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The pathway of MAP kinase mediation of CSF arrest in Xenopus oocytes
A cytoplasmic activity in mature oocytes responsible for second meiotic metaphase arrest was identified over 30 years ago in amphibian oocytes. In Xenopus oocytes CSF activity is initiated by the progesterone-dependent synthesis of Mos, a MAPK kinase kinase, which activates the MAPK pathway. CSF a...
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Published in: | Biology of the Cell 2001-09, Vol.93 (1), p.27-33 |
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container_title | Biology of the Cell |
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creator | Maller, James L. Schwab, Markus S. Roberts, B.Tibor Gross, Stefan D. Taieb, Frédéric E. Tunquist, Brian J. |
description | A cytoplasmic activity in mature oocytes responsible for second meiotic metaphase arrest was identified over 30 years ago in amphibian oocytes. In
Xenopus oocytes CSF activity is initiated by the progesterone-dependent synthesis of Mos, a MAPK kinase kinase, which activates the MAPK pathway. CSF arrest is mediated by a sole MAPK target, the protein kinase p90
Rsk which leads to inhibition of cyclin B degradation by the anaphase-promoting complex. Rsk phosphorylates and activates the Bub1 protein kinase, which may cause metaphase arrest due to inhibition of the anaphase-promoting complex (APC) by a conserved mechanism defined genetically in yeast and mammalian cells. CSF arrest in vertebrate oocytes by p90
Rsk provides a potential link between the MAPK pathway and the spindle assembly checkpoint in the cell cycle. |
doi_str_mv | 10.1016/S0248-4900(01)01127-3 |
format | article |
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Xenopus oocytes CSF activity is initiated by the progesterone-dependent synthesis of Mos, a MAPK kinase kinase, which activates the MAPK pathway. CSF arrest is mediated by a sole MAPK target, the protein kinase p90
Rsk which leads to inhibition of cyclin B degradation by the anaphase-promoting complex. Rsk phosphorylates and activates the Bub1 protein kinase, which may cause metaphase arrest due to inhibition of the anaphase-promoting complex (APC) by a conserved mechanism defined genetically in yeast and mammalian cells. CSF arrest in vertebrate oocytes by p90
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Xenopus oocytes CSF activity is initiated by the progesterone-dependent synthesis of Mos, a MAPK kinase kinase, which activates the MAPK pathway. CSF arrest is mediated by a sole MAPK target, the protein kinase p90
Rsk which leads to inhibition of cyclin B degradation by the anaphase-promoting complex. Rsk phosphorylates and activates the Bub1 protein kinase, which may cause metaphase arrest due to inhibition of the anaphase-promoting complex (APC) by a conserved mechanism defined genetically in yeast and mammalian cells. CSF arrest in vertebrate oocytes by p90
Rsk provides a potential link between the MAPK pathway and the spindle assembly checkpoint in the cell cycle.</description><subject>Anaphase-Promoting Complex-Cyclosome</subject><subject>Animals</subject><subject>Bub1</subject><subject>cytostatic factor</subject><subject>Life Sciences</subject><subject>Ligases - physiology</subject><subject>MAPK</subject><subject>Maturation-Promoting Factor - physiology</subject><subject>Mitogen-Activated Protein Kinases - physiology</subject><subject>oocyte maturation</subject><subject>Oocytes - growth & development</subject><subject>Oocytes - physiology</subject><subject>Protein Kinases - physiology</subject><subject>Proto-Oncogene Proteins c-mos - physiology</subject><subject>Ribosomal Protein S6 Kinases</subject><subject>Rsk</subject><subject>Spindle Apparatus</subject><subject>spindle assembly checkpoint</subject><subject>Ubiquitin-Protein Ligase Complexes</subject><subject>Xenopus</subject><issn>0248-4900</issn><issn>1768-322X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqNkV1v0zAUhi0EYmXwE0C5Quwim48df4SbqQvrhlQYUoeYuLEcx1HN0rjY6bb--yVL1V3ClaWj533t8xih94CPAQM_WWCSyTTLMf6E4QgDEJHSF2gCgsuUEnLzEk32yAF6E-MfjHGWS_YaHQAIiinkE_TlemmTte6W93qb-Dr5Nv2R3LpWR5usbOV053w7zIvFLNEh2Nglrk1ubOvXm5h4b7adjW_Rq1o30b7bnYfo5-z8urhM51cXX4vpPDWMYZ4CZSbjOa-oqVglCUBVYQ054SVjZQa5oLXJqJScVWUtAExV8tJKmQlMTAn0EB2NvUvdqHVwKx22ymunLqdzNcww4ULILL8b2I8juw7-76Z_t1q5aGzT6Nb6TVSCUABORQ-yETTBxxhsvW8GrAbV6km1GjwqDOpJtaJ97sPugk3Zq3pO7dz2wOcRuHeN3f5fqzq7KgimvA-nY9jFzj7swzrcKi6oYOrX9wt1lheyWPyeKdbzpyNve_93zgYVjbOt6f8wWNOpyrt_7PMIx9GqlQ</recordid><startdate>200109</startdate><enddate>200109</enddate><creator>Maller, James L.