Nilsen T W, Maroney P A
Mol Cell Biol. 1984 Oct;4(10):2235-8. doi: 10.1128/mcb.4.10.2235-2238.1984.
The translational efficiency of cMyc mRNAs was assessed in a variety of cell lines: HeLa cells and Epstein-Barr virus-transformed lymphocytes, both of which contain only the germ line cMyc allele; Daudi, a Burkitt cell line containing a translocated cMyc gene with no apparent alteration; and P3HR-1, a Burkitt line in which the 5' end of the translocated cMyc gene has been altered by the chromosomal translocation. Translational efficiency was inferred by measuring the number of ribosomes associated with the cMyc mRNA, using a procedure by which individual polysomal fractions were analyzed by blot hybridization. Since polysome size is a function of the length of the translated sequence as well as the rate of initiation of protein synthesis, we also determined the number of ribosomes associated with a control mRNA (alpha tubulin) which codes for a protein of similar size to cMyc. We found that the cMyc mRNA was associated with a number of ribosomes comparable to that associated with alpha tubulin mRNA in all the cell lines tested.
在多种细胞系中评估了cMyc mRNA的翻译效率:HeLa细胞和爱泼斯坦-巴尔病毒转化的淋巴细胞,这两种细胞系都仅含有种系cMyc等位基因;Daudi,一种含有易位cMyc基因且无明显改变的伯基特细胞系;以及P3HR-1,一种伯基特细胞系,其中易位cMyc基因的5'端已因染色体易位而改变。通过测量与cMyc mRNA相关的核糖体数量来推断翻译效率,使用的方法是通过印迹杂交分析各个多核糖体组分。由于多核糖体大小是翻译序列长度以及蛋白质合成起始速率的函数,我们还确定了与对照mRNA(α微管蛋白)相关的核糖体数量,该对照mRNA编码的蛋白质大小与cMyc相似。我们发现,在所有测试的细胞系中,cMyc mRNA与核糖体的数量与与α微管蛋白mRNA相关的核糖体数量相当。