Loading…

Regulatory evolution through divergence of a phosphoswitch in the transcription factor CEBPB

Evolution of gene regulation Changes in cis -regulatory regions of the genome play an important part in the evolution of gene regulation. Lynch et al . explore the influence of amino acid substitutions in transcription factors on gene regulation. They show how, over evolutionary time, amino acid sub...

Full description

Saved in:
Bibliographic Details
Published in:Nature (London) 2011-12, Vol.480 (7377), p.383-386
Main Authors: Lynch, Vincent J., May, Gemma, Wagner, Günter P.
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-c780t-c6a17490a51a7f3282d92d2116df91612275256f30d6c9e93f71570235a9f2633
cites cdi_FETCH-LOGICAL-c780t-c6a17490a51a7f3282d92d2116df91612275256f30d6c9e93f71570235a9f2633
container_end_page 386
container_issue 7377
container_start_page 383
container_title Nature (London)
container_volume 480
creator Lynch, Vincent J.
May, Gemma
Wagner, Günter P.
description Evolution of gene regulation Changes in cis -regulatory regions of the genome play an important part in the evolution of gene regulation. Lynch et al . explore the influence of amino acid substitutions in transcription factors on gene regulation. They show how, over evolutionary time, amino acid substitutions in the transcription factor CEBPB in the stem-lineage of placental mammals reorganize the location of key phosphorylation sites, thereby changing the way it responds to cAMP/PKA signalling. There is an emerging consensus that gene regulation evolves through changes in cis -regulatory elements 1 , 2 and transcription factors 3 , 4 , 5 , 6 . Although it is clear how nucleotide substitutions in cis -regulatory elements affect gene expression, it is not clear how amino-acid substitutions in transcription factors influence gene regulation 4 , 5 , 6 , 7 , 8 , 9 , 10 . Here we show that amino-acid changes in the transcription factor CCAAT/enhancer binding protein-β (CEBPB, also known as C/EBP-β) in the stem-lineage of placental mammals changed the way it responds to cyclic AMP/protein kinase A (cAMP/PKA) signalling. By functionally analysing resurrected ancestral proteins, we identify three amino-acid substitutions in an internal regulatory domain of CEBPB that are responsible for the novel function. These amino-acid substitutions reorganize the location of key phosphorylation sites, introducing a new site and removing two ancestral sites, reversing the response of CEBPB to GSK-3β-mediated phosphorylation from repression to activation. We conclude that changing the response of transcription factors to signalling pathways can be an important mechanism of gene regulatory evolution.
doi_str_mv 10.1038/nature10595
format article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_journals_914695280</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A626152071</galeid><sourcerecordid>A626152071</sourcerecordid><originalsourceid>FETCH-LOGICAL-c780t-c6a17490a51a7f3282d92d2116df91612275256f30d6c9e93f71570235a9f2633</originalsourceid><addsrcrecordid>eNqN0u9r1DAYB_Agijunr3wvZeIL0c78aNLk5XZMHQyUqe-EENOkl9FruiSd23-_nHe6Hpw6Sim0n3yfh_IF4DmChwgS_q5XaQwGQSroAzBDVc3KivH6IZhBiHkJOWF74EmMFxBCiurqMdjDGHIoKJqB7-emHTuVfLgpzJXvxuR8X6RF8GO7KBp3ZUJrem0KbwtVDAsfV_dPl_SicCtoihRUH3Vww6-jVukcVsxPjj8fPwWPrOqiebZ57oNv70--zj-WZ58-nM6Pzkpdc5hKzVReS0BFkaotwRw3AjcYIdZYgRjCuKaYMktgw7Qwgtga0RpiQpWwmBGyDw7WuUPwl6OJSV74MfR5pBSoYoJiDjN6uUat6ox0vfV5cb10UcsjhhmiGNbon4owWtFKIJ5VuUPlH2WC6nxvrMuvt1Lv46f5Bzu8HtylnIb-FU2TDnegfDVm6fTOVe91YDrh9daBbJK5Tq0aY5SnX863w_9np7lv1lYHH2MwVg7BLVW4kQjKVfHlpPhZv9hUYPyxNM0f-7vpGbzaABW16mwurXbxzuWOUMKr7N6uXcyf-taEuy7tmnsLcPoR1g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>914695280</pqid></control><display><type>article</type><title>Regulatory evolution through divergence of a phosphoswitch in the transcription factor CEBPB</title><source>Springer Nature - Connect here FIRST to enable access</source><creator>Lynch, Vincent J. ; May, Gemma ; Wagner, Günter P.