Loading…
Specificity of amino acid regulated gene expression: analysis of genes subjected to either complete or single amino acid deprivation
Amino acid deprivation activates the amino acid response (AAR) pathway that enhances transcription of genes containing an amino acid response element (AARE). The present data reveal a quantitative difference in the response to deprivation of individual amino acids. The AAR leads to increased eukaryo...
Saved in:
Published in: | Amino acids 2009-05, Vol.37 (1), p.79-88 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c625t-c903bf9cf391dde9b9935b83bf0ca5cc9ffa647f261f7a9a7946161bd3e008fe3 |
---|---|
cites | cdi_FETCH-LOGICAL-c625t-c903bf9cf391dde9b9935b83bf0ca5cc9ffa647f261f7a9a7946161bd3e008fe3 |
container_end_page | 88 |
container_issue | 1 |
container_start_page | 79 |
container_title | Amino acids |
container_volume | 37 |
creator | Palii, S. S Kays, C. E Deval, C Bruhat, A Fafournoux, P Kilberg, M. S |
description | Amino acid deprivation activates the amino acid response (AAR) pathway that enhances transcription of genes containing an amino acid response element (AARE). The present data reveal a quantitative difference in the response to deprivation of individual amino acids. The AAR leads to increased eukaryotic initiation factor 2α (eIF2α) phosphorylation and ATF4 translation. When HepG2 cells were deprived of an individual essential amino acid, p-eIF2α and activating transcription factor 4 were increased, but the correlation was relatively weak. Complete amino acid starvation in either Earle's balanced salt solution or Krebs-Ringer bicarbonate buffer (KRB) resulted in activation of transcription driven by a SNAT2 genomic fragment that contained an AARE. However, for the KRB, a proportion of the transcription was AARE-independent suggesting that amino acid-independent mechanisms were responsible. Therefore, activation of AARE-driven transcription is triggered by a deficiency in any one of the essential amino acids, but the response is not uniform. Furthermore, caution must be exercised when using a medium completely devoid of amino acids. |
doi_str_mv | 10.1007/s00726-008-0199-2 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3595573</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67195579</sourcerecordid><originalsourceid>FETCH-LOGICAL-c625t-c903bf9cf391dde9b9935b83bf0ca5cc9ffa647f261f7a9a7946161bd3e008fe3</originalsourceid><addsrcrecordid>eNp9ks-L1DAUx4Mo7uzqH-BFA8Kih2p-tGmzB2FZ1BUGPKx7Dmn60snQNmPSDs7dP9yUDjou6CUh733e9yUvX4ReUPKOElK-j2lhIiOkygiVMmOP0IrmvMpYOj1GKyK5zPK8oGfoPMYtIZRVVDxFZ1QSIhmrVujn3Q6Ms8648YC9xbp3g8fauAYHaKdOj9DgFgbA8GMXIEbnhyusB90dootzxZyMOE71FswMjx6DGzcQsPH9roMRsA84uqHt4FS-gV1wez0mwWfoidVdhOfH_QLdf_r47eY2W3_9_OXmep0ZwYoxM5Lw2kpjuaRNA7KWkhd1lWLE6MIYaa0WeWmZoLbUUpcyF1TQuuGQRmSBX6APi-5uqntoDAxj0J1K9-h1OCivnfo7M7iNav1e8UIWRcmTwNtFYPOg7PZ6reYYYUKUgvI9TezlsVnw3yeIo-pdNNB1egA_RSVKOovKBL75L0gJp5xUZcUS-voBuvVTSJ8xU7IQQhIhEkUXygQfYwD7-6qUqNk4ajGOSlNRs3HUrPzydDR_Ko5OSQBbgJhSQwvhtPW_VV8tRVZ7pdvgorq_YyQ9hwpWSV7xX-2F2ZI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1095669066</pqid></control><display><type>article</type><title>Specificity of amino acid regulated gene expression: analysis of genes subjected to either complete or single amino acid deprivation</title><source>Springer Nature</source><creator>Palii, S. S ; Kays, C. E ; Deval, C ; Bruhat, A ; Fafournoux, P ; Kilberg, M. S</creator><creatorcontrib>Palii, S. S ; Kays, C. E ; Deval, C ; Bruhat, A ; Fafournoux, P ; Kilberg, M. S</creatorcontrib><description>Amino acid deprivation activates the amino acid response (AAR) pathway that enhances transcription of genes containing an amino acid response element (AARE). The present data reveal a quantitative difference in the response to deprivation of individual amino acids. The AAR leads to increased eukaryotic initiation factor 2α (eIF2α) phosphorylation and ATF4 translation. When HepG2 cells were deprived of an individual essential amino acid, p-eIF2α and activating transcription factor 4 were increased, but the correlation was relatively weak. Complete amino acid starvation in either Earle's balanced salt solution or Krebs-Ringer bicarbonate buffer (KRB) resulted in activation of transcription driven by a SNAT2 genomic fragment that contained an AARE. However, for the KRB, a proportion of the transcription was AARE-independent suggesting that amino acid-independent mechanisms were responsible. Therefore, activation of AARE-driven transcription is triggered by a deficiency in any one of the essential amino acids, but the response is not uniform. Furthermore, caution must be exercised when using a medium completely devoid of amino acids.