The Glycerol-3-Phosphate Acyltransferase GPAT6 from Tomato Plays a Central Role in Fruit Cutin Biosynthesis
The thick cuticle covering and embedding the epidermal cells of tomato (Solanum lycopersicum) fruit acts not only as a protective barrier against pathogens and water loss but also influences quality traits such as brightness and postharvest shelf-life. In a recent study, we screened a mutant collect...
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Veröffentlicht in: | Plant physiology (Bethesda) 2016-06, Vol.171 (2), p.894-913 |
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creator | Petit, Johann Bres, Cécile Mauxion, Jean-Philippe Tai, Fabienne Wong Jun Martin, Laetitia B.B. Fich, Eric A. Joubès, Jérôme Rose, Jocelyn K.C. Domergue, Frédéric Rothan, Christophe |
description | The thick cuticle covering and embedding the epidermal cells of tomato (Solanum lycopersicum) fruit acts not only as a protective barrier against pathogens and water loss but also influences quality traits such as brightness and postharvest shelf-life. In a recent study, we screened a mutant collection of the miniature tomato cultivar Micro-Tom and isolated several glossy fruit mutants in which the abundance of cutin, the polyester component of the cuticle, was strongly reduced. We employed a newly developed mapping-by-sequencing strategy to identify the causal mutation underlying the cutin deficiency in a mutant thereafter named gpat6-a (for glycerol-3-phosphate acyltransferase6). To this end, a backcross population (BC₁F₂) segregating for the glossy trait was phenotyped. Individuals displaying either a wild-type or a glossy fruit trait were then pooled into bulked populations and submitted to whole-genome sequencing prior to mutation frequency analysis. This revealed that the causal point mutation in the gpat6-a mutant introduces a charged amino acid adjacent to the active site of a GPAT6 enzyme. We further showed that this mutation completely abolished the GPAT activity of the recombinant protein. The gpat6-a mutant showed perturbed pollen formation but, unlike a gpat6 mutant of Arabidopsis (Arabidopsis thaliana), was not male sterile. The most striking phenotype was observed in the mutant fruit, where cuticle thickness, composition, and properties were altered. RNA sequencing analysis highlighted the main processes and pathways that were affected by the mutation at the transcriptional level, which included those associated with lipid, secondary metabolite, and cell wall biosynthesis. |
doi_str_mv | 10.1104/pp.16.00409 |
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In a recent study, we screened a mutant collection of the miniature tomato cultivar Micro-Tom and isolated several glossy fruit mutants in which the abundance of cutin, the polyester component of the cuticle, was strongly reduced. We employed a newly developed mapping-by-sequencing strategy to identify the causal mutation underlying the cutin deficiency in a mutant thereafter named gpat6-a (for glycerol-3-phosphate acyltransferase6). To this end, a backcross population (BC₁F₂) segregating for the glossy trait was phenotyped. Individuals displaying either a wild-type or a glossy fruit trait were then pooled into bulked populations and submitted to whole-genome sequencing prior to mutation frequency analysis. This revealed that the causal point mutation in the gpat6-a mutant introduces a charged amino acid adjacent to the active site of a GPAT6 enzyme. We further showed that this mutation completely abolished the GPAT activity of the recombinant protein. The gpat6-a mutant showed perturbed pollen formation but, unlike a gpat6 mutant of Arabidopsis (Arabidopsis thaliana), was not male sterile. The most striking phenotype was observed in the mutant fruit, where cuticle thickness, composition, and properties were altered. RNA sequencing analysis highlighted the main processes and pathways that were affected by the mutation at the transcriptional level, which included those associated with lipid, secondary metabolite, and cell wall biosynthesis.