Characterization of a protein of the plastid inner envelope having homology to animal inorganic phosphate, chloride and organic-anion transporters.
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State: Public
Version: Final published version
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It was possible to publish this article open access thanks to a Swiss National Licence with the publisher.
State: Public
Version: Final published version
License: Not specified
It was possible to publish this article open access thanks to a Swiss National Licence with the publisher.
Serval ID
serval:BIB_3FE838835B1A
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Characterization of a protein of the plastid inner envelope having homology to animal inorganic phosphate, chloride and organic-anion transporters.
Journal
Planta
ISSN
0032-0935 (Print)
ISSN-L
0032-0935
Publication state
Published
Issued date
2004
Volume
218
Number
3
Pages
406-416
Language
english
Abstract
A protein from Arabidopsis thaliana (L.) Heynh. showing homology to animal proteins of the NaPi-1 family, involved in the transport of inorganic phosphate, chloride, glutamate and sialic acid, has been characterized. This protein, named ANTR2 (for anion transporters) was shown by chloroplast subfractionation to be localized to the plastid inner envelope in both A. thaliana and Spinacia oleracea (L.). Immunolocalization revealed that ANTR2 was expressed in the leaf mesophyll cells as well as in the developing embryo at the upturned-U stage. Five additional homologues of ANTR2 are found in the Arabidopsis genome, of which one was shown by green fluorescent protein (GFP) fusion to be also located in the chloroplast. All ANTR proteins share homology to the animal NaPi-1 family, as well as to other organic-anion transporters that are members of the Anion:Cation Symporter (ACS) family, and share the main features of transporters from this family, including the presence of 12 putative transmembrane domains and of a 7-amino acid motif in the fourth putative transmembrane domain. ANTR2 thus represent a novel protein of the plastid inner envelope that is likely to be involved in anion transport.
Keywords
Amino Acid Sequence, Animals, Anion Transport Proteins/chemistry, Anion Transport Proteins/genetics, Arabidopsis/genetics, Arabidopsis/metabolism, Arabidopsis Proteins/genetics, Arabidopsis Proteins/metabolism, Caenorhabditis elegans/genetics, Carrier Proteins/chemistry, Carrier Proteins/genetics, Cloning, Molecular, Escherichia coli/genetics, Escherichia coli/metabolism, Humans, Membrane Transport Proteins, Molecular Sequence Data, Phosphate Transport Proteins/chemistry, Phosphate Transport Proteins/genetics, Plastids/genetics, Sequence Alignment, Sequence Homology, Amino Acid, Symporters/chemistry, Symporters/genetics, Vesicular Glutamate Transport Protein 1, Vesicular Transport Proteins
Pubmed
Web of science
Open Access
Yes
Create date
24/01/2008 19:42
Last modification date
14/02/2022 7:54