Cell and tissue-type specific expression of Ras-related GTPase RhoB

被引:0
作者
Fritz, G [1 ]
Gnad, R [1 ]
Kaina, B [1 ]
机构
[1] Univ Mainz, Div Appl Toxicol, Inst Toxicol, D-55131 Mainz, Germany
关键词
Rho GTPases; DNA damage; gene expression; cell type specificity;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ras-homologous (Rho) GTPases are involved in the regulation of a variety of cellular processes such as the organization of the actin cytoskeleton, malignant transformation and genotoxic stress-induced signaling. Here we show that, among the family of Rho GTPases, specifically rhoB mRNA expression is rapidly induced upon UV-irradiation, whereas the level of rac 1 and cdc42 mRNA is not affected. Increase in rhoB mRNA was accompanied by a similar to 4-fold increase in the amount of membrane-bound RhoB protein. Basal expression of rhoB mRNA appears to be cell-type specific with low amounts in rodent NIH 3T3, V79, H4IIE, CHO and human HaCat cells and comparably high amounts in monkey COS, human HeLa and HepG2 cells. In rabbit tissues, exceptionally high levels of rhoB mRNA and RhoB protein were found in lung whereas its expression was quite low in heart, liver, spleen and kidney. Variations in rhoB mRNA expression level are nor due to cell-type specific differences in rhoB mRNA stability as shown by inhibitor experiments. However, transiently transfected rhoB promoter CAT construct was expressed at significantly higher level in HeLa and HepG2 as compared to NIH 3T3 and CHO cells. Thus, cell-type specific differences in the level of rhoB mRNA are likely to be due to variations in the transcriptional activity of the rhoB gene. The data indicate that, among the family of Rho GTPases, only the expression of rhoB is rapidly stimulated by genotoxic stress. Furthermore basal rhoB expression appears to be regulated in a cell and tissue-type specific manner. This may be related to yet unknown tissues-pecific physiological function of RhoB.
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收藏
页码:1681 / 1688
页数:8
相关论文
共 43 条
  • [1] INTRACELLULAR-LOCALIZATION OF THE P21(RHO) PROTEINS
    ADAMSON, P
    PATERSON, HF
    HALL, A
    [J]. JOURNAL OF CELL BIOLOGY, 1992, 119 (03) : 617 - 627
  • [2] ADAMSON P, 1992, J BIOL CHEM, V267, P20033
  • [3] CLOSTRIDIUM-BOTULINUM TYPE-C PRODUCES A NOVEL ADP-RIBOSYLTRANSFERASE DISTINCT FROM BOTULINUM-C2 TOXIN
    AKTORIES, K
    WELLER, U
    CHHATWAL, GS
    [J]. FEBS LETTERS, 1987, 212 (01) : 109 - 113
  • [4] BOTULINUM ADP-RIBOSYLTRANSFERASE C-3 - PURIFICATION OF THE ENZYME AND CHARACTERIZATION OF THE ADP-RIBOSYLATION REACTION IN PLATELET MEMBRANES
    AKTORIES, K
    ROSENER, S
    BLASCHKE, U
    CHHATWAL, GS
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 172 (02): : 445 - 450
  • [5] CHARACTERIZATION AND EXPRESSION OF THE HUMAN RHOH12 GENE-PRODUCT
    AVRAHAM, H
    WEINBERG, RA
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (05) : 2058 - 2066
  • [6] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [7] Signal transduction - Three paths to stress relief
    Canman, CE
    Kastan, MB
    [J]. NATURE, 1996, 384 (6606) : 213 - 214
  • [8] THE MAMMALIAN G-PROTEIN RHOC IS ADP-RIBOSYLATED BY CLOSTRIDIUM-BOTULINUM EXOENZYME C-3 AND AFFECTS ACTIN MICROFILAMENTS IN VERO CELLS
    CHARDIN, P
    BOQUET, P
    MADAULE, P
    POPOFF, MR
    RUBIN, EJ
    GILL, DM
    [J]. EMBO JOURNAL, 1989, 8 (04) : 1087 - 1092
  • [9] CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
  • [10] THE SMALL GTP-BINDING PROTEINS RAC1 AND CDC42 REGULATE THE ACTIVITY OF THE JNK/SAPK SIGNALING PATHWAY
    COSO, OA
    CHIARIELLO, M
    YU, JC
    TERAMOTO, H
    CRESPO, P
    XU, NG
    MIKI, T
    GUTKIND, JS
    [J]. CELL, 1995, 81 (07) : 1137 - 1146