Local and distal effects of arbuscular mycorrhizal colonization on direct pathway Pi uptake and root growth in Medicago truncatula.
Identifieur interne : 001470 ( Main/Corpus ); précédent : 001469; suivant : 001471Local and distal effects of arbuscular mycorrhizal colonization on direct pathway Pi uptake and root growth in Medicago truncatula.
Auteurs : Stephanie J. Watts-Williams ; Iver Jakobsen ; Timothy R. Cavagnaro ; Mette Gr NlundSource :
- Journal of experimental botany [ 1460-2431 ] ; 2015.
English descriptors
- KwdEn :
- Colony Count, Microbial (MeSH), Gene Expression Regulation, Plant (drug effects), Hyphae (drug effects), Hyphae (physiology), Medicago truncatula (drug effects), Medicago truncatula (growth & development), Medicago truncatula (microbiology), Mycorrhizae (drug effects), Mycorrhizae (physiology), Phosphorus (metabolism), Phosphorus (pharmacology), Plant Proteins (metabolism), Soil (chemistry).
- MESH :
- chemical , chemistry : Soil.
- chemical , metabolism : Phosphorus, Plant Proteins.
- drug effects : Gene Expression Regulation, Plant, Hyphae, Medicago truncatula, Mycorrhizae.
- growth & development : Medicago truncatula.
- microbiology : Medicago truncatula.
- chemical , pharmacology : Phosphorus.
- physiology : Hyphae, Mycorrhizae.
- Colony Count, Microbial.
Abstract
Two pathways exist for plant Pi uptake from soil: via root epidermal cells (direct pathway) or via associations with arbuscular mycorrhizal (AM) fungi, and the two pathways interact in a complex manner. This study investigated distal and local effects of AM colonization on direct root Pi uptake and root growth, at different soil P levels. Medicago truncatula was grown at three soil P levels in split-pots with or without AM fungal inoculation and where one root half grew into soil labelled with (33)P. Plant genotypes included the A17 wild type and the mtpt4 mutant. The mtpt4 mutant, colonized by AM fungi, but with no functional mycorrhizal pathway for Pi uptake, was included to better understand effects of AM colonization per se. Colonization by AM fungi decreased expression of direct Pi transporter genes locally, but not distally in the wild type. In mtpt4 mutant plants, direct Pi transporter genes and the Pi starvation-induced gene Mt4 were more highly expressed than in wild-type roots. In wild-type plants, less Pi was taken up via the direct pathway by non-colonized roots when the other root half was colonized by AM fungi, compared with non-mycorrhizal plants. Colonization by AM fungi strongly influenced root growth locally and distally, and direct root Pi uptake activity locally, but had only a weak influence on distal direct pathway activity. The responses to AM colonization in the mtpt4 mutant suggested that in the wild type, the increased P concentration of colonized roots was a major factor driving the effects of AM colonization on direct root Pi uptake.
DOI: 10.1093/jxb/erv202
PubMed: 25944927
PubMed Central: PMC4473995
Links to Exploration step
pubmed:25944927Le document en format XML
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Lyngby, Denmark.</nlm:affiliation></affiliation></author><author><name sortKey="Cavagnaro, Timothy R" sort="Cavagnaro, Timothy R" uniqKey="Cavagnaro T" first="Timothy R" last="Cavagnaro">Timothy R. Cavagnaro</name><affiliation><nlm:affiliation>School of Agriculture, Food and Wine, The University of Adelaide, Waite Campus, PMB1, Glen Osmond, SA 5064, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Gr Nlund, Mette" sort="Gr Nlund, Mette" uniqKey="Gr Nlund M" first="Mette" last="Gr Nlund">Mette Gr Nlund</name><affiliation><nlm:affiliation>Department of Chemical and Biochemical Engineering, Technical University of Denmark, 2800 Kgs. 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Department of Chemical and Biochemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark. sjw266@cornell.edu.</nlm:affiliation></affiliation></author><author><name sortKey="Jakobsen, Iver" sort="Jakobsen, Iver" uniqKey="Jakobsen I" first="Iver" last="Jakobsen">Iver Jakobsen</name><affiliation><nlm:affiliation>Department of Chemical and Biochemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark.</nlm:affiliation></affiliation></author><author><name sortKey="Cavagnaro, Timothy R" sort="Cavagnaro, Timothy R" uniqKey="Cavagnaro T" first="Timothy R" last="Cavagnaro">Timothy R. Cavagnaro</name><affiliation><nlm:affiliation>School of Agriculture, Food and Wine, The University of Adelaide, Waite Campus, PMB1, Glen Osmond, SA 5064, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Gr Nlund, Mette" sort="Gr Nlund, Mette" uniqKey="Gr Nlund M" first="Mette" last="Gr Nlund">Mette Gr Nlund</name><affiliation><nlm:affiliation>Department of Chemical and Biochemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Journal of experimental botany</title><idno type="eISSN">1460-2431</idno><imprint><date when="2015" type="published">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Colony Count, Microbial (MeSH)</term><term>Gene Expression Regulation, Plant (drug effects)</term><term>Hyphae (drug effects)</term><term>Hyphae (physiology)</term><term>Medicago truncatula (drug effects)</term><term>Medicago truncatula (growth & development)</term><term>Medicago truncatula (microbiology)</term><term>Mycorrhizae (drug effects)</term><term>Mycorrhizae (physiology)</term><term>Phosphorus (metabolism)</term><term>Phosphorus (pharmacology)</term><term>Plant Proteins (metabolism)</term><term>Soil (chemistry)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Soil</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Phosphorus</term><term>Plant Proteins</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Gene