Polymorphisms in plastoquinol oxidase (PTOX) from Arabidopsis accessions indicate SNP-induced structural variants associated with altitude and rainfall

Plant plastoquinol oxidase (PTOX) is a chloroplast oxidoreductase involved in carotenoid biosynthesis, chlororespiration, and response to environmental stresses. The present study aimed to gain insight of the potential role of nucleotide/amino acid changes linked to environmental adaptation in PTOX...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of bioenergetics and biomembranes 2019-04, Vol.51 (2), p.151-164
Hauptverfasser: Thiers, Karine Leitão Lima, da Silva, João Hermínio Martins, Sartori, Geraldo Rodrigues, dos Santos, Clesivan Pereira, Saraiva, Kátia Daniella da Cruz, Roque, André Luiz Maia, Arnholdt-Schmitt, Birgit, Costa, José Hélio
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 164
container_issue 2
container_start_page 151
container_title Journal of bioenergetics and biomembranes
container_volume 51
creator Thiers, Karine Leitão Lima
da Silva, João Hermínio Martins
Sartori, Geraldo Rodrigues
dos Santos, Clesivan Pereira
Saraiva, Kátia Daniella da Cruz
Roque, André Luiz Maia
Arnholdt-Schmitt, Birgit
Costa, José Hélio
description Plant plastoquinol oxidase (PTOX) is a chloroplast oxidoreductase involved in carotenoid biosynthesis, chlororespiration, and response to environmental stresses. The present study aimed to gain insight of the potential role of nucleotide/amino acid changes linked to environmental adaptation in PTOX gene/protein from Arabidopsis thaliana accessions. SNPs in the single-copy PTOX gene were identified in 1190 accessions of Arabidopsis using the Columbia-0 PTOX as a reference. The identified SNPs were correlated with geographical distribution of the accessions according to altitude, climate, and rainfall. Among the 32 identified SNPs in the coding region of the PTOX gene, 16 of these were characterized as non-synonymous SNPs (in which an AA is altered). A higher incidence of AA changes occurred in the mature protein at positions 78 (31%), 81 (31.4%), and 323 (49.9%). Three-dimensional structure prediction indicated that the AA change at position 323 (D323N) leads to a PTOX structure with the most favorable interaction with the substrate plastoquinol, when compared with the reference PTOX structure (Columbia-0). Molecular docking analysis suggested that the most favorable D323N PTOX-plastoquinol interaction is due to a better enzyme-substrate binding affinity. The molecular dynamics revealed that plastoquinol should be more stable in complex with D323N PTOX, likely due a restraint mechanism in this structure that stabilize plastoquinol inside of the reaction center. The integrated analysis made from accession geographical distribution and PTOX SNPs indicated that AA changes in PTOX are related to altitude and rainfall, potentially due to an adaptive positive environmental selection.
doi_str_mv 10.1007/s10863-018-9784-6
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2164401087</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2164401087</sourcerecordid><originalsourceid>FETCH-LOGICAL-c372t-656056ad3c8b635aa7a5d300cc8547b1066845d7d11c1943866480ca84d3dcb03</originalsourceid><addsrcrecordid>eNp1kctuFDEQRS0EIkPgA9ggS2zIwlAeP2cZReEhRWQkgpRdy217iKPuduNyB_Il_C4eTYAVq1Kpzr2lqkvISw5vOYB5hxysFgy4ZRtjJdOPyIorI5i2lj8mK-BSMWk210fkGeItAFhQ8JQcCdDcGKFX5Nc2D_djLvNNwhFpmug8OKz5-5KmPND8MwWHkb7ZXl1en9BdySM9La5PIc-YkDrvI2LK014aknc10i-ft6w1i4-BYi2Lr0txA71zJbmpNg1i9qmRgf5I9Ya6oaa6hEjdFGhxadq5YXhOnrSC8cVDPSZf359fnX1kF5cfPp2dXjAvzLoyrTQo7YLwttdCOWecCgLAe6uk6TlobaUKJnDu-UYKq7W04J2VQQTfgzgmrw--c2k3R6zdbV7K1FZ2a66lhPZi0yh-oHzJiCXuurmk0ZX7jkO3j6I7RNG1KLp9FJ1umlcPzks_xvBX8ef3DVgfAGyj6Vss_1b_3_U3zOyWuA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2164401087</pqid></control><display><type>article</type><title>Polymorphisms in plastoquinol oxidase (PTOX) from Arabidopsis accessions indicate SNP-induced structural variants associated with altitude and rainfall</title><source>MEDLINE</source><source>SpringerNature Journals</source><creator>Thiers, Karine Leitão Lima ; da Silva, João Hermínio Martins ; Sartori, Geraldo Rodrigues ; dos Santos, Clesivan Pereira ; Saraiva, Kátia Daniella da Cruz ; Roque, André Luiz Maia ; Arnholdt-Schmitt, Birgit ; Costa, José Hélio</creator><creatorcontrib>Thiers, Karine