</description><identifier>ISSN: 0032-0889</identifier><identifier>EISSN: 1532-2548</identifier><identifier>DOI: 10.1104/pp.16.00409</identifier><identifier>PMID: 27208295</identifier><language>eng</language><publisher>United States: American Society of Plant Biologists</publisher><subject><![CDATA[Amino Acid Sequence ; BIOCHEMISTRY AND METABOLISM ; Chromosome Mapping ; Fruit - anatomy & histology ; Fruit - enzymology ; Fruit - genetics ; Fruit - growth & development ; Glycerol-3-Phosphate O-Acyltransferase - genetics ; Glycerol-3-Phosphate O-Acyltransferase - metabolism ; Life Sciences ; Lycopersicon esculentum - anatomy & histology ; Lycopersicon esculentum - enzymology ; Lycopersicon esculentum - genetics ; Lycopersicon esculentum - growth & development ; Membrane Lipids - metabolism ; Models, Molecular ; Mutation ; Phenotype ; Phylogeny ; Plant Proteins - genetics ; Plant Proteins - metabolism ; Pollen - anatomy & histology ; Pollen - enzymology ; Pollen - genetics ; Pollen - growth & development ; Recombinant Proteins ; Sequence Alignment ; Sequence Analysis, RNA ; Vegetal Biology]]></subject><ispartof>Plant physiology (Bethesda), 2016-06, Vol.171 (2), p.894-913</ispartof><rights>Copyright © 2016 American Society of Plant Biologists</rights><rights>2016 American Society of Plant Biologists. All Rights Reserved.</rights><rights>Attribution</rights><rights>2016 American Society of Plant Biologists. All Rights Reserved. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-c9a77a4952305ea8d31c15ceda07aefe6ca143f5ff09c895ed09b9e5f2332d3f3</citedby><orcidid>0000-0002-0183-7000 ; 0000-0003-1881-9631 ; 0000-0001-6460-4637 ; 0000-0002-6921-7246 ; 0000-0001-5385-450X ; 0000-0002-6746-1755 ; 0000-0002-5665-2468 ; 0000-0002-2316-9947 ; 0000-0002-6831-2823</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/24809284$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/24809284$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,776,780,799,881,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27208295$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02637507$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Petit, Johann</creatorcontrib><creatorcontrib>Bres, Cécile</creatorcontrib><creatorcontrib>Mauxion, Jean-Philippe</creatorcontrib><creatorcontrib>Tai, Fabienne Wong Jun</creatorcontrib><creatorcontrib>Martin, Laetitia B.B.</creatorcontrib><creatorcontrib>Fich, Eric A.</creatorcontrib><creatorcontrib>Joubès, Jérôme</creatorcontrib><creatorcontrib>Rose, Jocelyn K.C.</creatorcontrib><creatorcontrib>Domergue, Frédéric</creatorcontrib><creatorcontrib>Rothan, Christophe</creatorcontrib><title>The Glycerol-3-Phosphate Acyltransferase GPAT6 from Tomato Plays a Central Role in Fruit Cutin Biosynthesis</title><title>Plant physiology (Bethesda)</title><addtitle>Plant Physiol</addtitle><description>The thick cuticle covering and embedding the epidermal cells of tomato (Solanum lycopersicum) fruit acts not only as a protective barrier against pathogens and water loss but also influences quality traits such as brightness and postharvest shelf-life. In a recent study, we screened a mutant collection of the miniature tomato cultivar Micro-Tom and isolated several glossy fruit mutants in which the abundance of cutin, the polyester component of the cuticle, was strongly reduced. We employed a newly developed mapping-by-sequencing strategy to identify the causal mutation underlying the cutin deficiency in a mutant thereafter named gpat6-a (for glycerol-3-phosphate acyltransferase6). To this end, a backcross population (BC₁F₂) segregating for the glossy trait was phenotyped. Individuals displaying either a wild-type or a glossy fruit trait were then pooled into bulked populations and submitted to whole-genome sequencing prior to mutation frequency analysis. This revealed that the causal point mutation in the gpat6-a mutant introduces a charged amino acid adjacent to the active site of a GPAT6 enzyme. We further showed that this mutation completely abolished the GPAT activity of the recombinant protein. The gpat6-a mutant showed perturbed pollen formation but, unlike a gpat6 mutant of Arabidopsis (Arabidopsis thaliana), was not male sterile. The most striking phenotype was observed in the mutant fruit, where cuticle thickness, composition, and properties were altered. RNA sequencing analysis highlighted the main processes and pathways that were affected by the mutation at the transcriptional level, which included those associated with lipid, secondary metabolite, and cell wall biosynthesis.</description><subject>Amino Acid Sequence</subject><subject>BIOCHEMISTRY AND METABOLISM</subject><subject>Chromosome Mapping</subject><subject>Fruit - anatomy & histology</subject><subject>Fruit - enzymology</subject><subject>Fruit - genetics</subject><subject>Fruit - growth & development</subject><subject>Glycerol-3-Phosphate O-Acyltransferase - genetics</subject><subject>Glycerol-3-Phosphate O-Acyltransferase - metabolism</subject><subject>Life Sciences</subject><subject>Lycopersicon esculentum - anatomy & histology</subject><subject>Lycopersicon esculentum - enzymology</subject><subject>Lycopersicon esculentum - genetics</subject><subject>Lycopersicon esculentum - growth & development</subject><subject>Membrane Lipids - metabolism</subject><subject>Models, Molecular</subject><subject>Mutation</subject><subject>Phenotype</subject><subject>Phylogeny</subject><subject>Plant Proteins - genetics</subject><subject>Plant Proteins - metabolism</subject><subject>Pollen - anatomy & histology</subject><subject>Pollen - enzymology</subject><subject>Pollen - genetics</subject><subject>Pollen - growth & development</subject><subject>Recombinant Proteins</subject><subject>Sequence Alignment</subject><subject>Sequence Analysis, RNA</subject><subject>Vegetal Biology</subject><issn>0032-0889</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0U1v1DAQBmALgei2cOIM8pEKZRl_JfYFaVnRFmklVmg5W65jk5RsnNpJpfx7XFLKx8kjz-PXtgahVwTWhAB_PwxrUq4BOKgnaEUEowUVXD5FK4Bcg5TqBJ2mdAMAhBH-HJ3QioKkSqzQj0Pj8GU3WxdDV7Bi34Q0NGZ0eGPnboymT95FkzLabw4l9jEc8SEczRjwvjNzwgZvXZ9hh7-GzuG2xxdxake8ncZcf2xDmvuxcalNL9Azb7rkXj6sZ-jbxafD9qrYfbn8vN3sCstZNRZWmaoyXAnKQDgja0YsEdbVBirjvCutIZx54T0oK5VwNahr5YSnjNGaeXaGPiy5w3R9dLVdnqeH2B5NnHUwrf6307eN_h7uNFdAS0pzwPkS0Px37Gqz0_d7mbFKQHVHsn37cFkMt5NLoz62ybquM70LU9KkUkJKwpjK9N1CbQwpRecfswno-1HqYdCk1L9GmfWbv3_xaH_PLoPXC7hJY4h_-lyCopKzn77Fo_Q</recordid><startdate>20160601</startdate><enddate>20160601</enddate><creator>Petit, Johann</creator><creator>Bres, Cécile</creator><creator>Mauxion, Jean-Philippe</creator><creator>Tai, Fabienne Wong Jun</creator><creator>Martin, Laetitia B.B.</creator><creator>Fich, Eric A.</creator><creator>Joubès, Jérôme</creator><creator>Rose, Jocelyn K.C.