Tissue-specific profiling of membrane proteins in the salicin sequestering juveniles of the herbivorous leaf beetle, Chrysomela populi.
Identifieur interne : 000662 ( Main/Exploration ); précédent : 000661; suivant : 000663Tissue-specific profiling of membrane proteins in the salicin sequestering juveniles of the herbivorous leaf beetle, Chrysomela populi.
Auteurs : Lydia Schmidt [Allemagne] ; Natalie Wielsch [Allemagne] ; Ding Wang [Allemagne] ; Wilhelm Boland [Allemagne] ; Antje Burse [Allemagne]Source :
- Insect biochemistry and molecular biology [ 1879-0240 ] ; 2019.
Descripteurs français
- KwdFr :
- Alcools benzyliques (métabolisme), Analyse de profil d'expression de gènes (MeSH), Animaux (MeSH), Coléoptères (croissance et développement), Coléoptères (génétique), Coléoptères (métabolisme), Glucosides (métabolisme), Herbivorie (MeSH), Larve (croissance et développement), Larve (génétique), Larve (métabolisme), Protéines d'insecte (génétique), Protéines d'insecte (métabolisme), Protéines membranaires (génétique), Protéines membranaires (métabolisme), Transcriptome (génétique).
- MESH :
- croissance et développement : Coléoptères, Larve.
- génétique : Coléoptères, Larve, Protéines d'insecte, Protéines membranaires, Transcriptome.
- métabolisme : Alcools benzyliques, Coléoptères, Glucosides, Larve, Protéines d'insecte, Protéines membranaires.
- Analyse de profil d'expression de gènes, Animaux, Herbivorie.
English descriptors
- KwdEn :
- Animals (MeSH), Benzyl Alcohols (metabolism), Coleoptera (genetics), Coleoptera (growth & development), Coleoptera (metabolism), Gene Expression Profiling (MeSH), Glucosides (metabolism), Herbivory (MeSH), Insect Proteins (genetics), Insect Proteins (metabolism), Larva (genetics), Larva (growth & development), Larva (metabolism), Membrane Proteins (genetics), Membrane Proteins (metabolism), Transcriptome (genetics).
- MESH :
- chemical , genetics : Insect Proteins, Membrane Proteins.
- chemical , metabolism : Benzyl Alcohols, Glucosides, Insect Proteins, Membrane Proteins.
- genetics : Coleoptera, Larva, Transcriptome.
- growth & development : Coleoptera, Larva.
- metabolism : Coleoptera, Larva.
- Animals, Gene Expression Profiling, Herbivory.
Abstract
Sequestration of plant secondary metabolites is a detoxification strategy widespread in herbivorous insects including not only storage, but also usage of these metabolites for the insects' own benefit. Larvae of the poplar leaf beetle Chrysomela populi sequester plant-derived salicin to produce the deterrent salicylaldehyde in specialized exocrine glands. To identify putative transporters involved in the sequestration process we investigated integral membrane proteins of several tissues from juvenile C. populi by using a proteomics approach. Computational analyses led to the identification of 122 transport proteins in the gut, 105 in the Malpighian tubules, 94 in the fat body and 27 in the defensive glands. Among these, primary active transporters as well as electrochemical potential-driven transporters were most abundant in all tissues, including ABC transporters (especially subfamilies B, C and G) and sugar porters as most interesting families facilitating the sequestration of plant glycosides. Whereas ABC transporters are predominantly expressed simultaneously in several tissues, sugar porters are often expressed in only one tissue, suggesting that sugar porters govern more distinct functions than members of the ABC family. The inventory of transporters presented in this study provides the base for further functional characterizations on transport processes of sequestered glycosides in insects.
DOI: 10.1016/j.ibmb.2019.03.009
PubMed: 30922827
Affiliations:
Links toward previous steps (curation, corpus...)
