| 2008 JASN IMPACT FACTOR 7.505 | HOME AUTHOR INFO EDITORIAL BOARD SUBSCRIBE FEEDBACK ALERTS HELP | |||
| CURRENT ISSUE | ARCHIVES | JASN Express | ONLINE SUBMISSION | |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Received July 14, 2006
Accepted on January 5, 2007
BASIC SCIENCE: Genetics and Development |
McGill Cancer Centre and Biochemistry Department, McGill University, Montreal, Quebec, Canada
1 To whom correspondence should be addressed. E-mail: maxime.bouchard{at}mcgill.ca.
| Abstract |
|---|
Pax genes are important regulators of kidney development. In the mouse, homozygous Pax2 inactivation results in renal agenesis, a phenotype that has largely precluded the analysis of Pax gene function during metanephric kidney development. To address this later function, kidney development was analyzed in embryos that were compound heterozygous for Pax2 and for Pax8, a closely related member of the Pax gene family. Both genes are coexpressed in differentiating nephrons and collecting ducts. At the morphological level, Pax2+/-Pax8+/- metanephric kidneys are severely hypodysplastic and characterized by a reduction in ureter tips and nephron number in comparison with wild-type or Pax2+/- kidneys. In developing nephrons, the molecular analysis of Pax2+/-Pax8+/- kidneys reveals a strong reduction in the expression levels of Lim1, a key regulator of nephron differentiation, accompanied by an increase in apoptosis. At a more mature stage, the reduction of Pax2/8 gene dosage severely affects distal tubule formation, revealing a role for Pax genes in the differentiation of specific nephron segments. At the ureter tips, the expression of Wnt11, a target of glial cell-derived neurotrophic factor-Ret signaling, is significantly reduced, whereas the expression levels of Ret and GDNF remain normal. Together, these results demonstrate a crucial role for Pax2 and Pax8 in nephron differentiation and branching morphogenesis of the metanephros.
This article has been cited by other articles:
![]() |
E. A. Ross, M. J. Williams, T. Hamazaki, N. Terada, W. L. Clapp, C. Adin, G. W. Ellison, M. Jorgensen, and C. D. Batich Embryonic Stem Cells Proliferate and Differentiate when Seeded into Kidney Scaffolds J. Am. Soc. Nephrol., November 1, 2009; 20(11): 2338 - 2347. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Gai, G. Zhou, S. Itoh, Y. Morimoto, H. Tanishima, I. Hatamura, K. Uetani, M. Ito, and Y. Muragaki Trps1 Functions Downstream of Bmp7 in Kidney Development J. Am. Soc. Nephrol., November 1, 2009; 20(11): 2403 - 2411. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. Wu, S. Kitamura, D. M. Truong, T. Rieg, V. Vallon, H. Sakurai, K. T. Bush, D. R. Vera, R. S. Ross, and S. K. Nigam {beta}1-Integrin is required for kidney collecting duct morphogenesis and maintenance of renal function Am J Physiol Renal Physiol, July 1, 2009; 297(1): F210 - F217. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. H.T. Nguyen, M. Beland, Y. Gaitan, and M. Bouchard Calcineurin A-Binding Protein, a Novel Modulator of the Calcineurin-Nuclear Factor of Activated T-Cell Signaling Pathway, Is Overexpressed in Wilms' Tumors and Promotes Cell Migration Mol. Cancer Res., June 1, 2009; 7(6): 821 - 831. [Abstract] [Full Text] [PDF] |
||||
![]() |
H.-G. O. Mesrobian Urinary Tract Anomalies Increased in Congenital Hypothyroidism AAP Grand Rounds, April 1, 2009; 21(4): 37 - 37. [Full Text] [PDF] |
||||
![]() |
S. Hartwig, D. Bridgewater, V. Di Giovanni, J. Cain, Y. Mishina, and N. D. Rosenblum BMP Receptor ALK3 Controls Collecting System Development J. Am. Soc. Nephrol., January 1, 2008; 19(1): 117 - 124. [Abstract] [Full Text] [PDF] |
||||
|
HOME
CURRENT ISSUE
ARCHIVES
JASN Express
ONLINE SUBMISSION
AUTHOR INFO
EDITORIAL BOARD SUBSCRIBE FEEDBACK ALERTS HELP |
Copyright © 2009 by the American Society of Nephrology. Online ISSN: 1533-3450 Print ISSN: 1046-6673