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Mark the Gene: a Method for Nondestructive Introduction of Marker Sequences Inside the Gene Frame of Transgenes

机译:标记基因:一种在转基因基因框架内无损引入标记序列的方法

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摘要

A specific marking and detection technique is a fundamental requirement for the safer use of genetically modified (GM) organisms. Here we propose a simple and effective method for directly marking functional transgenes in GM organisms. For that purpose, we introduced nucleotide substitutions (NS), based on the degeneracy of codons as markers (NS markers), into the bphC (2,3-dihydroxybiphenyl dioxygenase) and tomA3 (toluene-ortho-monooxygenase) gene frames using a PCR-based method. No change was observed in the enzyme activity of translated proteins, and alignments with homologous genes showed the uniqueness of the NS markers. Furthermore, we constructed tomA3 variations harboring NS markers in different positions. Although the translational products were identical, the constructed variation genes could be distinguished through their marker patterns by multiplex PCR, showing that NS markers could serve as product-specific tags for identifying individual GM organisms. This direct method of marking the functional transgene provides a simple, low-risk, and robust marking method without causing the gene functions to deteriorate.
机译:特定的标记和检测技术是安全使用转基因(GM)生物的基本要求。在这里,我们提出了一种简单有效的方法来直接标记转基因生物中的功能性转基因。为此,我们使用PCR将基于密码子简并性(NS标记)简并性的核苷酸取代(NS)引入了bphC(2,3-二羟基联苯双加氧酶)和tomA3(甲苯-单-单加氧酶)基因框架中基于方法。未观察到翻译蛋白的酶活性变化,并且与同源基因的比对显示NS标记的独特性。此外,我们构建了在不同位置带有NS标记的mA3变异。尽管翻译产物是相同的,但是构建的变异基因可以通过多重PCR通过其标记模式进行区分,这表明NS标记可以用作鉴定单个GM生物的产物特异性标记。标记功能性转基因的这种直接方法提供了一种简单,低风险和稳健的标记方法,而不会导致基因功能下降。

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