Mahmoudi M, Motoo Y, Vela G R, Bollon A P, Osther K
Cell Mol Biol. 1989;35(1):75-80.
We have studied the expression of c-myc and c-Ha-ras oncogenes in this cell line. Daudi lymphoblastoid cells and normal human leukocytes served as a positive and a negative control, respectively. The Northern blot analysis using a c-myc probe revealed a 2.7 kb transcript and two larger transcripts greater than 23 kb. In the Northern blot hybridization using a c-Ha-ras probe, two transcripts with sizes of 1.8 and 6.1 kb were observed. The affinity of the Namalva RNA hybridization to c-myc probe was about 10-fold lower than that in Daudi RNA, whereas no difference in the c-Ha-ras hybridization was observed between the two cell lines. These data indicate that c-myc and c-Ha-ras are expressed in Namalva cells. It is noteworthy to consider that the difference in oncogene expression between Namalva and Daudi cells might be due to the difference in interferon properties between the two cell lines.
我们研究了该细胞系中c-myc和c-Ha-ras癌基因的表达情况。Daudi淋巴母细胞和正常人白细胞分别作为阳性对照和阴性对照。使用c-myc探针进行的Northern印迹分析显示有一个2.7 kb的转录本以及两个大于23 kb的更大转录本。在使用c-Ha-ras探针的Northern印迹杂交中,观察到了大小分别为1.8 kb和6.1 kb的两个转录本。Namalva细胞RNA与c-myc探针的杂交亲和力比Daudi细胞RNA低约10倍,而在两种细胞系之间未观察到c-Ha-ras杂交的差异。这些数据表明c-myc和c-Ha-ras在Namalva细胞中表达。值得考虑的是,Namalva细胞和Daudi细胞之间癌基因表达的差异可能是由于两种细胞系之间干扰素特性的差异所致。