Comparative Functional Features of Plant Potassium HvHAK1 and HvHAK2 Transporters
Plant K + transporters of the HAK family belong to four rather divergent phylogenetic clusters, although most of the transporters belong to clusters I or II. A simple phylogenetic analysis of fungal and plant HAK transporters suggests that an original HAK gene duplicated even before fungi and plants...
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Veröffentlicht in: | The Journal of biological chemistry 2001-11, Vol.276 (48), p.44563-44569 |
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container_issue | 48 |
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container_title | The Journal of biological chemistry |
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creator | Senn, Marı́a E. Rubio, Francisco Bañuelos, Marı́a A. Rodrı́guez-Navarro, Alonso |
description | Plant K + transporters of the HAK family belong to four rather divergent phylogenetic clusters, although most of the transporters belong
to clusters I or II. A simple phylogenetic analysis of fungal and plant HAK transporters suggests that an original HAK gene duplicated even before fungi and plants diverged, generating transporters that at present fulfill different functions
in the plant. The HvHAK1 transporter belongs to cluster I and mediates high-affinity K + uptake in barley roots, but no function is known for the cluster II transporter, HvHAK2, which is not functional in yeast.
The function of HvHAK2 was investigated by constructing HvHAK1-HAK2 chimeric transporters, which were not functional even
when they included only short fragments of HvHAK2. Then, amino acids characteristic of cluster II in the N terminus and in
the first transmembrane domain were introduced into HvHAK1. All of these changes increased the Rb +
K
m , introducing minimal changes in the Na + K
m , which suggested that HvHAK2 is a low-affinity, Na + -sensitive K + transporter. Using a K + -defective Escherichia coli mutant, we functionally expressed HvHAK2 and found that the predicted characteristics were correct, as well as discovering
that the bacterial expression of HvHAK2 is functional at pH 5.5 but not at 7.5. We discuss whether HvHAK2 may be a tonoplast
transporter effective for vacuolar K + depletion in K + starved plants. |
doi_str_mv | 10.1074/jbc.M108129200 |
format | Article |
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to clusters I or II. A simple phylogenetic analysis of fungal and plant HAK transporters suggests that an original HAK gene duplicated even before fungi and plants diverged, generating transporters that at present fulfill different functions
in the plant. The HvHAK1 transporter belongs to cluster I and mediates high-affinity K + uptake in barley roots, but no function is known for the cluster II transporter, HvHAK2, which is not functional in yeast.
The function of HvHAK2 was investigated by constructing HvHAK1-HAK2 chimeric transporters, which were not functional even
when they included only short fragments of HvHAK2. Then, amino acids characteristic of cluster II in the N terminus and in
the first transmembrane domain were introduced into HvHAK1. All of these changes increased the Rb +
K
m , introducing minimal changes in the Na + K
m , which suggested that HvHAK2 is a low-affinity, Na + -sensitive K + transporter. Using a K + -defective Escherichia coli mutant, we functionally expressed HvHAK2 and found that the predicted characteristics were correct, as well as discovering
that the bacterial expression of HvHAK2 is functional at pH 5.5 but not at 7.5. We discuss whether HvHAK2 may be a tonoplast
transporter effective for vacuolar K + depletion in K + starved plants.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M108129200</identifier><identifier>PMID: 11562376</identifier><language>eng</language><publisher>United States: American Society for Biochemistry and Molecular Biology</publisher><subject>Amino Acid Sequence ; Arabinose - pharmacology ; Biological Transport ; Cation Transport Proteins - chemistry ; Dose-Response Relationship, Drug ; Escherichia coli - genetics ; Escherichia coli - metabolism ; HAK gene ; Hordeum - metabolism ; Hordeum vulgare ; HvHAK1 protein ; HvHAK2 protein ; Hydrogen-Ion Concentration ; Kinetics ; Molecular Sequence Data ; Mutagenesis ; Mutation ; Plant Proteins - metabolism ; Plasmids - metabolism ; Potassium - metabolism ; Potassium Chloride - pharmacology ; Protein Structure, Tertiary ; Sequence Homology, Amino Acid ; Time Factors ; Vacuoles</subject><ispartof>The Journal of biological chemistry, 2001-11, Vol.276 (48), p.44563-44569</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c502t-f34e2471624b00a835bc30936df93a650d007be2757d7c6f36865e9fd582e4a93</citedby><cites>FETCH-LOGICAL-c502t-f34e2471624b00a835bc30936df93a650d007be2757d7c6f36865e9fd582e4a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11562376$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Senn, Marı́a E.</creatorcontrib><creatorcontrib>Rubio, Francisco</creatorcontrib><creatorcontrib>Bañuelos, Marı́a A.</creatorcontrib><creatorcontrib>Rodrı́guez-Navarro, Alonso</creatorcontrib><title>Comparative Functional Features of Plant Potassium HvHAK1 and HvHAK2 Transporters</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Plant K + transporters of the HAK family belong to four rather divergent phylogenetic clusters, although most of the transporters belong
to clusters I or II. A simple phylogenetic analysis of fungal and plant HAK transporters suggests that an original HAK gene duplicated even before fungi and plants diverged, generating transporters that at present fulfill different functions
in the plant. The HvHAK1 transporter belongs to cluster I and mediates high-affinity K + uptake in barley roots, but no function is known for the cluster II transporter, HvHAK2, which is not functional in yeast.
