A C-terminally truncated human SRF cDNA encoding amino acid residues 1-412 was fused to the transcription activation domain of the herpes simplex virus protein VP16. This was preceeded by a splice acceptor site, a PGK-puromycin selection cassette, and a stop cassette composed of four SV40 polyadenylation signals. The selection cassette and stop cassette were flanked by loxP sites. This construct was then inserted following exon I of the endogenous gene. Despite the requirement of cre recombination to removed the stop cassette and achieve full SRF/VP16 expression, some leaky read-through transcript expression is detected in the retina. (J:172655)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
(129X1/SvJ x 129S1/Sv)F1-Kitl+
Targeted
Insertion
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--
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2

Phenotypes

Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes

References Literature

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PMID
Journal
Year
IF
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