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...
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Veröffentlicht in: | Cellular signalling 2010-05, Vol.22 (5), p.836-847 |
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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 |
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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 & 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 & 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 & 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> |
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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 |
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