinnia (Zinnia elegans) mesophyll cell culture system.

73 af surface while inducing both epidermal and mesophyll cell death.

74 evealed by transmission electron microscopy, mesophyll cells degrade chloroplasts, but degradation is

75 enhance photosynthetic capacity or increase mesophyll cell density.

76 nia, designated zIAA8, which is expressed by mesophyll cells differentiating as tracheary elements in

77 ing of subcellular compartments within plant mesophyll cells during haustoria ontogenesis.

78 GFP-fusion experiments in tobacco mesophyll cells established that the plant protein is ta

79 nforcement of the hinge through differential mesophyll cell expansion.

80 e metabolic cooperation of bundle sheath and mesophyll cells for C4 photosynthesis remains intact.

81 As a proof-of-concept approach, mesophyll cells from Arabidopsis thaliana were laser-mic

82 to study the physiology of ion transport in mesophyll cells from two Thlaspi spp. that differ signif

83 While the function of mesophyll cells, guard cells, phloem companion cells and

84 d classical Kranz anatomy with lightly lobed mesophyll cells having low chloroplast coverage.

85 ophyll cell system consists of isolated leaf mesophyll cells in culture that can be induced, by auxin

86 Expression was detected in mesophyll cells in leaves.

87 ein (MP), moved rapidly into the surrounding mesophyll cells in mature tobacco leaves of vector contr

88 h a fluorescent dye can traffic between leaf mesophyll cells in microinjection assays.

89 re readily detected in conducting as well as mesophyll cells in stems and source leaves.

90 lopment occurs between the bundle sheath and mesophyll cells in the Arabidopsis leaf.

91 n was strongest in all developing and mature mesophyll cells in the leaf, collar and sheath.

92 GUS activity was also detected in mesophyll cells in the outer husks of ear shoots and in

93 hnique to isolated vacuoles from Arabidopsis mesophyll cells in the whole-vacuole mode, we studied th

94 ell-specific metabolism, including guard and mesophyll cells, in order to elucidate mesophyll-derived

95 mechanism divided between bundle sheath and mesophyll cells increases photosynthetic efficiency.

96 leaf migrates from photosynthetically active mesophyll cells into the phloem down its concentration g

97 igrates passively through plasmodesmata from mesophyll cells into the sieve elements.

98 ated from Arabidopsis (Arabidopsis thaliana) mesophyll cells is mediated by two distinct membrane tra

99 er starch biosynthesis in guard cells and/or mesophyll cells is rate limiting for high CO2-induced st

100 mented transcriptional repression of RBCS in mesophyll cells is responsible for repressing LS synthes

101 Interestingly, mesophyll cells lacked the inward K+ current found in gu

102 ygenases (VLXs) accumulate in the paraveinal mesophyll cell layer of soybean (Glycine max L.) leaves

103 er major vein allocation, greater numbers of mesophyll cell layers and higher cell mass densities.

104 d for the three-dimensional (3D) geometry of mesophyll cells, leading to potential differences betwee

105 rker NADP-dependent malic enzyme but not the mesophyll cell marker phosphoenolpyruvate carboxylase, a

106 aize: bundle sheath cells (BSC) and adjacent mesophyll cells (MC).

107 ust above the ligule into highly specialized mesophyll cells (MCs) and bundle sheath cells (BSCs) at

108 different ABA responses in guard cell versus mesophyll cell metabolomes.

109 PSTVd injected into symplasmically connected mesophyll cells moved rapidly from cell to cell.

110 tation in TRY led to increased epidermal and mesophyll cell number, a reduction in endoreduplication

111 Mesophyll cells of 35S::Pto plants showed the accumulati

112 reductase in sap samples from epidermal and mesophyll cells of barley (Hordeum vulgare L.) and Arabi

113 In the presence of MV, isolated mesophyll cells of BS1-31 exhibited higher CO2 fixation

114 istance for diffusion of CO(2) to Rubisco in mesophyll cells of C(3) plants.

115 elop, TGA6 is expressed in aging cotyledons, mesophyll cells of hydathodes on leaf margins, vascular

116 GR protein was exclusively localized in the mesophyll cells of leaves at all growth temperatures, wh

117 However, in the mesophyll cells of leaves, AKT2 accounted for approximat

118 suberin-like lamellae in both epidermal and mesophyll cells of leaves.

119 2) activity was assayed in bundle sheath and mesophyll cells of maize (Zea mays L. var H99) from plan

120 Notably, the mesophyll cells of pgi1-2 leaves accumulated exceptional

121 Photosynthesis occurs in mesophyll cells of specialized organs such as leaves.

122 expressing a cytosolic GS1 isoenzyme in leaf mesophyll cells of tobacco.

