Pros and Cons of Genetic Engineering

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Pros and Cons of Genetic Engineering

Introduction

The first step to understanding genetic engineering and embracing its possibilities for society is to obtain a rough knowledge base of its history and method. The basis for altering the evolutionary process is dependant on the understanding of how individuals pass on characteristics to their offspring. Genetics achieved its first foothold on the secrets of nature's evolutionary process when an Austrian monk named Gregor Mendel developed the first "laws of heredity." Using these laws, scientists studied the characteristics of organisms for most of the next one hundred years following Mendel's discovery. These early studies concluded that each organism has two sets of character determinants, or genes. For instance, in regards to eye colour, a child could receive one set of genes from his or her father that were encoded one blue, and the other brown. The same child could also receive two brown genes from his or her mother. The conclusion for this inheritance would be the child has a three in four chance of having brown eyes, and a one in four chance of having blue.

Genes are transmitted through chromosomes which reside in the nucleus of every living organism's cells. Each chromosome is made up of fine strands of deoxyribonucleic acid, or DNA. The information carried on the DNA determines the cells function within the organism.

Sex cells are the only cells that contain a complete DNA map of the organism, therefore, "the structure of a DNA molecule or combination of DNA molecules determines the shape, form, and function of the [organism's] offspring . DNA discovery is attributed to the research of three scientists, Francis Crick, Maurice Wilkins, and James Dewey Watson in 1951. They were all later accredited with the Nobel Prize in physiology and medicine in 1962.

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The possibilities of genetic engineering are endless. Once the power to control the instructions, given to a single cell, are mastered anything can be accomplished. For example, insulin can be created and grown in large quantities by using an inexpensive gene manipulation method of growing a certain bacteria. This supply of insulin is also not dependant on the supply of pancreatic tissue from animals. Recombinant factor VIII, the blood clotting agent missing in people suffering from haemophilia, can also be created by genetic engineering. Virtually all people who were treated with factor VIII before 1985 acquired HIV, and later AIDS. Being completely pure, the bio engineered version of factor VIII eliminates any possibility of viral infection. Other uses of genetic engineering include creating disease resistant crops, formulating milk from cows already containing pharmaceutical compounds, generating vaccines, and altering livestock traits. In the not so distant future, genetic engineering will become a principal player in fighting genetic, bacterial, and viral disease, along with controlling aging, and providing replaceable parts for humans. Medicine has seen many new innovations in its history. The discovery of aesthetics permitted the birth of modern surgery, while the production of antibiotics in the 1920s minimized the threat from diseases such as pneumonia, tuberculosis and cholera. The creation of serums which build up the bodies immune system to specific infections, before being laid low with them, has also enhanced modern medicine greatly. All of these discoveries will fall under the broad shadow of genetic engineering when it reaches the medical community.
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Many people suffer from genetic diseases ranging from thousands of types of cancers, to blood, liver, and lung disorders. Amazingly, all of these will be able to be treated by genetic engineering, specifically, gene therapy. The basis of gene therapy is to supply a functional gene to cells lacking that particular function, thus correcting the genetic disorder or disease. There are two main categories of gene therapy: germ line therapy, or altering of sperm and egg cells, and somatic cell therapy, which is much like an organ transplant. Germ line therapy results in a permanent change for the ...

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This is a well researched report that covers a wide range of aspects surrounding genetic engineering. 1. The sources of information need to be referenced and an indication method needs to be used. 2. Be careful with language as several unsubstantiated claims are made. 3. The conclusion should be at the end of the report. 4. The source of quotes should be included. ****