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An Arabidopsis GPI-Anchor Plasmodesmal Neck Protein with Callose Binding Activity and Potential to Regulate Cell-to-Cell Trafficking
被引:240
作者:
Simpson, Clare
[1
]
Thomas, Carole
[1
]
Findlay, Kim
[1
]
Bayer, Emmanuelle
[1
]
Maule, Andrew J.
[1
]
机构:
[1] John Innes Ctr Plant Sci Res, Norwich NR4 7UH, Norfolk, England
来源:
关键词:
VIRUS MOVEMENT PROTEIN;
INTERCELLULAR PROTEIN;
FLUORESCENT PROTEIN;
MAJOR ALLERGEN;
MESSENGER-RNA;
TOBACCO BY-2;
POLLEN TUBES;
PLANT-CELLS;
X TGBP1;
EXPRESSION;
D O I:
10.1105/tpc.108.060145
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Plasmodesmata (Pds) traverse the cell wall to establish a symplastic continuum through most of the plant. Rapid and reversible deposition of callose in the cell wall surrounding the Pd apertures is proposed to provide a regulatory process through physical constriction of the symplastic channel. We identified members within a larger family of X8 domain-containing proteins that targeted to Pds. This subgroup of proteins contains signal sequences for a glycosylphosphatidylinositol linkage to the extracellular face of the plasma membrane. We focused our attention on three closely related members of this family, two of which specifically bind to 1,3-beta-glucans (callose) in vitro. We named this family of proteins Pd callose binding proteins (PDCBs). Yellow fluorescent protein-PDCB1 was found to localize to the neck region of Pds with potential to provide a structural anchor between the plasma membrane component of Pds and the cell wall. PDCB1, PDCB2, and PDCB3 had overlapping and widespread patterns of expression, but neither single nor combined insertional mutants for PDCB2 and PDCB3 showed any visible phenotype. However, increased expression of PDCB1 led to an increase in callose accumulation and a reduction of green fluorescent protein (GFP) movement in a GFP diffusion assay, identifying a potential association between PDCB-mediated callose deposition and plant cell-to-cell communication.
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页码:581 / 594
页数:14
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