Genetic engineering, recombinant DNA technology, genetic modification/manipulation (GM) and gene splicing are terms that apply to the direct manipulation of an organism's genes.[1] Genetic engineering is different from traditional breeding, where the organism's genes are manipulated indirectly; genetic engineering uses the techniques of molecular cloning and transformation to alter the structure and characteristics of genes directly. Genetic engineering techniques have found some successes in numerous applications. Some examples are in improving crop technology, the manufacture of synthetic human insulin through the use of modified bacteria, the manufacture of erythropoietin in hamster ovary cells, and the production of new types of experimental mice such as the oncomouse (cancer mouse) for research.
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There are a number of ways through which genetic engineering is accomplished. Essentially, the process has five main steps:
Isolation is achieved by identifying the gene of interest that the scientist wishes to insert into the organism, usually using existing knowledge of the various functions of genes. DNA information can be obtained from cDNA or gDNA libraries, and amplified using PCR techniques. If necessary, i.e. for insertion of eukaryotic genomic DNA into prokaryotes, further modification may be carried out such as removal of introns or ligating prokaryotic promoters.
Insertion of a gene into a vector such as a plasmid can be done once the gene of interest is isolated. Other vectors can also be used, such as viral vectors, and non-prokaryotic ones such as liposomes, or even direct insertion using DNA guns. Restriction enzymes and ligases are of great use in this crucial step if it is being inserted into prokaryotic or viral vectors. Daniel Nathans and Hamilton Smith received the 1978 Nobel Prize in Physiology or Medicine for their isolation of restriction endonucleases.
Once the vector is obtained, it can be used to transform the target organism. Depending on the vector used, it can be complex or simple. For example, using raw DNA with DNA guns is a fairly straightforward process but with low success rates, where the DNA is coated with molecules such as gold and fired directly into a cell. Other more complex methods, such as bacterial transformation or using viruses as vectors have higher success rates.
After transformation, the GMO can be isolated from those that have failed to take up the vector in various ways. One method is testing with DNA probes that can stick to the gene of interest that was supposed to have been transplanted, another would be to package resistance genes along with the vector, such that the resulting GMO is resistant to certain chemicals, and then they can be grown on agar dishes with the herbicide, to ensure only those that have taken up the vector will survive. Also those in the vector will only survive if the vector is not damaged.
The first genetically engineered medicine was synthetic human insulin, approved by the United States Food and Drug Administration in 1982. Another early application of genetic engineering was to create human growth hormone as replacement for a drug that was previously extracted from human cadavers. In 1987 the FDA approved the first genetically engineered vaccine for humans, for hepatitis B. Since these early uses of the technology in medicine, the use of GM has gradually expanded to supply a number of other drugs and vaccines.
One of the best known applications of genetic engineering is the creation of genetically modified organisms (GMOs) such as foods and vegetables that resist pest and bacteria infection and have longer freshness than otherwise.
Although there has been a revolution in the biological sciences in the past twenty years, there is still a great deal that remains to be discovered. The completion of the sequencing of the human genome, as well as the genomes of most agriculturally and scientifically important animals and plants, has increased the possibilities of genetic research immeasurably. Expedient and inexpensive access to comprehensive genetic data has become a reality with billions of sequenced nucleotides already online and annotated.
Human genetic engineering can be used to treat genetic disease, but there is a difference between treating the disease in an individual and in changing the genome that gets passed down to that person's descendants (germ-line genetic engineering).
Human genetic engineering is already being used on a small scale to allow infertile women with genetic defects in their mitochondria to have children.[2] Healthy human eggs from a second mother are used. The child produced this way has genetic information from two mothers and one father.[2] The changes made are germ line changes and will likely be passed down from generation to generation, thus are a permanent change to the human genome.[2]
Human genetic engineering has the potential to change human beings' appearance, adaptability, intelligence, character and behaviour. It may potentially be used in creating more dramatic changes in humans. There are many unresolved ethical issues and concerns surrounding this technology, and it remains a controversial topic.
The Roman Catholic Church, under the papacy of Benedict XVI, has condemned some particular cases of genetic engineering in the instruction Dignitas Personae, stating that in those situations it contradicts the fundamental truth of equality between all human beings. [3]