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[[Image:Genetic-engineering-wheat.jpg|thumb|right|200px|Elements of genetic engineering]]
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{{for|a non-technical introduction to the topic|Introduction to Genetics}}
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'''Genetic engineering''', '''[[recombinant DNA]] technology''', '''genetic modification/manipulation (GM)''' and '''gene splicing''' are terms that apply to the direct manipulation of an [[organism]]'s [[gene]]s.<ref>
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{{cite web
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|url=http://dictionary.reference.com/browse/Genetic%20engineering
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|title=Genetic engineering - Definitions from Dictionary.com
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|publisher=dictionary.reference.com
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|accessdate=2008-04-26
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|last='''Bold text'''
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|first=
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}}
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</ref> Genetic engineering is different from traditional [[breeding]], where the organism's genes are manipulated indirectly; genetic engineering uses the techniques of [[molecular cloning]] and [[transformation]] to alter the structure and characteristics of genes directly. Genetic engineering techniques have
  +
found some successes in MICK numerous applications. Some examples are in improving crop technology, the manufacture of synthetic human [[insulin]] through the use of modified bacteria, the manufacture of erythropoietin in hamster [[ovary]] cells, and the production of new types of experimental mice such as the oncomouse (cancer mouse) for research.
  +
  +
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== Engineering ==
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# Isolation of the genes of interest
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# Insertion of the genes into a transfer [[vector (biology)|vector]]
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# Transfer of the vector to the organism to be modified
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# [[Transformation (genetics)|Transformation]] of the cells of the organism
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# Separation of the genetically modified organism (GMO) from those that have not been successfully modified
  +
  +
'''Isolation''' is achieved by identifying the gene of interest that the scientist wishes to insert into the organism, usually using existing knowledge of the various functions of genes. DNA information can be obtained from [[cDNA]] or [[gDNA]] libraries, and amplified using [[PCR]] techniques. If necessary, i.e. for insertion of eukaryotic genomic DNA into [[prokaryotes]], further modification may be carried out such as removal of [[introns]] or ligating prokaryotic promoters.
  +
  +
'''Insertion''' of a gene into a vector such as a [[plasmid]] can be done once the gene of interest is isolated. Other vectors can also be used, such as viral vectors, and non-prokaryotic ones such as liposomes, or even direct insertion using DNA guns. [[Restriction enzyme]]s and [[ligases]] are of great use in this crucial step if it is being inserted into prokaryotic or viral vectors. [[Daniel Nathans]] and [[Hamilton Smith]] received the [[1978]] [[Nobel Prize]] [[Nobel Prize in Physiology or Medicine|in Physiology or Medicine]] for their isolation of [[restriction enzyme|restriction endonucleases]].
  +
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Once the vector is obtained, it can be used to '''transform''' the '''target organism'''. Depending on the vector used, it can be complex or simple. For example, using raw DNA with DNA guns is a fairly straightforward process but with low success rates, where the DNA is coated with molecules such as gold and fired directly into a cell. Other more complex methods, such as [[Transformation (genetics)|bacterial transformation]] or using viruses as vectors have higher success rates.
  +
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After transformation, the '''GMO''' can be '''isolated''' from those that have failed to take up the vector in various ways.
  +
  +
  +
=== Genetic Engineering ===
  +
Although there has been a revolution in the biological sciences in the past twenty years, there is still a great deal that remains to be discovered. The completion of the sequencing of the [[human genome]], as well as the genomes of most agriculturally and scientifically important animals and plants, has increased the possibilities of genetic research immeasurably. Expedient and inexpensive access to comprehensive genetic data has become a reality with billions of sequenced [[nucleotide]]s already online and annotated.
  +
  +
[[Image:PCWmice1.jpg|thumb|right|Knockout mice]]
  +
  +
* '''Loss of function experiments''', such as in a [[Gene knockout|gene knockout]] experiment, in which an organism is engineered to lack the activity of one or more genes. This allows the experimenter to analyze the defects caused by this [[mutation]], and can be considerably useful in unearthing the function of a gene. It is used especially frequently in [[developmental biology]]. A knockout experiment involves the creation and manipulation of a DNA construct ''[[in vitro]]'', which, in a simple knockout, consists of a copy of the desired gene which has been slightly altered such as to cripple its function. The construct is then taken up by [[embryonic stem cells]], where the engineered copy of the gene replaces the organism's own gene. These stem cells are injected into [[blastocyst]]s, which are implanted into surrogate mothers. Another method, useful in organisms such as [[Drosophila]] (fruitfly), is to induce mutations in a large population and then screen the progeny for the desired mutation. A similar process can be used in both plants and [[prokaryotes]].
  +
* '''Gain of function experiments''', the logical counterpart of knockouts. These are sometimes performed in conjunction with knockout experiments to more finely establish the function of the desired gene. The process is much the same as that in knockout engineering, except that the construct is designed to increase the function of the gene, usually by providing extra copies of the gene or inducing synthesis of the protein more frequently.
  +
  +
[[Image:GFP structure.png|thumb|right|175px|Green Fluorescent Protein ribbon diagram. From {{PDB|1EMA}}.]]
  +
  +
* '''Tracking experiments''', which seek to gain information about the localization and interaction of the desired protein. One way to do this is to replace the wild-type gene with a 'fusion' gene, which is a juxtaposition of the wild-type gene with a reporting element such as [[Green fluorescent protein|Green Fluorescent Protein]] (GFP) that will allow easy visualization of the products of the genetic modification. While this is a useful technique, the manipulation can destroy the function of the gene, creating secondary effects and possibly calling into question the results of the experiment. More sophisticated techniques are now in development that can track protein products without mitigating their function, such as the addition of small sequences which will serve as binding motifs to monoclonal antibodies.
  +
* '''Expression studies''' aim to discover where and when specific proteins are produced. In these experiments the DNA sequence before the DNA that codes for a protein, known as a gene's [[promoter]] is reintroduced into an organism with the protein coding region replaced by a reporter gene such as GFP or an enzyme that catalyzes the production of a dye. Thus the time and place where a particular protein is produced can be observed. Expression studies can be taken a step further by altering the promoter to find which pieces are crucial for the proper expression of the gene and are actually bound by transcription factor proteins; this process is known as [[promoter bashing]].
  +
  +
===Human genetic engineering===
  +
{{seealso|Human genetic engineering}}
  +
  +
Human genetic engineering can be used to treat [[genetic disease]], but there is a difference between treating the disease in an individual and in changing the genome that gets passed down to that person's descendants (germ-line genetic engineering).
  +
  +
Human genetic engineering is already being used on a small scale to allow infertile women with genetic defects in their [[mitochondria]] to have children.<ref name="bbc">
  +
{{cite web
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|url=http://news.bbc.co.uk/1/hi/sci/tech/1312708.stm
