pTurboYFP-C vector

cat.# FP611

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 pTurboYFP-C FP611 20 μg € 400.00 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 TurboYFP Reporter codon usage mammalian Promoter for TurboYFP PCMV IE Host cells mammalian Selection prokaryotic - kanamycin eukaryotic - neomycin (G418) Replication prokaryotic - pUC ori eukaryotic - SV40 ori Use TurboYFP expression in mammalian cells; generation of fusions to the TurboYFP C-terminus

Multiple cloning site (MCS)

TurboYFP		Bgl II				Sac I				EcoR I			Sal I		Kpn I			Apa I				BamH I				Stops
				Xho I				Hind III			Pst I					Sac II*				Sma I/Xma I					Xba I#					Bcl I#
...	GGT.CTC.	AGA.	T	CT.	C	GA.G	CT.C	AA.GCT.T	C	G.AAT.T	C	T.GCA.	G	TC.GAC.	GGT.A	CC	.GC	G.G	G	C.CC	G.	GG	A.TCC	.ACC.GGA.	TC	T.AG	A.	TAA	.C	TG.A	TC.A

Vector description

pTurboYFP-C is a mammalian expression vector encoding yellow fluorescent protein TurboYFP. The vector allows generation of fusions to the TurboYFP C-terminus and expression of TurboYFP fusions or TurboYFP alone in eukaryotic (mammalian) cells.

TurboYFP 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 the TurboYFP sequence [Kozak, 1987]. Multiple cloning site (MCS) is located between TurboYFP coding sequence and SV40 polyadenylation signal (SV40 polyA).

The vector backbone contains immediate early promoter of cytomegalovirus (P_{CMV IE}) for protein 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 TurboYFP-fusion proteins

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 TurboYFP C-terminus when inserted in the same reading frame as TurboYFP and no intervening stop codons are present. TurboYFP-tagged fusions retain fluorescent properties of the native protein allowing fusion localization in vivo. Unmodified vector will express TurboYFP, when transfected into eukaryotic (mammalian) cells.

Expression in mammalian cells

pTurboYFP-C can be transfected into mammalian cells by any known transfection method. CMV promoter provides strong, constitutive expression of TurboYFP 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
TurboYFP
Kozak consensus translation initiation site: 606-616
Start codon (ATG): 613-615
Stop codon: 1420-1422
Last amino acid in TurboYFP: 1339-1341
MCS: 1342-1419
SV40 early mRNA polyadenylation signal
Polyadenylation signals: 1562-1567 & 1591-1596
mRNA 3' ends: 1600 & 1612
f1 single-strand DNA origin: 1659-2114
Eukaryotic promoter for expression of Kan^r gene
-35 region: 2176-2181
-10 region: 2199-2204
Transcription start point: 2211
SV40 origin of replication: 2455-2590
SV40 early promoter
Enhancer (72-bp tandem repeats): 2288-2359 & 2360-2431
21-bp repeats: 2435-2455, 2456-2476 & 2478-2498
Early promoter element: 2511-2517
Major transcription start points: 2507, 2545, 2551 & 2556
Kanamycin/neomycin resistance gene
Neomycin phosphotransferase coding sequences:
Start codon (ATG): 2639-2641
Stop codon: 3431-3433
G->A mutation to remove Pst I site: 2821
C->A (Arg to Ser) mutation to remove BssH II site: 3167
Herpes simplex virus (HSV) thymidine kinase (TK) polyadenylation signal
Polyadenylation signals: 3669-3674 & 3682-3687
pUC plasmid replication origin: 4018-4661