Actin Turnover Is Required for Myosin-Dependent Mitochondrial Movements in Arabidopsis Root Hairs 英文参考文献.docVIP
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Actin Turnover Is Required for Myosin-Dependent Mitochondrial Movements in Arabidopsis Root Hairs 英文参考文献
ActinTurnoverIsRequiredforMyosin-Dependent
MitochondrialMovementsinArabidopsisRootHairs
MaozhongZheng1,2,MartinaBeck3,JensMu¨ller3,TongChen1,XiaohuaWang1,2,FengWang1,2 ,Qinli
Wang1,YuqingWang1,2,Frantisˇek Balusˇka3,4,DavidC.Logan5,JozefSamajˇ 3,6,7,JinxingLin1*
1Key Laboratory of Photosynthesis and Molecular Environmental Physiology, Institute of Botany, Chinese Academy of Sciences, Beijing, China, 2Graduate School of
Chinese Academy of Sciences, Beijing, China, 3Institute of Cellular and Molecular Botany, Rheinische Friedrich-Wilhelms-University Bonn, Department of Plant Cell
Biology,Bonn,Germany,4InstituteofBotany,SlovakAcademyofSciences,Bratislava,SlovakRepublic,5DepartmentofBiology,UniversityofSaskatchewan,Saskatoon,
Saskatchewan, Canada, 6Institute of Plant Genetics and Biotechnology, Slovak Academy of Sciences, Nitra, Slovak Republic, 7Faculty of Science, Palacky′ University
Olomouc,Olomouc,CzechRepublic
Abstract
Background: Previousstudies haveshown thatplantmitochondrial movementsaremyosin-basedalong actinfilaments,
which undergo continuous turnover by the exchange of actin subunits from existing filaments. Although earlier studies
revealed that actin filament dynamics are essential for many functions of the actin cytoskeleton, there are little data
connectingactindynamicsandmitochondrialmovements.
Methodology/Principal Findings: We addressed the role of actin filament dynamics in the control of mitochondrial
movementsbytreating cells withvarious pharmaceuticals thataffectactin filamentassemblyanddisassembly. Confocal
microscopy of Arabidopsis thaliana root hairs expressing GFP-FABD2 as an actin filament reporter showed that
mitochondrial distribution was in agreement with the arrangement of actin filaments in root hairs at different
developmental stages. Analyses of mitochondrial trajectories and instantaneous velocities immediately following
pharmacologicalperturbationofthecytoskeletonusingvariable-angleevanescentwavemicroscopyand/orsp
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