This transgene comprises a human growth hormone gene whose 5' regulatory elements have been replaced by nucleotides -4000 to +21 from the rat liver fatty-acid binding protein gene; the insertion also contains the pUC13 vector. Mice of this line (from founder G0#1) have ~66 transgene copies per haploid genome, as measured by densitometric analysis of Southern blots. Expression of human growth hormone mRNA, determined by dot-blot analysis, correlates generally with that of endogenous mouse Fabp1 mRNA in liver and intestine, including a proximal-to-distal intestinal expression gradient, highest in the proximal small intestine and declining progressively, though less rapidly for hGH than for Fabp1, through the distal colon. This Fabp1 5' regulatory segment suppresses the expression observed in colon and kidney of mice bearing similar transgenes with a shorter promoter (See Tg(Fabp1-GH1)7Bir, Tg(Fabp1-GH1)10Bir). (J:109939)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
(C57BL/6J x LT/Sv)F1
--
Insertion
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1
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5

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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