</creator><creatorcontrib>Lynch, Vincent J. ; May, Gemma ; Wagner, Günter P.</creatorcontrib><description>Evolution of gene regulation Changes in cis -regulatory regions of the genome play an important part in the evolution of gene regulation. Lynch et al . explore the influence of amino acid substitutions in transcription factors on gene regulation. They show how, over evolutionary time, amino acid substitutions in the transcription factor CEBPB in the stem-lineage of placental mammals reorganize the location of key phosphorylation sites, thereby changing the way it responds to cAMP/PKA signalling. There is an emerging consensus that gene regulation evolves through changes in cis -regulatory elements 1 , 2 and transcription factors 3 , 4 , 5 , 6 . Although it is clear how nucleotide substitutions in cis -regulatory elements affect gene expression, it is not clear how amino-acid substitutions in transcription factors influence gene regulation 4 , 5 , 6 , 7 , 8 , 9 , 10 . Here we show that amino-acid changes in the transcription factor CCAAT/enhancer binding protein-β (CEBPB, also known as C/EBP-β) in the stem-lineage of placental mammals changed the way it responds to cyclic AMP/protein kinase A (cAMP/PKA) signalling. By functionally analysing resurrected ancestral proteins, we identify three amino-acid substitutions in an internal regulatory domain of CEBPB that are responsible for the novel function. These amino-acid substitutions reorganize the location of key phosphorylation sites, introducing a new site and removing two ancestral sites, reversing the response of CEBPB to GSK-3β-mediated phosphorylation from repression to activation. We conclude that changing the response of transcription factors to signalling pathways can be an important mechanism of gene regulatory evolution.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/nature10595</identifier><identifier>PMID: 22080951</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/208/200 ; 631/337/572/2102 ; 631/45/612/822 ; 631/80/86 ; Amino Acid Substitution ; Amino acids ; Analysis ; Analytical, structural and metabolic biochemistry ; Animals ; Biological and medical sciences ; CCAAT-Enhancer-Binding Protein-beta - chemistry ; CCAAT-Enhancer-Binding Protein-beta - genetics ; CCAAT-Enhancer-Binding Protein-beta - metabolism ; Control ; Cyclic AMP - metabolism ; Cyclic AMP-Dependent Protein Kinases - metabolism ; Eutherians ; Evolution ; Evolution &amp; development ; Evolution, Molecular ; Female ; Forkhead Box Protein O1 ; Forkhead Transcription Factors - metabolism ; Fundamental and applied biological sciences. Psychology ; Gene expression ; Gene Expression Regulation ; Genetic aspects ; Genetic regulation ; Glycogen Synthase Kinase 3 - metabolism ; Glycogen Synthase Kinase 3 beta ; HeLa Cells ; Humanities and Social Sciences ; Humans ; Kinases ; letter ; Life sciences ; Mammals ; Models, Molecular ; Molecular and cellular biology ; multidisciplinary ; Mutation ; Natural history ; Phosphorylation ; Phosphorylation - genetics ; Physiological aspects ; Placenta ; Pregnancy ; Protein binding ; Protein Conformation ; Protein Structure, Tertiary ; Proteins ; Science ; Structure-Activity Relationship ; Transcription factors</subject><ispartof>Nature (London), 2011-12, Vol.480 (7377), p.383-386</ispartof><rights>Springer Nature Limited 2011</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2011 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Dec 15, 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c780t-c6a17490a51a7f3282d92d2116df91612275256f30d6c9e93f71570235a9f2633</citedby><cites>FETCH-LOGICAL-c780t-c6a17490a51a7f3282d92d2116df91612275256f30d6c9e93f71570235a9f2633</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=25285384$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22080951$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lynch, Vincent J.</creatorcontrib><creatorcontrib>May, Gemma</creatorcontrib><creatorcontrib>Wagner, Günter P.