MAP kinases have different functions in Dictyostelium G protein-mediated signaling

Extracellular signal regulated kinases (ERKs) are a class of MAP kinases that function in many signaling pathways in eukaryotic cells and in some cases, a single stimulus can activate more than one ERK suggesting functional redundancy or divergence from a common pathway. Dictyostelium discoideum enc...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cellular signalling 2010-05, Vol.22 (5), p.836-847
Hauptverfasser: Nguyen, Hoai-Nghia, Raisley, Brent, Hadwiger, Jeffrey A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 847
container_issue 5
container_start_page 836
container_title Cellular signalling
container_volume 22
creator Nguyen, Hoai-Nghia
Raisley, Brent
Hadwiger, Jeffrey A.
description Extracellular signal regulated kinases (ERKs) are a class of MAP kinases that function in many signaling pathways in eukaryotic cells and in some cases, a single stimulus can activate more than one ERK suggesting functional redundancy or divergence from a common pathway. Dictyostelium discoideum encodes only two MAP kinases, ERK1 and ERK2, that both function during the developmental life cycle. To determine if ERK1 and ERK2 have overlapping functions, chemotactic and developmental phenotypes of erk1 − and erk2 − mutants were assessed with respect to G protein-mediated signal transduction pathways. ERK1 was specifically required for Gα5-mediated tip morphogenesis and inhibition of folate chemotaxis but not for cAMP-stimulated chemotaxis or cGMP accumulation. ERK2 was the primary MAPK phosphorylated in response to folate or cAMP stimulation. Cell growth was not altered in erk1 − , erk2 − or erk1 − erk2 − mutants but each mutant displayed a different pattern of cell sorting in chimeric aggregates. The distribution of GFP-ERK1 or GFP-ERK2 fusion proteins in the cytoplasm and nucleus was not grossly altered in cells stimulated with cAMP or folate. These results suggest ERK1 and ERK2 have different roles in G protein-mediated signaling during growth and development.
doi_str_mv 10.1016/j.cellsig.2010.01.008
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2859692</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0898656810000148</els_id><sourcerecordid>745693526</sourcerecordid><originalsourceid>FETCH-LOGICAL-c498t-9f01c4533012af5a9be3c4f5741cf25ff843d9bec8fed67a01bbb6021220537f3</originalsourceid><addsrcrecordid>eNqFUcFu1DAUtBCIbls-AZQbpyzPduwkF1DV0oLUqgiVs-U4z1svWXuxnZX693i1SwUnTk96b2beaIaQtxSWFKj8sF4anKbkVksGZQd0CdC9IAvatbzmPeUvyQK6vqulkN0JOU1pDUAFSPaanDCAtm84LMj3u4tv1U_ndcJUPeodVqOzFiP6XNnZm-yCT5Xz1ZUz-SmkjJObN9VNtY0ho_P1BkenM45VseL15PzqnLyyekr45jjPyI_rzw-XX-rb-5uvlxe3tWn6Lte9BWoawTlQpq3Q_YDcNFa0DTWWCWu7ho9laTqLo2w10GEYJDDKGAjeWn5GPh50t_NQXJhiOepJbaPb6Pikgnbq34t3j2oVdop1opc9KwLvjwIx_JoxZbVxaZ-q9hjmpNpGyJ4LJgtSHJAmhpQi2ucvFNS-DrVWxzrUvg4FVJU6Cu_d3xafWX_yL4BPBwCWoHYOo0rGoTcl1IgmqzG4_7z4DfDNoHs</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>745693526</pqid></control><display><type>article</type><title>MAP kinases have different functions in Dictyostelium G protein-mediated signaling</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Nguyen, Hoai-Nghia ; Raisley, Brent ; Hadwiger, Jeffrey A.</creator><creatorcontrib>Nguyen, Hoai-Nghia ; Raisley, Brent ; Hadwiger, Jeffrey A.</creatorcontrib><description>Extracellular signal regulated kinases (ERKs) are a class of MAP kinases that function in many signaling pathways in eukaryotic cells and in some cases, a single stimulus can activate more than one ERK suggesting functional redundancy or divergence from a common pathway. Dictyostelium discoideum encodes only two MAP kinases, ERK1 and ERK2, that both function during the developmental life cycle. To determine if ERK1 and ERK2 have overlapping functions, chemotactic and developmental phenotypes of erk1 − and erk2 − mutants were assessed with respect to G protein-mediated