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Vector Maps

The MISSION research and development team, in collaboration with the RNAi Consortium (TRC) scientists, has generated a series of vectors to enable the successful implementation of your RNAi experiments. The base vector pLKO.1-puro was developed1 at the Broad Institute as part of TRC. Our contribution to TRC is a diverse set of vectors for critical control experiments, as well as vectors for custom shRNA production. This page contains information pertaining to these vectors.

pLKO.1-puro sequence (without shRNA insert)

TRC1.5 Vector: pLKO.1-puro
TRC1.5 Control Vectors
TRC1.5 Alternate Vector Backbones
TRC2 Vector: TRC2-pLKO-puro
Inducible shRNA Vectors
Lentiviral Packaging Vectors
References

TRC1.5 Vector: pLKO.1-puro Vector and Use

TRC1.5 clones are in the exact same vector backbone as the TRC1 clones

Features of the pLKO.1-puro vector allow for transient or stable transfection of the shRNA as well as production of lentiviral particles.1 Stable gene silencing is selected using the puromycin selectable marker while self-inactivating replication incompetent viral particles can be produced in packaging cells (HEK293T) by co-transfection with compatible packaging plasmids.2,3 Exclusive to our portfolio, TRC1.5 contains almost 200,000 clones including more than 49,000 validated clones. It combines all of the content from TRC1 plus an additional 39,212 clones targeting 2,661 new human genes and 2,395 mouse genes. Unlike adenovirus or murine-based MMLV or MSCV retroviral systems, lentiviral-based particles permit efficient infection and integration of the specific shRNA construct into differentiated and non-dividing cells, such as neurons and dendritic cells, overcoming low transfection and integration difficulties when using these cell lines. Compared to siRNA and other vector-based systems, pLKO.1-puro provides solutions for long-term knockdown and phenotypic observation, transduction of difficult or sensitive cell lines (non-dividing cells or primary cells), and is an economical renewable resource.

With an shRNA insert, the length of the pLKO.1-puro plasmid is 7,086 bp, as indicated in the vector map below. Without an shRNA insert, pLKO.1-puro vector has a length of 7,052 bp. The sequence file provided is the empty pLKO.1-puro vector (7,052 bp).

TRC1.5 Vector Map (pLKO.1-puro)

siRNA Vector

TRC1.5 Vector Description and Features

NameDescription
cpptCentral polypurine tract
hPGKHuman phosphoglycerate kinase eukaryotic promoter
puroRPuromycin resistance gene for mammalian selection
SIN/LTR3' self inactivating long terminal repeat
f1 orif1 origin of replication
ampRAmpicillin resistance gene for bacterial selection
pUC oripUC origin of replication
5' LTR5' long terminal repeat
PsiRNA packaging signal
RRERev response element

TRC1.5 Control Vectors

We offer a variety of controls for conducting the most rigorous and informative shRNA experiments possible. Visit the shRNA controls web page to learn more.

ProductPurposeVector MapVector File
SHC001Empty vector (no shRNA insert) ControlSHC001
SHC001
SHC002Non-Mammalian shRNA ControlSHC002
SHC002
SHC003TurboGFP ControlSHC003
SHC003
SHC004TurboGFP shRNA ControlSHC004
SHC004
SHC005eGFP shRNA ControlSHC005
SHC005
SHC007Luciferase shRNA ControlSHC007
SHC007
SHC008B2M shRNA ControlSHC008
SHC008
SHC009ARHGDIA shRNA ControlSHC009
SHC009
SHC010CMV-TagCFP™ ControlSHC010
SHC010
SHC011CMV-TagYFP™ ControlSHC011
SHC011
SHC012CMV-TagRFP™ ControlSHC012
SHC012
SHC013CMV-TagFP635™ ControlSHC013
SHC013
SHC014UbC-TurboGFP™ ControlSHC014
SHC014
SHC015UbC-TagFP635™ ControlSHC015
SHC015
SHC016Non-Target shRNA ControlSHC016
SHC016

TRC1.5 Alternate Vector Backbones

We offer a variety of alternate vector backbones as part of our standard shRNA offering. With our customizable MISSION shRNA ordering interface, it is possible to order TRC shRNAs in these vector backbones directly online on the clones detail pages for Plasmid DNA or Lentiviral Transduction Particles. For custom hairpins, please visit our custom cloning page for details on ordering.

ProductPurposeVector MapVector File
pLKO.1-CMV-NeoAlternate vector backbonepLKO.1-CMV-Neo
pLKO.1-CMV-Neo
pLKO.1-NeoAlternate vector backbonepLKO.1-Neo
pLKO.1-Neo
pLKO.1-CMV-tGFPAlternate vector backbonepLKO.1-CMV-tGFP
pLKO.1-CMV-tGFP
pLKO.1-Neo-CMV-tGFPAlternate vector backbonepLKO.1-Neo-CMV-tGFP
pLKO.1-Neo-CMV-tGFP
pLKO.1-puro-CMV-tGFPAlternate vector backbonepLKO.1-puro-CMV-tGFP
pLKO.1-puro-CMV-tGFP

We also offer several alternate vector backbones with fluorescent proteins or the UbC promoter. These constructs are available only as custom options. Please visit our custom cloning page for details on ordering.

