Lynch C M, Israel D I, Kaufman R J, Miller A D
Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
Hum Gene Ther. 1993 Jun;4(3):259-72. doi: 10.1089/hum.1993.4.3-259.
A variety of retroviral vectors for transduction and expression of clotting factor VIII (FVIII) were constructed by using truncated forms of a FVIII cDNA lacking part or all of the nonessential B-domain sequences. Both the titer of virus and FVIII protein production from the vectors was about 2 orders of magnitude lower than the virus titer and protein production from identical retroviral vectors containing other cDNAs, including clotting factor IX. These decreases could be entirely explained by an observed 100-fold lower accumulation of vector RNAs containing the FVIII sequences in comparison to vectors containing other cDNA sequences. Deletion analysis of one of the FVIII vectors demonstrated that diffuse sequences within the FVIII coding region had a deleterious effect upon vector titer and RNA accumulation. One inhibitory signal could be localized to a 1.2-kb stretch of DNA, but further localization was not possible as additional size reduction abolished the activity. These results indicate that expression of FVIII is regulated by signals within FVIII coding sequence that result in decreased RNA accumulation and FVIII protein production. Alteration of these inhibitory signals to permit high-level FVIII production may be difficult due to the wide distribution of these signals within the coding region of the protein.
通过使用缺失部分或全部非必需B结构域序列的凝血因子VIII(FVIII)cDNA截短形式,构建了多种用于转导和表达FVIII的逆转录病毒载体。这些载体产生的病毒滴度和FVIII蛋白产量比含有其他cDNA(包括凝血因子IX)的相同逆转录病毒载体的病毒滴度和蛋白产量低约2个数量级。与含有其他cDNA序列的载体相比,含有FVIII序列的载体RNA积累量降低了100倍,这可以完全解释这些降低情况。对其中一种FVIII载体的缺失分析表明,FVIII编码区内的分散序列对载体滴度和RNA积累有有害影响。一个抑制信号可定位到一段1.2 kb的DNA片段,但由于进一步减小尺寸会消除活性,所以无法进一步定位。这些结果表明,FVIII的表达受FVIII编码序列内信号的调节,这些信号导致RNA积累减少和FVIII蛋白产量降低。由于这些信号在该蛋白编码区内分布广泛,改变这些抑制信号以实现FVIII的高水平生产可能很困难。