Leitão Lima ; da Silva, João Hermínio Martins ; Sartori, Geraldo Rodrigues ; dos Santos, Clesivan Pereira ; Saraiva, Kátia Daniella da Cruz ; Roque, André Luiz Maia ; Arnholdt-Schmitt, Birgit ; Costa, José Hélio</creatorcontrib><description>Plant plastoquinol oxidase (PTOX) is a chloroplast oxidoreductase involved in carotenoid biosynthesis, chlororespiration, and response to environmental stresses. The present study aimed to gain insight of the potential role of nucleotide/amino acid changes linked to environmental adaptation in PTOX gene/protein from Arabidopsis thaliana accessions. SNPs in the single-copy PTOX gene were identified in 1190 accessions of Arabidopsis using the Columbia-0 PTOX as a reference. The identified SNPs were correlated with geographical distribution of the accessions according to altitude, climate, and rainfall. Among the 32 identified SNPs in the coding region of the PTOX gene, 16 of these were characterized as non-synonymous SNPs (in which an AA is altered). A higher incidence of AA changes occurred in the mature protein at positions 78 (31%), 81 (31.4%), and 323 (49.9%). Three-dimensional structure prediction indicated that the AA change at position 323 (D323N) leads to a PTOX structure with the most favorable interaction with the substrate plastoquinol, when compared with the reference PTOX structure (Columbia-0). Molecular docking analysis suggested that the most favorable D323N PTOX-plastoquinol interaction is due to a better enzyme-substrate binding affinity. The molecular dynamics revealed that plastoquinol should be more stable in complex with D323N PTOX, likely due a restraint mechanism in this structure that stabilize plastoquinol inside of the reaction center. The integrated analysis made from accession geographical distribution and PTOX SNPs indicated that AA changes in PTOX are related to altitude and rainfall, potentially due to an adaptive positive environmental selection.</description><identifier>ISSN: 0145-479X</identifier><identifier>EISSN: 1573-6881</identifier><identifier>DOI: 10.1007/s10863-018-9784-6</identifier><identifier>PMID: 30617736</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Acclimatization ; Adaptation ; Altitude ; Amino acid sequence ; Amino acids ; Animal Anatomy ; Animal Biochemistry ; Arabidopsis ; Arabidopsis - enzymology ; Arabidopsis - genetics ; Arabidopsis Proteins - chemistry ; Arabidopsis Proteins - genetics ; Arabidopsis Proteins - metabolism ; Binding sites ; Biochemistry ; Bioorganic Chemistry ; Biosynthesis ; Carotenoids ; Catalytic Domain ; Chemistry ; Chemistry and Materials Science ; Chloroplasts ; Consortia ; Environmental conditions ; Environmental stress ; Enzymes ; Flowers &amp; plants ; Genomes ; Geographical distribution ; Histology ; Molecular docking ; Molecular Docking Simulation ; Molecular dynamics ; Molecular structure ; Morphology ; Organic Chemistry ; Oxidase ; Oxidoreductase ; Oxidoreductases - chemistry ; Oxidoreductases - genetics ; Oxidoreductases - metabolism ; Peptides ; Plastoquinol ; Plastoquinone - analogs &amp; derivatives ; Plastoquinone - chemistry ; Plastoquinone - metabolism ; Polymorphism, Single Nucleotide ; Proteins ; Rainfall ; Servers ; Single-nucleotide polymorphism ; Software ; Substrates</subject><ispartof>Journal of bioenergetics and biomembranes, 2019-04, Vol.51 (2), p.151-164</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2019</rights><rights>Journal of Bioenergetics and Biomembranes is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-656056ad3c8b635aa7a5d300cc8547b1066845d7d11c1943866480ca84d3dcb03</citedby><cites>FETCH-LOGICAL-c372t-656056ad3c8b635aa7a5d300cc8547b1066845d7d11c1943866480ca84d3dcb03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10863-018-9784-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10863-018-9784-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,781,785,27929,27930,41493,42562,51324</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30617736$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thiers, Karine Leitão Lima</creatorcontrib><creatorcontrib>da Silva, João Hermínio Martins</creatorcontrib><creatorcontrib>Sartori, Geraldo Rodrigues</creatorcontrib><creatorcontrib>dos Santos, Clesivan Pereira</creatorcontrib><creatorcontrib>Saraiva, Kátia Daniella da