</description><identifier>ISSN: 0939-4451</identifier><identifier>EISSN: 1438-2199</identifier><identifier>DOI: 10.1007/s00726-008-0199-2</identifier><identifier>PMID: 19009228</identifier><language>eng</language><publisher>Vienna: Vienna : Springer Vienna</publisher><subject>Activating Transcription Factor 4 - genetics ; Activating Transcription Factor 4 - metabolism ; Amino Acid Transport System A - genetics ; Amino Acid Transport System A - metabolism ; Amino acids ; Amino Acids - deficiency ; Analytical Chemistry ; Animals ; Biochemical Engineering ; Biochemistry ; Biomedical and Life Sciences ; Cell Line ; Cell Line, Tumor ; Eukaryotic Initiation Factor-2 - genetics ; Eukaryotic Initiation Factor-2 - metabolism ; Fibroblasts - metabolism ; Gene Expression Profiling ; Gene Expression Regulation ; Humans ; Life Sciences ; Mice ; Neurobiology ; Nutrition research ; Oligonucleotide Array Sequence Analysis ; Original Article ; Phosphorylation - genetics ; Phosphorylation - physiology ; Proteins ; Proteomics ; Transcriptional Activation</subject><ispartof>Amino acids, 2009-05, Vol.37 (1), p.79-88</ispartof><rights>Springer-Verlag 2008</rights><rights>Springer-Verlag 2009</rights><rights>Copyright</rights><rights>Springer-Verlag 2008 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c625t-c903bf9cf391dde9b9935b83bf0ca5cc9ffa647f261f7a9a7946161bd3e008fe3</citedby><cites>FETCH-LOGICAL-c625t-c903bf9cf391dde9b9935b83bf0ca5cc9ffa647f261f7a9a7946161bd3e008fe3</cites><orcidid>0000-0001-5912-4591 ; 0000-0002-4900-4331</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19009228$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02667613$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Palii, S. S</creatorcontrib><creatorcontrib>Kays, C. E</creatorcontrib><creatorcontrib>Deval, C</creatorcontrib><creatorcontrib>Bruhat, A</creatorcontrib><creatorcontrib>Fafournoux, P</creatorcontrib><creatorcontrib>Kilberg, M. S</creatorcontrib><title>Specificity of amino acid regulated gene expression: analysis of genes subjected to either complete or single amino acid deprivation</title><title>Amino acids</title><addtitle>Amino Acids</addtitle><addtitle>Amino Acids</addtitle><description>Amino acid deprivation activates the amino acid response (AAR) pathway that enhances transcription of genes containing an amino acid response element (AARE). The present data reveal a quantitative difference in the response to deprivation of individual amino acids. The AAR leads to increased eukaryotic initiation factor 2α (eIF2α) phosphorylation and ATF4 translation. When HepG2 cells were deprived of an individual essential amino acid, p-eIF2α and activating transcription factor 4 were increased, but the correlation was relatively weak. Complete amino acid starvation in either Earle's balanced salt solution or Krebs-Ringer bicarbonate buffer (KRB) resulted in activation of transcription driven by a SNAT2 genomic fragment that contained an AARE. However, for the KRB, a proportion of the transcription was AARE-independent suggesting that amino acid-independent mechanisms were responsible. Therefore, activation of AARE-driven transcription is triggered by a deficiency in any one of the essential amino acids, but the response is not uniform. Furthermore, caution must be exercised when using a medium completely devoid of amino acids.