Yeast metabolic and signaling genes are required for heat-shock survival and have little overlap with the heat-induced genes
Genome-wide gene-expression studies have shown that hundreds of yeast genes are induced or repressed transiently by changes in temperature; many are annotated to stress response on this basis. To obtain a genome-scale assessment of which genes are functionally important for innate and/or acquired th...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2013-11, Vol.110 (46), p.E4393-E4402 |
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description | Genome-wide gene-expression studies have shown that hundreds of yeast genes are induced or repressed transiently by changes in temperature; many are annotated to stress response on this basis. To obtain a genome-scale assessment of which genes are functionally important for innate and/or acquired thermotolerance, we combined the use of a barcoded pool of ∼4,800 nonessential, prototrophic Saccharomyces cerevisiae deletion strains with Illumina-based deep-sequencing technology. As reported in other recent studies that have used deletion mutants to study stress responses, we observed that gene deletions resulting in the highest thermosensitivity generally are not the same as those transcriptionally induced in response to heat stress. Functional analysis of identified genes revealed that metabolism, cellular signaling, and chromatin regulation play roles in regulating thermotolerance and in acquired thermotolerance. However, for most of the genes identified, the molecular mechanism behind this action remains unclear. In fact, a large fraction of identified genes are annotated as having unknown functions, further underscoring our incomplete understanding of the response to heat shock. We suggest that survival after heat shock depends on a small number of genes that function in assessing the metabolic health of the cell and/or regulate its growth in a changing environment. |
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To obtain a genome-scale assessment of which genes are functionally important for innate and/or acquired thermotolerance, we combined the use of a barcoded pool of ∼4,800 nonessential, prototrophic Saccharomyces cerevisiae deletion strains with Illumina-based deep-sequencing technology. As reported in other recent studies that have used deletion mutants to study stress responses, we observed that gene deletions resulting in the highest thermosensitivity generally are not the same as those transcriptionally induced in response to heat stress. Functional analysis of identified genes revealed that metabolism, cellular signaling, and chromatin regulation play roles in regulating thermotolerance and in acquired thermotolerance. However, for most of the genes identified, the molecular mechanism behind this action remains unclear. In fact, a large fraction of identified genes are annotated as having unknown functions, further underscoring our incomplete understanding of the response to heat shock. We suggest that survival after heat shock depends on a small number of genes that function in assessing the metabolic health of the cell and/or regulate its growth in a changing environment.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1318100110</identifier><identifier>PMID: 24167267</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Biological Sciences ; cell communication ; Chromatin ; DNA Barcoding, Taxonomic ; DNA Primers - genetics ; Gene Deletion ; Gene expression ; Gene Expression Profiling - methods ; Gene Expression Regulation, Fungal - genetics ; Genes ; Genetic Markers - genetics ; Genetics ; Heat ; heat shock response ; heat tolerance ; Heat-Shock Response - genetics ; High-Throughput Nucleotide Sequencing ; Metabolic Networks and Pathways - genetics ; metabolism ; Molecular Sequence Annotation ; mutants ; PNAS Plus ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - genetics ; Signal Transduction - genetics ; Stress ; Systems Biology - methods ; temperature ; transcription (genetics) ; Yeast ; yeasts</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2013-11, Vol.110 (46), p.E4393-E4402</ispartof><rights>Copyright National Academy of Sciences Nov 12, 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c536t-f19a5790474d8492b1e230ba7d70c74591ce3ed6b835e80022ad18e57de528f33</citedby><cites>FETCH-LOGICAL-c536t-f19a5790474d8492b1e230ba7d70c74591ce3ed6b835e80022ad18e57de528f33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/110/46.cover.gif</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3831991/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3831991/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24167267$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gibney, Patrick A</creatorcontrib><creatorcontrib>Lu, Charles</creatorcontrib><creatorcontrib>Caudy, Amy A</creatorcontrib><creatorcontrib>Hess, David C</creatorcontrib><creatorcontrib>Botstein, David</creatorcontrib><title>Yeast metabolic and signaling genes are required for heat-shock survival and have little overlap with the heat-induced genes</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Genome-wide gene-expression studies have shown that hundreds of yeast genes are induced or repressed transiently by changes in temperature; many are annotated to stress response on this basis. To obtain a genome-scale assessment of which genes are functionally important for innate