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Animal biotechnology is used mainly for two purposes: to produce disease models
that mimic human diseases and can therefore be used both in the study of disease
and new - drug testing; and to produce animals that can be employed in basic
biological research into biological development and function.
Gene transfer methods is the factor determining where we carry out this purposes
successfully or not. Scientists have transfer genes across species, families, and
even kingdom. A lot of efficient transformation methods are now available to
generate transgenic animals, and animal cloning provides many chances in the
experimental science. Creating transgenic animals requires us to make sure the
transgene turns on at the right time and in the right tissues; otherwise, our body will
recognize those genes as the foreign genes and reject them.
Microinjection, first developed in the mouse, has been the method that are used to
transfer genes between animals and are popular technique for creating transgenic
organism, particularly mammals. It is a technique of delivering foreign DNA into a
living cell through a glass micropipette. Once a gene has been characterised and
appropriately expressed in eukaryotic cells, a transgenic animal can be made by
microinjection of the cloned gene into the fertilized eggs of a donor animal. The
foreign gene must be injected before the first cell division, or cleavage, occurs in
order that all cells of the organism harbor the gene.
It includes several steps: first, we have to identify a foreign gene of interest and
insert the foreign gene into an appropriate vector. Then, DNA must be injected
directly into the pronucleus of a single fertilized egg and we have to implant the
microinjected egg into a surrogate mother. After that, let the embryo develop to term
and demonstrate that the foreign gene has been stably incorporated into the host
genome and that it is heritable in at least one of the offspring. Finally, we have to
demonstrate that the gene is expressed and regulated correctly in the host organism.
However, there are still some problems, disadvantages in microinjection. Few
injected eggs survive, and not all of those retain the new DNA. If it is not targeted to
a specific chromosomal locus, that new DNA is integrated at random. As a
consequence, there will be an unexpected change in gene expression, especially
when the new DNA disrupts other genes. Another two methods also producing
transgenic animals are retrovirus-mediated gene transfer and embryonic stem cell-
mediated gene transfer.