Coordination of bacterial proteome with metabolism by cyclic AMP signalling

The cyclic AMP (cAMP)-dependent catabolite repression effect in Escherichia coli is among the most intensely studied regulatory processes in biology. However, the physiological function(s) of cAMP signalling and its molecular triggers remain elusive. Here we use a quantitative physiological approach...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nature (London) 2013-08, Vol.500 (7462), p.301-306
Hauptverfasser: You, Conghui, Okano, Hiroyuki, Hui, Sheng, Zhang, Zhongge, Kim, Minsu, Gunderson, Carl W., Wang, Yi-Ping, Lenz, Peter, Yan, Dalai, Hwa, Terence
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 306
container_issue 7462
container_start_page 301
container_title Nature (London)
container_volume 500
creator You, Conghui
Okano, Hiroyuki
Hui, Sheng
Zhang, Zhongge
Kim, Minsu
Gunderson, Carl W.
Wang, Yi-Ping
Lenz, Peter
Yan, Dalai
Hwa, Terence
description The cyclic AMP (cAMP)-dependent catabolite repression effect in Escherichia coli is among the most intensely studied regulatory processes in biology. However, the physiological function(s) of cAMP signalling and its molecular triggers remain elusive. Here we use a quantitative physiological approach to show that cAMP signalling tightly coordinates the expression of catabolic proteins with biosynthetic and ribosomal proteins, in accordance with the cellular metabolic needs during exponential growth. The expression of carbon catabolic genes increased linearly with decreasing growth rates upon limitation of carbon influx, but decreased linearly with decreasing growth rate upon limitation of nitrogen or sulphur influx. In contrast, the expression of biosynthetic genes showed the opposite linear growth-rate dependence as the catabolic genes. A coarse-grained mathematical model provides a quantitative framework for understanding and predicting gene expression responses to catabolic and anabolic limitations. A scheme of integral feedback control featuring the inhibition of cAMP signalling by metabolic precursors is proposed and validated. These results reveal a key physiological role of cAMP-dependent catabolite repression: to ensure that proteomic resources are spent on distinct metabolic sectors as needed in different nutrient environments. Our findings underscore the power of quantitative physiology in unravelling the underlying functions of complex molecular signalling networks. Cyclic AMP, one of the earliest discovered and most intensely studied signalling molecules in molecular biology, is widely believed to signal the carbon status in mediating catabolite repression in bacteria; here a quantitative approach reveals a much broader physiological role for cAMP signalling, whereby it coordinates the allocation of proteomic resources with the global metabolic needs of the cell, including, for example, nitrogen or sulphur. A global metabolic role for cyclic AMP Cyclic AMP, one of the earliest discovered and most intensely studied signalling molecules in molecular biology, is widely believed to be focused on carbon metabolism in bacteria. Now Terence Hwa and colleagues reveal a much broader physiological role, whereby cAMP signalling orchestrates the allocation of the whole genome's resources in response to global metabolic needs — including, for example, nitrogen and phosphorus. To achieve this rewrite of molecular biology textbooks, the researchers followed an
doi_str_mv 10.1038/nature12446
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_1560111211</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A632496160</galeid><sourcerecordid>A632496160</sourcerecordid><originalsourceid>FETCH-LOGICAL-c626t-67d6a156dd36966a1d735d811b90e5184346523b4a613e239767dc4d5fe6c5623</originalsourceid><addsrcrecordid>eNqF0ktv1DAUBtAIgehQWLFHEd1QQYrfSZajEY-q5SEoYmk5zk1w5cRT2xHMv69HbWEGBSEvbNnHn66tm2VPMTrBiFavRxUnD5gwJu5lC8xKUTBRlfezBUKkKlBFxUH2KIRLhBDHJXuYHRBaE45xvcjOVs751qQM48bcdXmjdARvlM3X3kVwA-Q_TfyRDxBV46wJQ95scr3R1uh8-eFzHkw_KmvN2D_OHnTKBnhyOx9m396-uVi9L84_vTtdLc8LLYiIhShboTAXbUtFLdKyLSlvK4ybGgHHFaNMcEIbpgSmkEot0w3NWt6B0FwQepi9uMlNFV5NEKIcTNBgrRrBTUGmbIQxJhj_nzIiOKoJ29Kjv-ilm3x62lalSjlDWPxRvbIgzdi56JXehsqloITVAguUVDGjehjBK-tG6Eza3vPPZ7xemyu5i05mUBotDEbPph7vXUgmwq_YqykEefr1y759-W-7vPi--jirtXcheOjk2ptB-Y3ESG6bUu40ZdLPbn92agZof9u7Lkzg1Q0I6Wjswe98_UzeNaaY5Ow</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1436954016</pqid></control><display><type>article</type><title>Coordination of bacterial proteome with metabolism by cyclic AMP