Literature DB >> 9806915

Early development of the zebrafish pronephros and analysis of mutations affecting pronephric function.

I A Drummond1, A Majumdar, H Hentschel, M Elger, L Solnica-Krezel, A F Schier, S C Neuhauss, D L Stemple, F Zwartkruis, Z Rangini, W Driever, M C Fishman.   

Abstract

The zebrafish pronephric kidney provides a simplified model of nephron development and epithelial cell differentiation which is amenable to genetic analysis. The pronephros consists of two nephrons with fused glomeruli and paired pronephric tubules and ducts. Nephron formation occurs after the differentiation of the pronephric duct with both the glomeruli and tubules being derived from a nephron primordium. Fluorescent dextran injection experiments demonstrate that vascularization of the zebrafish pronephros and the onset of glomerular filtration occurs between 40 and 48 hpf. We isolated fifteen recessive mutations that affect development of the pronephros. All have visible cysts in place of the pronephric tubule at 2-2.5 days of development. Mutants were grouped in three classes: (1) a group of twelve mutants with defects in body axis curvature and manifesting the most rapid and severe cyst formation involving the glomerulus, tubule and duct, (2) the fleer mutation with distended glomerular capillary loops and cystic tubules, and (3) the mutation pao pao tang with a normal glomerulus and cysts limited to the pronephric tubules. double bubble was analyzed as a representative of mutations that perturb the entire length of the pronephros and body axis curvature. Cyst formation begins in the glomerulus at 40 hpf at the time when glomerular filtration is established suggesting a defect associated with the onset of pronephric function. Basolateral membrane protein targeting in the pronephric duct epithelial cells is also severely affected, suggesting a failure in terminal epithelial cell differentiation and alterations in electrolyte transport. These studies reveal the similarity of normal pronephric development to kidney organogenesis in all vertebrates and allow for a genetic dissection of genes needed to establish the earliest renal function.

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Year:  1998        PMID: 9806915     DOI: 10.1242/dev.125.23.4655

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  176 in total

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Journal:  J Am Soc Nephrol       Date:  2010-06-24       Impact factor: 10.121

4.  Zebrafish cytosolic carboxypeptidases 1 and 5 are essential for embryonic development.

Authors:  Peter J Lyons; Matthew R Sapio; Lloyd D Fricker
Journal:  J Biol Chem       Date:  2013-09-10       Impact factor: 5.157

5.  The lineage-specific gene ponzr1 is essential for zebrafish pronephric and pharyngeal arch development.

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Journal:  Development       Date:  2012-02       Impact factor: 6.868

6.  The zebrafish fleer gene encodes an essential regulator of cilia tubulin polyglutamylation.

Authors:  Narendra Pathak; Tomoko Obara; Steve Mangos; Yan Liu; Iain A Drummond
Journal:  Mol Biol Cell       Date:  2007-08-29       Impact factor: 4.138

7.  Developmental localization of nephrin in zebrafish and medaka pronephric glomerulus.

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Journal:  J Histochem Cytochem       Date:  2013-01-15       Impact factor: 2.479

8.  Mutations in EMP2 cause childhood-onset nephrotic syndrome.

Authors:  Heon Yung Gee; Shazia Ashraf; Xiaoyang Wan; Virginia Vega-Warner; Julian Esteve-Rudd; Svjetlana Lovric; Humphrey Fang; Toby W Hurd; Carolin E Sadowski; Susan J Allen; Edgar A Otto; Emine Korkmaz; Joseph Washburn; Shawn Levy; David S Williams; Sevcan A Bakkaloglu; Anna Zolotnitskaya; Fatih Ozaltin; Weibin Zhou; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2014-05-08       Impact factor: 11.025

9.  Organization of the pronephric filtration apparatus in zebrafish requires Nephrin, Podocin and the FERM domain protein Mosaic eyes.

Authors:  Albrecht G Kramer-Zucker; Stephanie Wiessner; Abbie M Jensen; Iain A Drummond
Journal:  Dev Biol       Date:  2005-09-15       Impact factor: 3.582

10.  Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.

Authors:  Christina Austin-Tse; Jan Halbritter; Maimoona A Zariwala; Renée M Gilberti; Heon Yung Gee; Nathan Hellman; Narendra Pathak; Yan Liu; Jennifer R Panizzi; Ramila S Patel-King; Douglas Tritschler; Raqual Bower; Eileen O'Toole; Jonathan D Porath; Toby W Hurd; Moumita Chaki; Katrina A Diaz; Stefan Kohl; Svjetlana Lovric; Daw-Yang Hwang; Daniela A Braun; Markus Schueler; Rannar Airik; Edgar A Otto; Margaret W Leigh; Peadar G Noone; Johnny L Carson; Stephanie D Davis; Jessica E Pittman; Thomas W Ferkol; Jeffry J Atkinson; Kenneth N Olivier; Scott D Sagel; Sharon D Dell; Margaret Rosenfeld; Carlos E Milla; Niki T Loges; Heymut Omran; Mary E Porter; Stephen M King; Michael R Knowles; Iain A Drummond; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2013-10-03       Impact factor: 11.025

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