Not just the wall: the other ways to turn the yeast CWI pathway on.
Identifieur interne : 000077 ( Main/Exploration ); précédent : 000076; suivant : 000078Not just the wall: the other ways to turn the yeast CWI pathway on.
Auteurs : Elena Jiménez-Gutiérrez [Espagne] ; Estíbaliz Alegría-Carrasco [Espagne] ; Ángela Sellers-Moya [Espagne] ; María Molina [Espagne] ; Humberto Martín [Espagne]Source :
- International microbiology : the official journal of the Spanish Society for Microbiology [ 1618-1905 ] ; 2020.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Mitogen-Activated Protein Kinases.
- metabolism : Cell Membrane, Cell Wall, Cytoskeleton.
- physiology : Yeasts.
- DNA Damage, Endoplasmic Reticulum Stress, Signal Transduction, Stress, Physiological.
Abstract
The Saccharomyces cerevisiae cell wall integrity (CWI) pathway took this name when its role in the cell response to cell wall aggressions was clearly established. The receptors involved in sensing the damage, the relevant components operating in signaling to the MAPK Slt2, the transcription factors activated by this MAPK, as well as some key regulatory mechanisms have been identified and characterized along almost 30 years. However, other stimuli that do not alter specifically the yeast cell wall, including protein unfolding, low or high pH, or plasma membrane, oxidative and genotoxic stresses, have been also found to trigger the activation of this pathway. In this review, we compile almost forty non-cell wall-specific compounds or conditions, such as tunicamycin, hypo-osmotic shock, diamide, hydroxyurea, arsenate, and rapamycin, which induce these stresses. Relevant aspects of the CWI-mediated signaling in the response to these non-conventional pathway activators are discussed. The data presented here highlight the central and key position of the CWI pathway in the safeguard of yeast cells to a wide variety of external aggressions.
DOI: 10.1007/s10123-019-00092-2
PubMed: 31342212
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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Ramón y Cajal s/n, 28040, Madrid, Spain.</nlm:affiliation><country xml:lang="fr">Espagne</country><wicri:regionArea>Departamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense de Madrid (IRICIS), Pza. Ramón y Cajal s/n, 28040, Madrid</wicri:regionArea><placeName><settlement type="city">Madrid</settlement><region nuts="2" type="region">Communauté de Madrid</region></placeName><orgName type="university">Université complutense de Madrid</orgName></affiliation></author><author><name sortKey="Alegria Carrasco, Estibaliz" sort="Alegria Carrasco, Estibaliz" uniqKey="Alegria Carrasco E" first="Estíbaliz" last="Alegría-Carrasco">Estíbaliz Alegría-Carrasco</name><affiliation wicri:level="4"><nlm:affiliation>Departamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense de Madrid (IRICIS), Pza. 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Ramón y Cajal s/n, 28040, Madrid, Spain. humberto@ucm.es.</nlm:affiliation><country xml:lang="fr">Espagne</country><wicri:regionArea>Departamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense de Madrid (IRICIS), Pza. Ramón y Cajal s/n, 28040, Madrid</wicri:regionArea><placeName><settlement type="city">Madrid</settlement><region nuts="2" type="region">Communauté de Madrid</region></placeName><orgName type="university">Université complutense de Madrid</orgName></affiliation></author></analytic><series><title level="j">International microbiology : the official journal of the Spanish Society for Microbiology</title><idno type="eISSN">1618-1905</idno><imprint><date when="2020" type="published">2020</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cell Membrane (metabolism)</term><term>Cell Wall (metabolism)</term><term>Cytoskeleton (metabolism)</term><term>DNA Damage (MeSH)</term><term>Endoplasmic Reticulum Stress (MeSH)</term><term>Mitogen-Activated Protein Kinases (metabolism)</term><term>Signal Transduction (MeSH)</term><term>Stress, Physiological (MeSH)</term><term>Yeasts (physiology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Altération de l'ADN (MeSH)</term><term>Cytosquelette (métabolisme)</term><term>Levures (physiologie)</term><term>Membrane cellulaire (métabolisme)</term><term>Mitogen-Activated Protein Kinases (métabolisme)</term><term>Paroi cellulaire (métabolisme)</term><term>Stress du réticulum endoplasmique (MeSH)</term><term>Stress physiologique (MeSH)</term><term>Transduction du signal (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Mitogen-Activated Protein