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1.
Biochem J ; 356(Pt 2): 589-94, 2001 Jun 01.
Article in English | MEDLINE | ID: mdl-11368789

ABSTRACT

The sulphate transporter SHST1, from Stylosanthes hamata, features three tightly coupled transmembrane helices which include proline residues that are conserved in most related transporters. We used site-directed mutagenesis and expression of the mutant transporters in yeast to test whether these proline residues are important for function. Four proline residues were replaced by both alanine and leucine. Only one of these proline residues, Pro-144, was essential for sulphate transport. However, mutation of either Pro-133 or Pro-160 resulted in a severe decrease in sulphate transport activity; this was due more to a decrease in transport activity than to a decrease in the amount of mutant SHST1 in the plasma membrane. These results suggest that all three proline residues are important for transport, and that the conformation of the three tightly coupled helices may play a critical role in sulphate transport. We also show that SHST1 undergoes a post-translational modification that is required for trafficking to the plasma membrane.


Subject(s)
Carrier Proteins/chemistry , Carrier Proteins/metabolism , Membrane Transport Proteins , Plant Proteins/chemistry , Plant Proteins/metabolism , Amino Acid Sequence , Binding Sites , Carrier Proteins/genetics , Cell Membrane/metabolism , Fabaceae/genetics , Fabaceae/metabolism , Kinetics , Molecular Sequence Data , Mutagenesis, Site-Directed , Plant Proteins/genetics , Plants, Medicinal , Proline/chemistry , Protein Processing, Post-Translational , Protein Structure, Secondary , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae/growth & development , Saccharomyces cerevisiae/metabolism , Sequence Homology, Amino Acid , Sulfate Transporters
2.
FEBS Lett ; 477(1-2): 118-22, 2000 Jul 14.
Article in English | MEDLINE | ID: mdl-10899321

ABSTRACT

Mutations in the human sulphate transporter gene, DTDST, have been implicated in several diseases. Analysis of affected patients has linked disease symptoms to faulty sulphate transporter activity. We have reproduced two of these mutations in SHST1, a homologous member of the family isolated from the tropical legume, Stylosanthes hamata. Both mutations significantly reduce sulphate transport activity of SHST1. These results indicate that conserved residues between distinct members of the family may share essential roles in structure or function. The results also suggest that putative helix 9 may be important for stability and/or trafficking of SHST1 to the plasma membrane.


Subject(s)
Fabaceae , Mutation/genetics , Plants, Medicinal , Amino Acid Sequence , Amino Acid Substitution/genetics , Anion Transport Proteins , Biological Transport , Blotting, Western , Carrier Proteins/chemistry , Carrier Proteins/genetics , Carrier Proteins/metabolism , Cell Membrane/metabolism , Conserved Sequence/genetics , Genetic Complementation Test , Humans , Kinetics , Membrane Transport Proteins , Molecular Sequence Data , Saccharomyces cerevisiae/cytology , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae/growth & development , Saccharomyces cerevisiae/metabolism , Sequence Alignment , Structure-Activity Relationship , Sulfate Transporters , Thermodynamics
3.
FEBS Lett ; 467(2-3): 273-8, 2000 Feb 11.
Article in English | MEDLINE | ID: mdl-10675553

ABSTRACT

We have cloned and characterized the first member of a novel family of ammonium transporters in plants: AtAMT2 from Arabidopsis thaliana. AtAMT2 is more closely related to bacterial ammonium transporters than to plant transporters of the AMT1 family. The protein was expressed and functionally characterized in yeast. AtAMT2 transported ammonium in an energy-dependent manner. In contrast to transporters of the AMT1 family, however, AtAMT2 did not transport the ammonium analogue, methylammonium. AtAMT2 was expressed more highly in shoots than roots and was subject to nitrogen regulation.


Subject(s)
Arabidopsis/genetics , Plant Proteins/genetics , Amino Acid Sequence , Cloning, Molecular , DNA, Complementary/chemistry , Genetic Complementation Test , Molecular Sequence Data , Phylogeny , Plant Proteins/biosynthesis , Plant Proteins/chemistry , Quaternary Ammonium Compounds/metabolism , Sequence Alignment , Yeasts/metabolism
4.
Semin Speech Lang ; 17(2): 131-41; quiz 141-2, 1996 May.
Article in English | MEDLINE | ID: mdl-8727277

ABSTRACT

Early intervention services have expanded the concept of team participation for speech-language pathologists. Unlike traditional teams that grew out of the individual, direct service model of treatment, early intervention teams include the child's family along with professionals. Family members are invited to participate in assessing and treating their child, and the child is seen from a slightly different perspective by each team participant. Different viewpoints must be integrated and used to the benefit of the child. In this way, treatment options are expanded. Further, professionals may release their roles to other team members as well as learn new skills from other team members. The process of team development is illustrated through the experiences of one family-centered early intervention team.


Subject(s)
Patient Care Team , Speech-Language Pathology/organization & administration , Humans
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