Protein kinase B/Akt is essential for the insulin- but not progesterone-stimulated resumption of meiosis in Xenopus oocytes
In the present study, we have characterized the Xenopus Akt expressed in oocytes from the African clawed frog Xenopus laevis and tested whether its activity is required for the insulin- and progesterone-stimulated resumption of meiosis. A cDNA encoding the Xenopus Akt was isolated and sequenced, and...
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Veröffentlicht in: | Biochemical journal 2003-01, Vol.369 (Pt 2), p.227-238 |
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description | In the present study, we have characterized the Xenopus Akt expressed in oocytes from the African clawed frog Xenopus laevis and tested whether its activity is required for the insulin- and progesterone-stimulated resumption of meiosis. A cDNA encoding the Xenopus Akt was isolated and sequenced, and its expression in the Xenopus oocyte was confirmed by reverse transcription PCR and Northern blotting. Using phosphospecific antibodies and enzyme assays, a large and rapid activation of the Xenopus Akt was observed upon insulin stimulation of the oocytes. In contrast, progesterone caused a modest activation of this kinase with a slower time course. To test whether the activation of Akt was required in the stimulation of the resumption of meiosis, we have utilized two independent approaches: a functional dominant negative Akt mutant and an inhibitory monoclonal antibody. Both the mutant Akt, as well as the inhibitory monoclonal antibody, completely blocked the insulin-stimulated resumption of meiosis. In contrast, both treatments only partially inhibited (by approx. 30%) the progesterone-stimulated resumption of meiosis when submaximal doses of this hormone were utilized. These data demonstrate a crucial role for Akt in the insulin-stimulated cell cycle progression of Xenopus oocytes, whereas Akt may have an ancillary function in progesterone signalling. |
doi_str_mv | 10.1042/BJ20021243 |
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A cDNA encoding the Xenopus Akt was isolated and sequenced, and its expression in the Xenopus oocyte was confirmed by reverse transcription PCR and Northern blotting. Using phosphospecific antibodies and enzyme assays, a large and rapid activation of the Xenopus Akt was observed upon insulin stimulation of the oocytes. In contrast, progesterone caused a modest activation of this kinase with a slower time course. To test whether the activation of Akt was required in the stimulation of the resumption of meiosis, we have utilized two independent approaches: a functional dominant negative Akt mutant and an inhibitory monoclonal antibody. Both the mutant Akt, as well as the inhibitory monoclonal antibody, completely blocked the insulin-stimulated resumption of meiosis. In contrast, both treatments only partially inhibited (by approx. 30%) the progesterone-stimulated resumption of meiosis when submaximal doses of this hormone were utilized. These data demonstrate a crucial role for Akt in the insulin-stimulated cell cycle progression of Xenopus oocytes, whereas Akt may have an ancillary function in progesterone signalling.</description><identifier>ISSN: 0264-6021</identifier><identifier>EISSN: 1470-8728</identifier><identifier>DOI: 10.1042/BJ20021243</identifier><identifier>PMID: 12374568</identifier><language>eng</language><publisher>England</publisher><subject>Amino Acid Sequence ; Animals ; Antibodies, Monoclonal - metabolism ; COS Cells ; Dose-Response Relationship, Drug ; Female ; Insulin - metabolism ; Insulin - pharmacology ; Meiosis - drug effects ; Meiosis - physiology ; Microinjections ; Molecular Sequence Data ; Oocytes - drug effects ; Oocytes - physiology ; Phylogeny ; Progesterone - metabolism ; Progesterone - pharmacology ; Protein-Serine-Threonine Kinases ; Proto-Oncogene Proteins - classification ; Proto-Oncogene Proteins - genetics ; Proto-Oncogene Proteins - metabolism ; Proto-Oncogene Proteins c-akt ; RNA, Messenger - metabolism ; Sequence Alignment ; Signal Transduction - physiology ; Xenopus laevis - physiology</subject><ispartof>Biochemical journal, 2003-01, Vol.369 (Pt 2), p.227-238</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c374t-21b9d98dba32a6a4c067a2b610e2da3c2f07004f172639d446d423213a41d0be3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1223087/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1223087/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12374568$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Andersen, Carsten