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Electronic address: aburse@ice.mpg.de.</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Max Planck Institute for Chemical Ecology, Department of Bioorganic Chemistry, Hans-Knöll-Str. 8, D-07745, Jena</wicri:regionArea><wicri:noRegion>07745, Jena</wicri:noRegion><wicri:noRegion>07745, Jena</wicri:noRegion><wicri:noRegion>Jena</wicri:noRegion></affiliation></author></analytic><series><title level="j">Insect biochemistry and molecular biology</title><idno type="eISSN">1879-0240</idno><imprint><date when="2019" type="published">2019</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals (MeSH)</term><term>Benzyl Alcohols (metabolism)</term><term>Coleoptera (genetics)</term><term>Coleoptera (growth & development)</term><term>Coleoptera (metabolism)</term><term>Gene Expression Profiling (MeSH)</term><term>Glucosides (metabolism)</term><term>Herbivory (MeSH)</term><term>Insect Proteins (genetics)</term><term>Insect Proteins (metabolism)</term><term>Larva (genetics)</term><term>Larva (growth & development)</term><term>Larva (metabolism)</term><term>Membrane Proteins (genetics)</term><term>Membrane Proteins (metabolism)</term><term>Transcriptome (genetics)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Alcools benzyliques (métabolisme)</term><term>Analyse de profil d'expression de gènes (MeSH)</term><term>Animaux (MeSH)</term><term>Coléoptères (croissance et développement)</term><term>Coléoptères (génétique)</term><term>Coléoptères (métabolisme)</term><term>Glucosides (métabolisme)</term><term>Herbivorie (MeSH)</term><term>Larve (croissance et développement)</term><term>Larve (génétique)</term><term>Larve (métabolisme)</term><term>Protéines d'insecte (génétique)</term><term>Protéines d'insecte (métabolisme)</term><term>Protéines membranaires (génétique)</term><term>Protéines membranaires (métabolisme)</term><term>Transcriptome (génétique)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Insect Proteins</term><term>Membrane Proteins</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Benzyl Alcohols</term><term>Glucosides</term><term>Insect Proteins</term><term>Membrane Proteins</term></keywords><keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr"><term>Coléoptères</term><term>Larve</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Coleoptera</term><term>Larva</term><term>Transcriptome</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Coleoptera</term><term>Larva</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Coléoptères</term><term>Larve</term><term>Protéines d'insecte</term><term>Protéines membranaires</term><term>Transcriptome</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Coleoptera</term><term>Larva</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Alcools benzyliques</term><term>Coléoptères</term><term>Glucosides</term><term>Larve</term><term>Protéines d'insecte</term><term>Protéines membranaires</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Gene Expression Profiling</term><term>Herbivory</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Analyse de profil d'expression de gènes</term><term>Animaux</term><term>Herbivorie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Sequestration of plant secondary metabolites is a detoxification strategy widespread in herbivorous insects including not only storage, but also usage of these metabolites for the insects' own benefit. Larvae of the poplar leaf beetle Chrysomela populi sequester plant-derived salicin to produce the deterrent salicylaldehyde in specialized exocrine glands. To identify putative transporters involved in the sequestration process we investigated integral membrane proteins of several tissues from juvenile C. populi by using a proteomics approach. Computational analyses led to the identification of 122 transport proteins in the gut, 105 in the Malpighian tubules, 94 in the fat body and 27 in the defensive glands. Among these, primary active transporters as well as electrochemical potential-driven transporters were most abundant in all tissues, including ABC transporters (especially subfamilies B, C and G) and sugar porters as most interesting families facilitating the sequestration of plant glycosides. Whereas ABC transporters are predominantly expressed simultaneously in several tissues, sugar porters are often expressed in only one tissue, suggesting that sugar porters govern more distinct functions than members of the ABC family. The inventory of transporters presented in this study provides the base for further functional characterizations on transport processes of sequestered glycosides in insects.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">30922827</PMID><DateCompleted><Year>2020</Year><Month>01</Month><Day>10</Day></DateCompleted><DateRevised><Year>2020</Year><Month>01</Month><Day>10</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1879-0240</ISSN><JournalIssue CitedMedium="Internet"><Volume>109</Volume><PubDate><Year>2019</Year><Month>06</Month></PubDate></JournalIssue><Title>Insect biochemistry and molecular biology</Title><ISOAbbreviation>Insect Biochem Mol Biol</ISOAbbreviation></Journal><ArticleTitle>Tissue-specific profiling of membrane proteins in the salicin sequestering juveniles of the herbivorous leaf beetle, Chrysomela populi.