Cruz</creatorcontrib><creatorcontrib>Roque, André Luiz Maia</creatorcontrib><creatorcontrib>Arnholdt-Schmitt, Birgit</creatorcontrib><creatorcontrib>Costa, José Hélio</creatorcontrib><title>Polymorphisms in plastoquinol oxidase (PTOX) from Arabidopsis accessions indicate SNP-induced structural variants associated with altitude and rainfall</title><title>Journal of bioenergetics and biomembranes</title><addtitle>J Bioenerg Biomembr</addtitle><addtitle>J Bioenerg Biomembr</addtitle><description>Plant plastoquinol oxidase (PTOX) is a chloroplast oxidoreductase involved in carotenoid biosynthesis, chlororespiration, and response to environmental stresses. The present study aimed to gain insight of the potential role of nucleotide/amino acid changes linked to environmental adaptation in PTOX gene/protein from Arabidopsis thaliana accessions. SNPs in the single-copy PTOX gene were identified in 1190 accessions of Arabidopsis using the Columbia-0 PTOX as a reference. The identified SNPs were correlated with geographical distribution of the accessions according to altitude, climate, and rainfall. Among the 32 identified SNPs in the coding region of the PTOX gene, 16 of these were characterized as non-synonymous SNPs (in which an AA is altered). A higher incidence of AA changes occurred in the mature protein at positions 78 (31%), 81 (31.4%), and 323 (49.9%). Three-dimensional structure prediction indicated that the AA change at position 323 (D323N) leads to a PTOX structure with the most favorable interaction with the substrate plastoquinol, when compared with the reference PTOX structure (Columbia-0). Molecular docking analysis suggested that the most favorable D323N PTOX-plastoquinol interaction is due to a better enzyme-substrate binding affinity. The molecular dynamics revealed that plastoquinol should be more stable in complex with D323N PTOX, likely due a restraint mechanism in this structure that stabilize plastoquinol inside of the reaction center. The integrated analysis made from accession geographical distribution and PTOX SNPs indicated that AA changes in PTOX are related to altitude and rainfall, potentially due to an adaptive positive environmental selection.</description><subject>Acclimatization</subject><subject>Adaptation</subject><subject>Altitude</subject><subject>Amino acid sequence</subject><subject>Amino acids</subject><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Arabidopsis</subject><subject>Arabidopsis - enzymology</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis Proteins - chemistry</subject><subject>Arabidopsis Proteins - genetics</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Binding sites</subject><subject>Biochemistry</subject><subject>Bioorganic Chemistry</subject><subject>Biosynthesis</subject><subject>Carotenoids</subject><subject>Catalytic Domain</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chloroplasts</subject><subject>Consortia</subject><subject>Environmental conditions</subject><subject>Environmental stress</subject><subject>Enzymes</subject><subject>Flowers &amp; plants</subject><subject>Genomes</subject><subject>Geographical distribution</subject><subject>Histology</subject><subject>Molecular docking</subject><subject>Molecular Docking Simulation</subject><subject>Molecular dynamics</subject><subject>Molecular structure</subject><subject>Morphology</subject><subject>Organic Chemistry</subject><subject>Oxidase</subject><subject>Oxidoreductase</subject><subject>Oxidoreductases - chemistry</subject><subject>Oxidoreductases - genetics</subject><subject>Oxidoreductases - metabolism</subject><subject>Peptides</subject><subject>Plastoquinol</subject><subject>Plastoquinone - analogs &amp; derivatives</subject><subject>Plastoquinone - chemistry</subject><subject>Plastoquinone - metabolism</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Proteins</subject><subject>Rainfall</subject><subject>Servers</subject><subject>Single-nucleotide polymorphism</subject><subject>Software</subject><subject>Substrates</subject><issn>0145-479X</issn><issn>1573-6881</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kctuFDEQRS0EIkPgA9ggS2zIwlAeP2cZReEhRWQkgpRdy217iKPuduNyB_Il_C4eTYAVq1Kpzr2lqkvISw5vOYB5hxysFgy4ZRtjJdOPyIorI5i2lj8mK-BSMWk210fkGeItAFhQ8JQcCdDcGKFX5Nc2D_djLvNNwhFpmug8OKz5-5KmPND8MwWHkb7ZXl1en9BdySM9La5PIc-YkDrvI2LK014aknc10i-ft6w1i4-BYi2Lr0txA71zJbmpNg1i9qmRgf5I9Ya6oaa6hEjdFGhxadq5YXhOnrSC8cVDPSZf359fnX1kF5cfPp2dXjAvzLoyrTQo7YLwttdCOWecCgLAe6uk6TlobaUKJnDu-UYKq7W04J2VQQTfgzgmrw--c2k3R6zdbV7K1FZ2a66lhPZi0yh-oHzJiCXuurmk0ZX7jkO3j6I7RNG1KLp9FJ1umlcPzks_xvBX8ef3DVgfAGyj6Vss_1b_3_U3zOyWuA</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Thiers, Karine