signal transduction pathways. ERK1 was specifically required for Gα5-mediated tip morphogenesis and inhibition of folate chemotaxis but not for cAMP-stimulated chemotaxis or cGMP accumulation. ERK2 was the primary MAPK phosphorylated in response to folate or cAMP stimulation. Cell growth was not altered in erk1 − , erk2 − or erk1 − erk2 − mutants but each mutant displayed a different pattern of cell sorting in chimeric aggregates. The distribution of GFP-ERK1 or GFP-ERK2 fusion proteins in the cytoplasm and nucleus was not grossly altered in cells stimulated with cAMP or folate. These results suggest ERK1 and ERK2 have different roles in G protein-mediated signaling during growth and development.</description><identifier>ISSN: 0898-6568</identifier><identifier>EISSN: 1873-3913</identifier><identifier>DOI: 10.1016/j.cellsig.2010.01.008</identifier><identifier>PMID: 20079430</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Animals ; Cell Aggregation - drug effects ; Cell Shape - drug effects ; Cell Survival - drug effects ; Chemotaxis - drug effects ; Cyclic AMP - pharmacology ; Development ; Dictyostelium ; Dictyostelium - cytology ; Dictyostelium - drug effects ; Dictyostelium - enzymology ; Dictyostelium - growth &amp; development ; Dictyostelium discoideum ; Enzyme Activation - drug effects ; ERK1 ; ERK2 ; Folic Acid - pharmacology ; G protein ; GTP-Binding Protein alpha Subunits - metabolism ; GTP-Binding Proteins - metabolism ; MAP kinase ; MAP Kinase Signaling System - drug effects ; Mitogen-Activated Protein Kinase 1 - metabolism ; Mitogen-Activated Protein Kinase 3 - metabolism ; Morphogenesis - drug effects ; Mutation - genetics ; Phosphorylation - drug effects ; Subcellular Fractions - drug effects ; Subcellular Fractions - enzymology ; Transformation, Genetic - drug effects</subject><ispartof>Cellular signalling, 2010-05, Vol.22 (5), p.836-847</ispartof><rights>2010 Elsevier Inc.</rights><rights>2010 Elsevier Inc. All rights reserved.</rights><rights>2010 Elsevier Inc. All rights reserved. 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c498t-9f01c4533012af5a9be3c4f5741cf25ff843d9bec8fed67a01bbb6021220537f3</citedby><cites>FETCH-LOGICAL-c498t-9f01c4533012af5a9be3c4f5741cf25ff843d9bec8fed67a01bbb6021220537f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cellsig.2010.01.008$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20079430$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nguyen, Hoai-Nghia</creatorcontrib><creatorcontrib>Raisley, Brent</creatorcontrib><creatorcontrib>Hadwiger, Jeffrey A.</creatorcontrib><title>MAP kinases have different functions in Dictyostelium G protein-mediated signaling</title><title>Cellular signalling</title><addtitle>Cell Signal</addtitle><description>Extracellular signal regulated kinases (ERKs) are a class of MAP kinases that function in many signaling pathways in eukaryotic cells and in some cases, a single stimulus can activate more than one ERK suggesting functional redundancy or divergence from a common pathway. Dictyostelium discoideum encodes only two MAP kinases, ERK1 and ERK2, that both function during the developmental life cycle. To determine if ERK1 and ERK2 have overlapping functions, chemotactic and developmental phenotypes of erk1 − and erk2 − mutants were assessed with respect to G protein-mediated signal transduction pathways. ERK1 was specifically required for Gα5-mediated tip morphogenesis and inhibition of folate chemotaxis but not for cAMP-stimulated chemotaxis or cGMP accumulation. ERK2 was the primary MAPK phosphorylated in response to folate or cAMP stimulation. Cell growth was not altered in erk1 − , erk2 − or erk1 − erk2 − mutants but each mutant displayed a different pattern of cell sorting in chimeric aggregates. The distribution of GFP-ERK1 or GFP-ERK2 fusion proteins in the cytoplasm and nucleus was not grossly altered in cells stimulated with cAMP or folate. These results suggest ERK1 and ERK2 have different roles in G protein-mediated signaling during growth and development.