Growth factor-independent 32D-src and 32D-abl cell lines, established by infecting the interleukin-3-dependent myeloid precursor cell line (32D-123) with retroviruses containing the src or abl oncogene, were used to study transcriptional regulation of transforming growth factor Pl 32D-123, 32D-abl, and 32D-src cells were hybridized by using the TGF-131 probe. Ethidium bromide staining of the rRNA indicated that similar levels of undegraded RNA were present in all of the samples (data not shown).
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