Borisjuk N, Borisjuk L, Komarnytsky S, Timeva S, Hemleben V, Gleba Y, Raskin I
Biotech Center, Foran Hall, Cook College, Rutgers University, 59 Dudley Rd., New Brunswick, NJ 08901-8520, USA.
Nat Biotechnol. 2000 Dec;18(12):1303-6. doi: 10.1038/82430.
Here we show that the cis-acting genetic element aps (amplification-promoting sequence), isolated from the nontranscribed spacer region of tobacco ribosomal DNA (rDNA), increases the level of expression of recombinant proteins. Transgenic tobacco plants, transformed with expression cassettes containing the herbicide-resistant acetolactate synthase (hr-ALS) gene or the green fluorescent protein (GFP) gene fused to the aps sequence, had greater levels of corresponding messenger RNAs (mRNAs) and proteins compared to transformants lacking aps. Analysis of transgenic plants showed that aps increased the copy number and transcription of the adjacent heterologous genes and, in the case of hr-ALS, enhanced the herbicide resistance phenotype. Both the increased transgene copy number and enhanced expression were stably inherited. These data provide the first evidence that the aps sequence can be used for gene amplification in transgenic plants and possibly other multicellular organisms.
在此我们表明,从烟草核糖体DNA(rDNA)的非转录间隔区分离出的顺式作用遗传元件aps(扩增促进序列)可提高重组蛋白的表达水平。与缺乏aps的转化体相比,用含有与aps序列融合的抗除草剂乙酰乳酸合酶(hr-ALS)基因或绿色荧光蛋白(GFP)基因的表达盒转化的转基因烟草植株,其相应信使RNA(mRNA)和蛋白质水平更高。对转基因植株的分析表明,aps增加了相邻异源基因的拷贝数和转录,就hr-ALS而言,还增强了抗除草剂表型。转基因拷贝数的增加和表达增强均能稳定遗传。这些数据首次证明aps序列可用于转基因植物以及可能的其他多细胞生物中的基因扩增。