Abstract
Using proviral tagging in combination with in vitro selection for invasiveness, we have identified a gene, designated Tiam-1, that affects invasion. In the selected invasive T lymphoma variants, proviral insertions were found within coding exons of the Tiam-1 gene, resulting in both truncated 5'-end and 3'-end transcripts that give rise to N- and C-terminal Tiam-1 protein fragments. In one invasive variant, amplification of the Tiam-1 locus was observed with concomitant increase in the amount of normal Tiam-1 protein. Cell clones that were invasive in vitro produced experimental metastases in nude mice, and transfection of truncated Tiam-1 cDNAs into noninvasive cells made these cells invasive. The predicted Tiam-1 protein harbors a Dbl- and Pleckstrin-homologous domain, which it shares with GDP-GTP exchangers for Rho-like proteins that have been implicated in cytoskeletal organization.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Base Sequence
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DNA, Complementary / analysis
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DNA, Neoplasm / analysis
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Fungal Proteins / genetics
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GTP-Binding Proteins / metabolism
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Guanine Nucleotide Exchange Factors
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Lymphatic Metastasis
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Lymphoma, T-Cell / genetics*
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Lymphoma, T-Cell / microbiology
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Lymphoma, T-Cell / pathology
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Mice
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Mice, Inbred C3H
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Molecular Sequence Data
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Moloney murine leukemia virus / genetics
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Mutagenesis, Insertional
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Neoplasm Invasiveness / genetics*
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Oncogene Proteins / genetics
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Proteins / chemistry
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Proteins / genetics*
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Proto-Oncogene Proteins / genetics
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Restriction Mapping
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Sequence Alignment
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Sequence Analysis, DNA
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Sequence Homology, Amino Acid
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T-Lymphoma Invasion and Metastasis-inducing Protein 1
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Tumor Cells, Cultured
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Virus Integration / genetics
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rap GTP-Binding Proteins
Substances
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DNA, Complementary
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DNA, Neoplasm
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Fungal Proteins
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Guanine Nucleotide Exchange Factors
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Oncogene Proteins
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Proteins
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Proto-Oncogene Proteins
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T-Lymphoma Invasion and Metastasis-inducing Protein 1
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Tiam1 protein, mouse
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GTP-Binding Proteins
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rap GTP-Binding Proteins