B</creatorcontrib><creatorcontrib>Sakaue, Hiroshi</creatorcontrib><creatorcontrib>Nedachi, Taku</creatorcontrib><creatorcontrib>Kovacina, Kristina S</creatorcontrib><creatorcontrib>Clayberger, Carol</creatorcontrib><creatorcontrib>Conti, Marco</creatorcontrib><creatorcontrib>Roth, Richard A</creatorcontrib><title>Protein kinase B/Akt is essential for the insulin- but not progesterone-stimulated resumption of meiosis in Xenopus oocytes</title><title>Biochemical journal</title><addtitle>Biochem J</addtitle><description>In the present study, we have characterized the Xenopus Akt expressed in oocytes from the African clawed frog Xenopus laevis and tested whether its activity is required for the insulin- and progesterone-stimulated resumption of meiosis. A cDNA encoding the Xenopus Akt was isolated and sequenced, and its expression in the Xenopus oocyte was confirmed by reverse transcription PCR and Northern blotting. Using phosphospecific antibodies and enzyme assays, a large and rapid activation of the Xenopus Akt was observed upon insulin stimulation of the oocytes. In contrast, progesterone caused a modest activation of this kinase with a slower time course. To test whether the activation of Akt was required in the stimulation of the resumption of meiosis, we have utilized two independent approaches: a functional dominant negative Akt mutant and an inhibitory monoclonal antibody. Both the mutant Akt, as well as the inhibitory monoclonal antibody, completely blocked the insulin-stimulated resumption of meiosis. In contrast, both treatments only partially inhibited (by approx. 30%) the progesterone-stimulated resumption of meiosis when submaximal doses of this hormone were utilized. These data demonstrate a crucial role for Akt in the insulin-stimulated cell cycle progression of Xenopus oocytes, whereas Akt may have an ancillary function in progesterone signalling.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Antibodies, Monoclonal - metabolism</subject><subject>COS Cells</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Insulin - metabolism</subject><subject>Insulin - pharmacology</subject><subject>Meiosis - drug effects</subject><subject>Meiosis - physiology</subject><subject>Microinjections</subject><subject>Molecular Sequence Data</subject><subject>Oocytes - drug effects</subject><subject>Oocytes - physiology</subject><subject>Phylogeny</subject><subject>Progesterone - metabolism</subject><subject>Progesterone - pharmacology</subject><subject>Protein-Serine-Threonine Kinases</subject><subject>Proto-Oncogene Proteins - classification</subject><subject>Proto-Oncogene Proteins - genetics</subject><subject>Proto-Oncogene Proteins - metabolism</subject><subject>Proto-Oncogene Proteins c-akt</subject><subject>RNA, Messenger - metabolism</subject><subject>Sequence Alignment</subject><subject>Signal Transduction - physiology</subject><subject>Xenopus laevis - physiology</subject><issn>0264-6021</issn><issn>1470-8728</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUctu1TAQtRCIXi5s-ADkFYtKoeOxyWOD1FY8VQkWILGznGTSuk3s4HGQKn4eo15em5nFOToPHSGeKnihwODJ2QcEQIVG3xM7ZRqo2gbb-2IHWJuqLtCReMR8DaAMGHgojhTqxrys25348SnFTD7IGx8ckzw7Ob3J0rMkZgrZu1lOMcl8RdIH3mYfKtlvWYaY5ZriJXGmFANVnP2yzS7TKBPxtqzZxyDjJBfykYtg8fhKIa4byxiH20z8WDyY3Mz05PD34sub15_P31UXH9--Pz-9qIaSMleo-m7s2rF3Gl3tzAB147CvFRCOTg84QQNgJtVgrbvRmHo0qFFpZ9QIPem9eHWnu279QuNQeiU32zX5xaVbG523_yPBX9nL-N0qRA1tUwSeHwRS_LaVynbxPNA8u0BxY9tgpzssZy-O74hDisyJpj8mCuyvrWx__XurQn72b6y_1MM4-idQlZGv</recordid><startdate>20030115</startdate><enddate>20030115</enddate><creator>Andersen, Carsten B</creator><creator>Sakaue, Hiroshi</creator><creator>Nedachi, Taku</creator><creator>Kovacina, Kristina S</creator><creator>Clayberger, Carol</creator><creator>Conti, Marco</creator><creator>Roth, Richard A</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20030115</creationdate><title>Protein kinase B/Akt is essential for the insulin- but not progesterone-stimulated resumption of meiosis in Xenopus oocytes</title><author>Andersen, Carsten B ; Sakaue, Hiroshi ; Nedachi, Taku ; Kovacina, Kristina S ; Clayberger, Carol ; Conti, Marco ; Roth, Richard