Literature DB >> 15661758

Characterization of the nephrocystin/nephrocystin-4 complex and subcellular localization of nephrocystin-4 to primary cilia and centrosomes.

Géraldine Mollet1, Flora Silbermann, Marion Delous, Rémi Salomon, Corinne Antignac, Sophie Saunier.   

Abstract

Nephrocystin and nephrocystin-4 are newly identified proteins involved in familial juvenile nephronophthisis, an autosomal recessive nephropathy characterized by cyst formation and renal fibrosis. Nephrocystin is an adaptor protein that is able to associate with signaling molecules involved in cell adhesion and actin cytoskeleton organization, such as p130Cas, Pyk2, tensin and filamins. Nephrocystin was recently shown to interact and to co-localize with the microtubule component beta-tubulin to the primary cilia in renal epithelial cells, an organelle known to play a key role in the pathogenesis of cystic kidney diseases. In this study, we demonstrated that nephrocystin-4 also localizes to the primary cilia in polarized epithelial tubular cells, particularly at the basal bodies, and associates with microtubule component alpha-tubulin, suggesting a common role for the nephrocystin proteins in ciliary function. However, the co-localization of nephrocystin-4 with the microtubules is not restricted to the primary cilia, as nephrocystin-4 was also detected at the centrosomes of dividing cells and close to the cortical actin cytoskeleton in polarized cells. We also detected p130Cas and Pyk2 in the nephrocystin-4-containing complex, confirming the role of the nephrocystin proteins in cell-cell and cell-matrix adhesion signaling events. Finally, we refined the structural and functional regions involved in the interaction between nephrocystin and nephrocystin-4. These data suggest that nephrocystin and nephrocystin-4 belong to a multifunctional complex localized in actin- and microtubule-based structures involved in cell-cell and cell-matrix adhesion signaling as well as in cell division.

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Year:  2005        PMID: 15661758     DOI: 10.1093/hmg/ddi061

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  62 in total

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Authors:  Qicong Hu; W James Nelson
Journal:  Cytoskeleton (Hoboken)       Date:  2011-06-10

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Authors:  Peter G Czarnecki; Jagesh V Shah
Journal:  Trends Cell Biol       Date:  2012-03-06       Impact factor: 20.808

Review 3.  Mechanisms of nephronophthisis and related ciliopathies.

Authors:  Toby W Hurd; Friedhelm Hildebrandt
Journal:  Nephron Exp Nephrol       Date:  2010-11-11

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Journal:  Hum Mol Genet       Date:  2010-11-15       Impact factor: 6.150

5.  NPHP4 controls ciliary trafficking of membrane proteins and large soluble proteins at the transition zone.

Authors:  Junya Awata; Saeko Takada; Clive Standley; Karl F Lechtreck; Karl D Bellvé; Gregory J Pazour; Kevin E Fogarty; George B Witman
Journal:  J Cell Sci       Date:  2014-08-22       Impact factor: 5.285

6.  Uromodulin is expressed in renal primary cilia and UMOD mutations result in decreased ciliary uromodulin expression.

Authors:  Frank Zaucke; Joana M Boehnlein; Sarah Steffens; Roman S Polishchuk; Luca Rampoldi; Andreas Fischer; Andreas Pasch; Christoph W A Boehm; Anne Baasner; Massimo Attanasio; Bernd Hoppe; Helmut Hopfer; Bodo B Beck; John A Sayer; Friedhelm Hildebrandt; Matthias T F Wolf
Journal:  Hum Mol Genet       Date:  2010-02-18       Impact factor: 6.150

Review 7.  Insights into X-linked retinitis pigmentosa type 3, allied diseases and underlying pathomechanisms.

Authors:  Paulo A Ferreira
Journal:  Hum Mol Genet       Date:  2005-10-15       Impact factor: 6.150

8.  Nephronophthisis.

Authors:  Roslyn J Simms; Lorraine Eley; John A Sayer
Journal:  Eur J Hum Genet       Date:  2008-12-10       Impact factor: 4.246

Review 9.  Sending mixed signals: Cilia-dependent signaling during development and disease.

Authors:  Kelsey H Elliott; Samantha A Brugmann
Journal:  Dev Biol       Date:  2018-03-13       Impact factor: 3.582

Review 10.  Joubert syndrome: insights into brain development, cilium biology, and complex disease.

Authors:  Dan Doherty
Journal:  Semin Pediatr Neurol       Date:  2009-09       Impact factor: 1.636

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