LOCUS Exported 6087 bp ds-DNA circular SYN 18-DEC-2018
DEFINITION Cloning vector pXPG, complete sequence.
ACCESSION AF262031
VERSION .
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 6087)
AUTHORS Bert AG, Burrows J, Osborne CS, Cockerill PN.
TITLE Generation of an improved luciferase reporter gene plasmid that
employs a novel mechanism for high-copy replication
JOURNAL Plasmid 44 (2), 173-182 (2000)
PUBMED 10964627
REFERENCE 2 (bases 1 to 6087)
AUTHORS Bert AG, Burrows J, Osborne CS, Cockerill PN.
TITLE Direct Submission
JOURNAL Submitted (01-MAY-2000) Division of Human Immunology, Hanson Centre
For Cancer Research, Institute of Medical and Veterinary Science,
Frome Road, Adelaide, SA 5000, Australia
REFERENCE 3 (bases 1 to 6087)
AUTHORS Bert AG, Burrows J, Osborne CS, Cockerill PN.
TITLE Direct Submission
JOURNAL Submitted (04-AUG-2000) Division of Human Immunology, Hanson Centre
For Cancer Research, Institute of Medical and Veterinary Science,
Frome Road, Adelaide, SA 5000, Australia
REFERENCE 4 (bases 1 to 6087)
AUTHORS Cockerill PN.
TITLE Direct Submission
JOURNAL Submitted (25-MAR-2004) Molecular Medicine, University of Leeds,
Clinical Sciences Building, St. Jamess University Hospital, Leeds
LS9 7TF, UK
REFERENCE 5 (bases 1 to 6087)
AUTHORS .
TITLE Direct Submission
COMMENT On Mar 25, 2004 this sequence version replaced AF262031.2.
The reporter gene plasmid pXPG has been engineered by incorporating
a novel high copy origin of replication and the modified Luc+
luciferase gene into the pXP1 vector.
FEATURES Location/Qualifiers
source 1..6087
/organism="Cloning vector pXPG"
/mol_type="other DNA"
/note="high-copy number vector derived from cloning vectors
pXP1 and pGL3"
/db_xref="taxon:124098"
misc_feature 1..46
/label=multiple cloning site
/note="multiple cloning site"
misc_feature 47..1729
/label=pGL3 vector sequence
/note="pGL3 vector sequence"
regulatory 70..79
/regulatory_class="other"
/note="vertebrate consensus sequence for strong initiation
of translation (Kozak, 1987)"
gene 76..1734
/gene="Luc+"
/label=Luc+
/note="modified luciferase gene from plasmid pGL3"
CDS 76..1728
/codon_start=1
/gene="Luc+"
/product="luciferase"
/label=Luc+
/protein_id="AAF73967.1"
/translation="MEDAKNIKKGPAPFYPLEDGTAGEQLHKAMKRYALVPGTIAFTDA
HIEVDITYAEYFEMSVRLAEAMKRYGLNTNHRIVVCSENSLQFFMPVLGALFIGVAVAP
ANDIYNERELLNSMGISQPTVVFVSKKGLQKILNVQKKLPIIQKIIIMDSKTDYQGFQS
MYTFVTSHLPPGFNEYDFVPESFDRDKTIALIMNSSGSTGLPKGVALPHRTACVRFSHA
RDPIFGNQIIPDTAILSVVPFHHGFGMFTTLGYLICGFRVVLMYRFEEELFLRSLQDYK
IQSALLVPTLFSFFAKSTLIDKYDLSNLHEIASGGAPLSKEVGEAVAKRFHLPGIRQGY
GLTETTSAILITPEGDDKPGAVGKVVPFFEAKVVDLDTGKTLGVNQRGELCVRGPMIMS
GYVNNPEATNALIDKDGWLHSGDIAYWDEDEHFFIVDRLKSLIKYKGYQVAPAELESIL
LQHPNIFDAGVAGLPDDDAGELPAAVVVLEHGKTMTEKEIVDYVASQVTTAKKLRGGVV
FVDEVPKGLTGKLDARKIREILIKAKKGGKIAV"
misc_feature 1730..46
/label=pXP1 vector sequence
/note="pXP1 vector sequence"
intron 1739..2348
/note="SV40 small T intron"
intron 1813..1878
/label=small t intron
/note="SV40 (simian virus 40) small t antigen intron"
CDS 2008..2028
/codon_start=1
/product="nuclear localization signal of SV40 (simian virus
40) large T antigen"
/label=SV40 NLS
/translation="PKKKRKV"
regulatory 2349..3338
/regulatory_class="polyA_signal_sequence"
