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The most important advantage that retroviral vectors offer is their ability to transform their single stranded RNA genome into a double stranded DNA molecule that stably integrates into the target cell genome. This means that retroviral vectors can be used to permanently modify the host cell nuclear genome.
Structure. HTLVs are members of the oncovirus family of retroviruses, which are distinguished from other viruses by the presence of reverse transcriptase, an enzyme that transcribes RNA into DNA.
Definition. 00:00. A retrovirus is a virus that uses RNA as its genomic material. Upon infection with a retrovirus, a cell converts the retroviral RNA into DNA, which in turn is inserted into the DNA of the host cell. The cell then produces more retroviruses, which infect other cells.
Retrovirus Upon infection with a retrovirus, a cell converts the retroviral RNA into DNA, which in turn is inserted into the DNA of the host cell. The cell then produces more retroviruses, which infect other cells. Many retroviruses are associated with diseases, including AIDS and some forms of cancer.
As well as causing human and animal diseases, retroviruses are an important tool for gene therapy. By stripping out any harmful genes and replacing them with genetic instructions for producing a therapeutic protein, retroviruses can be used to insert these elements into human cells.
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In biotechnology, the retrovirus is used as a vector to transfer the gene of interest into the host. The retrovirus is modified into cloning vector this is done by deleting the genes that are responsible for pathogenicity.
Pervasive horizontal gene transfer between species mediated by retroviruses is such a defining factor of evolution [1]. Retroviral infections occurred in germline cells and were able to transfer the genomic codes vertically from parent to offspring.

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