</ArticleTitle><Pagination><MedlinePgn>81-91</MedlinePgn></Pagination><ELocationID EIdType="pii" ValidYN="Y">S0965-1748(18)30452-1</ELocationID><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.ibmb.2019.03.009</ELocationID><Abstract><AbstractText>Sequestration of plant secondary metabolites is a detoxification strategy widespread in herbivorous insects including not only storage, but also usage of these metabolites for the insects' own benefit. Larvae of the poplar leaf beetle Chrysomela populi sequester plant-derived salicin to produce the deterrent salicylaldehyde in specialized exocrine glands. To identify putative transporters involved in the sequestration process we investigated integral membrane proteins of several tissues from juvenile C. populi by using a proteomics approach. Computational analyses led to the identification of 122 transport proteins in the gut, 105 in the Malpighian tubules, 94 in the fat body and 27 in the defensive glands. Among these, primary active transporters as well as electrochemical potential-driven transporters were most abundant in all tissues, including ABC transporters (especially subfamilies B, C and G) and sugar porters as most interesting families facilitating the sequestration of plant glycosides. Whereas ABC transporters are predominantly expressed simultaneously in several tissues, sugar porters are often expressed in only one tissue, suggesting that sugar porters govern more distinct functions than members of the ABC family. The inventory of transporters presented in this study provides the base for further functional characterizations on transport processes of sequestered glycosides in insects.</AbstractText><CopyrightInformation>Copyright © 2019. Published by Elsevier Ltd.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Schmidt</LastName><ForeName>Lydia</ForeName><Initials>L</Initials><AffiliationInfo><Affiliation>Max Planck Institute for Chemical Ecology, Department of Bioorganic Chemistry, Hans-Knöll-Str. 8, D-07745, Jena, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wielsch</LastName><ForeName>Natalie</ForeName><Initials>N</Initials><AffiliationInfo><Affiliation>Max Planck Institute for Chemical Ecology, Research Group Mass Spectrometry/ Proteomics, Hans-Knöll-Str. 8, D-07745, Jena, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Ding</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Max Planck Institute for Chemical Ecology, Department of Bioorganic Chemistry, Hans-Knöll-Str. 8, D-07745, Jena, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Boland</LastName><ForeName>Wilhelm</ForeName><Initials>W</Initials><AffiliationInfo><Affiliation>Max Planck Institute for Chemical Ecology, Department of Bioorganic Chemistry, Hans-Knöll-Str. 8, D-07745, Jena, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Burse</LastName><ForeName>Antje</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Max Planck Institute for Chemical Ecology, Department of Bioorganic Chemistry, Hans-Knöll-Str. 8, D-07745, Jena, Germany. Electronic address: aburse@ice.mpg.de.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2019</Year><Month>03</Month><Day>25</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Insect Biochem Mol Biol</MedlineTA><NlmUniqueID>9207282</NlmUniqueID><ISSNLinking>0965-1748</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D001592">Benzyl Alcohols</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005960">Glucosides</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D019476">Insect Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D008565">Membrane Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>4649620TBZ</RegistryNumber><NameOfSubstance UI="C005696">salicin</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001592" MajorTopicYN="N">Benzyl Alcohols</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001517" MajorTopicYN="N">Coleoptera</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020869" MajorTopicYN="N">Gene Expression Profiling</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005960" MajorTopicYN="N">Glucosides</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D060434" MajorTopicYN="N">Herbivory</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D019476" MajorTopicYN="N">Insect Proteins</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007814" MajorTopicYN="N">Larva</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008565" MajorTopicYN="N">Membrane Proteins</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D059467" MajorTopicYN="N">Transcriptome</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="Y">ABC transporter</Keyword><Keyword MajorTopicYN="Y">Leaf beetle</Keyword><Keyword MajorTopicYN="Y">MFS</Keyword><Keyword MajorTopicYN="Y">Membrane proteome</Keyword><Keyword MajorTopicYN="Y">Proteomics</Keyword><Keyword MajorTopicYN="Y">Sequestration</Keyword><Keyword MajorTopicYN="Y">Sugar porters</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2018</Year><Month>12</Month><Day>12</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2019</Year><Month>03</Month><Day>21</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2019</Year><Month>03</Month><Day>21</Day></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2019</Year><Month>3</Month><Day>30</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2020</Year><Month>1</Month><Day>11</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2019</Year><Month>3</Month><Day>30</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">30922827</ArticleId><ArticleId IdType="pii">S0965-1748(18)30452-1</ArticleId><ArticleId IdType="doi">10.1016/j.ibmb.2019.03.009</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Allemagne</li></country></list><tree><country name="Allemagne"><noRegion><name sortKey="Schmidt, Lydia" sort="Schmidt, Lydia" uniqKey="Schmidt L" first="Lydia" last="Schmidt">Lydia Schmidt</name></noRegion><name sortKey="Boland, Wilhelm" sort="Boland, Wilhelm" uniqKey="Boland W" first="Wilhelm" last="Boland">Wilhelm Boland</name><name sortKey="Burse, Antje" sort="Burse, Antje" uniqKey="Burse A" first="Antje" last="Burse">Antje Burse</name><name sortKey="Wang, Ding" sort="Wang, Ding" uniqKey="Wang D" first="Ding" last="Wang">Ding Wang</name><name sortKey="Wielsch, Natalie" sort="Wielsch, Natalie" uniqKey="Wielsch N" first="Natalie" last="Wielsch">Natalie Wielsch</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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