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Gene therapy techniques have been developed to address genetic defects by inserting foreign genes into cells. Microinjection and electroporation have been attempted but have limitations in terms of time, expertise, and traumatic effects on cells. The most effective method to introduce foreign genes into cells is through the use of viral vectors. Retroviruses, in particular, show promise in gene therapy. Retroviruses have an outer protein envelope containing viral RNA and reverse transcriptase. The RNA genome of retroviruses is transcribed into DNA by reverse transcriptase and then integrated into the host's genome. Retroviral vectors are designed to replace certain viral genes with therapeutic genes. However, there are concerns with random integration, potential activation of oncogenes, limited target cells, and lack of precise control over gene expression.

Question for Practice Passage Test - 1
Try yourself:Why is electroporation considered traumatic to cells in gene therapy?
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Question for Practice Passage Test - 1
Try yourself:Which method of gene therapy involves the use of viral vectors?
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Question for Practice Passage Test - 1
Try yourself:What is the main advantage of retroviruses in gene therapy compared to DNA viruses or simple RNA viruses?
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Question for Practice Passage Test - 1
Try yourself:What is the role of reverse transcriptase in retroviruses?
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Question for Practice Passage Test - 1
Try yourself:What are the potential problems associated with retroviral vector gene therapy?
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