Expression Regulation, Plant</term><term>Hyphae</term><term>Medicago truncatula</term><term>Mycorrhizae</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Medicago truncatula</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Medicago truncatula</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Phosphorus</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Hyphae</term><term>Mycorrhizae</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Colony Count, Microbial</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Two pathways exist for plant Pi uptake from soil: via root epidermal cells (direct pathway) or via associations with arbuscular mycorrhizal (AM) fungi, and the two pathways interact in a complex manner. This study investigated distal and local effects of AM colonization on direct root Pi uptake and root growth, at different soil P levels. Medicago truncatula was grown at three soil P levels in split-pots with or without AM fungal inoculation and where one root half grew into soil labelled with (33)P. Plant genotypes included the A17 wild type and the mtpt4 mutant. The mtpt4 mutant, colonized by AM fungi, but with no functional mycorrhizal pathway for Pi uptake, was included to better understand effects of AM colonization per se. Colonization by AM fungi decreased expression of direct Pi transporter genes locally, but not distally in the wild type. In mtpt4 mutant plants, direct Pi transporter genes and the Pi starvation-induced gene Mt4 were more highly expressed than in wild-type roots. In wild-type plants, less Pi was taken up via the direct pathway by non-colonized roots when the other root half was colonized by AM fungi, compared with non-mycorrhizal plants. Colonization by AM fungi strongly influenced root growth locally and distally, and direct root Pi uptake activity locally, but had only a weak influence on distal direct pathway activity. The responses to AM colonization in the mtpt4 mutant suggested that in the wild type, the increased P concentration of colonized roots was a major factor driving the effects of AM colonization on direct root Pi uptake. </div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25944927</PMID><DateCompleted><Year>2016</Year><Month>03</Month><Day>28</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1460-2431</ISSN><JournalIssue CitedMedium="Internet"><Volume>66</Volume><Issue>13</Issue><PubDate><Year>2015</Year><Month>Jul</Month></PubDate></JournalIssue><Title>Journal of experimental botany</Title><ISOAbbreviation>J Exp Bot</ISOAbbreviation></Journal><ArticleTitle>Local and distal effects of arbuscular mycorrhizal colonization on direct pathway Pi uptake and root growth in Medicago truncatula.</ArticleTitle><Pagination><MedlinePgn>4061-73</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1093/jxb/erv202</ELocationID><Abstract><AbstractText>Two pathways exist for plant Pi uptake from soil: via root epidermal cells (direct pathway) or via associations with arbuscular mycorrhizal (AM) fungi, and the two pathways interact in a complex manner. This study investigated distal and local effects of AM colonization on direct root Pi uptake and root growth, at different soil P levels. Medicago truncatula was grown at three soil P levels in split-pots with or without AM fungal inoculation and where one root half grew into soil labelled with (33)P. Plant genotypes included the A17 wild type and the mtpt4 mutant. The mtpt4 mutant, colonized by AM fungi, but with no functional mycorrhizal pathway for Pi uptake, was included to better understand effects of AM colonization per se. Colonization by AM fungi decreased expression of direct Pi transporter genes locally, but not distally in the wild type. In mtpt4 mutant plants, direct Pi transporter genes and the Pi starvation-induced gene Mt4 were more highly expressed than in wild-type roots. In wild-type plants, less Pi was taken up via the direct pathway by non-colonized roots when the other root half was colonized by AM fungi, compared with non-mycorrhizal plants. Colonization by AM fungi strongly influenced root growth locally and distally, and direct root Pi uptake activity locally, but had only a weak influence on distal direct pathway activity. The responses to AM colonization in the mtpt4 mutant suggested that in the wild type, the increased P concentration of colonized roots was a major factor driving the effects of AM colonization on direct root Pi uptake. </AbstractText><CopyrightInformation>© The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Watts-Williams</LastName><ForeName>Stephanie J</ForeName><Initials>SJ</Initials><Identifier Source="ORCID">http://orcid.org/0000-0002-7359-8440</Identifier><AffiliationInfo><Affiliation>School of Biological Sciences, Monash University, Clayton, VIC 3800, Australia. Department of Chemical and Biochemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark. sjw266@cornell.edu.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Jakobsen</LastName><ForeName>Iver</ForeName><Initials>I</Initials><AffiliationInfo><Affiliation>Department of Chemical and Biochemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Cavagnaro</LastName><ForeName>Timothy R</ForeName><Initials>TR</Initials><AffiliationInfo><Affiliation>School of Agriculture, Food and Wine, The University of Adelaide, Waite Campus, PMB1, Glen Osmond, SA 5064, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Grønlund</LastName><ForeName>Mette</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Department of Chemical and Biochemical Engineering, Technical University of Denmark, 2800 Kgs. 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