signalling</title><source>MEDLINE</source><source>Springer Nature</source><source>Springer Nature - Connect here FIRST to enable access</source><creator>You, Conghui ; Okano, Hiroyuki ; Hui, Sheng ; Zhang, Zhongge ; Kim, Minsu ; Gunderson, Carl W. ; Wang, Yi-Ping ; Lenz, Peter ; Yan, Dalai ; Hwa, Terence</creator><creatorcontrib>You, Conghui ; Okano, Hiroyuki ; Hui, Sheng ; Zhang, Zhongge ; Kim, Minsu ; Gunderson, Carl W. ; Wang, Yi-Ping ; Lenz, Peter ; Yan, Dalai ; Hwa, Terence</creatorcontrib><description>The cyclic AMP (cAMP)-dependent catabolite repression effect in Escherichia coli is among the most intensely studied regulatory processes in biology. However, the physiological function(s) of cAMP signalling and its molecular triggers remain elusive. Here we use a quantitative physiological approach to show that cAMP signalling tightly coordinates the expression of catabolic proteins with biosynthetic and ribosomal proteins, in accordance with the cellular metabolic needs during exponential growth. The expression of carbon catabolic genes increased linearly with decreasing growth rates upon limitation of carbon influx, but decreased linearly with decreasing growth rate upon limitation of nitrogen or sulphur influx. In contrast, the expression of biosynthetic genes showed the opposite linear growth-rate dependence as the catabolic genes. A coarse-grained mathematical model provides a quantitative framework for understanding and predicting gene expression responses to catabolic and anabolic limitations. A scheme of integral feedback control featuring the inhibition of cAMP signalling by metabolic precursors is proposed and validated. These results reveal a key physiological role of cAMP-dependent catabolite repression: to ensure that proteomic resources are spent on distinct metabolic sectors as needed in different nutrient environments. Our findings underscore the power of quantitative physiology in unravelling the underlying functions of complex molecular signalling networks. Cyclic AMP, one of the earliest discovered and most intensely studied signalling molecules in molecular biology, is widely believed to signal the carbon status in mediating catabolite repression in bacteria; here a quantitative approach reveals a much broader physiological role for cAMP signalling, whereby it coordinates the allocation of proteomic resources with the global metabolic needs of the cell, including, for example, nitrogen or sulphur. A global metabolic role for cyclic AMP Cyclic AMP, one of the earliest discovered and most intensely studied signalling molecules in molecular biology, is widely believed to be focused on carbon metabolism in bacteria. Now Terence Hwa and colleagues reveal a much broader physiological role, whereby cAMP signalling orchestrates the allocation of the whole genome's resources in response to global metabolic needs — including, for example, nitrogen and phosphorus. To achieve this rewrite of molecular biology textbooks, the researchers followed an unusual top-down approach dubbed 'quantitative phenomenology', which could be applied to the systems biology of other signalling pathways, such as those producing cancer in mammalian cells.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/nature12446</identifier><identifier>PMID: 23925119</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/326/1320 ; 631/553/1833 ; Analysis ; Carbon ; Cell culture ; Cyclic adenylic acid ; Cyclic AMP - metabolism ; E coli ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - metabolism ; Escherichia coli Proteins - genetics ; Escherichia coli Proteins - metabolism ; Gene expression ; Gene Expression Regulation, Bacterial ; Glucose ; Humanities and Social Sciences ; Lactose ; Metabolic regulation ; Metabolism ; Metabolites ; Microbiology ; Models, Biological ; multidisciplinary ; Physiological aspects ; Physiology ; Proteins ; Proteome ; Proteomics ; Science ; Signal Transduction</subject><ispartof>Nature (London), 2013-08, Vol.500 (7462), p.301-306</ispartof><rights>Springer Nature Limited 2013</rights><rights>COPYRIGHT 2013 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Aug 15, 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c626t-67d6a156dd36966a1d735d811b90e5184346523b4a613e239767dc4d5fe6c5623</citedby><cites>FETCH-LOGICAL-c626t-67d6a156dd36966a1d735d811b90e5184346523b4a613e239767dc4d5fe6c5623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nature12446$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nature12446$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23925119$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>You, Conghui</creatorcontrib><creatorcontrib>Okano, Hiroyuki</creatorcontrib><creatorcontrib>Hui, Sheng</creatorcontrib><creatorcontrib>Zhang, Zhongge</creatorcontrib><creatorcontrib>Kim, Minsu</creatorcontrib><creatorcontrib>Gunderson, Carl W.