Sequence of plasmid pGT5 from the archaeon Pyrococcus abyssi: evidence for rolling-circle replication in a hyperthermophile
- PMID: 8655503
- PMCID: PMC178075
- DOI: 10.1128/jb.178.11.3232-3237.1996
Sequence of plasmid pGT5 from the archaeon Pyrococcus abyssi: evidence for rolling-circle replication in a hyperthermophile
Abstract
The plasmid pGT5 (3,444 bp) from the hyperthermophilic archaeon Pyrococcus abyssi GE5 has been completely sequenced. Two major open reading frames with a good coding probability are located on the same strand and cover 85% of the total sequence. The larger open reading frame encodes a putative polypeptide which exhibits sequence similarity with Rep proteins of plasmids using the rolling-circle mechanism for replication. Upstream of this open reading frame, we have detected an 11-bp motif identical to the double-stranded origin of several bacterial plasmids that replicate via the rolling-circle mechanism. A putative single-stranded origin exhibits similarities both to bacterial primosome-dependent single-stranded initiation sites and to bacterial primase (dnaG) start sites. A single-stranded form of pGT5 corresponding to the plus strand was detected in cells of P. abyssi. These data indicate that pGT5 replicates via the rolling-circle mechanism and suggest that members of the domain Archaea contain homologs of several bacterial proteins involved in chromosomal DNA replication. Phylogenetic analysis of Rep proteins from rolling-circle replicons suggest that diverse families diverged before the separation of the domains Archaea, Bacteria, and Eucarya.
Similar articles
-
Topoisomerase activity of the hyperthermophilic replication initiator protein Rep75.Nucleic Acids Res. 2000 Jun 1;28(11):2251-5. doi: 10.1093/nar/28.11.2251. Nucleic Acids Res. 2000. PMID: 10871346 Free PMC article.
-
A rolling circle replication initiator protein with a nucleotidyl-transferase activity encoded by the plasmid pGT5 from the hyperthermophilic archaeon Pyrococcus abyssi.Mol Microbiol. 1998 Mar;27(6):1183-92. doi: 10.1046/j.1365-2958.1998.00759.x. Mol Microbiol. 1998. PMID: 9570403
-
The active site of the rolling circle replication protein Rep75 is involved in site-specific nuclease, ligase and nucleotidyl transferase activities.Mol Microbiol. 1999 Aug;33(3):537-45. doi: 10.1046/j.1365-2958.1999.01498.x. Mol Microbiol. 1999. PMID: 10417644
-
Plasmid rolling-circle replication: highlights of two decades of research.Plasmid. 2005 Mar;53(2):126-36. doi: 10.1016/j.plasmid.2004.12.008. Epub 2005 Jan 22. Plasmid. 2005. PMID: 15737400 Review.
-
Rolling-circle replication of bacterial plasmids.Microbiol Mol Biol Rev. 1997 Dec;61(4):442-55. doi: 10.1128/mmbr.61.4.442-455.1997. Microbiol Mol Biol Rev. 1997. PMID: 9409148 Free PMC article. Review.
Cited by
-
Two novel families of plasmids from hyperthermophilic archaea encoding new families of replication proteins.Nucleic Acids Res. 2010 Aug;38(15):5088-104. doi: 10.1093/nar/gkq236. Epub 2010 Apr 18. Nucleic Acids Res. 2010. PMID: 20403814 Free PMC article.
-
Topoisomerase activity of the hyperthermophilic replication initiator protein Rep75.Nucleic Acids Res. 2000 Jun 1;28(11):2251-5. doi: 10.1093/nar/28.11.2251. Nucleic Acids Res. 2000. PMID: 10871346 Free PMC article.
-
Analysis of the first genome of a hyperthermophilic marine virus-like particle, PAV1, isolated from Pyrococcus abyssi.J Bacteriol. 2007 Jun;189(12):4510-9. doi: 10.1128/JB.01896-06. Epub 2007 Apr 20. J Bacteriol. 2007. PMID: 17449623 Free PMC article.
-
Living side by side with a virus: characterization of two novel plasmids from Thermococcus prieurii, a host for the spindle-shaped virus TPV1.Appl Environ Microbiol. 2013 Jun;79(12):3822-8. doi: 10.1128/AEM.00525-13. Epub 2013 Apr 12. Appl Environ Microbiol. 2013. PMID: 23584787 Free PMC article.
-
Archaeal extrachromosomal genetic elements.Microbiol Mol Biol Rev. 2015 Mar;79(1):117-52. doi: 10.1128/MMBR.00042-14. Microbiol Mol Biol Rev. 2015. PMID: 25694123 Free PMC article. Review.
References
Publication types
MeSH terms
Associated data
- Actions
- Actions
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases