Darveau A, Pelletier J, Sonenberg N
Proc Natl Acad Sci U S A. 1985 Apr;82(8):2315-9. doi: 10.1073/pnas.82.8.2315.
We have studied the in vitro translational efficiencies of two murine c-myc transcripts synthesized in vitro that differ in the lengths of their 5' noncoding regions (448 and 83 nucleotides) and also in their 3' noncoding regions. When translated in a reticulocyte translation system, the shorter transcript was translated 10-fold more efficiently. These results are consistent with the hypothesis of Saito et al. [Saito, H., Hayday, A. C., Wiman, K., Hayward, W. S. & Tonegawa, S. (1983) Proc. Natl. Acad. Sci. USA 80, 7476-7480] that translation of full-length human c-myc mRNA is normally repressed, whereas in several Burkitt lymphomas that have deletions of the mRNA 5' noncoding region (resulting from translocation of the c-myc gene), translation of the c-myc mRNA is more efficient. Our results suggest that activation of murine c-myc expression by production of a more efficient mRNA might in some cases play a role in neoplastic transformation.
我们研究了体外合成的两种小鼠c-myc转录本的体外翻译效率,这两种转录本在其5'非编码区长度(分别为448和83个核苷酸)以及3'非编码区均存在差异。当在网织红细胞翻译系统中进行翻译时,较短的转录本翻译效率要高出10倍。这些结果与Saito等人[斋藤浩、海迪、维曼、海沃德、利根川进(1983年)《美国国家科学院院刊》80, 7476 - 7480]的假设一致,即全长人类c-myc mRNA的翻译通常受到抑制,而在一些因c-myc基因易位导致mRNA 5'非编码区缺失的伯基特淋巴瘤中,c-myc mRNA的翻译效率更高。我们的结果表明,通过产生更高效的mRNA来激活小鼠c-myc表达在某些情况下可能在肿瘤转化中起作用。