IDENTIFICATION OF A NOVEL NUCLEAR-PROTEIN SYNTHESIZED IN GROWTH-ARRESTED HUMAN HEPATOBLASTOMA HEPG2 CELLS

被引:20
作者
DONADEL, G
GARZELLI, C
FRANK, R
GABRIELLI, F
机构
[1] UNIV PISA,INST BIOL CHEM,VIA ROMA 55,I-56126 PISA,ITALY
[2] UNIV PISA,DEPT BIOMED,I-56126 PISA,ITALY
[3] EUROPEAN MOLEC BIOL LAB,W-6900 HEIDELBERG,GERMANY
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1991年 / 195卷 / 03期
关键词
D O I
10.1111/j.1432-1033.1991.tb15759.x
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
DNA synthesis of human hepatoblastoma HepG2 cells is reversibly inhibited by butyrate. When butyrate is removed from the culture medium, cells re-enter the cell cycle, synthesizing DNA with a time lag of about 12 h. HepG2 cells, growth-inhibited for 30 h with butyrate, synthesize and accumulate a nuclear protein, called D. Protein D synthesis is inhibited in cells which, released from the butyrate block, have resumed DNA synthesis as well as in growing cells never exposed to butyrate. Protein D has been purified from growth-arrested cells and partially sequenced. The amino acid sequences of five internal trysin peptides indicate that protein D is a novel nuclear protein.
引用
收藏
页码:723 / 729
页数:7
相关论文
共 24 条
[1]   CONTROLLED SYNTHESIS OF HBSAG IN A DIFFERENTIATED HUMAN-LIVER CARCINOMA-DERIVED CELL-LINE [J].
ADEN, DP ;
FOGEL, A ;
PLOTKIN, S ;
DAMJANOV, I ;
KNOWLES, BB .
NATURE, 1979, 282 (5739) :615-616
[2]   RAPID REPRESSION OF QUIESCENCE-SPECIFIC GENE-EXPRESSION BY EPIDERMAL GROWTH-FACTOR, INSULIN, AND PP60V-SRC [J].
BEDARD, PA ;
YANNONI, Y ;
SIMMONS, DL ;
ERIKSON, RL .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (03) :1371-1375
[3]   REPRESSION OF QUIESCENCE-SPECIFIC POLYPEPTIDES IN CHICKEN HEART MESENCHYMAL CELLS TRANSFORMED BY ROUS-SARCOMA VIRUS [J].
BEDARD, PA ;
BALK, SD ;
GUNTHER, HS ;
MORISI, A ;
ERIKSON, RL .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (04) :1450-1458
[4]   MICROPREPARATIVE SEPARATION OF PEPTIDES DERIVED FROM SODIUM DODECYL SULFATE-SOLUBILIZED PROTEINS [J].
BOSSERHOFF, A ;
WALLACH, J ;
FRANK, RW .
JOURNAL OF CHROMATOGRAPHY, 1989, 473 (01) :71-77
[5]   RB AND THE CELL-CYCLE - ENTRANCE OR EXIT [J].
COOPER, JA ;
WHYTE, P .
CELL, 1989, 58 (06) :1009-1011
[6]   EXTENT OF HISTONE MODIFICATIONS AND H10 CONTENT DURING CELL-CYCLE PROGRESSION IN THE PRESENCE OF BUTYRATE [J].
DANNA, JA ;
GURLEY, LR ;
TOBEY, RA .
EXPERIMENTAL CELL RESEARCH, 1983, 147 (02) :407-417
[7]   THE P53 PROTO-ONCOGENE CAN ACT AS A SUPPRESSOR OF TRANSFORMATION [J].
FINLAY, CA ;
HINDS, PW ;
LEVINE, AJ .
CELL, 1989, 57 (07) :1083-1093
[8]   CHARACTERIZATION OF A CHROMATIN FRACTION BEARING PULSE-LABELED RNA - .2. QUANTIFICATION OF HISTONES AND HIGH-MOBILITY-GROUP PROTEINS [J].
GABRIELLI, F ;
HANCOCK, R ;
FABER, AJ .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1981, 120 (02) :363-369
[9]  
GABRIELLI F, 1989, HISTONES OTHER BASIC, P3
[10]  
GABRIELLI F, 1985, MOL CELL BIOCHEM, V65, P57