A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c374t-21b9d98dba32a6a4c067a2b610e2da3c2f07004f172639d446d423213a41d0be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Antibodies, Monoclonal - metabolism</topic><topic>COS Cells</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Insulin - metabolism</topic><topic>Insulin - pharmacology</topic><topic>Meiosis - drug effects</topic><topic>Meiosis - physiology</topic><topic>Microinjections</topic><topic>Molecular Sequence Data</topic><topic>Oocytes - drug effects</topic><topic>Oocytes - physiology</topic><topic>Phylogeny</topic><topic>Progesterone - metabolism</topic><topic>Progesterone - pharmacology</topic><topic>Protein-Serine-Threonine Kinases</topic><topic>Proto-Oncogene Proteins - classification</topic><topic>Proto-Oncogene Proteins - genetics</topic><topic>Proto-Oncogene Proteins - metabolism</topic><topic>Proto-Oncogene Proteins c-akt</topic><topic>RNA, Messenger - metabolism</topic><topic>Sequence Alignment</topic><topic>Signal Transduction - physiology</topic><topic>Xenopus laevis - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Andersen, Carsten B</creatorcontrib><creatorcontrib>Sakaue, Hiroshi</creatorcontrib><creatorcontrib>Nedachi, Taku</creatorcontrib><creatorcontrib>Kovacina, Kristina S</creatorcontrib><creatorcontrib>Clayberger, Carol</creatorcontrib><creatorcontrib>Conti, Marco</creatorcontrib><creatorcontrib>Roth, Richard 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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biochemical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Andersen, Carsten B</au><au>Sakaue, Hiroshi</au><au>Nedachi, Taku</au><au>Kovacina, Kristina S</au><au>Clayberger, Carol</au><au>Conti, Marco</au><au>Roth, Richard A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protein kinase B/Akt is essential for the insulin- but not progesterone-stimulated resumption of meiosis in Xenopus oocytes</atitle><jtitle>Biochemical journal</jtitle><addtitle>Biochem J</addtitle><date>2003-01-15</date><risdate>2003</risdate><volume>369</volume><issue>Pt 2</issue><spage>227</spage><epage>238</epage><pages>227-238</pages><issn>0264-6021</issn><eissn>1470-8728</eissn><abstract>In the present study, we have characterized the Xenopus Akt expressed in oocytes from the African clawed frog Xenopus laevis and tested whether its activity is required for the insulin- and progesterone-stimulated resumption of meiosis. A cDNA encoding the Xenopus Akt was isolated and sequenced, and its expression in the Xenopus oocyte was confirmed by reverse transcription PCR and Northern blotting. Using phosphospecific antibodies and enzyme assays, a large and rapid activation of the Xenopus Akt was observed upon insulin stimulation of the oocytes. In contrast, progesterone caused a modest activation of this kinase with a slower time course. To test whether the activation of Akt was required in the stimulation of the resumption of meiosis, we have utilized two independent approaches: a functional dominant negative Akt mutant and an inhibitory monoclonal antibody. Both the mutant Akt, as well as the inhibitory monoclonal antibody, completely blocked the insulin-stimulated resumption of meiosis. In contrast, both treatments only partially inhibited (by approx. 30%) the progesterone-stimulated resumption of meiosis when submaximal doses of this hormone were utilized. These data demonstrate a crucial role for Akt in the insulin-stimulated cell cycle progression of Xenopus oocytes, whereas Akt may have an ancillary function in progesterone signalling.</abstract><cop>England</cop><pmid>12374568</pmid><doi>10.1042/BJ20021243</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Animals Antibodies, Monoclonal - metabolism COS Cells Dose-Response Relationship, Drug Female Insulin - metabolism Insulin - pharmacology Meiosis - drug effects Meiosis - physiology Microinjections Molecular Sequence Data Oocytes - drug effects Oocytes - physiology Phylogeny Progesterone - metabolism Progesterone - pharmacology Protein-Serine-Threonine Kinases Proto-Oncogene Proteins - classification Proto-Oncogene Proteins - genetics Proto-Oncogene Proteins - metabolism Proto-Oncogene Proteins c-akt RNA, Messenger - metabolism Sequence Alignment Signal Transduction - physiology Xenopus laevis - physiology |
title | Protein kinase B/Akt is essential for the insulin- but not progesterone-stimulated resumption of meiosis in Xenopus oocytes |
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