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PMID: 10470101 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

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

Anticancer research ·Vol. 19 ·No. 3A ·1999-00-00 ·Pages 1681-8

Fritz G, Gnad R, Kaina B

Abstract

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 approximately 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 not 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 tissue-specific physiological function of RhoB.

MeSH Terms
3T3 Cells Animals CHO Cells COS Cells Cell Cycle Proteins/biosynthesis,genetics Cell Line/enzymology,radiation effects Chloramphenicol O-Acetyltransferase/biosynthesis,genetics Cricetinae Cricetulus Enzyme Induction/radiation effects Female Fibroblasts/enzymology,radiation effects GTP Phosphohydrolases/biosynthesis,genetics GTP-Binding Proteins/biosynthesis,genetics Gene Expression Regulation, Neoplastic/radiation effects HeLa Cells Humans Keratinocytes/enzymology,radiation effects Liver/enzymology Liver Neoplasms, Experimental/pathology Lung/enzymology Membrane Proteins/biosynthesis,genetics Mice Myocardium/enzymology Neoplasm Proteins/biosynthesis,genetics Organ Specificity Ovary/enzymology RNA, Messenger/biosynthesis,genetics Rabbits Rats Recombinant Fusion Proteins/biosynthesis,genetics Reverse Transcriptase Polymerase Chain Reaction Species Specificity Transfection Tumor Cells, Cultured/enzymology,radiation effects Ultraviolet Rays cdc42 GTP-Binding Protein rac GTP-Binding Proteins rhoB GTP-Binding Protein
Chemicals
Cell Cycle Proteins Membrane Proteins Neoplasm Proteins RNA, Messenger Recombinant Fusion Proteins Chloramphenicol O-Acetyltransferase GTP Phosphohydrolases GTP-Binding Proteins cdc42 GTP-Binding Protein rac GTP-Binding Proteins rhoB GTP-Binding Protein
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Fritz G
Institute of Toxicology, University of Mainz, Germany. Fritz@mail.uni-mainz.de
Gnad R
Kaina B
Article Info
Journal
Anticancer research
Abbr.
Anticancer Res
ISSN
0250-7005
Published
1999-00-00
Pages
1681-8
Language
English
Region
Greece
NLM ID
8102988
Subset
IM
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