The function of HvHAK2 was investigated by constructing HvHAK1-HAK2 chimeric transporters, which were not functional even
when they included only short fragments of HvHAK2. Then, amino acids characteristic of cluster II in the N terminus and in
the first transmembrane domain were introduced into HvHAK1. All of these changes increased the Rb +
K
m , introducing minimal changes in the Na + K
m , which suggested that HvHAK2 is a low-affinity, Na + -sensitive K + transporter. Using a K + -defective Escherichia coli mutant, we functionally expressed HvHAK2 and found that the predicted characteristics were correct, as well as discovering
that the bacterial expression of HvHAK2 is functional at pH 5.5 but not at 7.5. We discuss whether HvHAK2 may be a tonoplast
transporter effective for vacuolar K + depletion in K + starved plants.</description><subject>Amino Acid Sequence</subject><subject>Arabinose - pharmacology</subject><subject>Biological Transport</subject><subject>Cation Transport Proteins - chemistry</subject><subject>Dose-Response Relationship, Drug</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - metabolism</subject><subject>HAK gene</subject><subject>Hordeum - metabolism</subject><subject>Hordeum vulgare</subject><subject>HvHAK1 protein</subject><subject>HvHAK2 protein</subject><subject>Hydrogen-Ion Concentration</subject><subject>Kinetics</subject><subject>Molecular Sequence Data</subject><subject>Mutagenesis</subject><subject>Mutation</subject><subject>Plant Proteins - metabolism</subject><subject>Plasmids - metabolism</subject><subject>Potassium - metabolism</subject><subject>Potassium Chloride - pharmacology</subject><subject>Protein Structure, Tertiary</subject><subject>Sequence Homology, Amino Acid</subject><subject>Time Factors</subject><subject>Vacuoles</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkM9LwzAYhoMobk6vHqUH8daZ32mPMpwTJ06Y4C2kaeoy2mYm6cT_3koH-y7fe3i-l48HgGsEpwgKer8t9PQVwQzhHEN4AsZ9Jilh6PMUjCHEKM0xy0bgIoQt7Ifm6ByMEGIcE8HH4H3mmp3yKtq9SeZdq6N1raqTuVGx8yYkrkpWtWpjsnJRhWC7JlnsFw8vKFFtOUScrL1qw875aHy4BGeVqoO5OuwJ-Jg_rmeLdPn29Dx7WKaaQRzTilCDqUAc0wJClRFWaAJzwssqJ4ozWEIoCoMFE6XQvCI848zkVckybKjKyQTcDb077747E6JsbNCm7p81rgsSZYgiQlAPTgdQexeCN5Xcedso_ysRlP8SZS9RHiX2BzeH5q5oTHnED9Z64HYANvZr82O9kYV1emMaiQWXNJOUMk7IH2a9d3c</recordid><startdate>20011130</startdate><enddate>20011130</enddate><creator>Senn, Marı́a E.</creator><creator>Rubio, Francisco</creator><creator>Bañuelos, Marı́a A.</creator><creator>Rodrı́guez-Navarro, Alonso</creator><general>American Society for Biochemistry and Molecular Biology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20011130</creationdate><title>Comparative Functional Features of Plant Potassium HvHAK1 and HvHAK2 Transporters</title><author>Senn, Marı́a E. ; Rubio, Francisco ; Bañuelos, Marı́a A. ; Rodrı́guez-Navarro, Alonso</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c502t-f34e2471624b00a835bc30936df93a650d007be2757d7c6f36865e9fd582e4a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Amino Acid Sequence</topic><topic>Arabinose - pharmacology</topic><topic>Biological Transport</topic><topic>Cation Transport Proteins - chemistry</topic><topic>Dose-Response Relationship, Drug</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - metabolism</topic><topic>HAK gene</topic><topic>Hordeum - metabolism</topic><topic>Hordeum vulgare</topic><topic>HvHAK1 protein</topic><topic>HvHAK2 protein</topic><topic>Hydrogen-Ion Concentration</topic><topic>Kinetics</topic><topic>Molecular Sequence Data</topic><topic>Mutagenesis</topic><topic>Mutation</topic><topic>Plant Proteins - metabolism</topic><topic>Plasmids - metabolism</topic><topic>Potassium - metabolism</topic><topic>Potassium Chloride - pharmacology</topic><topic>Protein Structure, Tertiary</topic><topic>Sequence Homology, Amino Acid</topic><topic>Time Factors</topic><topic>Vacuoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Senn, Marı́a E.