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|title=BBC News | SCI/TECH | Genetically altered babies born
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|publisher=news.bbc.co.uk
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|accessdate=2008-04-26
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|last=
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|first=
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}}
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</ref> Healthy human eggs from a second mother are used. The child produced this way has genetic information from two mothers and one father.<ref name="bbc"/> The changes made are germ line changes and will likely be passed down from generation to generation, thus are a permanent change to the human genome.<ref name="bbc"/>
  +
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Human genetic engineering has the potential to change human beings' appearance, adaptability, intelligence, character and behaviour. It may potentially be used in creating more dramatic changes in humans. There are many unresolved ethical issues and concerns surrounding this technology, and it remains a controversial topic.
  +
  +
==Religious objections==
  +
The Roman Catholic Church, under the papacy of Benedict XVI, has condemned some particular cases of genetic engineering in the instruction ''Dignitas Personae'', stating that in those situations it ''contradicts the fundamental truth of equality between all human beings''. <ref>[http://www.washingtonpost.com/wp-dyn/content/article/2008/12/12/AR2008121200774.html Washington Post article]</ref>
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==References==
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{{refimprove|date=September 2007}}
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{{Reflist}}
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==Reading list==
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*{{cite book | author=British Medical Association | title=The Impact of Genetic Modification on Agriculture, Food and Health | publisher=BMJ Books | year=1999 | isbn=0-7279-1431-6}}
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*{{cite book | author=Donnellan, Craig | title=Genetic Modification (Issues) | publisher=Independence Educational Publishers | year=2004 | isbn=1-86168-288-3}}
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*{{cite book | author=Morgan, Sally | title=Superfoods: Genetic Modification of Foods (Science at the Edge) | publisher=Heinemann | year=2003 | isbn=1-4034-4123-5}}
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*{{cite book | author=Smiley, Sophie | title=Genetic Modification: Study Guide (Exploring the Issues) | publisher=Independence Educational Publishers | year=2005 | isbn=1-86168-307-3}}
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*{{cite book |last=Zaid |first=A |authorlink= |coauthors= H.G. Hughes, E. Porceddu, F. Nicholas|title= Glossary of Biotechnology for Food and Agriculture - A Revised and Augmented Edition of the Glossary of Biotechnology and Genetic Engineering. Available in English, French, Spanish, Arabic|url=http://www.fao.org/biotech/index_glossary.asp|year=2001|publisher=[[FAO]]|location=[[Rome, Italy]]|isbn= 92-5-104683-2}}
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==See also==
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<div style="-moz-column-count:3; column-count:3;">
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*[[Bioethics]]
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*[[Biotechnology]]
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*[[Biological engineering]]
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*[[Canola]]
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*[[Cloning]]
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*[[Ethics of technology]]
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*[[Eugenics]]
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*[[Experimental evolution]]
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*[[Genetic counselling]]
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*[[Genetic disorders]]
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*[[Genetic linkage]]
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*[[Gene flow]]
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*[[Genetic pollution]]
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*[[Gene pool]]
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*[[Genetically modified food]]
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*[[Genetically modified organisms]]
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*[[Transgene]]
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*[[Human genetic engineering]]
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*[[Population genetics]]
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*[[Recombinant DNA]]
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*[[Reproductive technology]]
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*[[Research ethics]]
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*[[Selective breeding]]
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*[[Stem cell]]
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</div>
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==External links==
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===General===
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*[http://www.mfe.govt.nz/publications/organisms/royal-commission-gm/ Ministry for the Environment NZ - Report of the Royal Commission on Genetic Modification]
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*[http://www.gmo-safety.eu/en/ GMO Safety - Information about research projects on the biological safety of genetically modified plants.]
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*[http://www.rsrevision.com/Alevel/ethics/genetic_engineering/index.htm Genetic Engineering] A UK site for students, with case studies and ethical responses
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*[http://www.bootstrike.com/Genetics/ Introduction to Genetic Engineering] Covers general information on Genetic Engineering including cloning, stem cells and DNA.
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*[http://www.mshri.on.ca/nagy/tt2008/ The 8th International Transgenic Technology Conference]
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[[Category:Bioengineering]]
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[[Category:Biotechnology]]
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[[Category:Genetic engineering| ]]
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[[Category:Molecular biology]]
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[[ar:هندسة الوراثة]]
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[[af:Genetiese manipulasie]]
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[[ca:Enginyeria genètica]]
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[[da:Gensplejsning]]
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[[de:Gentechnik]]
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[[es:Ingeniería genética]]
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[[eo:Gentekniko]]
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[[fr:Génie génétique]]
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[[gl:Enxeñería xenética]]
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[[ko:유전공학]]
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[[hr:Genetičko inženjerstvo]]
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[[id:Rekayasa genetika]]
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[[it:Ingegneria genetica]]
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[[he:הנדסה גנטית]]
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[[ku:Endazyariya bûmayîk]]
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[[nl:Genetische technologie]]
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[[ja:遺伝子工学]]
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[[pt:Engenharia genética]]
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[[ru:Генная инженерия]]
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[[simple:Genetic engineering]]
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[[sr:Генетички инжењеринг]]
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[[su:Rékayasa genetik]]
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[[fi:Geenitekniikka]]
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[[sv:Genetisk modifiering]]
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[[ta:மரபணு பொறியியல்]]
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[[th:พันธุวิศวกรรม]]
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-->
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{{EnWP|Genetic engineering}}

