Ramsay R G, Ishii S, Nishina Y, Soe G, Gonda T J
Ludwig Institute for Cancer Research, Royal Melbourne Hospital, Parkville, Australia.
Oncogene Res. 1989;4(4):259-69.
The expression of c-myb proteins in transformed and normal murine cells was investigated. Two c-myb proteins, p75c-myb and p90c-myb, were detected in normal thymocytes and cell lines with intact c-myb genes. These most likely differ by the inclusion of additional amino acids encoded by an alternatively spliced c-myb mRNA. The use of this alternative exon is therefore not a feature exclusively of those cells with viral integrations in their c-myb gene. Smaller c-myb proteins in myeloid leukemic cell lines with rearranged c-myb genes were also characterized. Viral integration into the 5' region of the c-myb gene in the W265 and W274 cell lines leads to the synthesis in each case of two amino-terminally truncated c-myb proteins. By contrast, in NFS60 cells, viral integration into a more 3' region of the c-myb locus (but upstream of an alternate exon) leads to the production of a single p50c-myb protein.
对转化的和正常的鼠细胞中c-myb蛋白的表达进行了研究。在正常胸腺细胞和具有完整c-myb基因的细胞系中检测到了两种c-myb蛋白,即p75c-myb和p90c-myb。它们很可能因包含由可变剪接的c-myb mRNA编码的额外氨基酸而有所不同。因此,这种可变外显子的使用并非是那些c-myb基因中有病毒整合的细胞所特有的特征。对c-myb基因重排的髓系白血病细胞系中的较小c-myb蛋白也进行了表征。病毒整合到W265和W274细胞系中c-myb基因的5'区域,在每种情况下都会导致合成两种氨基末端截短的c-myb蛋白。相比之下,在NFS60细胞中,病毒整合到c-myb基因座的更3'区域(但在可变外显子的上游)会导致产生单一的p50c-myb蛋白。