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In this study, we characterized and quantitated transcription from four c-\u003Cjats:italic>onc\u003C\u002Fjats:italic>genes, c-\u003Cjats:italic>myb\u003C\u002Fjats:italic>, c-\u003Cjats:italic>myc\u003C\u002Fjats:italic>, c-\u003Cjats:italic>erb\u003C\u002Fjats:italic>, and c-\u003Cjats:italic>src\u003C\u002Fjats:italic>, in a variety of chicken cells and tissues. Electrophoretic analysis of polyadenylated RNA, followed by transfer to nitrocellulose and hybridization to cloned\u003Cjats:italic>onc\u003C\u002Fjats:italic>probes showed that c-\u003Cjats:italic>myb\u003C\u002Fjats:italic>, c-\u003Cjats:italic>myc\u003C\u002Fjats:italic>, and c-\u003Cjats:italic>src\u003C\u002Fjats:italic>each give rise to a single mature transcript, whereas c-\u003Cjats:italic>erb\u003C\u002Fjats:italic>gives rise to multiple transcripts (B. Vennstrom and J. M. Bishop, Cell, in press) which vary in abundance among different cells and tissues. Transcription from c-\u003Cjats:italic>myb\u003C\u002Fjats:italic>, c-\u003Cjats:italic>myc\u003C\u002Fjats:italic>, c-\u003Cjats:italic>erb\u003C\u002Fjats:italic>, and c-\u003Cjats:italic>src\u003C\u002Fjats:italic>was quantitated by a “dot-blot” hybridization assay. We found that c-\u003Cjats:italic>myc\u003C\u002Fjats:italic>, c-\u003Cjats:italic>erb\u003C\u002Fjats:italic>, and c-\u003Cjats:italic>src\u003C\u002Fjats:italic>transcription could be detected in nearly all cells and tissues examined, whereas c-\u003Cjats:italic>myb\u003C\u002Fjats:italic>transcription was detected only in some hemopoietic cells; these cells, however, belong to several different lineages. Thus, in no case was expression of a c-\u003Cjats:italic>onc\u003C\u002Fjats:italic>gene restricted to a single cell lineage. There appeared to be a correlation between levels of c-\u003Cjats:italic>myb\u003C\u002Fjats:italic>expression and hemopoietic activity of the tissues and cells examined, which suggests that c-\u003Cjats:italic>myb\u003C\u002Fjats:italic>may be expressed primarily in immature hemopoietic cells. 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