293T: Difference between revisions
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{{technical|date=August 2016}} |
{{technical|date=August 2016}} |
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'''293T''' (or |
'''293T''' (or [[HEK 293T]]) is a human cell line, derived from the [[HEK 293]] cell line, that expresses a mutant version of the [[SV40 large T antigen]]. It is very commonly used in biology for protein expression and production of recombinant [[retroviruses]]. |
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== Origin == |
== Origin == |
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==External links== |
==External links== |
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*[https://www.atcc.org/Products/All/CRL-3216.aspx |
*[https://www.atcc.org/Products/All/CRL-3216.aspx ATCC entry for 293T] |
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*[https://web.expasy.org/cellosaurus/CVCL_0063 Cellosaurus entry for 293T] |
*[https://web.expasy.org/cellosaurus/CVCL_0063 Cellosaurus entry for 293T] |
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Revision as of 02:45, 22 June 2019
 | This article may be too technical for most readers to understand. (August 2016) |
293T (or HEK 293T) is a human cell line, derived from the HEK 293 cell line, that expresses a mutant version of the SV40 large T antigen. It is very commonly used in biology for protein expression and production of recombinant retroviruses.
Origin
293T was created in Michele Calos's lab at Stanford by stable transfection of the HEK 293 cell line with a plasmid encoding a temperature-sensitive mutant of the SV40 large T antigen; it was originally referred to as 293/tsA1609neo.[1] The first reference to the cell line as "293T" may be its use to create the BOSC23 packaging cell line for producing retroviral particles.[2]
Characteristics
The transfection used to create 293T (involving plasmid pRSV-1609) conferred neomycin/G418 resistance and expression of the tsA1609 allele of SV40 large T antigen; this allele is fully active at 33 °C (its permissive temperature), has substantial function at 37 °C, and is inactive at 40 °C.[3] 293T is very efficiently transfectable with DNA (like its parent HEK 293). Due to the expression of SV40 large T antigen, transfected plasmid DNAs that carry the SV40 origin of replication can replicate in 293T and will transiently maintain a high copy number; this can greatly increase the amount of recombinant protein or retrovirus that can be produced from the cells.
Genome
The full genome sequences of three different isolates of 293T have been determined. They are quite similar to each other but show detectable divergence from the parental HEK 293 cell line.[4]
References
- ^ DuBridge RB, Tang P, Hsia HC, Leong PM, Miller JH, Calos MP (Jan 1987). "Analysis of mutation in human cells by using an Epstein-Barr virus shuttle system". Mol. Cell. Biol. 7 (1): 379–387. doi:10.1128/MCB.7.1.379. PMC 365079. PMID 3031469.
- ^ Pear WS, Nolan GP, Scott ML, Baltimore D (15 Sep 1993). "Production of high-titer helper-free retroviruses by transient transfection". Proc. Natl. Acad. Sci. USA. 90 (18): 8392–8396. doi:10.1073/pnas.90.18.8392. PMC 47362. PMID 7690960.
- ^ Rio DC, Clark SG, Tjian R (4 Jan 1985). "A mammalian host-vector system that regulates expression and amplification of transfected genes by temperature induction". Science. 227 (4682): 23–28. doi:10.1126/science.2981116. PMID 2981116.
- ^ Lin YC, Boone M, Meuris L, Lemmens I, Van Roy N, Soete A, Reumers J, Moisse M, Plaisance S, Drmanac R, Chen J, Speleman F, Lambrechts D, Van de Peer Y, Tavernier J, Callewaert N (3 Sep 2014). "Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations". Nat. Commun. 5. 4767. doi:10.1038/ncomms5767. PMC 4166678. PMID 25182477.