Leitão Lima</creator><creator>da Silva, João Hermínio Martins</creator><creator>Sartori, Geraldo Rodrigues</creator><creator>dos Santos, Clesivan Pereira</creator><creator>Saraiva, Kátia Daniella da Cruz</creator><creator>Roque, André Luiz Maia</creator><creator>Arnholdt-Schmitt, Birgit</creator><creator>Costa, José Hélio</creator><general>Springer US</general><general>Springer Nature B.V</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>3V.</scope><scope>7QO</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>20190401</creationdate><title>Polymorphisms in plastoquinol oxidase (PTOX) from Arabidopsis accessions indicate SNP-induced structural variants associated with altitude and rainfall</title><author>Thiers, Karine Leitão Lima ; da Silva, João Hermínio Martins ; Sartori, Geraldo Rodrigues ; dos Santos, Clesivan Pereira ; Saraiva, Kátia Daniella da Cruz ; Roque, André Luiz Maia ; Arnholdt-Schmitt, Birgit ; Costa, José Hélio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-656056ad3c8b635aa7a5d300cc8547b1066845d7d11c1943866480ca84d3dcb03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acclimatization</topic><topic>Adaptation</topic><topic>Altitude</topic><topic>Amino acid sequence</topic><topic>Amino acids</topic><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Arabidopsis</topic><topic>Arabidopsis - enzymology</topic><topic>Arabidopsis - genetics</topic><topic>Arabidopsis Proteins - chemistry</topic><topic>Arabidopsis Proteins - genetics</topic><topic>Arabidopsis Proteins - metabolism</topic><topic>Binding sites</topic><topic>Biochemistry</topic><topic>Bioorganic Chemistry</topic><topic>Biosynthesis</topic><topic>Carotenoids</topic><topic>Catalytic Domain</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chloroplasts</topic><topic>Consortia</topic><topic>Environmental conditions</topic><topic>Environmental stress</topic><topic>Enzymes</topic><topic>Flowers &amp; plants</topic><topic>Genomes</topic><topic>Geographical distribution</topic><topic>Histology</topic><topic>Molecular docking</topic><topic>Molecular Docking Simulation</topic><topic>Molecular dynamics</topic><topic>Molecular structure</topic><topic>Morphology</topic><topic>Organic Chemistry</topic><topic>Oxidase</topic><topic>Oxidoreductase</topic><topic>Oxidoreductases - chemistry</topic><topic>Oxidoreductases - genetics</topic><topic>Oxidoreductases - metabolism</topic><topic>Peptides</topic><topic>Plastoquinol</topic><topic>Plastoquinone - analogs &amp; derivatives</topic><topic>Plastoquinone - chemistry</topic><topic>Plastoquinone - metabolism</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Proteins</topic><topic>Rainfall</topic><topic>Servers</topic><topic>Single-nucleotide polymorphism</topic><topic>Software</topic><topic>Substrates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thiers, Karine Leitão Lima</creatorcontrib><creatorcontrib>da Silva, João Hermínio Martins</creatorcontrib><creatorcontrib>Sartori, Geraldo Rodrigues</creatorcontrib><creatorcontrib>dos Santos, Clesivan Pereira</creatorcontrib><creatorcontrib>Saraiva, Kátia Daniella da Cruz</creatorcontrib><creatorcontrib>Roque, André Luiz Maia</creatorcontrib><creatorcontrib>Arnholdt-Schmitt, Birgit</creatorcontrib><creatorcontrib>Costa, José Hélio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection (ProQuest)</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database (ProQuest)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><jtitle>Journal of bioenergetics and biomembranes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thiers, Karine Leitão Lima</au><au>da Silva, João Hermínio Martins</au><au>Sartori, Geraldo Rodrigues</au><au>dos Santos, Clesivan Pereira</au><au>Saraiva, Kátia Daniella da Cruz</au><au>Roque, André Luiz Maia</au><au>Arnholdt-Schmitt, Birgit</au><au>Costa, José Hélio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymorphisms in plastoquinol oxidase (PTOX) from Arabidopsis accessions indicate SNP-induced structural