The SAGA Histone Acetyltransferase Complex Regulates Leucine Uptake through the Agp3 Permease in Fission Yeast

Metabolic responses of unicellular organisms are mostly acute, transient, and cell-autonomous. Regulation of nutrient uptake in yeast is one such rapid response. High quality nitrogen sources such as NH4+ inhibit uptake of poor nitrogen sources, such as amino acids. Both transcriptional and posttran...

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Veröffentlicht in:The Journal of biological chemistry 2012-11, Vol.287 (45), p.38158-38167
Hauptverfasser: Takahashi, Hidekazu, Sun, Xiaoying, Hamamoto, Makiko, Yashiroda, Yoko, Yoshida, Minoru
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container_end_page 38167
container_issue 45
container_start_page 38158
container_title The Journal of biological chemistry
container_volume 287
creator Takahashi, Hidekazu
Sun, Xiaoying
Hamamoto, Makiko
Yashiroda, Yoko
Yoshida, Minoru
description Metabolic responses of unicellular organisms are mostly acute, transient, and cell-autonomous. Regulation of nutrient uptake in yeast is one such rapid response. High quality nitrogen sources such as NH4+ inhibit uptake of poor nitrogen sources, such as amino acids. Both transcriptional and posttranscriptional mechanisms operate in nutrient uptake regulation; however, many components of this system remain uncharacterized in the fission yeast, Schizosaccharomyces pombe. Here, we demonstrate that the Spt-Ada-Gcn acetyltransferase (SAGA) complex modulates leucine uptake. Initially, we noticed that a branched-chain amino acid auxotroph exhibits a peculiar adaptive growth phenotype on solid minimal media containing certain nitrogen sources. In fact, the growth of many auxotrophic strains is inhibited by excess NH4Cl, possibly through nitrogen-mediated uptake inhibition of the corresponding nutrients. Surprisingly, DNA microarray analysis revealed that the transcriptional reprogramming during the adaptation of the branched-chain amino acid auxotroph was highly correlated with reprogramming observed in deletions of the SAGA histone acetyltransferase module genes. Deletion of gcn5+ increased leucine uptake in the prototrophic background and rendered the leucine auxotroph resistant to NH4Cl. Deletion of tra1+ caused the opposite phenotypes. The increase in leucine uptake in the gcn5Δ mutant was dependent on an amino acid permease gene, SPCC965.11c+. The closest budding yeast homolog of this permease is a relatively nonspecific amino acid permease AGP3, which functions in poor nutrient conditions. Our analysis identified the regulation of nutrient uptake as a physiological function for the SAGA complex, providing a potential link between cellular metabolism and chromatin regulation. Background: SAGA is a multiprotein complex that possesses histone acetyltransferase activity. Results: Fission yeast strains with deletions in the SAGA acetyltransferase subunit exhibited increased leucine uptake in a manner dependent on an amino acid permease gene. Conclusion: SAGA regulates amino acid uptake in fission yeast. Significance: Regulation of nutrient uptake by SAGA provides a potential link between cellular metabolism and chromatin regulation.
doi_str_mv 10.1074/jbc.M112.411165
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Regulation of nutrient uptake in yeast is one such rapid response. High quality nitrogen sources such as NH4+ inhibit uptake of poor nitrogen sources, such as amino acids. Both transcriptional and posttranscriptional mechanisms operate in nutrient uptake regulation; however, many components of this system remain uncharacterized in the fission yeast, Schizosaccharomyces pombe. Here, we demonstrate that the Spt-Ada-Gcn acetyltransferase (SAGA) complex modulates leucine uptake. Initially, we noticed that a branched-chain amino acid auxotroph exhibits a peculiar adaptive growth phenotype on solid minimal media containing certain nitrogen sources. In fact, the growth of many auxotrophic strains is inhibited by excess NH4Cl, possibly through nitrogen-mediated uptake inhibition of the corresponding nutrients. Surprisingly, DNA microarray analysis revealed that the transcriptional reprogramming during the adaptation of the branched-chain amino acid auxotroph was highly correlated with reprogramming observed in deletions of the SAGA histone acetyltransferase module genes. Deletion of gcn5+ increased leucine uptake in the prototrophic background and rendered the leucine auxotroph resistant to