Kinases</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Cell Membrane</term><term>Cell Wall</term><term>Cytoskeleton</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Cytosquelette</term><term>Membrane cellulaire</term><term>Mitogen-Activated Protein Kinases</term><term>Paroi cellulaire</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Levures</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Yeasts</term></keywords><keywords scheme="MESH" xml:lang="en"><term>DNA Damage</term><term>Endoplasmic Reticulum Stress</term><term>Signal Transduction</term><term>Stress, Physiological</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Altération de l'ADN</term><term>Stress du réticulum endoplasmique</term><term>Stress physiologique</term><term>Transduction du signal</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The Saccharomyces cerevisiae cell wall integrity (CWI) pathway took this name when its role in the cell response to cell wall aggressions was clearly established. The receptors involved in sensing the damage, the relevant components operating in signaling to the MAPK Slt2, the transcription factors activated by this MAPK, as well as some key regulatory mechanisms have been identified and characterized along almost 30 years. However, other stimuli that do not alter specifically the yeast cell wall, including protein unfolding, low or high pH, or plasma membrane, oxidative and genotoxic stresses, have been also found to trigger the activation of this pathway. In this review, we compile almost forty non-cell wall-specific compounds or conditions, such as tunicamycin, hypo-osmotic shock, diamide, hydroxyurea, arsenate, and rapamycin, which induce these stresses. Relevant aspects of the CWI-mediated signaling in the response to these non-conventional pathway activators are discussed. The data presented here highlight the central and key position of the CWI pathway in the safeguard of yeast cells to a wide variety of external aggressions.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">31342212</PMID><DateCompleted><Year>2020</Year><Month>10</Month><Day>07</Day></DateCompleted><DateRevised><Year>2020</Year><Month>10</Month><Day>07</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1618-1905</ISSN><JournalIssue CitedMedium="Internet"><Volume>23</Volume><Issue>1</Issue><PubDate><Year>2020</Year><Month>Jan</Month></PubDate></JournalIssue><Title>International microbiology : the official journal of the Spanish Society for Microbiology</Title><ISOAbbreviation>Int Microbiol</ISOAbbreviation></Journal><ArticleTitle>Not just the wall: the other ways to turn the yeast CWI pathway on.</ArticleTitle><Pagination><MedlinePgn>107-119</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1007/s10123-019-00092-2</ELocationID><Abstract><AbstractText>The Saccharomyces cerevisiae cell wall integrity (CWI) pathway took this name when its role in the cell response to cell wall aggressions was clearly established. The receptors involved in sensing the damage, the relevant components operating in signaling to the MAPK Slt2, the transcription factors activated by this MAPK, as well as some key regulatory mechanisms have been identified and characterized along almost 30 years. However, other stimuli that do not alter specifically the yeast cell wall, including protein unfolding, low or high pH, or plasma membrane, oxidative and genotoxic stresses, have been also found to trigger the activation of this pathway. In this review, we compile almost forty non-cell wall-specific compounds or conditions, such as tunicamycin, hypo-osmotic shock, diamide, hydroxyurea, arsenate, and rapamycin, which induce these stresses. Relevant aspects of the CWI-mediated signaling in the response to these non-conventional pathway activators are discussed. The data presented here highlight the central and key position of the CWI pathway in the safeguard of yeast cells to a wide variety of external aggressions.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Jiménez-Gutiérrez</LastName><ForeName>Elena</ForeName><Initials>E</Initials><AffiliationInfo><Affiliation>Departamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense de Madrid (IRICIS), Pza. Ramón y Cajal s/n, 28040, Madrid, Spain.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Alegría-Carrasco</LastName><ForeName>Estíbaliz</ForeName><Initials>E</Initials><AffiliationInfo><Affiliation>Departamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense de Madrid (IRICIS), Pza. Ramón y Cajal s/n, 28040, Madrid, Spain.