Sandell L J
Washington University School of Medicine, Department of Orthopaedic Surgery, St Louis, MO 63110, USA.
Clin Orthop Relat Res. 2000 Oct(379 Suppl):S9-16. doi: 10.1097/00003086-200010001-00003.
Gene therapy is the process whereby a therapeutic protein is synthesized from a DNA molecule (gene) that has been inserted into the cells. The goal is to produce the desired protein in the proper quantity in the proper location. Successful designing of vectors for gene therapy requires knowledge of gene structure and regulation. The gene is comprised of protein-coding sequences (called exons) that are interrupted by noncoding sequences (called introns). The expression of a gene in a tissue is regulated by proteins that bind to specific deoxyribonucleic acid sequences generally upstream from the first exon, in the deoxyribonucleic acid promoter domain. Understanding the mechanisms of gene regulation provides the deoxyribonucleic acid sequences necessary to direct expression of specific genes in the right tissue at the proper time in the desired amount.
基因治疗是指从已插入细胞的DNA分子(基因)合成治疗性蛋白质的过程。目标是在适当的位置以适当的数量产生所需的蛋白质。成功设计用于基因治疗的载体需要了解基因结构和调控。基因由被非编码序列(称为内含子)中断的蛋白质编码序列(称为外显子)组成。基因在组织中的表达受与特定脱氧核糖核酸序列结合的蛋白质调控,这些序列通常位于脱氧核糖核酸启动子结构域中第一个外显子上游。了解基因调控机制可提供必要的脱氧核糖核酸序列,以在适当的时间、以所需的量在正确的组织中指导特定基因的表达。