Detailed Information on Publication Record
2013
Overexpression of the Auxin Binding PROTEIN1 Modulates PIN-Dependent Auxin Transport in Tobacco Cells
COVANOVA, Milada, Michael SAUER, Jan RYCHTAR, Jiří FRIML, Jan PETRASEK et. al.Basic information
Original name
Overexpression of the Auxin Binding PROTEIN1 Modulates PIN-Dependent Auxin Transport in Tobacco Cells
Authors
COVANOVA, Milada (203 Czech Republic), Michael SAUER (56 Belgium), Jan RYCHTAR (840 United States of America), Jiří FRIML (203 Czech Republic, guarantor, belonging to the institution), Jan PETRASEK (203 Czech Republic) and Eva ZAŽÍMALOVÁ (203 Czech Republic)
Edition
Plos One, SAN FRANCISCO, PUBLIC LIBRARY SCIENCE, 2013, 1932-6203
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
Genetics and molecular biology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 3.534
RIV identification code
RIV/00216224:14740/13:00072089
Organization unit
Central European Institute of Technology
UT WoS
000325211000181
Keywords in English
ZEA-MAYS-L; PLANT HORMONE AUXIN; MEMBRANE H+-ATPASE; PLASMA-MEMBRANE; COLEOPTILE MEMBRANES; MOLECULAR-CLONING; POLAR TRANSPORT; ARABIDOPSIS; EFFLUX; DIVISION
Tags
International impact, Reviewed
Změněno: 13/2/2014 21:45, Olga Křížová
Abstract
V originále
Background: Auxin binding protein 1 (ABP1) is a putative auxin receptor and its function is indispensable for plant growth and development. ABP1 has been shown to be involved in auxin-dependent regulation of cell division and expansion, in plasma-membrane-related processes such as changes in transmembrane potential, and in the regulation of clathrin-dependent endocytosis. However, the ABP1-regulated downstream pathway remains elusive. Methodology/Principal Findings: Using auxin transport assays and quantitative analysis of cellular morphology we show that ABP1 regulates auxin efflux from tobacco BY-2 cells. The overexpression of ABP1can counterbalance increased auxin efflux and auxin starvation phenotypes caused by the overexpression of PIN auxin efflux carrier. Relevant mechanism involves the ABP1-controlled vesicle trafficking processes, including positive regulation of endocytosis of PIN auxin efflux carriers, as indicated by fluorescence recovery after photobleaching (FRAP) and pharmacological manipulations. Conclusions/Significance: The findings indicate the involvement of ABP1 in control of rate of auxin transport across plasma membrane emphasizing the role of ABP1 in regulation of PIN activity at the plasma membrane, and highlighting the relevance of ABP1 for the formation of developmentally important, PIN-dependent auxin gradients.