Protein kinase B/Akt is essential for the insulin- but not progesterone-stimulated resumption of meiosis in Xenopus oocytes

被引:40
作者
Andersen, CB
Sakaue, H
Nedachi, T
Kovacina, KS
Clayberger, C
Conti, M
Roth, RA [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Mol Pharmacol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Gynecol & Obstet, Div Reprod Biol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Cardiothorac Surg, Stanford, CA 94305 USA
关键词
cell cycle; insulin action; phosphatase; progesterone signalling;
D O I
10.1042/BJ20021243
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:227 / 238
页数:12
相关论文
共 53 条
[1]   Mechanism of activation and function of protein kinase B [J].
Alessi, DR ;
Cohen, P .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1998, 8 (01) :55-62
[2]   3-phosphoinositide-dependent protein kinase-1 (PDK1): structural and functional homology with the Drosophila DSTPK61 kinase [J].
Alessi, DR ;
Deak, M ;
Casamayor, A ;
Caudwell, FB ;
Morrice, N ;
Norman, DG ;
Gaffney, P ;
Reese, CB ;
MacDougall, CN ;
Harbison, D ;
Ashworth, A ;
Bownes, M .
CURRENT BIOLOGY, 1997, 7 (10) :776-789
[3]   Protein kinase B/Akt induces resumption of meiosis in Xenopus oocytes [J].
Andersen, CB ;
Roth, RA ;
Conti, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (30) :18705-18708
[4]   The classical progesterone receptor associates with p42 MAPK and is involved in phosphatidylinositol 3-kinase signaling in Xenopus oocytes [J].
Bagowski, CP ;
Myers, JW ;
Ferrell, JE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (40) :37708-37714
[5]   HA-RASVAL-12,THR-59 ACTIVATES S6 KINASE AND P34CDC2 KINASE IN XENOPUS OOCYTES - EVIDENCE FOR C-MOSXE-DEPENDENT AND C-MOSXE-INDEPENDENT PATHWAYS [J].
BARRETT, CB ;
SCHROETKE, RM ;
VANDERHOORN, FA ;
NORDEEN, SK ;
MALLER, JL .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (01) :310-315
[6]   The classical progesterone receptor mediates Xenopus oocyte maturation through a nongenomic mechanism [J].
Bayaa, M ;
Booth, RA ;
Sheng, YL ;
Liu, XJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) :12607-12612
[7]   INSULIN-STIMULATED OOCYTE MATURATION REQUIRES INSULIN-RECEPTOR SUBSTRATE-1 AND INTERACTION WITH THE SH2 DOMAINS OF PHOSPHATIDYLINOSITOL 3-KINASE [J].
CHUANG, LM ;
MYERS, MG ;
BACKER, JM ;
SHOELSON, SE ;
WHITE, MF ;
BIRNBAUM, MJ ;
KAHN, CR .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (11) :6653-6660
[8]  
CLAYBERGER C, 1987, J IMMUNOL, V138, P1510
[9]   INHIBITION OF GLYCOGEN-SYNTHASE KINASE-3 BY INSULIN-MEDIATED BY PROTEIN-KINASE-B [J].
CROSS, DAE ;
ALESSI, DR ;
COHEN, P ;
ANDJELKOVICH, M ;
HEMMINGS, BA .
NATURE, 1995, 378 (6559) :785-789
[10]   PIP2 and PIP3: Complex roles at the cell surface [J].
Czech, MP .
CELL, 2000, 100 (06) :603-606