Genetic Cloning

1547 Words4 Pages

Cloning

Cloning is a process that creates exact genetic copies of an existing cell.Cloning is a more general term that describes a number of different processes that can be used to produce genetically identical copies. The process of cloning can happen either naturally, for instance, when identical twins develop or it can be induced through synthetic conditions in a laboratory. There are three different types of artificial cloning: gene cloning, reproductive cloning and therapeutic cloning.

Gene cloning works by first isolating the desired gene and ‘cutting’ it from the original chromosome using restriction enzymes. The piece of DNA is ‘pasted’ into a vector and the ends of the DNA are joined with the vector DNA by ligation. The vector is introduced into a host cell, often a bactera or yeast, by a process called transformation. The host cells copy the vector DNA along with their own DNA, creating multiple copies of the inserted DNA. The vector DNA is separated from the host cells’ DNA and purified. Gene cloning is used to create a large number of copies of a gene. The cloned DNA can be used to decipher the function of the gene, Investigate a gene’s characteristics like size, or expression, look at how mutations may affect a gene’s function or make large concentrations of the protein coded for by the gene.

Reproductive cloning is a type of cloning which is performed for the purpose of creating a duplicate copy of another organism. It creates exact genetic copy, or clone, of an individual. It is accomplished using a process called somatic cell nuclear transfer(SCNT). SCNT when done on a mouse for instance, functions by taking the nucleus out of a somatic cell(any non gamete cell) of one mouse and then that nucleus is put into ...

... middle of paper ...

...y into a cell it usually will not function the desired way. Instead, a carrier called a vector is genetically engineered to deliver the gene. Certain viruses are often used as vectors because they can deliver the new gene by infecting the cell. The viruses are modified so they can’t cause disease and will not be fought off by the patient’s immune system. The vector can be injected or given by IV directly into a specific place in the patient’s body. The vector can also be introduced after , a sample of the patient’s cells are removed and exposed to the vector in a lab. The cells with the vector are then returned to the patient.
In conclusion, all three of these practices offer the opportunity for great medical advancement but struggle with ethical issues and possible risks as well as questions of their viablity as legitimate treatments to benefit medical problems.

Open Document