RNA-dependent RNA polymerase: Difference between revisions
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Many RDRPs are associated tightly with membranes and are therefore difficult to study. The best known RDRPs are polioviral 3Dpol, vesicular stomatitis virus L, and [[hepatitis C virus]] NS5b protein. |
Many RDRPs are associated tightly with membranes and are therefore difficult to study. The best known RDRPs are polioviral 3Dpol, vesicular stomatitis virus L, and [[hepatitis C virus]] NS5b protein. |
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[[Eukaryote]]s also have RDRPs, these amplify [[microRNA]]s.<ref>[http://www.ebi.ac.uk/interpro/IEntry?ac=IPR007855 InterPro: RNA-dependent RNA polymerase, eukaryotic-type], retrieved 6 April 2008</ref> |
[[Eukaryote]]s also have RDRPs involved in [[RNA interference]], these amplify [[microRNA]]s and [[small temporal RNA]]s, and produce double-stranded RNA using [[small interfering RNA]]s as primers<ref>{{cite journal |author=Iyer LM, Koonin EV, Aravind L |title=Evolutionary connection between the catalytic subunits of DNA-dependent RNA polymerases and eukaryotic RNA-dependent RNA polymerases and the origin of RNA polymerases |journal=BMC Struct. Biol. |volume=3 |issue= |pages=1 |year=2003 |month=January |pmid=12553882 |doi= |url=http://www.biomedcentral.com/1472-6807/3/1}}</ref><ref>[http://www.ebi.ac.uk/interpro/IEntry?ac=IPR007855 InterPro: RNA-dependent RNA polymerase, eukaryotic-type], retrieved 6 April 2008</ref> |
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== See also == |
== See also == |
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Revision as of 10:57, 30 May 2008
RNA-dependent RNA polymerase (RDRP), or RNA replicase, is an enzyme that catalyzes the replication of RNA from an RNA template. In contrast to a typical RNA polymerase, which uses DNA as a template, RDRP is, as its name suggests, dependent on RNA.
Viral RDRPs were discovered in the early 1960s from studies on mengovirus and polio virus when it was observed that these viruses were not sensitive to actinomycin D, a drug that inhibits cellular DNA directed RNA synthesis.This lack of sensitivity suggested that there was a virus specific enzyme that could copy RNA from an RNA template and not from a DNA template.
The most famous example of RDRP is the polio virus. The virus is made up of RNA which enters the cell through receptor-mediated endocytosis. From there, the RNA is able to act as a template for complementary RNA synthesis, immediately. The complementary strand is then, itself, able to act as a template for the production of new viral genomes which are further packaged and released from the cell ready to infect more host cells. The advantage of this method of replication is that there is no DNA stage, replication is quick and easy. The disadvantage is that there is no 'back-up' DNA copy.
Many RDRPs are associated tightly with membranes and are therefore difficult to study. The best known RDRPs are polioviral 3Dpol, vesicular stomatitis virus L, and hepatitis C virus NS5b protein.
Eukaryotes also have RDRPs involved in RNA interference, these amplify microRNAs and small temporal RNAs, and produce double-stranded RNA using small interfering RNAs as primers[1][2]
See also
References
- ^ Iyer LM, Koonin EV, Aravind L (2003). "Evolutionary connection between the catalytic subunits of DNA-dependent RNA polymerases and eukaryotic RNA-dependent RNA polymerases and the origin of RNA polymerases". BMC Struct. Biol. 3: 1. PMID 12553882.
{{cite journal}}: Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link) - ^ InterPro: RNA-dependent RNA polymerase, eukaryotic-type, retrieved 6 April 2008
External links
- RNA+Replicase at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- EC 2.7.7.48
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