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Angus Murphy answers a few questions about this month's
new hot paper in the field of Plant & Animal Science.
From
•>>March 2007
Field:
Plant & Animal Science
Article Title: Cellular efflux of auxin catalyzed by the
Arabidopsis
MDR/PGP transporter AtPGP1
Authors: Geisler, M;Blakeslee, JJ;Bouchard, R;Lee,
OR;Vincenzetti, V;Bandyopadhyay, A;Titapiwatanakun, B;Peer,
WA;Bailly, A;Richards, EL;Ejenda, KFK;Smith, AP;Baroux,
C;Grossniklaus, U;Muller, A;Hrycyna, CA;Dudler, R;Murphy,
AS;Martinoia, E
Journal: PLANT J
Volume: 44
Issue: 2
Page: 179-194
Year: OCT 2005
* Purdue Univ, Dept Hort, W Lafayette, IN 47907 USA.
* Purdue Univ, Dept Hort, W Lafayette, IN 47907 USA.
* Univ Zurich, Inst Plant Biol, Basel Zurich Plant Sci Ctr, CH-8007 Zurich, Switzerland.
* Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA.
* Ruhr Univ Bochum, Lehrstuhl Pflanzenphysiol, D-44801
Bochum, Germany.
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Why
do you think your paper is highly cited?
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“In this paper, we showed that PGPs directly mediated cellular auxin transport. This is quite significant, as PGP1 was found to have much narrower substrate specificity than its mammalian
homologs.”
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Until the publication of this paper, there was no clear
documentation of cellular efflux of the plant hormone auxin.
Physiological and developmental studies had strongly implicated the
PIN efflux carriers and P-glycoproteins (PGPs) in auxin efflux, but
the mechanism had not been demonstrated. The PIN proteins had been
shown to be required for normal polar development and to align with
the transport vector, so it was presumed that PGPs regulated PIN
activity and/or membrane stability.
In this paper, we showed that PGPs directly mediated cellular
auxin transport. This is quite significant, as PGP1 was found to
have much narrower substrate specificity than its mammalian homologs.
The paper is also very thorough, as it reports on a collaborative
effort between Professor Enrico Martinoia’s group at the
University of Zurich and my own.
Does
it describe a new discovery, methodology, or synthesis of knowledge?
The paper described new applications and refinements of existing
methodologies. PGPs were successfully expressed in yeast and human
HeLa cell lines. A HeLa cell is an immortal cell line used in
medical research. The HeLa cell line was derived from cervical
cancer cells taken from Henrietta Lacks, who died from her cancer in
1951.
A method developed in our lab to track radiolabelled auxin
applied in nanoliter quantities was refined to track hormone
movement through small tissues, and protoplast transport assays were
used to monitor cellular auxin efflux. PGPs were also
immunolocalized in plant tissues for the first time.
Could
you summarize the significance of your paper in layman’s terms?
This and successive papers using its methodology have removed the
word "putative" from the designation of the auxin efflux
and influx proteins, thus paving the way for a new understanding of
how this hormone functions in plant development.
How
did you become involved in this research, and were there obstacles
along the way?
I had no intention of working in the area of auxin transport. A
mistake made while working on anion transporters and their role in
metal ion homeostasis produced a startling outcome that resulted in
the identification of PGPs as components of auxin transport
complexes.
Are
there any social or political implications for your research?
Manipulation of plant form is one of the most expensive aspects
of horticulture. More recently, we have shown that manipulation of
plant architecture via modulation of auxin transport streams can be
used to produce crop plants with enhanced mineral nutrition and
water-stress tolerance.
Angus Murphy
Associate Professor
Department of Horticulture
Purdue University
West Lafayette, IN, USA
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ESI Special Topics,
March 2007
Citing URL - http://www.esi-topics.com/nhp/2007/march-07-AngusMurphy.html
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