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ARA7(Q69L) 在转基因拟南芥细胞中的表达诱导形成扩大的多泡体。

ARA7(Q69L) expression in transgenic Arabidopsis cells induces the formation of enlarged multivesicular bodies.

机构信息

School of Life Sciences, Centre for Cell and Developmental Biology, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China.

出版信息

J Exp Bot. 2013 Jul;64(10):2817-29. doi: 10.1093/jxb/ert125. Epub 2013 May 16.

DOI:10.1093/jxb/ert125
PMID:23682115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3697957/
Abstract

Arabidopsis thaliana ARA7 (AtRabF2b), a member of the plant Rab5 small GTPases functioning in the vacuolar transport pathway, localizes to pre-vacuolar compartments (PVCs), known as multivesicular bodies (MVBs) in plant cells. Overexpression of the constitutively active GTP-bound mutant of ARA7, ARA7(Q69L), induces the formation of large ring-like structures (1-2 µm in diameter). To better understand the biology of these ARA7(Q69L)-induced ring-like structures, transgenic Arabidopsis cell lines expressing ARA7(Q69L) tagged with green fluorescent protein (GFP) under the control of a heat shock-inducible promoter were generated. In these transgenic cells, robust ring-like structures were formed after 4 h of heat shock induction. Transient co-expression, confocal imaging, and immunogold electron microscopy (immunogold-EM) experiments demonstrated that these GFP-ARA7(Q69L)-labelled ring-like structures were distinct from the Golgi apparatus and trans-Golgi network, but were labelled with an antibody against an MVB marker protein. In addition, live cell imaging and detailed EM analysis showed that the GFP-ARA7(Q69L)-induced spherical structures originated from the homotypic fusion of MVBs. In summary, it was demonstrated that GFP-ARA7(Q69L) expression is an efficient tool for studying PVC/MVB-mediated protein trafficking and vacuolar degradation in plant cells.

摘要

拟南芥 ARA7(AtRabF2b)是植物 Rab5 小 GTPases 家族的一员,在液泡运输途径中发挥作用,定位于前液泡区室(PVC),在植物细胞中称为多泡体(MVB)。ARA7 的组成型活性 GTP 结合突变体 ARA7(Q69L)的过表达诱导大环状结构(直径 1-2µm)的形成。为了更好地理解这些 ARA7(Q69L)诱导的环状结构的生物学特性,生成了在热休克诱导启动子控制下表达 GFP 标记的 ARA7(Q69L)的转基因拟南芥细胞系。在这些转基因细胞中,热休克诱导 4 小时后形成了强烈的环状结构。瞬时共表达、共聚焦成像和免疫金电子显微镜(免疫金电镜)实验表明,这些 GFP-ARA7(Q69L)标记的环状结构与高尔基体和反式高尔基体网络不同,但与 MVB 标记蛋白的抗体标记。此外,活细胞成像和详细的 EM 分析表明,GFP-ARA7(Q69L)诱导的球形结构来源于 MVB 的同源融合。总之,证明 GFP-ARA7(Q69L)的表达是研究植物细胞中 PVC/MVB 介导的蛋白质运输和液泡降解的有效工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/432fd4921413/exbotj_ert125_f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/af9b8d803188/exbotj_ert125_f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/652d8a7c2edc/exbotj_ert125_f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/ef5186ed895b/exbotj_ert125_f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/ac8b89a51904/exbotj_ert125_f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/2e007599ebda/exbotj_ert125_f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/3678cd669528/exbotj_ert125_f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/7146fbf75a79/exbotj_ert125_f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/89d9dec3f848/exbotj_ert125_f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/432fd4921413/exbotj_ert125_f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/af9b8d803188/exbotj_ert125_f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/652d8a7c2edc/exbotj_ert125_f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/ef5186ed895b/exbotj_ert125_f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/ac8b89a51904/exbotj_ert125_f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/2e007599ebda/exbotj_ert125_f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/3678cd669528/exbotj_ert125_f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/7146fbf75a79/exbotj_ert125_f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/89d9dec3f848/exbotj_ert125_f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/897b/3697957/432fd4921413/exbotj_ert125_f0009.jpg

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