Transgenic Organism: Difference between revisions

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A transgenic organism is a genetically engineered [[organism|organism]]. They are created by firstly isolating the [[DNA|DNA]] and then fragmenting it using [[Restriction enzyme|restriction enzymes]] before recombining the [[DNA|DNA]] in a new controlled way. The [[restriction enzyme|restriction enzymes]] cleave the DNA at a specific restriction site and mainly create [[‘sticky’ ends|sticky ends]] that have complementary sequences to each other and can therefore adhere together.   
A transgenic organism is a genetically engineered [[Organism|organism]]. They are created by isolating [[DNA|DNA]] and then fragmenting it using [[Restriction enzyme|restriction enzymes]], before recombining it in a new, controlled way. The [[Restriction enzyme|restriction enzymes]] cleave the DNA at a specific restriction site and mainly create [[‘sticky’ ends|sticky ends]] that have complementary sequences to each other and can therefore adhere together.   


The recombined DNA is reintroduced to a [[cell|cell]] or [[organism|organism]]. The main use of this technology is for experimental studies, however a very importatant aspect of the application is developing and improving varities of crop plants and domesticated animals&nbsp;<ref>Page 440, Hartl D.L and Ruvolo M (2012) Genetics, Analysis of Genes and Genomes, 8th edition, USA: Jones and Bartlett</ref>.<br>  
The recombined DNA is reintroduced to a [[Cell|cell]] or [[Organism|organism]]. The main use of this technology is for experimental studies, however a very important aspect of the application is developing and improving varities of crop plants and domesticated animals&nbsp;<ref>Page 440, Hartl D.L and Ruvolo M (2012) Genetics, Analysis of Genes and Genomes, 8th edition, USA: Jones and Bartlett</ref>.<br>  


=== References  ===
=== References  ===


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<references />

Revision as of 20:17, 6 December 2011

A transgenic organism is a genetically engineered organism. They are created by isolating DNA and then fragmenting it using restriction enzymes, before recombining it in a new, controlled way. The restriction enzymes cleave the DNA at a specific restriction site and mainly create sticky ends that have complementary sequences to each other and can therefore adhere together. 

The recombined DNA is reintroduced to a cell or organism. The main use of this technology is for experimental studies, however a very important aspect of the application is developing and improving varities of crop plants and domesticated animals [1].

References

  1. Page 440, Hartl D.L and Ruvolo M (2012) Genetics, Analysis of Genes and Genomes, 8th edition, USA: Jones and Bartlett