Out-Lab Therapy Approach Based on Elected A Restriction Enzyme to Transfer Target Gene

Ayad Ismaeel
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Abstract

An important approach of therapy the target gene sequence causes diseases via repair/recombine the mutated gene (gene transfer) using a restriction enzymes in the laboratory. This approach will cause multiple problems happening accompany to biological laboratory if ruled out problems outside of it like the digested DNA ran as a smear on an agarose gel, incomplete restriction enzyme digestion, extra bands in the gel, etc. The paper suggested new approach of therapy via repair/replacement mutated gene caused disease by detecting primers and finding restriction enzymes using bioinformatics tools, software, packages etc. then achieving the repair/ recombine of mutations before going to the biologic lab (out-lab) to avoid the problems associated these laboratories. Implement and apply this a proposed therapy approach on TP53 gene (which caused more than 50% of human cancers) and after confirming there is mutations on P53 tumor protein shows an effective cost, friendly therapy methodology and comprehensive.
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基于选择性限缩酶转移靶基因的实验室外治疗方法
在实验室中利用限制性内切酶对突变基因进行修复/重组(基因转移)是治疗靶基因序列引起疾病的重要方法。这种方法如果排除了外部问题,如消化后的DNA在琼脂糖凝胶上涂片,限制性内切酶消化不完全,凝胶中有额外的条带等,将会导致生物实验室出现多种问题。本文提出了利用生物信息学工具、软件、软件包等检测引物和寻找限制性内切酶,在进入生物实验室(外实验室)之前实现突变的修复/重组,以避免这些实验室相关问题,通过修复/替换突变基因引起的疾病的新方法。将这一提出的治疗方法应用于TP53基因(导致超过50%的人类癌症),并在确认P53肿瘤蛋白存在突变后,显示出一种有效、成本高、友好且全面的治疗方法。
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