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sellers-Moya</LastName><ForeName>Ángela</ForeName><Initials>Á</Initials><AffiliationInfo><Affiliation>Departamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense de Madrid (IRICIS), Pza. Ramón y Cajal s/n, 28040, Madrid, Spain.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Molina</LastName><ForeName>María</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Departamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense de Madrid (IRICIS), Pza. Ramón y Cajal s/n, 28040, Madrid, Spain. molmifa@ucm.es.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Martín</LastName><ForeName>Humberto</ForeName><Initials>H</Initials><Identifier Source="ORCID">http://orcid.org/0000-0002-6736-3602</Identifier><AffiliationInfo><Affiliation>Departamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense de Madrid (IRICIS), Pza. Ramón y Cajal s/n, 28040, Madrid, Spain. humberto@ucm.es.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>BIO2016-75030-P</GrantID><Agency>Ministry of Science, Innovation and Universities</Agency><Country></Country></Grant><Grant><GrantID>S2017/BMD-3691-InGEMICS-CM</GrantID><Agency>Comunidad de Madrid</Agency><Country></Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2019</Year><Month>07</Month><Day>24</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Int Microbiol</MedlineTA><NlmUniqueID>9816585</NlmUniqueID><ISSNLinking>1139-6709</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>EC 2.7.11.24</RegistryNumber><NameOfSubstance UI="D020928">Mitogen-Activated Protein Kinases</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D002462" MajorTopicYN="N">Cell Membrane</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002473" MajorTopicYN="N">Cell Wall</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003599" MajorTopicYN="N">Cytoskeleton</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004249" MajorTopicYN="N">DNA Damage</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D059865" MajorTopicYN="N">Endoplasmic Reticulum Stress</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D020928" MajorTopicYN="N">Mitogen-Activated Protein Kinases</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015398" MajorTopicYN="Y">Signal Transduction</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013312" MajorTopicYN="N">Stress, Physiological</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015003" MajorTopicYN="N">Yeasts</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">CWI pathway</Keyword><Keyword MajorTopicYN="N">MAPK</Keyword><Keyword MajorTopicYN="N">Slt2</Keyword><Keyword MajorTopicYN="N">Stress response</Keyword><Keyword MajorTopicYN="N">Yeast cell wall</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2019</Year><Month>06</Month><Day>14</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2019</Year><Month>07</Month><Day>11</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2019</Year><Month>07</Month><Day>10</Day></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2019</Year><Month>7</Month><Day>26</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2020</Year><Month>10</Month><Day>8</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2019</Year><Month>7</Month><Day>26</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">31342212</ArticleId><ArticleId IdType="doi">10.1007/s10123-019-00092-2</ArticleId><ArticleId IdType="pii">10.1007/s10123-019-00092-2</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Espagne</li></country><region><li>Communauté de Madrid</li></region><settlement><li>Madrid</li></settlement><orgName><li>Université complutense de Madrid</li></orgName></list><tree><country name="Espagne"><region name="Communauté de Madrid"><name sortKey="Jimenez Gutierrez, Elena" sort="Jimenez Gutierrez, Elena" uniqKey="Jimenez Gutierrez E" first="Elena" last="Jiménez-Gutiérrez">Elena Jiménez-Gutiérrez</name></region><name sortKey="Alegria Carrasco, Estibaliz" sort="Alegria Carrasco, Estibaliz" uniqKey="Alegria Carrasco E" first="Estíbaliz" last="Alegría-Carrasco">Estíbaliz Alegría-Carrasco</name><name sortKey="Martin, Humberto" sort="Martin, Humberto" uniqKey="Martin H" first="Humberto" last="Martín">Humberto Martín</name><name sortKey="Molina, Maria" sort="Molina, Maria" uniqKey="Molina M" first="María" last="Molina">María Molina</name><name sortKey="Sellers Moya, Angela" sort="Sellers Moya, Angela" uniqKey="Sellers Moya A" first="Ángela" last="Sellers-Moya">Ángela Sellers-Moya</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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