Latest revision as of 21:00, 18 December 2008

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File:Genetic-engineering-wheat.jpg

Elements of genetic engineering

For a non-technical introduction to the topic, see Introduction to Genetics.

Genetic engineering, recombinant DNA technology, genetic modification/manipulation (GM) and gene splicing are terms that apply to the direct manipulation of an organism's genes.[1] Genetic engineering is different from traditional breeding, where the organism's genes are manipulated indirectly; genetic engineering uses the techniques of molecular cloning and transformation to alter the structure and characteristics of genes directly. Genetic engineering techniques have found some successes in MICK numerous applications. Some examples are in improving crop technology, the manufacture of synthetic human insulin through the use of modified bacteria, the manufacture of erythropoietin in hamster ovary cells, and the production of new types of experimental mice such as the oncomouse (cancer mouse) for research.


Engineering

  1. Isolation of the genes of interest
  2. Insertion of the genes into a transfer vector
  3. Transfer of the vector to the organism to be modified
  4. Transformation of the cells of the organism
  5. Separation of the genetically modified organism (GMO) from those that have not been successfully modified

Isolation is achieved by identifying the gene of interest that the scientist wishes to insert into the organism, usually using existing knowledge of the various functions of genes. DNA information can be obtained from cDNA or gDNA libraries, and amplified using PCR techniques. If necessary, i.e. for insertion of eukaryotic genomic DNA into prokaryotes, further modification may be carried out such as removal of introns or ligating prokaryotic promoters.

Insertion of a gene into a vector such as a plasmid can be done once the gene of interest is isolated. Other vectors can also be used, such as viral vectors, and non-prokaryotic ones such as liposomes, or even direct insertion using DNA guns. Restriction enzymes and ligases are of great use in this crucial step if it is being inserted into prokaryotic or viral vectors. Daniel Nathans and Hamilton Smith received the 1978 Nobel Prize in Physiology or Medicine for their isolation of restriction endonucleases.

