CHANGES OF CELL CYCLE-REGULATING GENES IN INTERFERON-TREATED DAUDI CELLS

被引:21
作者
YAMADA, H
OCHI, K
NAKADA, S
NEMOTO, T
HORIGUCHIYAMADA, J
机构
[1] Department of Internal Medicine, Aoto Hospital, The Jikei University School of Medicine, Tokyo, 125, 6-41-2 Aoto, Katsushika-ku
关键词
CELL CYCLE; INTERFERON; CYCLIN; CYCLIN-DEPENDENT KINASE; CDC25; WEE1;
D O I
10.1007/BF00926071
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Interferon (IFN) modulates the expression of several genes and some of them are considered to be responsible for the inhibition of cellular growth. However, the alterations of cell cycle-regulating genes produced by IFN still remain unclear. Accordingly, we studied the expression of cell; cycle-regulating genes during IFN-induced growth arrest. Cell cycle synchronized and unsynchronized Daudi Burkitt lymphoma cells were treated with IFN. Both the cell cycle distribution and the expression of cell cycle-regulating genes (cdk2, cdc2, cyclins A, B, C, D3, cdc25, and wee1) were studied by flow cytometry and by Northern blot hybridization or the reverse-transcription polymerase chain reaction, respectively. Treated cells passed through the first G1 phase and gradually accumulated in the following G1 phase. Expression of cyclins A, B, and D3 oscillated along with the cell cycle progression in control cells, and the alterations of cyclin B expression were especially prominent. Both cdc2 and cdk2 also showed changes, but these were not so distinct as observed with cyclin B. Expression of cdc25 and wee1 was little affected by cell cycle progression. In IFN-treated cells, expression of cyclins A and B were down-regulated, while that of cyclin C was not. Cyclin D3 expression was also down-regulated at 48 h, followed by an increase at 72 h. Expression of both cdc2 and cdk2 was down-regulated, especially that of the later. Wee1 expression was down-regulated by IFN but, the expression of cdc25 remained stable. These findings suggest that the modulation of cell cycle-regulating genes, particular by cyclin A and cdk2, plays an important role in IFN-induced cellular growth arrest.
引用
收藏
页码:117 / 123
页数:7
相关论文
共 46 条
[1]   CYCLIN-A AND THE RETINOBLASTOMA GENE-PRODUCT COMPLEX WITH A COMMON TRANSCRIPTION FACTOR [J].
BANDARA, LR ;
ADAMCZEWSKI, JP ;
HUNT, T ;
LATHANGUE, NB .
NATURE, 1991, 352 (6332) :249-251
[2]   PHOSPHORYLATION OF THE RETINOBLASTOMA GENE-PRODUCT IS MODULATED DURING THE CELL-CYCLE AND CELLULAR-DIFFERENTIATION [J].
CHEN, PL ;
SCULLY, P ;
SHEW, JY ;
WANG, JYJ ;
LEE, WH .
CELL, 1989, 58 (06) :1193-1198
[3]   REGULATION OF CELL-PROLIFERATION AND DIFFERENTIATION BY INTERFERONS [J].
CLEMENS, MJ ;
MCNURLAN, MA .
BIOCHEMICAL JOURNAL, 1985, 226 (02) :345-360
[4]   THE PRODUCT OF THE RETINOBLASTOMA SUSCEPTIBILITY GENE HAS PROPERTIES OF A CELL-CYCLE REGULATORY ELEMENT [J].
DECAPRIO, JA ;
LUDLOW, JW ;
LYNCH, D ;
FURUKAWA, Y ;
GRIFFIN, J ;
PIWNICAWORMS, H ;
HUANG, CM ;
LIVINGSTON, DM .
CELL, 1989, 58 (06) :1085-1095
[5]   A CYCLIN-A-PROTEIN KINASE COMPLEX POSSESSES SEQUENCE-SPECIFIC DNA-BINDING ACTIVITY - P33CDK2 IS A COMPONENT OF THE E2F-CYCLIN-A COMPLEX [J].
DEVOTO, SH ;
MUDRYJ, M ;
PINES, J ;
HUNTER, T ;
NEVINS, JR .
CELL, 1992, 68 (01) :167-176
[6]   PHYSICAL INTERACTION OF THE RETINOBLASTOMA PROTEIN WITH HUMAN D-CYCLINS [J].
DOWDY, SF ;
HINDS, PW ;
LOUIE, K ;
REED, SI ;
ARNOLD, A ;
WEINBERG, RA .
CELL, 1993, 73 (03) :499-511
[7]   CLOSE LINK BETWEEN REDUCTION OF C-MYC EXPRESSION BY INTERFERON AND G0/G1 ARREST [J].
EINAT, M ;
RESNITZKY, D ;
KIMCHI, A .
NATURE, 1985, 313 (6003) :597-600
[8]   FUNCTIONAL INTERACTIONS OF THE RETINOBLASTOMA PROTEIN WITH MAMMALIAN D-TYPE CYCLINS [J].
EWEN, ME ;
SLUSS, HK ;
SHERR, CJ ;
MATSUSHIME, H ;
KATO, JY ;
LIVINGSTON, DM .
CELL, 1993, 73 (03) :487-497
[9]   THE RETINOBLASTOMA GENE-PRODUCT REGULATES PROGRESSION THROUGH THE G1 PHASE OF THE CELL-CYCLE [J].
GOODRICH, DW ;
WANG, NP ;
QIAN, YW ;
LEE, EYHP ;
LEE, WH .
CELL, 1991, 67 (02) :293-302
[10]   STRUCTURALLY SIMILAR BUT FUNCTIONALLY DISTINCT FACTORS, IRF-1 AND IRF-2, BIND TO THE SAME REGULATORY ELEMENTS OF IFN AND IFN-INDUCIBLE GENES [J].
HARADA, H ;
FUJITA, T ;
MIYAMOTO, M ;
KIMURA, Y ;
MARUYAMA, M ;
FURIA, A ;
MIYATA, T ;
TANIGUCHI, T .
CELL, 1989, 58 (04) :729-739