Milland J, Christiansen D, Thorley B R, McKenzie I F, Loveland B E
Austin Research Institute, Heidelberg, Australia.
Eur J Biochem. 1996 May 15;238(1):221-30. doi: 10.1111/j.1432-1033.1996.0221q.x.
Specific sequences in the coding region of CD46 (membrane cofactor protein) transcripts have been shown to have a marked effect on translation. Two A+T-rich regions of CD46 cDNA were altered by mutation without changing the CD46 amino acid sequence (silent nucleotide substitution). In one region, the A+T content was reduced from 78% to 55% and in the other a putative polyadenylation addition sequence was disrupted. In each example, mutated sequences transfected into COS-7 cells produced significantly more soluble or cell surface protein (up to a 20-fold increase) than wild-type sequences. The amount of cellular plasmid DNA and CD46 mRNA was not increased, suggesting that the effect was not due to increased transfection efficiency, or transcript synthesis or stability. Biosynthetically labelled transfected cells showed an increase in translation rate but cell-free in vitro translation studies demonstrated that wild-type and mutated transcripts were translated with similar efficiency. The data show that translation of CD46 is affected by specific mRNA coding sequences, 400-540 bases from the initiation codon, and suggest that these sequences require the structural integrity of the cell to exert their effect.
已证明CD46(膜辅因子蛋白)转录本编码区的特定序列对翻译有显著影响。通过突变改变了CD46 cDNA的两个富含A+T的区域,而不改变CD46氨基酸序列(沉默核苷酸替换)。在一个区域中,A+T含量从78%降至55%,在另一个区域中,一个假定的聚腺苷酸化附加序列被破坏。在每个例子中,转染到COS-7细胞中的突变序列产生的可溶性或细胞表面蛋白比野生型序列显著更多(增加高达20倍)。细胞内质粒DNA和CD46 mRNA的量没有增加,这表明该效应不是由于转染效率提高、转录本合成或稳定性增加所致。生物合成标记的转染细胞显示翻译速率增加,但无细胞体外翻译研究表明野生型和突变转录本的翻译效率相似。数据表明,CD46的翻译受起始密码子400-540个碱基处特定mRNA编码序列的影响,并表明这些序列需要细胞的结构完整性来发挥其作用。