</creator><creator>Schwab, Markus S.</creator><creator>Roberts, B.Tibor</creator><creator>Gross, Stefan D.</creator><creator>Taieb, Frédéric E.</creator><creator>Tunquist, Brian J.</creator><general>Elsevier SAS</general><general>Blackwell Publishing Ltd</general><general>Wiley</general><scope>BSCLL</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>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0001-9612-2069</orcidid></search><sort><creationdate>200109</creationdate><title>The pathway of MAP kinase mediation of CSF arrest in Xenopus oocytes</title><author>Maller, James L. ; Schwab, Markus S. ; Roberts, B.Tibor ; Gross, Stefan D. ; Taieb, Frédéric E. ; Tunquist, Brian J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5506-135c4696d3cd5d8211dd0a1926b55b41973fc438865dbf711cdb6be884702cb13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Anaphase-Promoting Complex-Cyclosome</topic><topic>Animals</topic><topic>Bub1</topic><topic>cytostatic factor</topic><topic>Life Sciences</topic><topic>Ligases - physiology</topic><topic>MAPK</topic><topic>Maturation-Promoting Factor - physiology</topic><topic>Mitogen-Activated Protein Kinases - physiology</topic><topic>oocyte maturation</topic><topic>Oocytes - growth & development</topic><topic>Oocytes - physiology</topic><topic>Protein Kinases - physiology</topic><topic>Proto-Oncogene Proteins c-mos - physiology</topic><topic>Ribosomal Protein S6 Kinases</topic><topic>Rsk</topic><topic>Spindle Apparatus</topic><topic>spindle assembly checkpoint</topic><topic>Ubiquitin-Protein Ligase Complexes</topic><topic>Xenopus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maller, James L.</creatorcontrib><creatorcontrib>Schwab, Markus S.</creatorcontrib><creatorcontrib>Roberts, B.Tibor</creatorcontrib><creatorcontrib>Gross, Stefan D.</creatorcontrib><creatorcontrib>Taieb, Frédéric E.</creatorcontrib><creatorcontrib>Tunquist, Brian J.</creatorcontrib><collection>Istex</collection><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>Hyper Article en Ligne (HAL)</collection><jtitle>Biology of the Cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maller, James L.</au><au>Schwab, Markus S.</au><au>Roberts, B.Tibor</au><au>Gross, Stefan D.</au><au>Taieb, Frédéric E.</au><au>Tunquist, Brian J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The pathway of MAP kinase mediation of CSF arrest in Xenopus oocytes</atitle><jtitle>Biology of the Cell</jtitle><addtitle>Biol Cell</addtitle><date>2001-09</date><risdate>2001</risdate><volume>93</volume><issue>1</issue><spage>27</spage><epage>33</epage><pages>27-33</pages><issn>0248-4900</issn><eissn>1768-322X</eissn><abstract>A cytoplasmic activity in mature oocytes responsible for second meiotic metaphase arrest was identified over 30 years ago in amphibian oocytes. In
Xenopus oocytes CSF activity is initiated by the progesterone-dependent synthesis of Mos, a MAPK kinase kinase, which activates the MAPK pathway. CSF arrest is mediated by a sole MAPK target, the protein kinase p90
Rsk which leads to inhibition of cyclin B degradation by the anaphase-promoting complex. Rsk phosphorylates and activates the Bub1 protein kinase, which may cause metaphase arrest due to inhibition of the anaphase-promoting complex (APC) by a conserved mechanism defined genetically in yeast and mammalian cells. CSF arrest in vertebrate oocytes by p90
Rsk provides a potential link between the MAPK pathway and the spindle assembly checkpoint in the cell cycle.</abstract><cop>Oxford, UK</cop><pub>Elsevier SAS</pub><pmid>11730319</pmid><doi>10.1016/S0248-4900(01)01127-3</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-9612-2069</orcidid></addata></record> |
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source | ScienceDirect Journals; Wiley-Blackwell Read & Publish Collection |
subjects | Anaphase-Promoting Complex-Cyclosome Animals Bub1 cytostatic factor Life Sciences Ligases - physiology MAPK Maturation-Promoting Factor - physiology Mitogen-Activated Protein Kinases - physiology oocyte maturation Oocytes - growth & development Oocytes - physiology Protein Kinases - physiology Proto-Oncogene Proteins c-mos - physiology Ribosomal Protein S6 Kinases Rsk Spindle Apparatus spindle assembly checkpoint Ubiquitin-Protein Ligase Complexes Xenopus |
title | The pathway of MAP kinase mediation of CSF arrest in Xenopus oocytes |
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