</creatorcontrib><title>Regulatory evolution through divergence of a phosphoswitch in the transcription factor CEBPB</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>Evolution of gene regulation Changes in cis -regulatory regions of the genome play an important part in the evolution of gene regulation. Lynch et al . explore the influence of amino acid substitutions in transcription factors on gene regulation. They show how, over evolutionary time, amino acid substitutions in the transcription factor CEBPB in the stem-lineage of placental mammals reorganize the location of key phosphorylation sites, thereby changing the way it responds to cAMP/PKA signalling. There is an emerging consensus that gene regulation evolves through changes in cis -regulatory elements 1 , 2 and transcription factors 3 , 4 , 5 , 6 . Although it is clear how nucleotide substitutions in cis -regulatory elements affect gene expression, it is not clear how amino-acid substitutions in transcription factors influence gene regulation 4 , 5 , 6 , 7 , 8 , 9 , 10 . Here we show that amino-acid changes in the transcription factor CCAAT/enhancer binding protein-β (CEBPB, also known as C/EBP-β) in the stem-lineage of placental mammals changed the way it responds to cyclic AMP/protein kinase A (cAMP/PKA) signalling. By functionally analysing resurrected ancestral proteins, we identify three amino-acid substitutions in an internal regulatory domain of CEBPB that are responsible for the novel function. These amino-acid substitutions reorganize the location of key phosphorylation sites, introducing a new site and removing two ancestral sites, reversing the response of CEBPB to GSK-3β-mediated phosphorylation from repression to activation. We conclude that changing the response of transcription factors to signalling pathways can be an important mechanism of gene regulatory evolution.</description><subject>631/208/200</subject><subject>631/337/572/2102</subject><subject>631/45/612/822</subject><subject>631/80/86</subject><subject>Amino Acid Substitution</subject><subject>Amino acids</subject><subject>Analysis</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>CCAAT-Enhancer-Binding Protein-beta - chemistry</subject><subject>CCAAT-Enhancer-Binding Protein-beta - genetics</subject><subject>CCAAT-Enhancer-Binding Protein-beta - metabolism</subject><subject>Control</subject><subject>Cyclic AMP - metabolism</subject><subject>Cyclic AMP-Dependent Protein Kinases - metabolism</subject><subject>Eutherians</subject><subject>Evolution</subject><subject>Evolution &amp; development</subject><subject>Evolution, Molecular</subject><subject>Female</subject><subject>Forkhead Box Protein O1</subject><subject>Forkhead Transcription Factors - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Genetic aspects</subject><subject>Genetic regulation</subject><subject>Glycogen Synthase Kinase 3 - metabolism</subject><subject>Glycogen Synthase Kinase 3 beta</subject><subject>HeLa Cells</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Kinases</subject><subject>letter</subject><subject>Life sciences</subject><subject>Mammals</subject><subject>Models, Molecular</subject><subject>Molecular and cellular biology</subject><subject>multidisciplinary</subject><subject>Mutation</subject><subject>Natural history</subject><subject>Phosphorylation</subject><subject>Phosphorylation - genetics</subject><subject>Physiological aspects</subject><subject>Placenta</subject><subject>Pregnancy</subject><subject>Protein binding</subject><subject>Protein Conformation</subject><subject>Protein Structure, Tertiary</subject><subject>Proteins</subject><subject>Science</subject><subject>Structure-Activity Relationship</subject><subject>Transcription factors</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqN0u9r1DAYB_Agijunr3wvZeIL0c78aNLk5XZMHQyUqe-EENOkl9FruiSd23-_nHe6Hpw6Sim0n3yfh_IF4DmChwgS_q5XaQwGQSroAzBDVc3KivH6IZhBiHkJOWF74EmMFxBCiurqMdjDGHIoKJqB7-emHTuVfLgpzJXvxuR8X6RF8GO7KBp3ZUJrem0KbwtVDAsfV_dPl_SicCtoihRUH3Vww6-jVukcVsxPjj8fPwWPrOqiebZ57oNv70--zj-WZ58-nM6Pzkpdc5hKzVReS0BFkaotwRw3AjcYIdZYgRjCuKaYMktgw7Qwgtga0RpiQpWwmBGyDw7WuUPwl6OJSV74MfR5pBSoYoJiDjN6uUat6ox0vfV5cb10UcsjhhmiGNbon4owWtFKIJ5VuUPlH2WC6nxvrMuvt1Lv46f5Bzu8HtylnIb-FU2TDnegfDVm6fTOVe91YDrh9daBbJK5Tq0aY5SnX863w_9np7lv1lYHH2MwVg7BLVW4kQjKVfHlpPhZv9hUYPyxNM0f-7vpGbzaABW16mwurXbxzuWOUMKr7N6uXcyf-taEuy7tmnsLcPoR1g</recordid><startdate>20111215</startdate><enddate>20111215</enddate><creator>Lynch, Vincent J.