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	<title>Reverse transcriptase - Revision history</title>
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	<updated>2026-09-27T18:52:58Z</updated>
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		<title>Bpwhite: Created page with &quot;&#039;&#039;&#039;Reverse transcriptase&#039;&#039;&#039; (RT) is an enzyme used to generate complementary DNA (cDNA) from an RNA template, a process termed reverse transcription. Its discovery fundamentally altered the understanding of molecular biology by demonstrating a permanent exception to the classical Central Dogma of molecular biology, which previously modeled the flow of genetic information strictly as moving from DNA to RNA to proteins.  == Discovery ==  Reverse tra...&quot;</title>
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		<updated>2026-09-27T03:49:45Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;&amp;#039;&amp;#039;&amp;#039;Reverse transcriptase&amp;#039;&amp;#039;&amp;#039; (RT) is an &lt;a href=&quot;/index.php?title=Enzyme&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;Enzyme (page does not exist)&quot;&gt;enzyme&lt;/a&gt; used to generate complementary DNA (&lt;a href=&quot;/index.php?title=CDNA&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;CDNA (page does not exist)&quot;&gt;cDNA&lt;/a&gt;) from an &lt;a href=&quot;/index.php/RNA&quot; title=&quot;RNA&quot;&gt;RNA&lt;/a&gt; template, a process termed reverse transcription. Its discovery fundamentally altered the understanding of molecular biology by demonstrating a permanent exception to the classical &lt;a href=&quot;/index.php/Central_Dogma_of_molecular_biology&quot; class=&quot;mw-redirect&quot; title=&quot;Central Dogma of molecular biology&quot;&gt;Central Dogma of molecular biology&lt;/a&gt;, which previously modeled the flow of genetic information strictly as moving from &lt;a href=&quot;/index.php/DNA&quot; title=&quot;DNA&quot;&gt;DNA&lt;/a&gt; to RNA to &lt;a href=&quot;/index.php/Proteins&quot; title=&quot;Proteins&quot;&gt;proteins&lt;/a&gt;.  == Discovery ==  Reverse tra...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Reverse transcriptase&amp;#039;&amp;#039;&amp;#039; (RT) is an [[enzyme]] used to generate complementary DNA ([[cDNA]]) from an [[RNA]] template, a process termed reverse transcription. Its discovery fundamentally altered the understanding of molecular [[biology]] by demonstrating a permanent exception to the classical [[Central Dogma of molecular biology]], which previously modeled the flow of genetic information strictly as moving from [[DNA]] to RNA to [[proteins]].&lt;br /&gt;
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== Discovery ==&lt;br /&gt;
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Reverse transcriptase was discovered independently in 1970 by [[Howard Temin]] at the University of Wisconsin and [[David Baltimore]] at MIT. Both researchers isolated the enzyme from different RNA tumor viruses. For this paradigm-shifting discovery, Temin and Baltimore shared the 1975 [[Nobel Prize in Physiology or Medicine]] alongside [[Renato Dulbecco]].&lt;br /&gt;
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== Function in Viruses ==&lt;br /&gt;
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Reverse transcriptase is most heavily associated with &amp;#039;&amp;#039;&amp;#039;[[retroviruses]]&amp;#039;&amp;#039;&amp;#039;, such as the [[Human Immunodeficiency Virus]] (HIV) and the [[Human T-lymphotropic virus]] (HTLV).&lt;br /&gt;
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When a retrovirus infects a target [[cell]], it releases its single-stranded RNA genome into the host&amp;#039;s [[cytoplasm]]. Because host cells lack the machinery to replicate RNA directly or integrate RNA into their chromosomes, the virus relies on its own pre-packaged reverse transcriptase. The enzyme reads the viral RNA and converts it into a stable, double-stranded DNA molecule. This newly synthesized viral DNA is then transported into the [[cell nucleus]] and permanently spliced into the host&amp;#039;s [[genome]] by the enzyme [[integrase]], establishing a [[provirus]] that forces the cell to manufacture new viral particles.&lt;br /&gt;
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== Enzymatic Mechanics ==&lt;br /&gt;
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Reverse transcriptase is a multifunctional enzyme that executes three distinct, sequential biochemical activities to convert single-stranded RNA into double-stranded DNA:&lt;br /&gt;