</creatorcontrib><creatorcontrib>Wang, Yi-Ping</creatorcontrib><creatorcontrib>Lenz, Peter</creatorcontrib><creatorcontrib>Yan, Dalai</creatorcontrib><creatorcontrib>Hwa, Terence</creatorcontrib><title>Coordination of bacterial proteome with metabolism by cyclic AMP signalling</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>The cyclic AMP (cAMP)-dependent catabolite repression effect in Escherichia coli is among the most intensely studied regulatory processes in biology. However, the physiological function(s) of cAMP signalling and its molecular triggers remain elusive. Here we use a quantitative physiological approach to show that cAMP signalling tightly coordinates the expression of catabolic proteins with biosynthetic and ribosomal proteins, in accordance with the cellular metabolic needs during exponential growth. The expression of carbon catabolic genes increased linearly with decreasing growth rates upon limitation of carbon influx, but decreased linearly with decreasing growth rate upon limitation of nitrogen or sulphur influx. In contrast, the expression of biosynthetic genes showed the opposite linear growth-rate dependence as the catabolic genes. A coarse-grained mathematical model provides a quantitative framework for understanding and predicting gene expression responses to catabolic and anabolic limitations. A scheme of integral feedback control featuring the inhibition of cAMP signalling by metabolic precursors is proposed and validated. These results reveal a key physiological role of cAMP-dependent catabolite repression: to ensure that proteomic resources are spent on distinct metabolic sectors as needed in different nutrient environments. Our findings underscore the power of quantitative physiology in unravelling the underlying functions of complex molecular signalling networks. Cyclic AMP, one of the earliest discovered and most intensely studied signalling molecules in molecular biology, is widely believed to signal the carbon status in mediating catabolite repression in bacteria; here a quantitative approach reveals a much broader physiological role for cAMP signalling, whereby it coordinates the allocation of proteomic resources with the global metabolic needs of the cell, including, for example, nitrogen or sulphur. A global metabolic role for cyclic AMP Cyclic AMP, one of the earliest discovered and most intensely studied signalling molecules in molecular biology, is widely believed to be focused on carbon metabolism in bacteria. Now Terence Hwa and colleagues reveal a much broader physiological role, whereby cAMP signalling orchestrates the allocation of the whole genome's resources in response to global metabolic needs — including, for example, nitrogen and phosphorus. To achieve this rewrite of molecular biology textbooks, the researchers followed an unusual top-down approach dubbed 'quantitative phenomenology', which could be applied to the systems biology of other signalling pathways, such as those producing cancer in mammalian cells.</description><subject>631/326/1320</subject><subject>631/553/1833</subject><subject>Analysis</subject><subject>Carbon</subject><subject>Cell culture</subject><subject>Cyclic adenylic acid</subject><subject>Cyclic AMP - metabolism</subject><subject>E coli</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - metabolism</subject><subject>Escherichia coli Proteins - genetics</subject><subject>Escherichia coli Proteins - metabolism</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Glucose</subject><subject>Humanities and Social Sciences</subject><subject>Lactose</subject><subject>Metabolic regulation</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Microbiology</subject><subject>Models, Biological</subject><subject>multidisciplinary</subject><subject>Physiological aspects</subject><subject>Physiology</subject><subject>Proteins</subject><subject>Proteome</subject><subject>Proteomics</subject><subject>Science</subject><subject>Signal Transduction</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqF0ktv1DAUBtAIgehQWLFHEd1QQYrfSZajEY-q5SEoYmk5zk1w5cRT2xHMv69HbWEGBSEvbNnHn66tm2VPMTrBiFavRxUnD5gwJu5lC8xKUTBRlfezBUKkKlBFxUH2KIRLhBDHJXuYHRBaE45xvcjOVs751qQM48bcdXmjdARvlM3X3kVwA-Q_TfyRDxBV46wJQ95scr3R1uh8-eFzHkw_KmvN2D_OHnTKBnhyOx9m396-uVi9L84_vTtdLc8LLYiIhShboTAXbUtFLdKyLSlvK4ybGgHHFaNMcEIbpgSmkEot0w3NWt6B0FwQepi9uMlNFV5NEKIcTNBgrRrBTUGmbIQxJhj_nzIiOKoJ29Kjv-ilm3x62lalSjlDWPxRvbIgzdi56JXehsqloITVAguUVDGjehjBK-tG6Eza3vPPZ7xemyu5i05mUBotDEbPph7vXUgmwq_YqykEefr1y759-W-7vPi--jirtXcheOjk2ptB-Y3ESG6bUu40ZdLPbn92agZof9u7Lkzg1Q0I6Wjswe98_UzeNaaY5Ow</recordid><startdate>20130801</startdate><enddate>20130801</enddate><creator>You, Conghui</creator><creator>Okano, Hiroyuki</creator><creator>Hui, Sheng</creator><creator>Zhang, Zhongge</creator><creator>Kim, Minsu</creator><creator>Gunderson, Carl W.