Once the vector is obtained, it can be used to transform the target organism. Depending on the vector used, it can be complex or simple. For example, using raw DNA with DNA guns is a fairly straightforward process but with low success rates, where the DNA is coated with molecules such as gold and fired directly into a cell. Other more complex methods, such as bacterial transformation or using viruses as vectors have higher success rates.

After transformation, the GMO can be isolated from those that have failed to take up the vector in various ways.


Genetic Engineering

Although there has been a revolution in the biological sciences in the past twenty years, there is still a great deal that remains to be discovered. The completion of the sequencing of the human genome, as well as the genomes of most agriculturally and scientifically important animals and plants, has increased the possibilities of genetic research immeasurably. Expedient and inexpensive access to comprehensive genetic data has become a reality with billions of sequenced nucleotides already online and annotated.

File:PCWmice1.jpg

Knockout mice

  • Loss of function experiments, such as in a gene knockout experiment, in which an organism is engineered to lack the activity of one or more genes. This allows the experimenter to analyze the defects caused by this mutation, and can be considerably useful in unearthing the function of a gene. It is used especially frequently in developmental biology. A knockout experiment involves the creation and manipulation of a DNA construct in vitro, which, in a simple knockout, consists of a copy of the desired gene which has been slightly altered such as to cripple its function. The construct is then taken up by embryonic stem cells, where the engineered copy of the gene replaces the organism's own gene. These stem cells are injected into blastocysts, which are implanted into surrogate mothers. Another method, useful in organisms such as Drosophila (fruitfly), is to induce mutations in a large population and then screen the progeny for the desired mutation. A similar process can be used in both plants and prokaryotes.
  • Gain of function experiments, the logical counterpart of knockouts. These are sometimes performed in conjunction with knockout experiments to more finely establish the function of the desired gene. The process is much the same as that in knockout engineering, except that the construct is designed to increase the function of the gene, usually by providing extra copies of the gene or inducing synthesis of the protein more frequently.
File:GFP structure.png

Green Fluorescent Protein ribbon diagram. From PDB 1EMA.

  • Tracking experiments, which seek to gain information about the localization and interaction of the desired protein. One way to do this is to replace the wild-type gene with a 'fusion' gene, which is a juxtaposition of the wild-type gene with a reporting element such as Green Fluorescent Protein (GFP) that will allow easy visualization of the products of the genetic modification. While this is a useful technique, the manipulation can destroy the function of the gene, creating secondary effects and possibly calling into question the results of the experiment. More sophisticated techniques are now in development that can track protein products without mitigating their function, such as the addition of small sequences which will serve as binding motifs to monoclonal antibodies.
  • Expression studies aim to discover where and when specific proteins are produced. In these experiments the DNA sequence before the DNA that codes for a protein, known as a gene's promoter is reintroduced into an organism with the protein coding region replaced by a reporter gene such as GFP or an enzyme that catalyzes the production of a dye. Thus the time and place where a particular protein is produced can be observed. Expression studies can be taken a step further by altering the promoter to find which pieces are crucial for the proper expression of the gene and are actually bound by transcription factor proteins; this process is known as promoter bashing.

Human genetic engineering

See also: Human genetic engineering

Human genetic engineering can be used to treat genetic disease, but there is a difference between treating the disease in an individual and in changing the genome that gets passed down to that person's descendants (germ-line genetic engineering).

Human genetic engineering is already being used on a small scale to allow infertile women with genetic defects in their mitochondria to have children.[2] Healthy human eggs from a second mother are used. The child produced this way has genetic information from two mothers and one father.[2] The changes made are germ line changes and will likely be passed down from generation to generation, thus are a permanent change to the human genome.[2]

Human genetic engineering has the potential to change human beings' appearance, adaptability, intelligence, character and behaviour. It may potentially be used in creating more dramatic changes in humans. There are many unresolved ethical issues and concerns surrounding this technology, and it remains a controversial topic.

Religious objections

The Roman Catholic Church, under the papacy of Benedict XVI, has condemned some particular cases of genetic engineering in the instruction Dignitas Personae, stating that in those situations it contradicts the fundamental truth of equality between all human beings. [3]

References

This article needs additional citations for verification.
Please help improve this article by adding reliable references. Unsourced material may be challenged and removed. (September 2007)
  1. ↑ Bold text Genetic engineering - Definitions from Dictionary.com. dictionary.reference.com. URL accessed on 2008-04-26.
  2. ↑ 2.0 2.1 2.2 BBC News. news.bbc.co.uk. URL accessed on 2008-04-26.
  3. ↑ Washington Post article

Reading list

See also

External links

General


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