</creatorcontrib><creatorcontrib>Rubio, Francisco</creatorcontrib><creatorcontrib>Bañuelos, Marı́a A.</creatorcontrib><creatorcontrib>Rodrı́guez-Navarro, Alonso</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Senn, Marı́a E.</au><au>Rubio, Francisco</au><au>Bañuelos, Marı́a A.</au><au>Rodrı́guez-Navarro, Alonso</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative Functional Features of Plant Potassium HvHAK1 and HvHAK2 Transporters</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2001-11-30</date><risdate>2001</risdate><volume>276</volume><issue>48</issue><spage>44563</spage><epage>44569</epage><pages>44563-44569</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Plant K + transporters of the HAK family belong to four rather divergent phylogenetic clusters, although most of the transporters belong
to clusters I or II. A simple phylogenetic analysis of fungal and plant HAK transporters suggests that an original HAK gene duplicated even before fungi and plants diverged, generating transporters that at present fulfill different functions
in the plant. The HvHAK1 transporter belongs to cluster I and mediates high-affinity K + uptake in barley roots, but no function is known for the cluster II transporter, HvHAK2, which is not functional in yeast.
The function of HvHAK2 was investigated by constructing HvHAK1-HAK2 chimeric transporters, which were not functional even
when they included only short fragments of HvHAK2. Then, amino acids characteristic of cluster II in the N terminus and in
the first transmembrane domain were introduced into HvHAK1. All of these changes increased the Rb +
K
m , introducing minimal changes in the Na + K
m , which suggested that HvHAK2 is a low-affinity, Na + -sensitive K + transporter. Using a K + -defective Escherichia coli mutant, we functionally expressed HvHAK2 and found that the predicted characteristics were correct, as well as discovering
that the bacterial expression of HvHAK2 is functional at pH 5.5 but not at 7.5. We discuss whether HvHAK2 may be a tonoplast
transporter effective for vacuolar K + depletion in K + starved plants.</abstract><cop>United States</cop><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>11562376</pmid><doi>10.1074/jbc.M108129200</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Amino Acid Sequence Arabinose - pharmacology Biological Transport Cation Transport Proteins - chemistry Dose-Response Relationship, Drug Escherichia coli - genetics Escherichia coli - metabolism HAK gene Hordeum - metabolism Hordeum vulgare HvHAK1 protein HvHAK2 protein Hydrogen-Ion Concentration Kinetics Molecular Sequence Data Mutagenesis Mutation Plant Proteins - metabolism Plasmids - metabolism Potassium - metabolism Potassium Chloride - pharmacology Protein Structure, Tertiary Sequence Homology, Amino Acid Time Factors Vacuoles |
title | Comparative Functional Features of Plant Potassium HvHAK1 and HvHAK2 Transporters |
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