</creator><creator>Wang, Yi-Ping</creator><creator>Lenz, Peter</creator><creator>Yan, Dalai</creator><creator>Hwa, Terence</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><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>ATWCN</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T5</scope><scope>7TG</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>R05</scope><scope>RC3</scope><scope>S0X</scope><scope>SOI</scope><scope>7X8</scope><scope>7T7</scope></search><sort><creationdate>20130801</creationdate><title>Coordination of bacterial proteome with metabolism by cyclic AMP signalling</title><author>You, Conghui ; Okano, Hiroyuki ; Hui, Sheng ; Zhang, Zhongge ; Kim, Minsu ; Gunderson, Carl W. ; Wang, Yi-Ping ; Lenz, Peter ; Yan, Dalai ; Hwa, Terence</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c626t-67d6a156dd36966a1d735d811b90e5184346523b4a613e239767dc4d5fe6c5623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>631/326/1320</topic><topic>631/553/1833</topic><topic>Analysis</topic><topic>Carbon</topic><topic>Cell culture</topic><topic>Cyclic adenylic acid</topic><topic>Cyclic AMP - metabolism</topic><topic>E coli</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - metabolism</topic><topic>Escherichia coli Proteins - genetics</topic><topic>Escherichia coli Proteins - metabolism</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Glucose</topic><topic>Humanities and Social Sciences</topic><topic>Lactose</topic><topic>Metabolic regulation</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Microbiology</topic><topic>Models, Biological</topic><topic>multidisciplinary</topic><topic>Physiological aspects</topic><topic>Physiology</topic><topic>Proteins</topic><topic>Proteome</topic><topic>Proteomics</topic><topic>Science</topic><topic>Signal Transduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>You, Conghui</creatorcontrib><creatorcontrib>Okano, Hiroyuki</creatorcontrib><creatorcontrib>Hui, Sheng</creatorcontrib><creatorcontrib>Zhang, Zhongge</creatorcontrib><creatorcontrib>Kim, Minsu</creatorcontrib><creatorcontrib>Gunderson, Carl W.</creatorcontrib><creatorcontrib>Wang, Yi-Ping</creatorcontrib><creatorcontrib>Lenz, Peter</creatorcontrib><creatorcontrib>Yan, Dalai</creatorcontrib><creatorcontrib>Hwa, Terence</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Middle School</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>ProQuest Nursing &amp; Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical 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>Agricultural Science Collection</collection><collection>ProQuest Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Technology Research Database</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>Research Library (Alumni Edition)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Earth, Atmospheric &amp; Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>Biological Sciences</collection><collection>Agriculture Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database (ProQuest)</collection><collection>Research Library</collection><collection>ProQuest Science Journals</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Earth, Atmospheric &amp; Aquatic Science Database</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 One Psychology</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>University of Michigan</collection><collection>Genetics Abstracts</collection><collection>SIRS Editorial</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>You, Conghui</au><au>Okano, Hiroyuki</au><au>Hui, Sheng</au><au>Zhang, Zhongge</au><au>Kim, Minsu</au><au>Gunderson, Carl W.