/note="SV40 early polyA signal; compiled from the pXP1 SV40
sequence except for deletion of TTG which is missing in the
equivalent SV40 elements upstream of the multiple cloning
site"
polyA_signal 2450..2584
/label=SV40 poly(A) signal
/note="SV40 polyadenylation signal"
misc_feature 2584
/note="BamHI site destroyed and a ClaI site created by
end-filling and religation of the BamHI site"
promoter 3441..3545
/gene="bla"
/label=AmpR promoter
CDS 3546..4406
/codon_start=1
/gene="b-lactamase"
/product="beta-lactamase"
/label=b-lactamase
/protein_id="AAF73968.1"
/translation="MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGYI
ELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRVDAGQEQLGRRIHYSQNDLVEYS
PVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRW
EPELNEAIPNDERDTTMPAAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSA
LPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGAS
LIKHW"
gene 3546..4406
/gene="b-lactamase"
/label=b-lactamase
/note="AMP-R"
rep_origin 4577..5165
/direction=RIGHT
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
variation 4604
/replace="a"
/label=high-copy number origin of replication mutation
/note="high-copy number origin of replication mutation"
rep_origin 5168
misc_feature 5351..5491
/label=bom
/note="basis of mobility region from pBR322"
regulatory 5633..5862
/regulatory_class="polyA_signal_sequence"
/note="SV40 early polyA signal"
polyA_signal 5730..5864
/label=SV40 poly(A) signal
/note="SV40 polyadenylation signal"
regulatory 5863..6087
/regulatory_class="polyA_signal_sequence"
/note="SV40 early polyA signal"
polyA_signal 5958..5
/label=SV40 poly(A) signal
/note="SV40 polyadenylation signal"
LOCUS Exported 6087 bp ds-DNA circular SYN 18-DEC-2018
DEFINITION Cloning vector pXPG, complete sequence.
ACCESSION AF262031
VERSION .
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 6087)
AUTHORS Bert AG, Burrows J, Osborne CS, Cockerill PN.
TITLE Generation of an improved luciferase reporter gene plasmid that
employs a novel mechanism for high-copy replication
JOURNAL Plasmid 44 (2), 173-182 (2000)
PUBMED 10964627
REFERENCE 2 (bases 1 to 6087)
AUTHORS Bert AG, Burrows J, Osborne CS, Cockerill PN.
TITLE Direct Submission
JOURNAL Submitted (01-MAY-2000) Division of Human Immunology, Hanson Centre
For Cancer Research, Institute of Medical and Veterinary Science,
Frome Road, Adelaide, SA 5000, Australia
REFERENCE 3 (bases 1 to 6087)
AUTHORS Bert AG, Burrows J, Osborne CS, Cockerill PN.
TITLE Direct Submission
JOURNAL Submitted (04-AUG-2000) Division of Human Immunology, Hanson Centre
For Cancer Research, Institute of Medical and Veterinary Science,
Frome Road, Adelaide, SA 5000, Australia
REFERENCE 4 (bases 1 to 6087)
AUTHORS Cockerill PN.
TITLE Direct Submission
JOURNAL Submitted (25-MAR-2004) Molecular Medicine, University of Leeds,
Clinical Sciences Building, St. Jamess University Hospital, Leeds
LS9 7TF, UK
REFERENCE 5 (bases 1 to 6087)
AUTHORS .
TITLE Direct Submission
COMMENT On Mar 25, 2004 this sequence version replaced AF262031.2.
The reporter gene plasmid pXPG has been engineered by incorporating
a novel high copy origin of replication and the modified Luc+
luciferase gene into the pXP1 vector.