and/or acquired thermotolerance, we combined the use of a barcoded pool of ∼4,800 nonessential, prototrophic Saccharomyces cerevisiae deletion strains with Illumina-based deep-sequencing technology. As reported in other recent studies that have used deletion mutants to study stress responses, we observed that gene deletions resulting in the highest thermosensitivity generally are not the same as those transcriptionally induced in response to heat stress. Functional analysis of identified genes revealed that metabolism, cellular signaling, and chromatin regulation play roles in regulating thermotolerance and in acquired thermotolerance. However, for most of the genes identified, the molecular mechanism behind this action remains unclear. In fact, a large fraction of identified genes are annotated as having unknown functions, further underscoring our incomplete understanding of the response to heat shock. 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Lu, Charles ; Caudy, Amy A ; Hess, David C ; Botstein, David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c536t-f19a5790474d8492b1e230ba7d70c74591ce3ed6b835e80022ad18e57de528f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Biological Sciences</topic><topic>cell communication</topic><topic>Chromatin</topic><topic>DNA Barcoding, Taxonomic</topic><topic>DNA Primers - genetics</topic><topic>Gene Deletion</topic><topic>Gene expression</topic><topic>Gene Expression Profiling - methods</topic><topic>Gene Expression Regulation, Fungal - genetics</topic><topic>Genes</topic><topic>Genetic Markers - genetics</topic><topic>Genetics</topic><topic>Heat</topic><topic>heat shock response</topic><topic>heat tolerance</topic><topic>Heat-Shock Response - genetics</topic><topic>High-Throughput Nucleotide Sequencing</topic><topic>Metabolic Networks and Pathways - genetics</topic><topic>metabolism</topic><topic>Molecular Sequence Annotation</topic><topic>mutants</topic><topic>PNAS Plus</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Signal Transduction - genetics</topic><topic>Stress</topic><topic>Systems Biology - methods</topic><topic>temperature</topic><topic>transcription (genetics)</topic><topic>Yeast</topic><topic>yeasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gibney, Patrick A</creatorcontrib><creatorcontrib>Lu, Charles</creatorcontrib><creatorcontrib>Caudy, Amy A</creatorcontrib><creatorcontrib>Hess, David C</creatorcontrib><creatorcontrib>Botstein, David</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gibney, Patrick A</au><au>Lu, Charles</au><au>Caudy, Amy A</au><au>Hess, David C</au><au>Botstein, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Yeast metabolic and signaling genes are required for heat-shock survival and have little overlap with the heat-induced genes</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2013-11-12</date><risdate>2013</risdate><volume>110</volume><issue>46</issue><spage>E4393</spage><epage>E4402</epage><pages>E4393-E4402</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Genome-wide gene-expression studies have shown that hundreds of yeast genes are induced or repressed transiently by changes in temperature; 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To obtain a genome-scale assessment of which genes are functionally important for innate and/or acquired thermotolerance, we combined the use of a barcoded pool of ∼4,800 nonessential, prototrophic Saccharomyces cerevisiae deletion strains with Illumina-based deep-sequencing technology. As reported in other recent studies that have used deletion mutants to study stress responses, we observed that gene deletions resulting in the highest thermosensitivity generally are not the same as those transcriptionally induced in response to heat stress. Functional analysis of identified genes revealed that metabolism, cellular signaling, and chromatin regulation play roles in regulating thermotolerance and in acquired thermotolerance. However, for most of the genes identified, the molecular mechanism behind this action remains unclear. In fact, a large fraction of identified genes are annotated as having unknown functions, further underscoring our incomplete understanding of the response to heat shock. We suggest that survival after heat shock depends on a small number of genes that function in assessing the metabolic health of the cell and/or regulate its growth in a changing environment.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>24167267</pmid><doi>10.1073/pnas.1318100110</doi><oa>free_for_read</oa></addata></record> |
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subjects | Biological Sciences cell communication Chromatin DNA Barcoding, Taxonomic DNA Primers - genetics Gene Deletion Gene expression Gene Expression Profiling - methods Gene Expression Regulation, Fungal - genetics Genes Genetic Markers - genetics Genetics Heat heat shock response heat tolerance Heat-Shock Response - genetics High-Throughput Nucleotide Sequencing Metabolic Networks and Pathways - genetics metabolism Molecular Sequence Annotation mutants PNAS Plus Saccharomyces cerevisiae Saccharomyces cerevisiae - genetics Signal Transduction - genetics Stress Systems Biology - methods temperature transcription (genetics) Yeast yeasts |
title | Yeast metabolic and signaling genes are required for heat-shock survival and have little overlap with the heat-induced genes |
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