A Membrane Microdomain-Associated Protein, Arabidopsis Flot1, Is Involved in a Clathrin-Independent Endocytic Pathway and Is Required for Seedling Development

被引:162
作者
Li, Ruili [1 ,2 ]
Liu, Peng [1 ,2 ]
Wan, Yinglang [1 ]
Chen, Tong [1 ]
Wang, Qinli [1 ]
Mettbach, Ursula [3 ]
Baluska, Frantisek [3 ]
Samaj, Jozef [4 ]
Fang, Xiaohong [5 ]
Lucas, William J. [6 ]
Lin, Jinxing [1 ]
机构
[1] Chinese Acad Sci, Inst Bot, Key Lab Plant Mol Physiol, Beijing 100093, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
[3] Univ Bonn, Dept Plant Cell Biol, Inst Cellular & Mol Bot, D-53115 Bonn, Germany
[4] Palacky Univ, Fac Sci, Ctr Reg Hana Biotechnol & Agr Res, Olomouc 78301, Czech Republic
[5] Chinese Acad Sci, Inst Chem, Key Lab Mol Nanostruct & Nanotechnol, Beijing 100190, Peoples R China
[6] Univ Calif Davis, Dept Plant Biol, Coll Biol Sci, Davis, CA 95616 USA
基金
中国国家自然科学基金;
关键词
DETERGENT-RESISTANT MEMBRANES; LIPID RAFTS; PROTEOMIC ANALYSIS; ARTIFICIAL MICRORNAS; POLLEN TUBES; PLANT-CELLS; DYNAMICS; GENE; CYTOSKELETON; TRAFFICKING;
D O I
10.1105/tpc.112.095695
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
Endocytosis is essential for the maintenance of protein and lipid compositions in the plasma membrane and for the acquisition of materials from the extracellular space. Clathrin-dependent and -independent endocytic processes are well established in yeast and animals; however, endocytic pathways involved in cargo internalization and intracellular trafficking remain to be fully elucidated for plants. Here, we used transgenic green fluorescent protein-flotillin1 (GFP-Flot1) Arabidopsis thaliana plants in combination with confocal microscopy analysis and transmission electron microscopy immunogold labeling to study the spatial and dynamic aspects of GFP-Flot1-positive vesicle formation. Vesicle size, as outlined by the gold particles, was; similar to 100 nm, which is larger than the 30-nm size of clathrin-coated vesicles. GFP-Flot1 also did not colocalize with clathrin light chain-mOrange. Variable-angle total internal reflection fluorescence microscopy also revealed that the dynamic behavior of GFP-Flot1-positive puncta was different from that of clathrin light chain-mOrange puncta. Furthermore, disruption of membrane microdomains caused a significant alteration in the dynamics of Flot1-positive puncta. Analysis of artificial microRNA Flot1 transgenic Arabidopsis lines established that a reduction in Flot1 transcript levels gave rise to a reduction in shoot and root meristem size plus retardation in seedling growth. Taken together, these findings support the hypothesis that, in plant cells, Flot1 is involved in a clathrin-independent endocytic pathway and functions in seedling development.
引用
收藏
页码:2105 / 2122
页数:18
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