123 idopsis was constructed and expressed in the mesophyll cells of transgenic tobacco plants.

124 auxin-induced gene were examined in isolated mesophyll cells of Zinnia and in the organs of Zinnia pl

125 Mechanically isolated mesophyll cells of Zinnia elegans L. cv Envy differentia

126 Two systems analyzed, cultured mesophyll cells of Zinnia elegans L. var. Envy and etiol

127 acheary elements (TEs) induced from isolated mesophyll cells of Zinnia elegans.

128 leaves, stems and sepals but not in petals, mesophyll cells or roots.

129 vation, or to H2O2 challenge in the cultured mesophyll cells, or to senescence in the leaves.

130 dles (perivascular), from the photosynthetic mesophyll cells, or within the vicinity of the stomatal

131 Mesophyll cells plasmolyzed in 600 mM sorbitol, whereas

132 n in guard cells but are starch deficient in mesophyll cells (plastidial phosphoglucose isomerase [pP

133 oted starch synthesis, restoring granules in mesophyll cell plastids.

134 Furthermore, dtx50 mutant mesophyll cells preloaded with ABA released less ABA com

135 When mesophyll cell protoplast mRNA (mesophyll mRNA) was expr

136 JUB1 transactivates DREB2A expression in mesophyll cell protoplasts and transgenic plants and bin

137 Here we applied patch clamp techniques to mesophyll cell protoplasts of fava bean (Vicia faba cv L

138 rom Arabidopsis thaliana leaf guard cell and mesophyll cell protoplasts was studied using the patch c

139 NAP transactivated the promoter of AAO3 in mesophyll cell protoplasts, and electrophoretic mobility

140 to I(Kout) observed from direct analysis of mesophyll cell protoplasts.

141 ental gradient and between bundle sheath and mesophyll cells, respectively.

142 ression profiles were compared with those of mesophyll cells, resulting in identification of 64 trans

143 the overexpression of cytosolic GS1 in leaf mesophyll cells seems to provide an alternate route to c

144 L2-5 and IL4-3 in detail and found increased mesophyll cell size and leaf ploidy levels, suggesting t

145 ltered in the green and white sectors of im: Mesophyll cell sizes are dramatically enlarged in the gr

146 ikinase and phosphoenolpyruvate carboxylase (mesophyll cell specific).

147 Expression of ZmPPCK1 in leaves is mesophyll cell-specific and light-induced, indicating th

148 ator in metabolic partitioning and reveals a mesophyll cell-specific requirement for the translocator

149 ealed significant accumulation of Rubisco in mesophyll cells, suggesting a continuing cell type-speci

150 The Zinnia mesophyll cell system consists of isolated leaf mesophyl

151 The Zinnia mesophyll cell system is a remarkable tool with which to

152 roplasts are more evenly distributed in leaf mesophyll cells than in the wild type.

153 In the isolated mesophyll cells, the mRNA accumulates in 48 hr of cultur

154 rated in the cytosol than in the vacuoles of mesophyll cells, thus increasing the driving force for p

155 ncluding an entirely symplastic pathway from mesophyll cells to sink tissues.

156 nergy is used to transfer sucrose (Suc) from mesophyll cells to the phloem of leaf minor veins agains

157 Chloroplasts in mesophyll cells typically contain five to seven granules

158 retention of substantial amounts of ptDNA in mesophyll cells until leaf necrosis.

159 uginosa pathogenesis are that the surface of mesophyll cell walls adopt an unusual convoluted or undu

160 lves perpendicularly to the outer surface of mesophyll cell walls, and that PA14 cells make circular

161 y equal to the diameter of P. aeruginosa, in mesophyll cell walls.

162 ABA signal transduction pathway observed in mesophyll cells was preserved in the frog oocytes.

163 hosphoenolpyruvate carboxylase (PEPC) in the mesophyll cells was studied.

164 Sucrose concentrations in mesophyll cells were greater than those reported in the

165 Highly pure preparations of guard cells and mesophyll cells were isolated in the presence of transcr

166 tion; we also observed severe alterations in mesophyll cells, which lack oil bodies and normal plasti

167 the vacuoles of bundle sheath and paraveinal mesophyll cells, while VLXA, B and C localized to the cy

168 Tobacco mesophyll cells will provide a useful model for function

169 is obligatory, because one can assay whether mesophyll cells with defective bundle sheath neighbors r

170 accumulates primarily phytoglycogen in leaf mesophyll cells, with only small amounts of starch in ot

171 alls of vascular parenchyma cells and spongy mesophyll cells within 4 hr after wounding of wild-type