GENE EXPRESSIONS AND ACTIVITIES OF PROTEIN PHOSPHATASES PP1 AND PP2A IN RAT-LIVER REGENERATION AFTER PARTIAL-HEPATECTOMY

被引:26
作者
KAKINOKI, Y
KITAMURA, K
MATSUZAWA, S
MIZUNO, Y
MIYAZAKI, T
KIKUCHI, K
机构
[1] HOKKAIDO UNIV,SCH MED,INST IMMUNOL SCI,BIOCHEM SECT,KITA 15,NISHI 7,KITA KU,SAPPORO,HOKKAIDO 060,JAPAN
[2] HOKKAIDO UNIV,SCH MED,DEPT INTERNAL MED 3,SAPPORO,HOKKAIDO 060,JAPAN
关键词
D O I
10.1016/S0006-291X(05)80989-1
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
We have examined the levels of gene expressions and activities of protein phosphatases, PP1 and PP2A, in rat regenerating livers. PP1α mRNA started to increase from 6 h after partial hepatectomy (PH) and showed two peaks at 12 and 48 h. PP2A mRNA level showed two peaks at 6 and 10∼12 h. Protein phosphatase activities were determined both in non-nuclear fraction and in nuclei. While spontaneous PP1 activity in non-nuclear fraction was nearly constant, potential PP1 activity revealed by Co2+-trypsin treatment showed a small peak between 7 and 12 h. In nuclei, both spontaneous and potential PP1 activity began to increase from 4∼7 h after PH, reached a maximum (about 2.5-fold over control levels) at 12 h, the time which corresponds to the G1 to S transition in the cell cycle, and then declined back to control levels by 7 days. PP2A activity in non-nuclear fraction was nearly constant in both spontaneous and potential forms. PP2A activity in both forms in nuclei was very low throughout. These results suggest the possibility that PP1 in nuclei plays some role in the G1 to S transition in the cell cycle of hepatocyte proliferation. © 1992 Academic Press, Inc.
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页码:291 / 297
页数:7
相关论文
共 31 条
[11]  
Higgins GM, 1931, ARCH PATHOL, V12, P186
[12]   PURIFICATION AND CHARACTERIZATION OF MG2+-DEPENDENT GLYCOGEN-SYNTHASE PHOSPHATASE (PHOSPHOPROTEIN PHOSPHATASE IA) FROM RAT-LIVER [J].
HIRAGA, A ;
KIKUCHI, K ;
TAMURA, S ;
TSUIKI, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1981, 119 (03) :503-510
[13]   THE PROTEIN PHOSPHATASES INVOLVED IN CELLULAR-REGULATION .2. GLYCOGEN-METABOLISM [J].
INGEBRITSEN, TS ;
FOULKES, JG ;
COHEN, P .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1983, 132 (02) :263-274
[14]   ISOLATION AND CHARACTERIZATION OF AN INHIBITOR-SENSITIVE AND A POLYCATION-STIMULATED PROTEIN PHOSPHATASE FROM RAT-LIVER NUCLEI [J].
JAKES, S ;
MELLGREN, RL ;
SCHLENDER, KK .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 888 (01) :135-142
[15]   GLYCOGEN SYNTHASE PHOSPHATASE OF RAT-LIVER - ITS SEPARATION FROM PHOSPHORYLASE PHOSPHATASE ON DE-52 COLUMNS [J].
KIKUCHI, K ;
TAMURA, S ;
HIRAGA, A ;
TSUIKI, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1977, 75 (01) :29-37
[16]   MOLECULAR-CLONING OF CDNA FOR THE CATALYTIC SUBUNIT OF RAT-LIVER TYPE-2A PROTEIN PHOSPHATASE, AND DETECTION OF HIGH-LEVELS OF EXPRESSION OF THE GENE IN NORMAL AND CANCER-CELLS [J].
KITAGAWA, Y ;
TAHIRA, T ;
IKEDA, I ;
KIKUCHI, K ;
TSUIKI, S ;
SUGIMURA, T ;
NAGAO, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 951 (01) :123-129
[17]  
KITAMURA K, 1991, J BIOCHEM-TOKYO, V109, P307
[18]   MESSENGER-RNA LEVELS OF CATALYTIC SUBUNITS OF PROTEIN PHOSPHATASE-1, PHOSPHATASE-2A, AND PHOSPHATASE-2C IN HEPATOCARCINOGENESIS [J].
KITAMURA, K ;
MIZUNO, Y ;
HATAYAMA, I ;
SATO, K ;
TAMURA, S ;
NAGAO, M ;
TSUIKI, S ;
KIKUCHI, K .
JAPANESE JOURNAL OF CANCER RESEARCH, 1992, 83 (01) :66-71
[19]   DIFFERENTIAL PHOSPHORYLATION OF VERTEBRATE P34CDC2 KINASE AT THE G1/S AND G2/M TRANSITIONS OF THE CELL-CYCLE - IDENTIFICATION OF MAJOR PHOSPHORYLATION SITES [J].
KREK, W ;
NIGG, EA .
EMBO JOURNAL, 1991, 10 (02) :305-316
[20]   IDENTIFICATION OF HIGH-LEVELS OF PROTEIN PHOSPHATASE-1 IN RAT-LIVER NUCLEI [J].
KURET, J ;
BELL, H ;
COHEN, P .
FEBS LETTERS, 1986, 203 (02) :197-202