</description><subject>Activating Transcription Factor 4 - genetics</subject><subject>Activating Transcription Factor 4 - metabolism</subject><subject>Amino Acid Transport System A - genetics</subject><subject>Amino Acid Transport System A - metabolism</subject><subject>Amino acids</subject><subject>Amino Acids - deficiency</subject><subject>Analytical Chemistry</subject><subject>Animals</subject><subject>Biochemical Engineering</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Cell Line</subject><subject>Cell Line, Tumor</subject><subject>Eukaryotic Initiation Factor-2 - genetics</subject><subject>Eukaryotic Initiation Factor-2 - metabolism</subject><subject>Fibroblasts - metabolism</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Mice</subject><subject>Neurobiology</subject><subject>Nutrition research</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Original Article</subject><subject>Phosphorylation - genetics</subject><subject>Phosphorylation - physiology</subject><subject>Proteins</subject><subject>Proteomics</subject><subject>Transcriptional Activation</subject><issn>0939-4451</issn><issn>1438-2199</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9ks-L1DAUx4Mo7uzqH-BFA8Kih2p-tGmzB2FZ1BUGPKx7Dmn60snQNmPSDs7dP9yUDjou6CUh733e9yUvX4ReUPKOElK-j2lhIiOkygiVMmOP0IrmvMpYOj1GKyK5zPK8oGfoPMYtIZRVVDxFZ1QSIhmrVujn3Q6Ms8648YC9xbp3g8fauAYHaKdOj9DgFgbA8GMXIEbnhyusB90dootzxZyMOE71FswMjx6DGzcQsPH9roMRsA84uqHt4FS-gV1wez0mwWfoidVdhOfH_QLdf_r47eY2W3_9_OXmep0ZwYoxM5Lw2kpjuaRNA7KWkhd1lWLE6MIYaa0WeWmZoLbUUpcyF1TQuuGQRmSBX6APi-5uqntoDAxj0J1K9-h1OCivnfo7M7iNav1e8UIWRcmTwNtFYPOg7PZ6reYYYUKUgvI9TezlsVnw3yeIo-pdNNB1egA_RSVKOovKBL75L0gJp5xUZcUS-voBuvVTSJ8xU7IQQhIhEkUXygQfYwD7-6qUqNk4ajGOSlNRs3HUrPzydDR_Ko5OSQBbgJhSQwvhtPW_VV8tRVZ7pdvgorq_YyQ9hwpWSV7xX-2F2ZI</recordid><startdate>20090501</startdate><enddate>20090501</enddate><creator>Palii, S. S</creator><creator>Kays, C. E</creator><creator>Deval, C</creator><creator>Bruhat, A</creator><creator>Fafournoux, P</creator><creator>Kilberg, M. S</creator><general>Vienna : Springer Vienna</general><general>Springer Vienna</general><general>Springer Nature B.V</general><general>Springer Verlag</general><scope>FBQ</scope><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>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</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>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>M7P</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5912-4591</orcidid><orcidid>https://orcid.org/0000-0002-4900-4331</orcidid></search><sort><creationdate>20090501</creationdate><title>Specificity of amino acid regulated gene expression: analysis of genes subjected to either complete or single amino acid deprivation</title><author>Palii, S. S ; Kays, C. E ; Deval, C ; Bruhat, A ; Fafournoux, P ; Kilberg, M. S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c625t-c903bf9cf391dde9b9935b83bf0ca5cc9ffa647f261f7a9a7946161bd3e008fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Activating Transcription Factor 4 - genetics</topic><topic>Activating Transcription Factor 4 - metabolism</topic><topic>Amino Acid Transport System A - genetics</topic><topic>Amino Acid Transport System A - metabolism</topic><topic>Amino acids</topic><topic>Amino Acids - deficiency</topic><topic>Analytical Chemistry</topic><topic>Animals</topic><topic>Biochemical Engineering</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Cell Line</topic><topic>Cell Line, Tumor</topic><topic>Eukaryotic Initiation Factor-2 - genetics</topic><topic>Eukaryotic Initiation Factor-2 - metabolism</topic><topic>Fibroblasts - metabolism</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Mice</topic><topic>Neurobiology</topic><topic>Nutrition research</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Original Article</topic><topic>Phosphorylation - genetics</topic><topic>Phosphorylation - physiology</topic><topic>Proteins</topic><topic>Proteomics</topic><topic>Transcriptional Activation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Palii, S. S</creatorcontrib><creatorcontrib>Kays, C. E</creatorcontrib><creatorcontrib>Deval, C</creatorcontrib><creatorcontrib>Bruhat, A</creatorcontrib><creatorcontrib>Fafournoux, P</creatorcontrib><creatorcontrib>Kilberg, M. S</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>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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 & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</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 & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Biological Science Journals</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 China</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Amino acids</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Palii, S. S</au><au>Kays, C. E</au><au>Deval, C</au><au>Bruhat, A</au><au>Fafournoux, P</au><au>Kilberg, M. S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Specificity of amino acid regulated gene expression: analysis of genes subjected to either complete or single amino acid deprivation</atitle><jtitle>Amino acids</jtitle><stitle>Amino Acids</stitle><addtitle>Amino Acids</addtitle><date>2009-05-01</date><risdate>2009</risdate><volume>37</volume><issue>1</issue><spage>79</spage><epage>88</epage><pages>79-88</pages><issn>0939-4451</issn><eissn>1438-2199</eissn><abstract>Amino acid deprivation activates the amino acid response (AAR) pathway that enhances transcription of genes containing an amino acid response element (AARE). The present data reveal a quantitative difference in the response to deprivation of individual amino acids. The AAR leads to increased eukaryotic initiation factor 2α (eIF2α) phosphorylation and ATF4 translation. When HepG2 cells were deprived of an individual essential amino acid, p-eIF2α and activating transcription factor 4 were increased, but the correlation was relatively weak. Complete amino acid starvation in either Earle's balanced salt solution or Krebs-Ringer bicarbonate buffer (KRB) resulted in activation of transcription driven by a SNAT2 genomic fragment that contained an AARE. However, for the KRB, a proportion of the transcription was AARE-independent suggesting that amino acid-independent mechanisms were responsible. Therefore, activation of AARE-driven transcription is triggered by a deficiency in any one of the essential amino acids, but the response is not uniform. Furthermore, caution must be exercised when using a medium completely devoid of amino acids.</abstract><cop>Vienna</cop><pub>Vienna : Springer Vienna</pub><pmid>19009228</pmid><doi>10.1007/s00726-008-0199-2</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-5912-4591</orcidid><orcidid>https://orcid.org/0000-0002-4900-4331</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0939-4451 |
ispartof | Amino acids, 2009-05, Vol.37 (1), p.79-88 |
issn | 0939-4451 1438-2199 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3595573 |
source | Springer Nature |
subjects | Activating Transcription Factor 4 - genetics Activating Transcription Factor 4 - metabolism Amino Acid Transport System A - genetics Amino Acid Transport System A - metabolism Amino acids Amino Acids - deficiency Analytical Chemistry Animals Biochemical Engineering Biochemistry Biomedical and Life Sciences Cell Line Cell Line, Tumor Eukaryotic Initiation Factor-2 - genetics Eukaryotic Initiation Factor-2 - metabolism Fibroblasts - metabolism Gene Expression Profiling Gene Expression Regulation Humans Life Sciences Mice Neurobiology Nutrition research Oligonucleotide Array Sequence Analysis Original Article Phosphorylation - genetics Phosphorylation - physiology Proteins Proteomics Transcriptional Activation |
title | Specificity of amino acid regulated gene expression: analysis of genes subjected to either complete or single amino acid deprivation |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T13%3A12%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Specificity%20of%20amino%20acid%20regulated%20gene%20expression:%20analysis%20of%20genes%20subjected%20to%20either%20complete%20or%20single%20amino%20acid%20deprivation&rft.jtitle=Amino%20acids&rft.au=Palii,%20S.%20S&rft.date=2009-05-01&rft.volume=37&rft.issue=1&rft.spage=79&rft.epage=88&rft.pages=79-88&rft.issn=0939-4451&rft.eissn=1438-2199&rft_id=info:doi/10.1007/s00726-008-0199-2&rft_dat=%3Cproquest_pubme%3E67195579%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c625t-c903bf9cf391dde9b9935b83bf0ca5cc9ffa647f261f7a9a7946161bd3e008fe3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1095669066&rft_id=info:pmid/19009228&rfr_iscdi=true |