Matches in SemOpenAlex for { <https://semopenalex.org/work/W2136180536> ?p ?o ?g. }
- W2136180536 endingPage "1999" @default.
- W2136180536 startingPage "1990" @default.
- W2136180536 abstract "The Mos protein kinase is a key regulator of vertebrate oocyte maturation. Oocyte-specific Mos protein expression is subject to translational control. In the frog Xenopus, the translation of Mos protein requires the progesterone-induced polyadenylation of the maternal Mos mRNA, which is present in the oocyte cytoplasm. Both theXenopus p42 mitogen-activated protein kinase (MAPK) and maturation-promoting factor (MPF) signaling pathways have been proposed to mediate progesterone-stimulated oocyte maturation. In this study, we have determined the relative contributions of the MAPK and MPF signaling pathways to Mos mRNA polyadenylation. We report that progesterone-induced Mos mRNA polyadenylation was attenuated in oocytes expressing the MAPK phosphatase rVH6. Moreover, inhibition of MAPK signaling blocked progesterone-induced Mos protein accumulation. Activation of the MAPK pathway by injection of RNA encoding Mos was sufficient to induce both the polyadenylation of synthetic Mos mRNA substrates and the accumulation of endogenous Mos protein in the absence of MPF signaling. Activation of MPF, by injection of cyclin B1 RNA or purified cyclin B1 protein, also induced both Mos protein accumulation and Mos mRNA polyadenylation. However, this action of MPF required MAPK activity. By contrast, the cytoplasmic polyadenylation of maternal cyclin B1 mRNA was stimulated by MPF in a MAPK-independent manner, thus revealing a differential regulation of maternal mRNA polyadenylation by the MAPK and MPF signaling pathways. We propose that MAPK-stimulated Mos mRNA cytoplasmic polyadenylation is a key component of the positive-feedback loop, which contributes to the all-or-none process of oocyte maturation." @default.
- W2136180536 created "2016-06-24" @default.
- W2136180536 creator A5047232306 @default.
- W2136180536 creator A5063253877 @default.
- W2136180536 creator A5074008409 @default.
- W2136180536 creator A5084812887 @default.
- W2136180536 date "1999-03-01" @default.
- W2136180536 modified "2023-10-11" @default.
- W2136180536 title "The Mitogen-Activated Protein Kinase Signaling Pathway Stimulates Mos mRNA Cytoplasmic Polyadenylation during <i>Xenopus</i> Oocyte Maturation" @default.
- W2136180536 cites W126837237 @default.
- W2136180536 cites W139618738 @default.
- W2136180536 cites W1489207129 @default.
- W2136180536 cites W1545350340 @default.
- W2136180536 cites W1579500886 @default.
- W2136180536 cites W1604978548 @default.
- W2136180536 cites W177280810 @default.
- W2136180536 cites W1935296246 @default.
- W2136180536 cites W1961615758 @default.
- W2136180536 cites W1966006041 @default.
- W2136180536 cites W1968174450 @default.
- W2136180536 cites W1972979813 @default.
- W2136180536 cites W1973772302 @default.
- W2136180536 cites W1974559056 @default.
- W2136180536 cites W1981001162 @default.
- W2136180536 cites W1984269514 @default.
- W2136180536 cites W1993995783 @default.
- W2136180536 cites W1995294841 @default.
- W2136180536 cites W2003542182 @default.
- W2136180536 cites W2008855387 @default.
- W2136180536 cites W2009629503 @default.
- W2136180536 cites W2010394043 @default.
- W2136180536 cites W2012781224 @default.
- W2136180536 cites W2013549179 @default.
- W2136180536 cites W2018636110 @default.
- W2136180536 cites W2028275151 @default.
- W2136180536 cites W2030629284 @default.
- W2136180536 cites W2032984787 @default.
- W2136180536 cites W2035936653 @default.
- W2136180536 cites W2037426608 @default.
- W2136180536 cites W2043335974 @default.
- W2136180536 cites W2044145281 @default.
- W2136180536 cites W2047799300 @default.
- W2136180536 cites W2055037221 @default.
- W2136180536 cites W2055157702 @default.
- W2136180536 cites W2059155490 @default.
- W2136180536 cites W2059623287 @default.
- W2136180536 cites W2066235505 @default.
- W2136180536 cites W2067064841 @default.
- W2136180536 cites W2067621854 @default.
- W2136180536 cites W2067656276 @default.
- W2136180536 cites W2070404387 @default.
- W2136180536 cites W2076860978 @default.
- W2136180536 cites W2078119356 @default.
- W2136180536 cites W2082190322 @default.
- W2136180536 cites W2084136914 @default.
- W2136180536 cites W2084659331 @default.
- W2136180536 cites W2089784855 @default.
- W2136180536 cites W2091759633 @default.
- W2136180536 cites W2093205464 @default.
- W2136180536 cites W2096733041 @default.
- W2136180536 cites W2101500464 @default.
- W2136180536 cites W2102242413 @default.
- W2136180536 cites W2106251845 @default.
- W2136180536 cites W2114476704 @default.
- W2136180536 cites W2115701574 @default.
- W2136180536 cites W2117939247 @default.
- W2136180536 cites W2130084958 @default.
- W2136180536 cites W2132300009 @default.
- W2136180536 cites W2145312934 @default.
- W2136180536 cites W2152090841 @default.
- W2136180536 cites W2154625613 @default.
- W2136180536 cites W2196561685 @default.
- W2136180536 cites W2244032147 @default.
- W2136180536 cites W247355068 @default.
- W2136180536 cites W278363641 @default.
- W2136180536 cites W4251911047 @default.
- W2136180536 cites W66625613 @default.
- W2136180536 doi "https://doi.org/10.1128/mcb.19.3.1990" @default.
- W2136180536 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/83992" @default.
- W2136180536 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10022886" @default.
- W2136180536 hasPublicationYear "1999" @default.
- W2136180536 type Work @default.
- W2136180536 sameAs 2136180536 @default.
- W2136180536 citedByCount "84" @default.
- W2136180536 countsByYear W21361805362012 @default.
- W2136180536 countsByYear W21361805362013 @default.
- W2136180536 countsByYear W21361805362014 @default.
- W2136180536 countsByYear W21361805362016 @default.
- W2136180536 countsByYear W21361805362017 @default.
- W2136180536 countsByYear W21361805362020 @default.
- W2136180536 crossrefType "journal-article" @default.
- W2136180536 hasAuthorship W2136180536A5047232306 @default.
- W2136180536 hasAuthorship W2136180536A5063253877 @default.
- W2136180536 hasAuthorship W2136180536A5074008409 @default.
- W2136180536 hasAuthorship W2136180536A5084812887 @default.
- W2136180536 hasBestOaLocation W21361805362 @default.
- W2136180536 hasConcept C104317684 @default.
- W2136180536 hasConcept C105580179 @default.