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genetics
Reverse genetics has been an extremely useful tool to study the functions of individual viral genes. It enables researchers to rationally design improved recombinant viruses for use in clinical applications such as vaccination and experimental oncolytic-virus therapy. Especially, reverse genetics has revolutionized the study of RNA viruses.
Introduction of Reverse Genetics
Reverse genetics is opposite to forward genetics. In forward genetics, regular genetics begins with a mutant phenotype, proceeds to show the existence of the relevant gene by progeny ratio analysis, and finally clones and sequences the gene to determine its DNA and protein sequence. However, reverse genetics starts from DNA (cDNA) mutants and helps understand the functions of a gene by analyzing the phenotypic effects caused by genetically engineering specific nucleic acid sequences. Typically, the genetic sequence is changed by directed deletions (gene knockout), insertions (knock-ins), point mutations (site-directed mutagenesis to create null alleles (non-functional)), gene knockdowns (RNAi). Besides, various recombinant oncolytic viruses have been engineered via reverse genetics to improve onco-selectivity, safety, onco-toxicity and stimulation of tumor-specific immunity. Reverse genetics also plays a crucial role in the development of highly specific live attenuated versions of vaccines against specific viruses.