</creator><creator>Domergue, Frédéric</creator><creator>Rothan, Christophe</creator><general>American Society of Plant Biologists</general><general>Oxford University Press ; American Society of Plant Biologists</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>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0183-7000</orcidid><orcidid>https://orcid.org/0000-0003-1881-9631</orcidid><orcidid>https://orcid.org/0000-0001-6460-4637</orcidid><orcidid>https://orcid.org/0000-0002-6921-7246</orcidid><orcidid>https://orcid.org/0000-0001-5385-450X</orcidid><orcidid>https://orcid.org/0000-0002-6746-1755</orcidid><orcidid>https://orcid.org/0000-0002-5665-2468</orcidid><orcidid>https://orcid.org/0000-0002-2316-9947</orcidid><orcidid>https://orcid.org/0000-0002-6831-2823</orcidid></search><sort><creationdate>20160601</creationdate><title>The Glycerol-3-Phosphate Acyltransferase GPAT6 from Tomato Plays a Central Role in Fruit Cutin Biosynthesis</title><author>Petit, Johann ; Bres, Cécile ; Mauxion, Jean-Philippe ; 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In a recent study, we screened a mutant collection of the miniature tomato cultivar Micro-Tom and isolated several glossy fruit mutants in which the abundance of cutin, the polyester component of the cuticle, was strongly reduced. We employed a newly developed mapping-by-sequencing strategy to identify the causal mutation underlying the cutin deficiency in a mutant thereafter named gpat6-a (for glycerol-3-phosphate acyltransferase6). To this end, a backcross population (BC₁F₂) segregating for the glossy trait was phenotyped. Individuals displaying either a wild-type or a glossy fruit trait were then pooled into bulked populations and submitted to whole-genome sequencing prior to mutation frequency analysis. This revealed that the causal point mutation in the gpat6-a mutant introduces a charged amino acid adjacent to the active site of a GPAT6 enzyme. We further showed that this mutation completely abolished the GPAT activity of the recombinant protein. The gpat6-a mutant showed perturbed pollen formation but, unlike a gpat6 mutant of Arabidopsis (Arabidopsis thaliana), was not male sterile. The most striking phenotype was observed in the mutant fruit, where cuticle thickness, composition, and properties were altered. RNA sequencing analysis highlighted the main processes and pathways that were affected by the mutation at the transcriptional level, which included those associated with lipid, secondary metabolite, and cell wall biosynthesis.</abstract><cop>United States</cop><pub>American Society of Plant Biologists</pub><pmid>27208295</pmid><doi>10.1104/pp.16.00409</doi><tpages>20</tpages><orcidid>https://orcid.org/0000-0002-0183-7000</orcidid><orcidid>https://orcid.org/0000-0003-1881-9631</orcidid><orcidid>https://orcid.org/0000-0001-6460-4637</orcidid><orcidid>https://orcid.org/0000-0002-6921-7246</orcidid><orcidid>https://orcid.org/0000-0001-5385-450X</orcidid><orcidid>https://orcid.org/0000-0002-6746-1755</orcidid><orcidid>https://orcid.org/0000-0002-5665-2468</orcidid><orcidid>https://orcid.org/0000-0002-2316-9947</orcidid><orcidid>https://orcid.org/0000-0002-6831-2823</orcidid><oa>free_for_read</oa></addata></record> |
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source | Jstor Complete Legacy; Oxford University Press Journals All Titles (1996-Current); MEDLINE; EZB-FREE-00999 freely available EZB journals |
subjects | Amino Acid Sequence BIOCHEMISTRY AND METABOLISM Chromosome Mapping Fruit - anatomy & histology Fruit - enzymology Fruit - genetics Fruit - growth & development Glycerol-3-Phosphate O-Acyltransferase - genetics Glycerol-3-Phosphate O-Acyltransferase - metabolism Life Sciences Lycopersicon esculentum - anatomy & histology Lycopersicon esculentum - enzymology Lycopersicon esculentum - genetics Lycopersicon esculentum - growth & development Membrane Lipids - metabolism Models, Molecular Mutation Phenotype Phylogeny Plant Proteins - genetics Plant Proteins - metabolism Pollen - anatomy & histology Pollen - enzymology Pollen - genetics Pollen - growth & development Recombinant Proteins Sequence Alignment Sequence Analysis, RNA Vegetal Biology |
title | The Glycerol-3-Phosphate Acyltransferase GPAT6 from Tomato Plays a Central Role in Fruit Cutin Biosynthesis |
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