What does Mos do in oocytes and somatic cells?

被引:229
作者
Sagata, N
机构
[1] Department of Biology, Faculty of Science, Kyushu University, Fukuoka 812-81
关键词
D O I
10.1002/bies.950190105
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
Mos, a protein kinase, is specifically expressed and functions during meiotic maturation (or G(2)/M progression) of vertebrate oocytes. When expressed ectopically, however, it can also readily induce oncogenic transformation (or uncontrolled G(1)/S transitions) in somatic cells. In both of these cell types, Mos activates mitogen-activated protein kinase (MAPK), which seems largely to mediate its different functions in both oocyte maturation and cellular transformation, In oocyte maturation, the Mos-MAPK pathway probably serves to activate and stabilize M-phase promoting factor (MPF) (possibly by inhibiting some negative regulator(s) of this factor), while in cellular transformation, it seems to stabilize and activate the nuclear oncoprotein c-Fos as well as to induce transcription of its gene. Thus, the different functions of Mos in oocytes and somatic cells may arise chiefly from its different MAPK-mediated targets in the respective cell types. This review discusses the cellular basis that may enable Mos to act differently in oocytes and somatic cells.
引用
收藏
页码:13 / 21
页数:9
相关论文
共 70 条
[1]  
Chen RH, 1996, ONCOGENE, V12, P1493
[2]   The mitogen-activated protein kinase phosphatases PAC1, MKP-1, and MKP-2 have unique substrate specificities and reduced activity in vivo toward the ERK2 sevenmaker mutation [J].
Chu, YF ;
Solski, PA ;
KhosraviFar, R ;
Der, CJ ;
Kelly, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (11) :6497-6501
[3]   DISRUPTION OF C-MOS CAUSES PARTHENOGENETIC DEVELOPMENT OF UNFERTILIZED MOUSE EGGS [J].
COLLEDGE, WH ;
CARLTON, MBL ;
UDY, GB ;
EVANS, MJ .
NATURE, 1994, 370 (6484) :65-68
[4]   A CHARACTERIZATION OF CYTOSTATIC FACTOR ACTIVITY FROM XENOPUS EGGS AND C-MOS-TRANSFORMED CELLS [J].
DAAR, I ;
PAULES, RS ;
VANDEWOUDE, GF .
JOURNAL OF CELL BIOLOGY, 1991, 114 (02) :329-335
[5]  
Davidson EH., 1986, GENE ACTIVITY EARLY
[6]  
DAVIS RJ, 1993, J BIOL CHEM, V268, P14553
[7]   CELL-CYCLE TYROSINE PHOSPHORYLATION OF P34CDC2 AND A MICROTUBULE-ASSOCIATED PROTEIN-KINASE HOMOLOG IN XENOPUS OOCYTES AND EGGS [J].
FERRELL, JE ;
WU, M ;
GERHART, JC ;
MARTIN, GS .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (04) :1965-1971
[8]   XENOPUS HOMOLOG OF THE MOS PROTOONCOGENE TRANSFORMS MAMMALIAN FIBROBLASTS AND INDUCES MATURATION OF XENOPUS OOCYTES [J].
FREEMAN, RS ;
PICKHAM, KM ;
KANKI, JP ;
LEE, BA ;
PENA, SV ;
DONOGHUE, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (15) :5805-5809
[9]   MEIOTIC INDUCTION BY XENOPUS CYCLIN B IS ACCELERATED BY COEXPRESSION WITH MOSXE [J].
FREEMAN, RS ;
BALLANTYNE, SM ;
DONOGHUE, DJ .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (03) :1713-1717
[10]   MOS OVEREXPRESSION IN SWISS 3T3 CELLS INDUCES MEIOTIC-LIKE ALTERATIONS OF THE MITOTIC SPINDLE [J].
FUKASAWA, K ;
VANDEWOUDE, GF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (08) :3430-3434