</au><au>Wang, Yi-Ping</au><au>Lenz, Peter</au><au>Yan, Dalai</au><au>Hwa, Terence</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coordination of bacterial proteome with metabolism by cyclic AMP signalling</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2013-08-01</date><risdate>2013</risdate><volume>500</volume><issue>7462</issue><spage>301</spage><epage>306</epage><pages>301-306</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><coden>NATUAS</coden><abstract>The cyclic AMP (cAMP)-dependent catabolite repression effect in Escherichia coli is among the most intensely studied regulatory processes in biology. However, the physiological function(s) of cAMP signalling and its molecular triggers remain elusive. Here we use a quantitative physiological approach to show that cAMP signalling tightly coordinates the expression of catabolic proteins with biosynthetic and ribosomal proteins, in accordance with the cellular metabolic needs during exponential growth. The expression of carbon catabolic genes increased linearly with decreasing growth rates upon limitation of carbon influx, but decreased linearly with decreasing growth rate upon limitation of nitrogen or sulphur influx. In contrast, the expression of biosynthetic genes showed the opposite linear growth-rate dependence as the catabolic genes. A coarse-grained mathematical model provides a quantitative framework for understanding and predicting gene expression responses to catabolic and anabolic limitations. A scheme of integral feedback control featuring the inhibition of cAMP signalling by metabolic precursors is proposed and validated. These results reveal a key physiological role of cAMP-dependent catabolite repression: to ensure that proteomic resources are spent on distinct metabolic sectors as needed in different nutrient environments. Our findings underscore the power of quantitative physiology in unravelling the underlying functions of complex molecular signalling networks. Cyclic AMP, one of the earliest discovered and most intensely studied signalling molecules in molecular biology, is widely believed to signal the carbon status in mediating catabolite repression in bacteria; here a quantitative approach reveals a much broader physiological role for cAMP signalling, whereby it coordinates the allocation of proteomic resources with the global metabolic needs of the cell, including, for example, nitrogen or sulphur. A global metabolic role for cyclic AMP Cyclic AMP, one of the earliest discovered and most intensely studied signalling molecules in molecular biology, is widely believed to be focused on carbon metabolism in bacteria. Now Terence Hwa and colleagues reveal a much broader physiological role, whereby cAMP signalling orchestrates the allocation of the whole genome's resources in response to global metabolic needs — including, for example, nitrogen and phosphorus. To achieve this rewrite of molecular biology textbooks, the researchers followed an unusual top-down approach dubbed 'quantitative phenomenology', which could be applied to the systems biology of other signalling pathways, such as those producing cancer in mammalian cells.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>23925119</pmid><doi>10.1038/nature12446</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0028-0836
ispartof Nature (London), 2013-08, Vol.500 (7462), p.301-306
issn 0028-0836
1476-4687
language eng
recordid cdi_proquest_miscellaneous_1560111211
source MEDLINE; Springer Nature; Springer Nature - Connect here FIRST to enable access
subjects 631/326/1320
631/553/1833
Analysis
Carbon
Cell culture
Cyclic adenylic acid
Cyclic AMP - metabolism
E coli
Escherichia coli
Escherichia coli - genetics
Escherichia coli - metabolism
Escherichia coli Proteins - genetics
Escherichia coli Proteins - metabolism
Gene expression
Gene Expression Regulation, Bacterial
Glucose
Humanities and Social Sciences
Lactose
Metabolic regulation
Metabolism
Metabolites
Microbiology
Models, Biological
multidisciplinary
Physiological aspects
Physiology
Proteins
Proteome
Proteomics
Science
Signal Transduction
title Coordination of bacterial proteome with metabolism by cyclic AMP signalling
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T18%3A14%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Coordination%20of%20bacterial%20proteome%20with%20metabolism%20by%20cyclic%20AMP%20signalling&rft.jtitle=Nature%20(London)&rft.au=You,%20Conghui&rft.date=2013-08-01&rft.volume=500&rft.issue=7462&rft.spage=301&rft.epage=306&rft.pages=301-306&rft.issn=0028-0836&rft.eissn=1476-4687&rft.coden=NATUAS&rft_id=info:doi/10.1038/nature12446&rft_dat=%3Cgale_proqu%3EA632496160%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1436954016&rft_id=info:pmid/23925119&rft_galeid=A632496160&rfr_iscdi=true