
pmid: 2584718
Abstract Using DNA-mediated gene transfer, we have studied the TL protein products encoded by both the T3c and T13c BALB/c genes. Biochemically, the proteins differed in their m.w. and pI points; serologically, although both molecules were recognized by TL alloantiserum, only the T13c protein was recognized by monoclonal TL antibodies. Interestingly, both proteins were serologically and immunochemically recognized by leukemia-specific TL.4 antiserum. The quantity of cell surface T13 was significantly greater than T3 possibly due to the less efficient splicing of T3 transcripts in the L cell nucleus; both genes directed the synthesis of cytoplasmic RNA containing an unspliced intron 3 as assessed by S1 analysis. In toto, the results suggest that T3c is similar or perhaps identical with the novel TL product previously identified on the surface of certain x-ray-induced BALB/c leukemias.
Mice, Inbred BALB C, Leukemia, T-Cell, Membrane Glycoproteins, Enzyme-Linked Immunosorbent Assay, DNA, Neoplasm, Transfection, Precipitin Tests, Neoplasm Proteins, Mice, Phenotype, Animals, Cloning, Molecular, Genes, Neoplasm
Mice, Inbred BALB C, Leukemia, T-Cell, Membrane Glycoproteins, Enzyme-Linked Immunosorbent Assay, DNA, Neoplasm, Transfection, Precipitin Tests, Neoplasm Proteins, Mice, Phenotype, Animals, Cloning, Molecular, Genes, Neoplasm
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