DNA synthesis: Difference between revisions
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'''DNA synthesis''' is the natural or artificial creation of [[deoxyribonucleic acid]] (DNA) molecules. In nature, such molecules are created by all living cells through the process of [[DNA replication]], with replication initiator proteins splitting the existing DNA of the cell and making a copy of each split segment, with the copied segments then being joined together into a new DNA molecule. Various means also exist to artificially stimulate the replication of naturally occurring DNA, or to create artificial gene sequences. A [[polymerase chain reaction]] is a form of enzymatic DNA synthesis, using cycles of repeated heating and cooling of the reaction for DNA melting and enzymatic replication of the DNA. [[Artificial gene synthesis]] is the process of synthesizing a [[gene]] ''[[in vitro]]'' without the need for initial template [[DNA]] samples. The main method is currently by [[oligonucleotide synthesis]] (also used for other applications) from [[Digital genetic sequence|digital genetic sequences]] and subsequent annealing of the resultant fragments. |
'''DNA synthesis''' is the natural or artificial creation of [[deoxyribonucleic acid]] (DNA) molecules. In nature, such molecules are created by all living cells through the process of [[DNA replication]], with replication initiator proteins splitting the existing DNA of the cell and making a copy of each split segment, with the copied segments then being joined together into a new DNA molecule. Various means also exist to artificially stimulate the replication of naturally occurring DNA, or to create artificial gene sequences. A [[polymerase chain reaction]] is a form of enzymatic DNA synthesis, using cycles of repeated heating and cooling of the reaction for DNA melting and enzymatic replication of the DNA. [[Artificial gene synthesis]] is the process of synthesizing a [[gene]] ''[[in vitro]]'' without the need for initial template [[DNA]] samples. The main method is currently by [[oligonucleotide synthesis]] (also used for other applications) from [[Digital genetic sequence|digital genetic sequences]] and subsequent annealing of the resultant fragments. |
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The Carlson Curve is a term coined by The Economist <ref>Life 2.0. (2006, August 31). The Economist</ref> to describe the biotechnological equivalent of [[Moore's Law]], and is named after author Rob Carlson. <ref>Carlson, Robert H. Biology Is Technology: The Promise, Peril, and New Business of Engineering Life. Cambridge, MA: Harvard UP, 2010. Print</ref> Carlson accurately predicted that the doubling time of [[DNA sequencing]] technologies (measured by cost and performance) would be at least as fast as Moore's Law <ref>"The Pace and Proliferation of Biological Technologies" Robert Carlson. Biosecurity and Bioterrorism: Biodefense Strategy, Practice, and Science. September 2003, 1(3): 203-214. doi:10.1089/153871303769201851</ref>. Carlson Curves illustrate the rapid (in some cases hyperexponential) decreases in cost, and increases in performance, of a variety of technologies, including DNA sequencing, DNA synthesis and a range of physical and computational tools used in [[protein expression]] and in determining protein structures. |
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[[Category:DNA replication]] |
[[Category:DNA replication]] |
Revision as of 14:00, 25 April 2013
DNA synthesis is the natural or artificial creation of deoxyribonucleic acid (DNA) molecules. In nature, such molecules are created by all living cells through the process of DNA replication, with replication initiator proteins splitting the existing DNA of the cell and making a copy of each split segment, with the copied segments then being joined together into a new DNA molecule. Various means also exist to artificially stimulate the replication of naturally occurring DNA, or to create artificial gene sequences. A polymerase chain reaction is a form of enzymatic DNA synthesis, using cycles of repeated heating and cooling of the reaction for DNA melting and enzymatic replication of the DNA. Artificial gene synthesis is the process of synthesizing a gene in vitro without the need for initial template DNA samples. The main method is currently by oligonucleotide synthesis (also used for other applications) from digital genetic sequences and subsequent annealing of the resultant fragments.
The Carlson Curve is a term coined by The Economist [1] to describe the biotechnological equivalent of Moore's Law, and is named after author Rob Carlson. [2] Carlson accurately predicted that the doubling time of DNA sequencing technologies (measured by cost and performance) would be at least as fast as Moore's Law [3]. Carlson Curves illustrate the rapid (in some cases hyperexponential) decreases in cost, and increases in performance, of a variety of technologies, including DNA sequencing, DNA synthesis and a range of physical and computational tools used in protein expression and in determining protein structures.
- ^ Life 2.0. (2006, August 31). The Economist
- ^ Carlson, Robert H. Biology Is Technology: The Promise, Peril, and New Business of Engineering Life. Cambridge, MA: Harvard UP, 2010. Print
- ^ "The Pace and Proliferation of Biological Technologies" Robert Carlson. Biosecurity and Bioterrorism: Biodefense Strategy, Practice, and Science. September 2003, 1(3): 203-214. doi:10.1089/153871303769201851