ProductPurposeVector MapVector File
pLKO.1-puro-CMV-TagCFP™Alternate vector backbonepLKO.1-puro-CMV-TagCFP
pLKO.1-puro-CMV-TagCFP
pLKO.1-puro-CMV-TagYFP™Alternate vector backbonepLKO.1-puro-CMV-TagYFP
pLKO.1-puro-CMV-TagYFP
pLKO.1-puro-CMV-TagRFP™Alternate vector backbonepLKO.1-puro-CMV-TagRFP
pLKO.1-puro-CMV-TagRFP
pLKO.1-puro-CMV-TagFP635™Alternate vector backbonepLKO.1-puro-CMV-TagFP635
pLKO.1-puro-CMV-TagFP635
pLKO.1-puro-UbC-TurboGFP™Alternate vector backbonepLKO.1-puro-UbC-TurboGFP
pLKO.1-puro-UbC-TurboGFP
pLKO.1-puro-UbC-TagFP635™Alternate vector backbonepLKO.1-puro-UbC-TagFP635
pLKO.1-puro-UbC-TagFP635

TRC2 Vector: TRC2-pLKO-puro Vector and Use

The TRC2-pLKO-puro vector also allows for transient or stable transfection of the shRNA as well as the production of lentiviral particles. The only change between the TRC1.5 vector and the TRC2 vector is the addition of the WPRE (or the Woodchuck Hepatitis Post-Transcriptional Regulatory Element).4 This allows for enhanced expression of transgenes delivered by lentivirus.5 As with TRC1.5, stable gene silencing is achieved by using the puromycin selectable marker. Self-inactivating replication incompetent viral particles can be produced in packaging cells (HEK293T) by co-transfection with compatible packaging plasmids. TRC2-pLKO-puro provides solutions for stable long-term knockdown and phenotypic observation, transduction of difficult or sensitive cell lines (non-dividing cells or primary cells), and enhanced expression of transgenes.

With an shRNA insert, the length of the TRC2-pLKO-puro plasmid is 7,518 bp, as indicated in the vector map below. Without an shRNA insert, the TRC2-pLKO-puro vector has a length of 7,484 bp. The sequence file provided is the empty TRC2-pLKO-puro vector (7,484 bp).

TRC2-pLKO-puro sequence (without shRNA insert)

TRC2 Vector Map (TRC2-pLKO-puro)

trc2-plko-puro
NameDescription
cpptCentral polypurine tract
hPGKHuman phosphoglycerate kinase eukaryotic promoter
puroRPuromycin resistance gene for mammalian selection
WPREWoodchuck Hepatitis Post-Transcriptional Regulatory Element
SIN/LTR3' self inactivating long terminal repeat
f1 orif1 origin of replication
ampRAmpicillin resistance gene for bacterial selection
pUC oripUC origin of replication
5' LTR5' long terminal repeat
PsiRNA packaging signal
RRERev response element
TRC2 Vector Description and Features
ProductPurposeVector MapVector File
SHC201Empty TRC2 vector (no shRNA insert) ControlSHC201
SHC201
SHC202Non-Target shRNA ControlSHC202
SHC202
SHC203TurboGFP ControlSHC203
SHC203
SHC204TurboGFP shRNA ControlSHC204
SHC204
TRC2 Control Vectors

Please note: At this time, there are no alternate vector backbones available for TRC2.

Inducible shRNA Vectors

The pLKO vector has been redesigned to contain a LacI (repressor) and a modified human U6 shRNA promoter with LacO (operator) sequences. In the absence of IPTG (isopropyl-β-D-thio-galactoside), an analogue of lactose, LacI binds to LacO preventing expression of the shRNA. When IPTG is present, the allosteric LacI repressor changes conformation, releasing itself from lacO modified human U6 promoter, and subsequently allows expression of the shRNA.

We are proud to offer two different IPTG inducible vectors for your research. The preferred inducible vector, pLKO-puro-IPTG-3xLacO, contains three lac operon sequences (two in the U6 promoter and one 3' of the promoter) affording both tight regulation and great gene silencing. Whereas, the pLKO-puro-IPTG-1xLacO vector contains a single lac operon sequence in the U6 promoter, which allows for an advantage to shRNA expression, but looser control of the promoter when not induced.

ProductPurposeVector MapVector File
pLKO-puro-IPTG-1xLacOAlternate vector backbonepLKO-puro-IPTG-1xLacO
pLKO-puro-IPTG-1xLacO
pLKO-puro-IPTG-3xLacOAlternate vector backbonepLKO-puro-IPTG-3xLacO
pLKO-puro-IPTG-3xLacO

Lentiviral Packaging Vectors

Finally, for those wanting to package their own lentivirus, we offer the optimized packaging mix. Visit the Lentiviral packaging mix web page to learn more.

ProductPurposeVector MapVector File
SHP001
pMISSIONgagpol
Packaging Vector #1pMISSIONgagpol
pMISSIONgagpol
SHP001
pMISSIONvsvg
Packaging Vector #2pMISSIONvsvg
pMISSIONvsvg

References

1.
Stewart, S. A. et al. Lentivirus-delivered stable gene silencing by RNAi in primary cells. RNA 2003, 9, 493–501.. https://doi.org/10.1261/rna.2192803
2.
Zufferey, R. et al. Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo. Nat. Biotechnol 1997, 15, 871–85.. https://doi.org/10.1038/nbt0997-871
3.
Zufferey, R. et al. Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery. J. Virol. 1998, 72, 9873–80.. https://doi.org/10.1128/JVI.72.12.9873-9880.1998
4.
Donello J. E. et al. Woodchuck hepatitis virus contains a tripartite posttranscriptional regulatory element. J. Virol. 1998, 72, 5085-92.. https://doi.org/10.1128/JVI.72.6.5085-5092.1998
5.
Zufferey, R. et al. Woodchuck hepatitis virus posttranscriptional regulatory element enhances expression of transgenes delivered by retroviral vectors. J. Virol. 1999, 73, 2886-92.. https://doi.org/10.1128/JVI.73.4.2886-2892.1999

Contact Us

For questions about the library, pricing and quotes or other concerns, please e-mail us at: MISSIONRNAi@sial.com.

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