Abstract
Overexpression of the budding yeast RAS2 gene in Nicotiana plumbaginifolia cells revealed that RAS2 acted as 'suicide' gene in freshly isolated protoplasts from leaves and blocked cell proliferation in cell suspension-derived protoplasts. Among a series of genes tested (such as npt II, CDC35, PDE2), RAS2 was the only one to block the expression of the cat gene, as measured in a transient gene expression assay. Another ras gene, v-Ha-ras, had similar effects. Furthermore, the RAS2 effect was species-specific and depended on the modulation of hormonal metabolism in the transfected cells, while no differences were noticed between the normal and the activated val19 gene. Transfected plant cells are shown to synthesize a RAS2 protein of the same electrophoretic mobility as the yeast RAS2 product. The results are discussed in the broader context of the evolutionarily conserved ras genes involved in vital cellular functions.
MeSH Terms
Cell Differentiation/genetics
Cell Survival/genetics
Fungal Proteins/biosynthesis,genetics
Gene Expression
Genes, Fungal
Genes, ras
Genetic Engineering
Mitosis/genetics
Plant Cells
Plants/genetics,metabolism
Plants, Toxic
Plasmids
Saccharomyces cerevisiae/genetics
Saccharomyces cerevisiae Proteins
Tobacco/cytology,genetics
Transformation, Genetic
ras Proteins
Chemicals
Fungal Proteins
Saccharomyces cerevisiae Proteins
RAS2 protein, S cerevisiae
ras Proteins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Hilson P
Unité de Biologie Moléculaire et de Physiologie Animale, Faculté des Sciences Agronomiques de l'Etat, Gembloux, Belgium.
Dewulf J
Delporte F
Installé P
Jacquemin J M
Jacobs M
Negrutiu I
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