NH4Cl. Deletion of tra1+ caused the opposite phenotypes. The increase in leucine uptake in the gcn5Δ mutant was dependent on an amino acid permease gene, SPCC965.11c+. The closest budding yeast homolog of this permease is a relatively nonspecific amino acid permease AGP3, which functions in poor nutrient conditions. Our analysis identified the regulation of nutrient uptake as a physiological function for the SAGA complex, providing a potential link between cellular metabolism and chromatin regulation. Background: SAGA is a multiprotein complex that possesses histone acetyltransferase activity. Results: Fission yeast strains with deletions in the SAGA acetyltransferase subunit exhibited increased leucine uptake in a manner dependent on an amino acid permease gene. Conclusion: SAGA regulates amino acid uptake in fission yeast. 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Regulation of nutrient uptake in yeast is one such rapid response. High quality nitrogen sources such as NH4+ inhibit uptake of poor nitrogen sources, such as amino acids. Both transcriptional and posttranscriptional mechanisms operate in nutrient uptake regulation; however, many components of this system remain uncharacterized in the fission yeast, Schizosaccharomyces pombe. Here, we demonstrate that the Spt-Ada-Gcn acetyltransferase (SAGA) complex modulates leucine uptake. Initially, we noticed that a branched-chain amino acid auxotroph exhibits a peculiar adaptive growth phenotype on solid minimal media containing certain nitrogen sources. In fact, the growth of many auxotrophic strains is inhibited by excess NH4Cl, possibly through nitrogen-mediated uptake inhibition of the corresponding nutrients. Surprisingly, DNA microarray analysis revealed that the transcriptional reprogramming during the adaptation of the branched-chain amino acid auxotroph was highly correlated with reprogramming observed in deletions of the SAGA histone acetyltransferase module genes. Deletion of gcn5+ increased leucine uptake in the prototrophic background and rendered the leucine auxotroph resistant to NH4Cl. Deletion of tra1+ caused the opposite phenotypes. The increase in leucine uptake in the gcn5Δ mutant was dependent on an amino acid permease gene, SPCC965.11c+. The closest budding yeast homolog of this permease is a relatively nonspecific amino acid permease AGP3, which functions in poor nutrient conditions. Our analysis identified the regulation of nutrient uptake as a physiological function for the SAGA complex, providing a potential link between cellular metabolism and chromatin regulation. Background: SAGA is a multiprotein complex that possesses histone acetyltransferase activity. Results: Fission yeast strains with deletions in the SAGA acetyltransferase subunit exhibited increased leucine uptake in a manner dependent on an amino acid permease gene. Conclusion: SAGA regulates amino acid uptake in fission yeast. 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development</subject><subject>Schizosaccharomyces - metabolism</subject><subject>Schizosaccharomyces pombe</subject><subject>Schizosaccharomyces pombe Proteins - genetics</subject><subject>Schizosaccharomyces pombe Proteins - metabolism</subject><subject>Transaminases - genetics</subject><subject>Transaminases - metabolism</subject><subject>Yeast Genetics</subject><subject>Yeast Metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1vEzEQxS0EoqFw5oZ85LKpx_Z--IIURbRFSgWCVoKT5fXOJi6b9WJ7K_rf4yilKgd8Gcn-vTeeeYS8BbYEVsuz29YurwD4UgJAVT4jC2CNKEQJ35-TBWMcCsXL5oS8ivGW5SMVvCQnnCvFa14tyHi9Q_ptdbGily4mPyJdWUz3QwpmjD0GE5Gu_X4a8Df9itt5MAkj3eBsXWZvpmR-Ik274OftLtcs306CfsGwx4PUjfTcxej8SH_ki_SavOjNEPHNQz0lN-cfr9eXxebzxaf1alPYkqlUtEoBa7FpSy5U11qwpUILBnnfIaugLQXWUvS2NlhJrJg0Tdk3xkglewmdOCUfjr7T3O6xszjmgQY9Bbc34V574_S_L6Pb6a2_00I2DWvKbPD-wSD4XzPGpPcuWhwGM6KfowYQquJCyjqjZ0fUBh9jwP6xDTB9SEnnlPQhJX1MKSvePf3dI_83lgyoI4B5R3cOg47W4WixcwFt0p13_zX_A2Cwo3A</recordid><startdate>20121102</startdate><enddate>20121102</enddate><creator>Takahashi, Hidekazu</creator><creator>Sun, Xiaoying</creator><creator>Hamamoto, Makiko</creator><creator>Yashiroda, Yoko</creator><creator>Yoshida, Minoru</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20121102</creationdate><title>The SAGA Histone Acetyltransferase Complex Regulates Leucine Uptake through the Agp3 Permease in Fission Yeast</title><author>Takahashi, Hidekazu ; 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development</topic><topic>Schizosaccharomyces - metabolism</topic><topic>Schizosaccharomyces