</creator><creator>May, Gemma</creator><creator>Wagner, Günter P.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>IQODW</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>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></search><sort><creationdate>20111215</creationdate><title>Regulatory evolution through divergence of a phosphoswitch in the transcription factor CEBPB</title><author>Lynch, Vincent J. ; May, Gemma ; Wagner, Günter P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c780t-c6a17490a51a7f3282d92d2116df91612275256f30d6c9e93f71570235a9f2633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>631/208/200</topic><topic>631/337/572/2102</topic><topic>631/45/612/822</topic><topic>631/80/86</topic><topic>Amino Acid Substitution</topic><topic>Amino acids</topic><topic>Analysis</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>CCAAT-Enhancer-Binding Protein-beta - chemistry</topic><topic>CCAAT-Enhancer-Binding Protein-beta - genetics</topic><topic>CCAAT-Enhancer-Binding Protein-beta - metabolism</topic><topic>Control</topic><topic>Cyclic AMP - metabolism</topic><topic>Cyclic AMP-Dependent Protein Kinases - metabolism</topic><topic>Eutherians</topic><topic>Evolution</topic><topic>Evolution &amp; development</topic><topic>Evolution, Molecular</topic><topic>Female</topic><topic>Forkhead Box Protein O1</topic><topic>Forkhead Transcription Factors - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Genetic aspects</topic><topic>Genetic regulation</topic><topic>Glycogen Synthase Kinase 3 - metabolism</topic><topic>Glycogen Synthase Kinase 3 beta</topic><topic>HeLa Cells</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Kinases</topic><topic>letter</topic><topic>Life sciences</topic><topic>Mammals</topic><topic>Models, Molecular</topic><topic>Molecular and cellular biology</topic><topic>multidisciplinary</topic><topic>Mutation</topic><topic>Natural history</topic><topic>Phosphorylation</topic><topic>Phosphorylation - genetics</topic><topic>Physiological aspects</topic><topic>Placenta</topic><topic>Pregnancy</topic><topic>Protein binding</topic><topic>Protein Conformation</topic><topic>Protein Structure, Tertiary</topic><topic>Proteins</topic><topic>Science</topic><topic>Structure-Activity Relationship</topic><topic>Transcription factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lynch, Vincent J.</creatorcontrib><creatorcontrib>May, Gemma</creatorcontrib><creatorcontrib>Wagner, Günter P.</creatorcontrib><collection>Pascal-Francis</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>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>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 Complete</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>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>AUTh Library subscriptions: 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>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>ProQuest research library</collection><collection>Science Database</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><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lynch, Vincent J.