pTurboGFP-dest1 vector

cat.# FP519

The vector sequence has been compiled using the information from sequence databases, published literature, and other sources, together with partial sequences obtained by Evrogen. This vector has not been completely sequenced.

Download vector information: Data sheet (pdf) Sequence (txt) Restriction map (pdf) Restriction table (pdf)

Product Cat.# Size Price pTurboGFP-dest1 FP519 20 μg € 400 The price does not include delivery. The price varies in different countries. Please contact your local distributor for exact prices and delivery information. Vector type mammalian expression vector Reporter TurboGFP Reporter codon usage mammalian Promoter for TurboGFP PCMV IE Host cells mammalian Selection prokaryotic - kanamycin eukaryotic - neomycin (G418) Replication prokaryotic - pUC ori eukaryotic - SV40 ori Use TurboGFP expression in mammalian cells; generation of fusions to the TurboGFP-dest1 N-terminus

Multiple cloning site (MCS)

Nhe I				Bgl II*			Sac I		Hind III		EcoR I			Sal I		Kpn I			Apa I*				BamH I		Age I			TurboGFP
	Afe I				Xho I*							Pst I*					Sac II				Sma I/Xma I						Nco I*
GCT	A.GC	G.CT	A.CCG.GAC.TC	A.GAT.	CT	C.	GAG.	CTC.	AAG.CTT.	C	GA.ATT.	C	TG.CA	G.	TCG.AC	G.GTA.	CC	G.C	GG.	G	CC.C	G	G.G	AT.CC	A.CCG.GT	C.GCC.A	CC.	ATG.G	AG.AGC

Vector description

pTurboGFP-dest1 is a mammalian expression vector encoding destabilized green fluorescent protein TurboGFP-dest1 (see reporter description). To generate TurboGFP-dest1 variant, residues 422-461 of mouse ornithine decarboxylase (MODC) were fused to the TurboGFP C-terminus. This MODC region contains a PEST amino acid sequence that targets the protein for degradation and provides for rapid protein turnover [Li et al., 1998]. TurboGFP-dest1 retains fluorescent properties of the native protein and has a half-life of approximately 1-1.5 hours, as measured by fluorescence intensity of cells treated with the protein synthesis inhibitor, cycloheximide.

pTurboGFP-dest1 carries synthetic version of the TurboGFP-dest1 gene which codon usage is optimized for high expression in mammalian cells (humanized) [Haas et al., 1996]. To increase mRNA translation efficiency, Kozak consensus translation initiation site is generated upstream of TurboGFP-dest1 coding sequence [Kozak, 1987].

pTurboGFP-dest1 vector can be used to express TurboGFP-dest1 in eukaryotic (mammalian) cells. For example it can be used as a positive control with a pTurboGFP-PRL-dest1 promoterless vector (Cat.# FP518). The vector can be also used to generate destabilized TurboGFP-tagged fusion proteins. Multiple cloning site (MCS) is located upstream of TurboGFP-dest1 coding sequence.

The vector backbone contains immediate early promoter of cytomegalovirus (P_{CMV IE}) for reporter expression, SV40 origin for replication in mammalian cells expressing SV40 T-antigen, pUC origin of replication for propagation in E. coli and f1 origin for single-stranded DNA production. SV40 polyadenylation signals (SV40 poly A) direct proper processing of the 3'-end of the reporter mRNA.

SV40 early promoter (P_SV40) provides neomycin resistance gene (Neo^r) expression to select stably transfected eukaryotic cells using G418. Bacterial promoter (P) provides kanamycin resistance gene expression (Kan^r) in E. coli. Kan^r/Neo^r gene is linked with herpes simplex virus (HSV) thymidine kinase (TK) polyadenylation signals.

Generation of TurboGFP-dest1-tagged fusions

A localization signal or a gene of interest should be cloned into MCS of the vector. It will be expressed as a fusion to the TurboGFP-dest1 N-terminus when inserted in the same reading frame as TurboGFP and no in-frame stop codons are present. TurboGFP-dest1-tagged fusions retain fluorescent properties of the native protein allowing fusion localization in vivo. Unmodified pTurboGFP-dest1 vector will express TurboGFP-dest1 when transfected into eukaryotic (mammalian) cells.

Expression in mammalian cells

pTurboGFP-dest1 can be transfected into mammalian cells by any known transfection method. CMV promoter provides strong, constitutive expression of TurboGFP-dest1 or its fusions in many cell types. If required, stable transformants can be selected using G418 [Gorman, 1985].

Propagation in E. coli

Suitable host strains for propagation in E. coli include DH5alpha, HB101, XL1-Blue, and other general purpose strains. Plasmid incompatibility group is pMB1/ColE1. The vector confers resistance to kanamycin (30 μg/ml) to E. coli hosts. Copy number in E. coli is about 500.

Location of features

P_{CMV IE}: 1-589
Enhancer region: 59-465
TATA box: 554-560
Transcription start point: 583
MCS: 591-671
TurboGFP
Kozak consensus translation initiation site: 672-682
Start codon (ATG): 679-681
Last amino acid in TurboGFP: 1372-1374
Stop codon: 1510-1512
MODC PEST sequence: 1390-1512
SV40 early mRNA polyadenylation signal
Polyadenylation signals: 1667-1672 & 1696-1701
mRNA 3' ends: 1705 & 1717
f1 single-strand DNA origin: 1764-2219
Eukaryotic promoter for expression of Kan^r gene
-35 region: 2281-2286
-10 region: 2304-2309
Transcription start point: 2316
SV40 origin of replication: 2560-2695
SV40 early promoter
Enhancer (72-bp tandem repeats): 2393-2464 & 2465-2536
21-bp repeats: 2540-2560, 2561-2581 & 2583-2603
Early promoter element: 2616-2622
Major transcription start points: 2612, 2650, 2656 & 2661
Kanamycin/neomycin resistance gene
Neomycin phosphotransferase coding sequences:
Start codon (ATG): 2744-2746
Stop codon: 3536-3538
G->A mutation to remove Pst I site: 2926
C->A (Arg to Ser) mutation to remove BssH II site: 3272
Herpes simplex virus (HSV) thymidine kinase (TK) polyadenylation signal
Polyadenylation signals: 3774-3779 & 3787-3792
pUC plasmid replication origin: 4123-4766