Abstract
We describe the isolation, growth-suppressing activity, and chromosomal localization of the human homologue of the murine growth-arrest-specific gene gas1. Overexpression of h-gas1 is able to block cell proliferation in the A549 lung carcinoma and the T24 bladder carcinoma cell lines. No effect was observed when h-gas1 was introduced into the osteosarcoma cell line SAOS-2 and into the adenovirus-type-5 transformed cell line 293. This finding is related to our previous evidence that simian virus 40-transformed NIH 3T3 cells are also refractory to murine gas1 overexpression, suggesting that the retinoblastoma and/or p53 gene products have an active role in mediating the growth-suppressing effect of gas1. We also show that h-gas1 is on chromosome 9q21.3-22.1, in a region considered to be a fragile site. Altogether, the results raise the possibility that h-gas1 may be a target for genetic alterations leading to its inactivation in tumor cells.
MeSH Terms
Amino Acid Sequence
Animals
Base Sequence
Cell Cycle Proteins
Cell Division/genetics
Cell Line
Chromosome Mapping
Chromosomes, Human, Pair 9
DNA, Complementary/genetics
GPI-Linked Proteins
Gene Expression
Growth Inhibitors/genetics,physiology
Humans
In Situ Hybridization
Membrane Glycoproteins/genetics,physiology
Membrane Proteins
Mice
Molecular Sequence Data
Saccharomyces cerevisiae Proteins
Sequence Homology, Nucleic Acid
Species Specificity
Chemicals
Cell Cycle Proteins
DNA, Complementary
GAS1 protein, S cerevisiae
GAS1 protein, human
GPI-Linked Proteins
Gas1 protein, mouse
Growth Inhibitors
Membrane Glycoproteins
Membrane Proteins
Saccharomyces cerevisiae Proteins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Del Sal G
Laboratoire Nazionale, Consorzio Interuniversitario per le Biotechnologie, Trieste, Italy.
Collavin L
Ruaro M E
Edomi P
Saccone S
Valle G D
Schneider C
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