</au><au>May, Gemma</au><au>Wagner, Günter P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulatory evolution through divergence of a phosphoswitch in the transcription factor CEBPB</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2011-12-15</date><risdate>2011</risdate><volume>480</volume><issue>7377</issue><spage>383</spage><epage>386</epage><pages>383-386</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><coden>NATUAS</coden><abstract>Evolution of gene regulation Changes in cis -regulatory regions of the genome play an important part in the evolution of gene regulation. Lynch et al . explore the influence of amino acid substitutions in transcription factors on gene regulation. They show how, over evolutionary time, amino acid substitutions in the transcription factor CEBPB in the stem-lineage of placental mammals reorganize the location of key phosphorylation sites, thereby changing the way it responds to cAMP/PKA signalling. There is an emerging consensus that gene regulation evolves through changes in cis -regulatory elements 1 , 2 and transcription factors 3 , 4 , 5 , 6 . Although it is clear how nucleotide substitutions in cis -regulatory elements affect gene expression, it is not clear how amino-acid substitutions in transcription factors influence gene regulation 4 , 5 , 6 , 7 , 8 , 9 , 10 . Here we show that amino-acid changes in the transcription factor CCAAT/enhancer binding protein-β (CEBPB, also known as C/EBP-β) in the stem-lineage of placental mammals changed the way it responds to cyclic AMP/protein kinase A (cAMP/PKA) signalling. By functionally analysing resurrected ancestral proteins, we identify three amino-acid substitutions in an internal regulatory domain of CEBPB that are responsible for the novel function. These amino-acid substitutions reorganize the location of key phosphorylation sites, introducing a new site and removing two ancestral sites, reversing the response of CEBPB to GSK-3β-mediated phosphorylation from repression to activation. We conclude that changing the response of transcription factors to signalling pathways can be an important mechanism of gene regulatory evolution.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>22080951</pmid><doi>10.1038/nature10595</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0028-0836
ispartof Nature (London), 2011-12, Vol.480 (7377), p.383-386
issn 0028-0836
1476-4687
language eng
recordid cdi_proquest_journals_914695280
source Springer Nature - Connect here FIRST to enable access
subjects 631/208/200
631/337/572/2102
631/45/612/822
631/80/86
Amino Acid Substitution
Amino acids
Analysis
Analytical, structural and metabolic biochemistry
Animals
Biological and medical sciences
CCAAT-Enhancer-Binding Protein-beta - chemistry
CCAAT-Enhancer-Binding Protein-beta - genetics
CCAAT-Enhancer-Binding Protein-beta - metabolism
Control
Cyclic AMP - metabolism
Cyclic AMP-Dependent Protein Kinases - metabolism
Eutherians
Evolution
Evolution & development
Evolution, Molecular
Female
Forkhead Box Protein O1
Forkhead Transcription Factors - metabolism
Fundamental and applied biological sciences. Psychology
Gene expression
Gene Expression Regulation
Genetic aspects
Genetic regulation
Glycogen Synthase Kinase 3 - metabolism
Glycogen Synthase Kinase 3 beta
HeLa Cells
Humanities and Social Sciences
Humans
Kinases
letter
Life sciences
Mammals
Models, Molecular
Molecular and cellular biology
multidisciplinary
Mutation
Natural history
Phosphorylation
Phosphorylation - genetics
Physiological aspects
Placenta
Pregnancy
Protein binding
Protein Conformation
Protein Structure, Tertiary
Proteins
Science
Structure-Activity Relationship
Transcription factors
title Regulatory evolution through divergence of a phosphoswitch in the transcription factor CEBPB
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T05%3A19%3A50IST&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=Regulatory%20evolution%20through%20divergence%20of%20a%20phosphoswitch%20in%20the%20transcription%20factor%20CEBPB&rft.jtitle=Nature%20(London)&rft.au=Lynch,%20Vincent%20J.&rft.date=2011-12-15&rft.volume=480&rft.issue=7377&rft.spage=383&rft.epage=386&rft.pages=383-386&rft.issn=0028-0836&rft.eissn=1476-4687&rft.coden=NATUAS&rft_id=info:doi/10.1038/nature10595&rft_dat=%3Cgale_proqu%3EA626152071%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c780t-c6a17490a51a7f3282d92d2116df91612275256f30d6c9e93f71570235a9f2633%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=914695280&rft_id=info:pmid/22080951&rft_galeid=A626152071&rfr_iscdi=true