pombe</topic><topic>Schizosaccharomyces pombe Proteins - genetics</topic><topic>Schizosaccharomyces pombe Proteins - metabolism</topic><topic>Transaminases - genetics</topic><topic>Transaminases - metabolism</topic><topic>Yeast Genetics</topic><topic>Yeast Metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takahashi, Hidekazu</creatorcontrib><creatorcontrib>Sun, Xiaoying</creatorcontrib><creatorcontrib>Hamamoto, Makiko</creatorcontrib><creatorcontrib>Yashiroda, Yoko</creatorcontrib><creatorcontrib>Yoshida, Minoru</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takahashi, Hidekazu</au><au>Sun, Xiaoying</au><au>Hamamoto, Makiko</au><au>Yashiroda, Yoko</au><au>Yoshida, Minoru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The SAGA Histone Acetyltransferase Complex Regulates Leucine Uptake through the Agp3 Permease in Fission Yeast</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2012-11-02</date><risdate>2012</risdate><volume>287</volume><issue>45</issue><spage>38158</spage><epage>38167</epage><pages>38158-38167</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Metabolic responses of unicellular organisms are mostly acute, transient, and cell-autonomous. Regulation of nutrient uptake in yeast is one such rapid response. High quality nitrogen sources such as NH4+ inhibit uptake of poor nitrogen sources, such as amino acids. Both transcriptional and posttranscriptional mechanisms operate in nutrient uptake regulation; however, many components of this system remain uncharacterized in the fission yeast, Schizosaccharomyces pombe. Here, we demonstrate that the Spt-Ada-Gcn acetyltransferase (SAGA) complex modulates leucine uptake. Initially, we noticed that a branched-chain amino acid auxotroph exhibits a peculiar adaptive growth phenotype on solid minimal media containing certain nitrogen sources. In fact, the growth of many auxotrophic strains is inhibited by excess NH4Cl, possibly through nitrogen-mediated uptake inhibition of the corresponding nutrients. Surprisingly, DNA microarray analysis revealed that the transcriptional reprogramming during the adaptation of the branched-chain amino acid auxotroph was highly correlated with reprogramming observed in deletions of the SAGA histone acetyltransferase module genes. Deletion of gcn5+ increased leucine uptake in the prototrophic background and rendered the leucine auxotroph resistant to NH4Cl. Deletion of tra1+ caused the opposite phenotypes. The increase in leucine uptake in the gcn5Δ mutant was dependent on an amino acid permease gene, SPCC965.11c+. The closest budding yeast homolog of this permease is a relatively nonspecific amino acid permease AGP3, which functions in poor nutrient conditions. Our analysis identified the regulation of nutrient uptake as a physiological function for the SAGA complex, providing a potential link between cellular metabolism and chromatin regulation. Background: SAGA is a multiprotein complex that possesses histone acetyltransferase activity. Results: Fission yeast strains with deletions in the SAGA acetyltransferase subunit exhibited increased leucine uptake in a manner dependent on an amino acid permease gene. Conclusion: SAGA regulates amino acid uptake in fission yeast. Significance: Regulation of nutrient uptake by SAGA provides a potential link between cellular metabolism and chromatin regulation.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22992726</pmid><doi>10.1074/jbc.M112.411165</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Acetyltransferases - genetics
Acetyltransferases - metabolism
Amino Acid Transport
Amino Acid Transport Systems - genetics
Amino Acid Transport Systems - metabolism
Amino Acids - metabolism
Amino Acids - pharmacology
Ammonium Chloride - pharmacology
Biological Transport - drug effects
Culture Media - pharmacology
Gene Expression Profiling
Leucine - metabolism
Leucine - pharmacology
Lysine Acetyltransferase
Metabolism
Molecular Cell Biology
Mutation
Nutrient Regulation
Oligonucleotide Array Sequence Analysis
Protein Acylation
Schizosaccharomyces - genetics
Schizosaccharomyces - growth & development
Schizosaccharomyces - metabolism
Schizosaccharomyces pombe
Schizosaccharomyces pombe Proteins - genetics
Schizosaccharomyces pombe Proteins - metabolism
Transaminases - genetics
Transaminases - metabolism
Yeast Genetics
Yeast Metabolism
title The SAGA Histone Acetyltransferase Complex Regulates Leucine Uptake through the Agp3 Permease in Fission Yeast
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