variants associated with altitude and rainfall</atitle><jtitle>Journal of bioenergetics and biomembranes</jtitle><stitle>J Bioenerg Biomembr</stitle><addtitle>J Bioenerg Biomembr</addtitle><date>2019-04-01</date><risdate>2019</risdate><volume>51</volume><issue>2</issue><spage>151</spage><epage>164</epage><pages>151-164</pages><issn>0145-479X</issn><eissn>1573-6881</eissn><abstract>Plant plastoquinol oxidase (PTOX) is a chloroplast oxidoreductase involved in carotenoid biosynthesis, chlororespiration, and response to environmental stresses. The present study aimed to gain insight of the potential role of nucleotide/amino acid changes linked to environmental adaptation in PTOX gene/protein from Arabidopsis thaliana accessions. SNPs in the single-copy PTOX gene were identified in 1190 accessions of Arabidopsis using the Columbia-0 PTOX as a reference. The identified SNPs were correlated with geographical distribution of the accessions according to altitude, climate, and rainfall. Among the 32 identified SNPs in the coding region of the PTOX gene, 16 of these were characterized as non-synonymous SNPs (in which an AA is altered). A higher incidence of AA changes occurred in the mature protein at positions 78 (31%), 81 (31.4%), and 323 (49.9%). Three-dimensional structure prediction indicated that the AA change at position 323 (D323N) leads to a PTOX structure with the most favorable interaction with the substrate plastoquinol, when compared with the reference PTOX structure (Columbia-0). Molecular docking analysis suggested that the most favorable D323N PTOX-plastoquinol interaction is due to a better enzyme-substrate binding affinity. The molecular dynamics revealed that plastoquinol should be more stable in complex with D323N PTOX, likely due a restraint mechanism in this structure that stabilize plastoquinol inside of the reaction center. The integrated analysis made from accession geographical distribution and PTOX SNPs indicated that AA changes in PTOX are related to altitude and rainfall, potentially due to an adaptive positive environmental selection.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>30617736</pmid><doi>10.1007/s10863-018-9784-6</doi><tpages>14</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0145-479X
ispartof Journal of bioenergetics and biomembranes, 2019-04, Vol.51 (2), p.151-164
issn 0145-479X
1573-6881
language eng
recordid cdi_proquest_journals_2164401087
source MEDLINE; SpringerNature Journals
subjects Acclimatization
Adaptation
Altitude
Amino acid sequence
Amino acids
Animal Anatomy
Animal Biochemistry
Arabidopsis
Arabidopsis - enzymology
Arabidopsis - genetics
Arabidopsis Proteins - chemistry
Arabidopsis Proteins - genetics
Arabidopsis Proteins - metabolism
Binding sites
Biochemistry
Bioorganic Chemistry
Biosynthesis
Carotenoids
Catalytic Domain
Chemistry
Chemistry and Materials Science
Chloroplasts
Consortia
Environmental conditions
Environmental stress
Enzymes
Flowers & plants
Genomes
Geographical distribution
Histology
Molecular docking
Molecular Docking Simulation
Molecular dynamics
Molecular structure
Morphology
Organic Chemistry
Oxidase
Oxidoreductase
Oxidoreductases - chemistry
Oxidoreductases - genetics
Oxidoreductases - metabolism
Peptides
Plastoquinol
Plastoquinone - analogs & derivatives
Plastoquinone - chemistry
Plastoquinone - metabolism
Polymorphism, Single Nucleotide
Proteins
Rainfall
Servers
Single-nucleotide polymorphism
Software
Substrates
title Polymorphisms in plastoquinol oxidase (PTOX) from Arabidopsis accessions indicate SNP-induced structural variants associated with altitude and rainfall
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-13T09%3A40%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Polymorphisms%20in%20plastoquinol%20oxidase%20(PTOX)%20from%20Arabidopsis%20accessions%20indicate%20SNP-induced%20structural%20variants%20associated%20with%20altitude%20and%20rainfall&rft.jtitle=Journal%20of%20bioenergetics%20and%20biomembranes&rft.au=Thiers,%20Karine%20Leit%C3%A3o%20Lima&rft.date=2019-04-01&rft.volume=51&rft.issue=2&rft.spage=151&rft.epage=164&rft.pages=151-164&rft.issn=0145-479X&rft.eissn=1573-6881&rft_id=info:doi/10.1007/s10863-018-9784-6&rft_dat=%3Cproquest_cross%3E2164401087%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2164401087&rft_id=info:pmid/30617736&rfr_iscdi=true