</description><subject>Animals</subject><subject>Cell Aggregation - drug effects</subject><subject>Cell Shape - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Chemotaxis - drug effects</subject><subject>Cyclic AMP - pharmacology</subject><subject>Development</subject><subject>Dictyostelium</subject><subject>Dictyostelium - cytology</subject><subject>Dictyostelium - drug effects</subject><subject>Dictyostelium - enzymology</subject><subject>Dictyostelium - growth &amp; development</subject><subject>Dictyostelium discoideum</subject><subject>Enzyme Activation - drug effects</subject><subject>ERK1</subject><subject>ERK2</subject><subject>Folic Acid - pharmacology</subject><subject>G protein</subject><subject>GTP-Binding Protein alpha Subunits - metabolism</subject><subject>GTP-Binding Proteins - metabolism</subject><subject>MAP kinase</subject><subject>MAP Kinase Signaling System - drug effects</subject><subject>Mitogen-Activated Protein Kinase 1 - metabolism</subject><subject>Mitogen-Activated Protein Kinase 3 - metabolism</subject><subject>Morphogenesis - drug effects</subject><subject>Mutation - genetics</subject><subject>Phosphorylation - drug effects</subject><subject>Subcellular Fractions - drug effects</subject><subject>Subcellular Fractions - enzymology</subject><subject>Transformation, Genetic - drug effects</subject><issn>0898-6568</issn><issn>1873-3913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUcFu1DAUtBCIbls-AZQbpyzPduwkF1DV0oLUqgiVs-U4z1svWXuxnZX693i1SwUnTk96b2beaIaQtxSWFKj8sF4anKbkVksGZQd0CdC9IAvatbzmPeUvyQK6vqulkN0JOU1pDUAFSPaanDCAtm84LMj3u4tv1U_ndcJUPeodVqOzFiP6XNnZm-yCT5Xz1ZUz-SmkjJObN9VNtY0ho_P1BkenM45VseL15PzqnLyyekr45jjPyI_rzw-XX-rb-5uvlxe3tWn6Lte9BWoawTlQpq3Q_YDcNFa0DTWWCWu7ho9laTqLo2w10GEYJDDKGAjeWn5GPh50t_NQXJhiOepJbaPb6Pikgnbq34t3j2oVdop1opc9KwLvjwIx_JoxZbVxaZ-q9hjmpNpGyJ4LJgtSHJAmhpQi2ucvFNS-DrVWxzrUvg4FVJU6Cu_d3xafWX_yL4BPBwCWoHYOo0rGoTcl1IgmqzG4_7z4DfDNoHs</recordid><startdate>20100501</startdate><enddate>20100501</enddate><creator>Nguyen, Hoai-Nghia</creator><creator>Raisley, Brent</creator><creator>Hadwiger, Jeffrey A.</creator><general>Elsevier Inc</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>M7N</scope><scope>5PM</scope></search><sort><creationdate>20100501</creationdate><title>MAP kinases have different functions in Dictyostelium G protein-mediated signaling</title><author>Nguyen, Hoai-Nghia ; Raisley, Brent ; Hadwiger, Jeffrey A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c498t-9f01c4533012af5a9be3c4f5741cf25ff843d9bec8fed67a01bbb6021220537f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Cell Aggregation - drug effects</topic><topic>Cell Shape - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>Chemotaxis - drug effects</topic><topic>Cyclic AMP - pharmacology</topic><topic>Development</topic><topic>Dictyostelium</topic><topic>Dictyostelium - cytology</topic><topic>Dictyostelium - drug effects</topic><topic>Dictyostelium - enzymology</topic><topic>Dictyostelium - growth &amp; development</topic><topic>Dictyostelium discoideum</topic><topic>Enzyme Activation - drug effects</topic><topic>ERK1</topic><topic>ERK2</topic><topic>Folic Acid - pharmacology</topic><topic>G protein</topic><topic>GTP-Binding Protein alpha Subunits - metabolism</topic><topic>GTP-Binding Proteins - metabolism</topic><topic>MAP kinase</topic><topic>MAP Kinase Signaling System - drug effects</topic><topic>Mitogen-Activated Protein Kinase 1 - metabolism</topic><topic>Mitogen-Activated Protein Kinase 3 - metabolism</topic><topic>Morphogenesis - drug effects</topic><topic>Mutation - genetics</topic><topic>Phosphorylation - drug effects</topic><topic>Subcellular Fractions - drug effects</topic><topic>Subcellular Fractions - enzymology</topic><topic>Transformation, Genetic - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nguyen, Hoai-Nghia</creatorcontrib><creatorcontrib>Raisley, Brent</creatorcontrib><creatorcontrib>Hadwiger, Jeffrey A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cellular signalling</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nguyen, Hoai-Nghia</au><au>Raisley, Brent</au><au>Hadwiger, Jeffrey A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MAP kinases have different functions in Dictyostelium G protein-mediated signaling</atitle><jtitle>Cellular signalling</jtitle><addtitle>Cell Signal</addtitle><date>2010-05-01</date><risdate>2010</risdate><volume>22</volume><issue>5</issue><spage>836</spage><epage>847</epage><pages>836-847</pages><issn>0898-6568</issn><eissn>1873-3913</eissn><abstract>Extracellular signal regulated kinases (ERKs) are a class of MAP kinases that function in many signaling pathways in eukaryotic cells and in some cases, a single stimulus can activate more than one ERK suggesting functional redundancy or divergence from a common pathway. Dictyostelium discoideum encodes only two MAP kinases, ERK1 and ERK2, that both function during the developmental life cycle. To determine if ERK1 and ERK2 have overlapping functions, chemotactic and developmental phenotypes of erk1 − and erk2 − mutants were assessed with respect to G protein-mediated signal transduction pathways. ERK1 was specifically required for Gα5-mediated tip morphogenesis and inhibition of folate chemotaxis but not for cAMP-stimulated chemotaxis or cGMP accumulation. ERK2 was the primary MAPK phosphorylated in response to folate or cAMP stimulation. Cell growth was not altered in erk1 − , erk2 − or erk1 − erk2 − mutants but each mutant displayed a different pattern of cell sorting in chimeric aggregates. The distribution of GFP-ERK1 or GFP-ERK2 fusion proteins in the cytoplasm and nucleus was not grossly altered in cells stimulated with cAMP or folate. These results suggest ERK1 and ERK2 have different roles in G protein-mediated signaling during growth and development.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>20079430</pmid><doi>10.1016/j.cellsig.2010.01.008</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0898-6568
ispartof Cellular signalling, 2010-05, Vol.22 (5), p.836-847
issn 0898-6568
1873-3913
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2859692
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Animals
Cell Aggregation - drug effects
Cell Shape - drug effects
Cell Survival - drug effects
Chemotaxis - drug effects
Cyclic AMP - pharmacology
Development
Dictyostelium
Dictyostelium - cytology
Dictyostelium - drug effects
Dictyostelium - enzymology
Dictyostelium - growth & development
Dictyostelium discoideum
Enzyme Activation - drug effects
ERK1
ERK2
Folic Acid - pharmacology
G protein
GTP-Binding Protein alpha Subunits - metabolism
GTP-Binding Proteins - metabolism
MAP kinase
MAP Kinase Signaling System - drug effects
Mitogen-Activated Protein Kinase 1 - metabolism
Mitogen-Activated Protein Kinase 3 - metabolism
Morphogenesis - drug effects
Mutation - genetics
Phosphorylation - drug effects
Subcellular Fractions - drug effects
Subcellular Fractions - enzymology
Transformation, Genetic - drug effects
title MAP kinases have different functions in Dictyostelium G protein-mediated signaling
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T00%3A07%3A32IST&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=MAP%20kinases%20have%20different%20functions%20in%20Dictyostelium%20G%20protein-mediated%20signaling&rft.jtitle=Cellular%20signalling&rft.au=Nguyen,%20Hoai-Nghia&rft.date=2010-05-01&rft.volume=22&rft.issue=5&rft.spage=836&rft.epage=847&rft.pages=836-847&rft.issn=0898-6568&rft.eissn=1873-3913&rft_id=info:doi/10.1016/j.cellsig.2010.01.008&rft_dat=%3Cproquest_pubme%3E745693526%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=745693526&rft_id=info:pmid/20079430&rft_els_id=S0898656810000148&rfr_iscdi=true