FEATURES Location/Qualifiers
source 1..6087
/organism="Cloning vector pXPG"
/mol_type="other DNA"
/note="high-copy number vector derived from cloning vectors
pXP1 and pGL3"
/db_xref="taxon:124098"
misc_feature 1..46
/label=multiple cloning site
/note="multiple cloning site"
misc_feature 47..1729
/label=pGL3 vector sequence
/note="pGL3 vector sequence"
regulatory 70..79
/regulatory_class="other"
/note="vertebrate consensus sequence for strong initiation
of translation (Kozak, 1987)"
gene 76..1734
/gene="Luc+"
/label=Luc+
/note="modified luciferase gene from plasmid pGL3"
CDS 76..1728
/codon_start=1
/gene="Luc+"
/product="luciferase"
/label=Luc+
/protein_id="AAF73967.1"
/translation="MEDAKNIKKGPAPFYPLEDGTAGEQLHKAMKRYALVPGTIAFTDA
HIEVDITYAEYFEMSVRLAEAMKRYGLNTNHRIVVCSENSLQFFMPVLGALFIGVAVAP
ANDIYNERELLNSMGISQPTVVFVSKKGLQKILNVQKKLPIIQKIIIMDSKTDYQGFQS
MYTFVTSHLPPGFNEYDFVPESFDRDKTIALIMNSSGSTGLPKGVALPHRTACVRFSHA
RDPIFGNQIIPDTAILSVVPFHHGFGMFTTLGYLICGFRVVLMYRFEEELFLRSLQDYK
IQSALLVPTLFSFFAKSTLIDKYDLSNLHEIASGGAPLSKEVGEAVAKRFHLPGIRQGY
GLTETTSAILITPEGDDKPGAVGKVVPFFEAKVVDLDTGKTLGVNQRGELCVRGPMIMS
GYVNNPEATNALIDKDGWLHSGDIAYWDEDEHFFIVDRLKSLIKYKGYQVAPAELESIL
LQHPNIFDAGVAGLPDDDAGELPAAVVVLEHGKTMTEKEIVDYVASQVTTAKKLRGGVV
FVDEVPKGLTGKLDARKIREILIKAKKGGKIAV"
misc_feature 1730..46
/label=pXP1 vector sequence
/note="pXP1 vector sequence"
intron 1739..2348
/note="SV40 small T intron"
intron 1813..1878
/label=small t intron
/note="SV40 (simian virus 40) small t antigen intron"
CDS 2008..2028
/codon_start=1
/product="nuclear localization signal of SV40 (simian virus
40) large T antigen"
/label=SV40 NLS
/translation="PKKKRKV"
regulatory 2349..3338
/regulatory_class="polyA_signal_sequence"
/note="SV40 early polyA signal; compiled from the pXP1 SV40
sequence except for deletion of TTG which is missing in the
equivalent SV40 elements upstream of the multiple cloning
site"
polyA_signal 2450..2584
/label=SV40 poly(A) signal
/note="SV40 polyadenylation signal"
misc_feature 2584
/note="BamHI site destroyed and a ClaI site created by
end-filling and religation of the BamHI site"
promoter 3441..3545
/gene="bla"
/label=AmpR promoter
CDS 3546..4406
/codon_start=1
/gene="b-lactamase"
/product="beta-lactamase"
/label=b-lactamase
/protein_id="AAF73968.1"
/translation="MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGYI
ELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRVDAGQEQLGRRIHYSQNDLVEYS
PVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRW
EPELNEAIPNDERDTTMPAAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSA
LPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGAS
LIKHW"
gene 3546..4406
/gene="b-lactamase"
/label=b-lactamase
/note="AMP-R"
rep_origin 4577..5165
/direction=RIGHT
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
variation 4604
/replace="a"
/label=high-copy number origin of replication mutation
/note="high-copy number origin of replication mutation"
rep_origin 5168
misc_feature 5351..5491
/label=bom
/note="basis of mobility region from pBR322"
regulatory 5633..5862
/regulatory_class="polyA_signal_sequence"
/note="SV40 early polyA signal"
polyA_signal 5730..5864
/label=SV40 poly(A) signal
/note="SV40 polyadenylation signal"
regulatory 5863..6087
/regulatory_class="polyA_signal_sequence"
/note="SV40 early polyA signal"
polyA_signal 5958..5
/label=SV40 poly(A) signal
/note="SV40 polyadenylation signal"