Gene Isolation: The gene responsible for producing insulin (proinsulin gene) is isolated from human DNA. Gene Insertion: The isolated gene is inserted into a plasmid (a small, circular DNA molecule) that can replicate within bacteria or yeast cells. Transformation: The plasmid is introduced into bacterial or yeast cells through a process called transformation. These cells are then cultured in large fermentation tanks. Protein Production: The bacteria or yeast cells use the inserted gene to produce insulin. Afterward, the insulin is extracted and purified.
Benefits: This method provides a consistent and safe supply of insulin, reducing the risk of allergic reactions and allowing for large-scale production.
Genetic engineering has revolutionized medicine, particularly in the production of therapeutic proteins like insulin and in the development of gene therapy. Here's how it's used:1. Production of Insulin: Recombinant DNA Technology: One of the most well-known applications of genetic engineering is the production of human insulin. Before genetic engineering, insulin for diabetic patients was extracted from the pancreases of animals like pigs or cows, which had limitations in terms of supply and compatibility with the human body. Process:Gene Identification: Scientists first identify and isolate the human gene responsible for insulin production. Insertion into Bacteria: This gene is inserted into a plasmid (a small circular DNA molecule) which is then introduced into a bacterium, typically Escherichia coli. Bacterial Production: The bacteria are cultured in large quantities, where they use the inserted human gene to produce insulin. Purification: The insulin is then harvested and purified for medical use. Outcome: This method produces "recombinant human insulin," which is chemically identical to insulin naturally produced by the human pancreas, leading to better control of diabetes with fewer side effects. 2. Gene Therapy: Concept: Gene therapy involves the direct modification of a patient's genes to treat or prevent disease. This can involve replacing a faulty gene with a healthy one, inactivating a malfunctioning gene, or introducing a new gene to help fight a disease. Types of Gene Therapy:Somatic Gene Therapy: The therapeutic genes are introduced into the somatic (non-reproductive) cells. The effects of this therapy are limited to the individual patient and are not passed on to offspring. It is used to treat conditions like cystic fibrosis, hemophilia, and certain types of cancer. Germline Gene Therapy: This involves altering genes in germ cells (sperm or eggs), meaning changes would be passed on to future generations. This type is highly controversial and is not widely practiced due to ethical concerns. Methods of Delivery:Viral Vectors: Viruses are often used as carriers (vectors) to deliver the therapeutic gene into the patient's cells. These viruses are modified to be safe and are engineered to carry the therapeutic DNA. Non-Viral Methods: Other methods include direct injection of DNA, use of liposomes (fat-based vesicles), or CRISPR-Cas9 technology, which can precisely edit specific parts of the genome. Examples:Treatment of Genetic Disorders: Gene therapy has been used to treat disorders like severe combined immunodeficiency (SCID), where a gene defect prevents the immune system from functioning properly. Cancer Therapy: Techniques like CAR-T cell therapy, where a patient’s T-cells are genetically engineered to better fight cancer cells, have shown significant promise. Hereditary Blindness: In some cases, gene therapy has restored vision in patients with certain forms of inherited blindness by introducing functional copies of genes into retinal cells. 3. Production of Other Therapeutic Proteins: Clotting Factors: Genetic engineering is used to produce clotting factors for patients with hemophilia, reducing reliance on blood donations and decreasing the risk of blood-borne infections. Growth Hormones: Recombinant human growth hormone is produced similarly to insulin and is used to treat growth disorders in children and adults. Monoclonal Antibodies: These are engineered proteins that can specifically target certain cells, such as cancer cells or pathogens, and are used in treatments for various diseases, including cancer, autoimmune disorders, and infectious diseases. 4. Personalized Medicine: Pharmacogenomics: Genetic engineering contributes to the field of pharmacogenomics, where an individual’s genetic profile is used to tailor medical treatments. This allows for more effective and less toxic treatments, as drugs can be customized to the patient’s unique genetic makeup. CRISPR and Beyond: The development of CRISPR-Cas9 and similar technologies has opened new avenues in gene editing, offering the potential to not only treat but potentially cure genetic disorders by correcting mutations at their source. 5. Vaccine Development: Genetically Engineered Vaccines: Genetic engineering is also used to develop vaccines, such as the mRNA vaccines for COVID-19, which use engineered genetic material to instruct cells to produce a protein that triggers an immune response. These applications of genetic engineering in medicine highlight its transformative potential, offering new treatments and hope for conditions that were once considered untreatable.4o
Genetic engineering has revolutionized medicine in various ways, including:
1. Insulin production: Genetic engineering enabled the production of human insulin in bacteria, making it widely available and affordable for diabetes treatment.
2. Gene therapy: Genetic engineering allows for the introduction of healthy copies of a gene to replace faulty or missing ones, treating genetic disorders like sickle cell anemia and cystic fibrosis.
3. Vaccine development: Genetic engineering facilitates the creation of vaccines, such as the HPV vaccine, by producing specific viral proteins in yeast or bacteria.
4. Cancer treatment: Genetic engineering is used to develop targeted therapies, like CAR-T cell therapy, which reprograms immune cells to attack cancer cells.
5. Gene editing: CRISPR-Cas9 and other gene editing tools enable precise modifications to genes, holding promise for treating genetic diseases.
6. Regenerative medicine: Genetic engineering is used to create stem cells for tissue engineering and regenerative medicine, potentially treating conditions like Parkinson's disease.
7. Pharmacogenomics: Genetic engineering helps develop personalized medicine by tailoring treatments to an individual's genetic profile.
8. Antibody production: Genetic engineering enables the production of monoclonal antibodies for treating various diseases, including cancer and autoimmune disorders.
9. Viral vector development: Genetic engineering creates viral vectors for gene therapy, vaccine delivery, and gene editing.
10. Synthetic biology: Genetic engineering enables the design of new biological pathways, organisms, or biological functions for medical applications.
These advancements have transformed the field of medicine, offering new hope for treating and potentially curing genetic diseases.