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Molecular and Cellular Biology, February 2006, p. 1538-1548, Vol. 26, No. 4
0270-7306/06/$08.00+0 doi:10.1128/MCB.26.4.1538-1548.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Overexpression of PKD1 Causes Polycystic Kidney Disease
Caroline Thivierge,
Almira Kurbegovic,
Martin Couillard,
Richard Guillaume,
Olivier Coté, and
Marie Trudel*
Institut de Recherches Cliniques de Montreal, Molecular Genetics and Development, Faculte de Medecine de l'Universite de Montreal, Montreal, Quebec, Canada
Received 7 October 2005/
Returned for modification 3 November 2005/
Accepted 4 December 2005
The pathogenetic mechanisms underlying autosomal dominant polycystic kidney disease (ADPKD) remain to be elucidated. While there is evidence that Pkd1 gene haploinsufficiency and loss of heterozygosity can cause cyst
formation in mice, paradoxically high levels of Pkd1 expression have
been detected in the kidneys of ADPKD patients. To determine whether
Pkd1 gain of function can be a pathogenetic process, a Pkd1 bacterial
artificial chromosome (Pkd1-BAC) was modified by homologous
recombination to solely target a sustained Pkd1 expression
preferentially to the adult kidney. Several transgenic lines were
generated that specifically overexpressed the Pkd1 transgene in the
kidneys 2- to 15-fold over Pkd1 endogenous levels. All transgenic mice
reproducibly developed tubular and glomerular cysts and renal
insufficiency and died of renal failure. This model demonstrates that
overexpression of wild-type Pkd1 alone is sufficient to trigger
cystogenesis resembling human ADPKD. Our results also uncovered a
striking increased renal c-myc expression in mice from all
transgenic lines, indicating that c-myc is a critical in vivo
downstream effector of Pkd1 molecular pathways. This study not only
produced an invaluable and first PKD model to evaluate molecular
pathogenesis and therapies but also provides evidence that gain of
function could be a pathogenetic mechanism in
ADPKD.
* Corresponding author. Mailing address: Molecular Genetics and Development, IRCM, 110 ave. des Pins ouest, Montreal, Quebec, Canada H2W 1R7. Phone: (514) 987-5712. Fax: (514) 987-5585. E-mail:
trudelm{at}ircm.qc.ca.
Molecular and Cellular Biology, February 2006, p. 1538-1548, Vol. 26, No. 4
0022-538X/06/$08.00+0 doi:10.1128/MCB.26.4.1538-1548.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
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