Genetic Engineering.

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Genetic Engineering

Genetic engineering seems to be one of the incredible breakthroughs in science. It was discovered in the 1900’s by Mendel, who used to study peas by creating different species at one time. Genetic engineering can be described as the non-natural alteration of the genetic code. Genes are parts of the DNA (deoxyribonucleic acid) that control the characteristics of individuals (e.g. hair colour); these are different for every individual. Normally genes are passed along generations but now scientists are now able to classify an individual gene and insert it into an organism that will carry the trait of that certain gene. This organism is seen to be transgenic which is a term used to describe that the organisms DNA has been changed. Different genes from different organisms are able to be inserted into different species genes (e.g. a human gene can be placed in a bacteria gene). Genetic engineering is used for a number of different things. (Watson et al 1992)

The typical genetic procedure goes as follows first the gene that will be taken has to be located and isolated. The messenger RNA from the gene needed has to be isolated and a simple complementary copy is done using an enzyme called transcriptase. One more copy is made by adding another enzyme called polymerase, this creates a double stranded piece of DNA. DNA is a long strand and can be isolated from the mixture by precipitating it with ethanol. (Bill Indge et al 2000)

The DNA is then suspended in a solution which contains a Ph buffer; the DNA is then cut using the restriction enzyme. The DNA parts are then inserted into a host. There are a number of ways in which this can be done the most common way is using viruses as vectors. The most frequent vector is bacterial plasmids.  A bacterium has two types of genetic material. There is a long strand of DNA in a form of a ring which is referred to a single circular chromosome. The second is a number of small rings of double stranded DNA called plasmids. These can be removed from the bacterium and inserted into a new bacterial cell quite easily. In the bacterium the plasmids are able to copy themselves. So any gene added to a plasmid is also copied, this is called cloning. (Bill Indge et al 2000)

An isolated plasmid has to be cut open to be used as a vector using an enzyme, this causes ‘sticky ends’.  The same restriction enzyme is used (the one that was used to cut out the DNA). These two are then joined together using an enzyme called ligase.  This happens naturally in the nuclei, and it repairs any DNA that has been damaged in replication.  Ligase then speeds both the complementary strand of DNA after the sticky ends of the strand have been joined. The genetically made plasmids are reinserted into the bacterium, where some of the recombinant plasmids enter the cytoplasm of the bacteria. (Bill Indge et al 2000)

The first mammal to be cloned was a sheep called Dolly who was made by a ewe and ram mating. She was an exact genetic replica of her donor a six year old female sheep. Sheep are just the start of animals being cloned. In Oregon they are cloning monkeys from embryonic cells. ()

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A clone is an organism or cell that has been identically copied genetically to another cell or organism. Simple organisms like bacteria reproduce themselves by copying their own DNA and splitting. The two bacteria that come from this form asexual reproduction and are clones of each other as they are genetically the same. The difference in sexual reproduction is that the nucleus of a sperm cell (this carries the father’s DNA) comes together with the nucleus of the egg cell (this contains the mother’s DNA). This gives the result of an offspring which contains genetic material from the mother and ...

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