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1. &amp;#039;&amp;#039;&amp;#039;RNA-dependent DNA polymerase activity:&amp;#039;&amp;#039;&amp;#039; The enzyme reads the viral RNA template and synthesizes a complementary, single-stranded DNA molecule. This process requires a short strand of host [[tRNA]] to act as a starting [[primer]].&lt;br /&gt;
2. &amp;#039;&amp;#039;&amp;#039;Ribonuclease H (RNase H) activity:&amp;#039;&amp;#039;&amp;#039; Once the RNA-DNA hybrid is formed, the RNase H domain of the enzyme selectively degrades the original RNA template strand, leaving only the newly synthesized single strand of DNA.&lt;br /&gt;
3. &amp;#039;&amp;#039;&amp;#039;DNA-dependent DNA polymerase activity:&amp;#039;&amp;#039;&amp;#039; The enzyme then uses the newly made single-stranded DNA as a template to synthesize a second, complementary DNA strand, resulting in a complete double-stranded DNA double helix.&lt;br /&gt;
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Crucially, viral reverse transcriptase lacks the 3&amp;#039; to 5&amp;#039; exonuclease proofreading capability found in standard cellular [[DNA polymerase]]. As a result, it makes frequent transcription errors. This high [[mutation rate]] is a primary driver of rapid viral evolution, allowing retroviruses to quickly evade the host&amp;#039;s immune system and develop resistance to antiviral medications.&lt;br /&gt;
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== Function in Eukaryotes ==&lt;br /&gt;
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While famous for its viral origins, reverse transcription is also essential to normal cellular biology in [[eukaryotes]], including humans:&lt;br /&gt;
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* &amp;#039;&amp;#039;&amp;#039;Telomerase:&amp;#039;&amp;#039;&amp;#039; The ends of linear [[chromosomes]] contain repetitive protective sequences called [[telomeres]], which naturally shorten with each cell division. &amp;#039;&amp;#039;&amp;#039;[[Telomerase]]&amp;#039;&amp;#039;&amp;#039; is a specialized ribonucleoprotein complex that acts as a cellular reverse transcriptase. It uses a built-in RNA template to add DNA sequence repeats back onto the chromosome ends, preventing the loss of vital genetic information and playing a key role in cellular aging and [[cancer]] immortalization.&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Retrotransposons:&amp;#039;&amp;#039;&amp;#039; A significant portion of the eukaryotic genome consists of mobile genetic elements called &amp;#039;&amp;#039;&amp;#039;[[retrotransposons]]&amp;#039;&amp;#039;&amp;#039; (such as Alu elements and LINEs in humans). These &amp;quot;jumping genes&amp;quot; transcribe themselves into RNA, use an internally encoded reverse transcriptase to convert back into DNA, and insert the new copy at a different location in the genome. This copy-and-paste mechanism has been a major engine of genomic expansion and evolutionary change over millions of years.&lt;br /&gt;
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== Applications in Biotechnology ==&lt;br /&gt;
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Because of its unique ability to link the transient RNA transcriptome to the stable DNA genome, reverse transcriptase has become an indispensable tool in modern biotechnology and medicine:&lt;br /&gt;
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* &amp;#039;&amp;#039;&amp;#039;RT-PCR:&amp;#039;&amp;#039;&amp;#039; Reverse transcription [[polymerase chain reaction]] (RT-PCR) uses the enzyme to convert fragile messenger RNA ([[mRNA]]) into stable cDNA. This allows researchers to accurately measure [[gene expression]] levels in tissues or detect the presence of RNA viruses (such as SARS-CoV-2) in patient samples.&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;cDNA Libraries:&amp;#039;&amp;#039;&amp;#039; Biologists use the enzyme to construct &amp;#039;&amp;#039;&amp;#039;[[cDNA libraries]]&amp;#039;&amp;#039;&amp;#039;. By reverse-transcribing mature mRNA, researchers can isolate the exact protein-coding sequences of genes, completely free of the non-coding [[introns]] that clutter the raw genomic DNA.&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Pharmacology:&amp;#039;&amp;#039;&amp;#039; Because RT is essential for retroviral replication but generally not required for day-to-day host cell survival, it is a primary pharmacological target. Reverse transcriptase inhibitors (such as AZT) are the cornerstone of [[antiretroviral therapy]] used to manage HIV infections, working by physically blocking the enzyme&amp;#039;s active site or prematurely terminating the growing DNA chain.&lt;/div&gt;</summary>
		<author><name>Bpwhite</name></author>
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