Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities - PubMed (original) (raw)
. 1993 Mar 4;362(6415):65-7.
doi: 10.1038/362065a0.
Affiliations
- PMID: 8383297
- DOI: 10.1038/362065a0
Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities
G R Dressler et al. Nature. 1993.
Abstract
The Pax genes comprise a family of transcription factors active in specific tissues during embryonic development and are associated with at least three developmental mutations in mouse and man. In the developing kidney, Pax-2 is expressed in the induced mesenchyme, in the ureter epithelium, and in early epithelial structures derived from the mesenchyme. Pax-2 expression is repressed upon terminal differentiation of the renal tubule epithelium, but persists in the undifferentiated epithelium of human Wilms' tumours. We have produced a dominant gain-of-function mutation in transgenic mice by deregulating the expression of the mouse Pax-2 gene. The data obtained with four independently derived transgenic embryos and with one transgenic line demonstrate that deregulated Pax-2 expression results in histologically abnormal and dysfunctional renal epithelium with properties similar to congenital nephrotic syndrome. Thus, repression of Pax-2 is required for normal kidney development and persistent expression of Pax-2 may restrict the differentiation potential of renal epithelial cells.
Similar articles
- Aberrant expression of Pax-2 in Danforth's short tail (Sd) mice.
Phelps DE, Dressler GR. Phelps DE, et al. Dev Biol. 1993 May;157(1):251-8. doi: 10.1006/dbio.1993.1129. Dev Biol. 1993. PMID: 8482415 - Characterization of Pax-2 regulatory sequences that direct transgene expression in the Wolffian duct and its derivatives.
Kuschert S, Rowitch DH, Haenig B, McMahon AP, Kispert A. Kuschert S, et al. Dev Biol. 2001 Jan 1;229(1):128-40. doi: 10.1006/dbio.2000.9971. Dev Biol. 2001. PMID: 11133159 - Pax-2, kidney development, and oncogenesis.
Dressler GR. Dressler GR. Med Pediatr Oncol. 1996 Nov;27(5):440-4. doi: 10.1002/(SICI)1096-911X(199611)27:5<440::AID-MPO9>3.0.CO;2-M. Med Pediatr Oncol. 1996. PMID: 8827071 Review. - Pax2 in development and renal disease.
Dressler GR, Woolf AS. Dressler GR, et al. Int J Dev Biol. 1999;43(5):463-8. Int J Dev Biol. 1999. PMID: 10535325 Review. - The paired-box transcription factor, PAX2, positively modulates expression of the Wilms' tumor suppressor gene (WT1).
Dehbi M, Ghahremani M, Lechner M, Dressler G, Pelletier J. Dehbi M, et al. Oncogene. 1996 Aug 1;13(3):447-53. Oncogene. 1996. PMID: 8760285
Cited by
- Placenta defects and embryonic lethality resulting from disruption of mouse hydroxysteroid (17-beta) dehydrogenase 2 gene.
Rantakari P, Strauss L, Kiviranta R, Lagerbohm H, Paviala J, Holopainen I, Vainio S, Pakarinen P, Poutanen M. Rantakari P, et al. Mol Endocrinol. 2008 Mar;22(3):665-75. doi: 10.1210/me.2007-0257. Epub 2007 Nov 29. Mol Endocrinol. 2008. PMID: 18048640 Free PMC article. - We, the developing rete testis, efferent ducts, and Wolffian duct, all hereby agree that we need to connect.
de Mello Santos T, Hinton BT. de Mello Santos T, et al. Andrology. 2019 Sep;7(5):581-587. doi: 10.1111/andr.12631. Epub 2019 Apr 29. Andrology. 2019. PMID: 31033257 Free PMC article. - Patterning and early cell lineage decisions in the developing kidney: the role of Pax genes.
Dressler GR. Dressler GR. Pediatr Nephrol. 2011 Sep;26(9):1387-94. doi: 10.1007/s00467-010-1749-x. Epub 2011 Jan 11. Pediatr Nephrol. 2011. PMID: 21221999 Free PMC article. Review. - Lineage-specific responses to reduced embryonic Pax3 expression levels.
Zhou HM, Wang J, Rogers R, Conway SJ. Zhou HM, et al. Dev Biol. 2008 Mar 15;315(2):369-82. doi: 10.1016/j.ydbio.2007.12.020. Epub 2007 Dec 27. Dev Biol. 2008. PMID: 18243171 Free PMC article. - The role of Pax2 in mouse prostate development.
Xu B, Hariharan A, Rakshit S, Dressler GR, Wellik DM. Xu B, et al. Prostate. 2012 Feb 1;72(2):217-24. doi: 10.1002/pros.21424. Epub 2011 May 18. Prostate. 2012. PMID: 21594883 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases