Mouse albumin (Alb) promoter

Mouse albumin (Alb) gene promoter paired with its far-upstream enhancer, directing transgene expression almost exclusively to differentiated hepatocytes in transgenic mice. Standard promoter for liver-specific Cre driver lines (Alb-Cre) and hepatic transgene expression in mouse models of liver disease, drug metabolism, and lipid biology.

Length: 2336 bp

Strength: strong

Tissue: Differentiated hepatocytes; requires the far-upstream enhancer for efficient liver-specific expression

Expression: constitutive

Origin: Mouse albumin gene, proximal promoter plus far-upstream enhancer

Characteristics

The albumin proximal promoter alone gives only weak expression in transgenic mice; a far-upstream enhancer located 8.5-10.4 kb 5' of the promoter is required together with it for efficient, high-level liver-specific expression, while the intervening -8.5 to -0.3 kb region is dispensable. Alb-Cre transgenic mice, which express Cre recombinase from this promoter/enhancer combination, are the standard line for hepatocyte-specific gene knockouts crossed against loxP-flanked alleles. Cre-mediated excision in Alb-Cre liver is not complete at birth — recombination proceeds progressively over the first several weeks of postnatal life rather than occurring immediately in all hepatocytes.

Applications: Hepatocyte-specific Cre expression (Alb-Cre) for conditional gene knockouts in mouse models of liver disease, drug metabolism, and lipid biology, crossed against loxP-flanked target alleles. Also used directly to drive liver-restricted transgene expression in non-Cre constructs.

Limitations: The proximal promoter alone gives only weak expression; efficient liver-specific activity requires pairing with the far-upstream (8.5-10.4 kb) enhancer, so a minimal promoter-only construct will underperform. In Alb-Cre mice, recombination of loxP-flanked alleles is incomplete at birth and increases progressively with postnatal age, so experiments requiring complete embryonic or neonatal knockout should not assume immediate full excision.

Sequence

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References

  1. Pinkert et al. (1987). An albumin enhancer located 10 kb upstream functions along with its promoter to direct efficient, liver-specific expression in transgenic mice. Genes Dev - Pinkert 1987 Albumin Enhancer