Literature DB >> 21071979

Mechanisms of nephronophthisis and related ciliopathies.

Toby W Hurd1, Friedhelm Hildebrandt.   

Abstract

An emerging group of human genetic diseases termed 'ciliopathies' are caused by dysfunction of two functionally and physically associated organelles, the centrosome and cilium. These organelles are central to perception of the physical environment through detection of a diverse variety of extracellular signals such as growth factors, chemicals, light and fluid flow. Many of the described ciliopathies display multi-organ involvement, with renal and retina being the most commonly affected. Nephronophthisis is a recessive disorder of the kidney that is the leading cause of end-stage renal failure in children. Through positional cloning, many of the causative mutations have been mapped to genes involved in centrosome and cilia function. In this review, we discuss the identified causative mutations that give rise to nephronophthisis and how these are related to the disease etiology in both the kidney and other organs.
Copyright © 2010 S. Karger AG, Basel.

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Year:  2010        PMID: 21071979      PMCID: PMC2992643          DOI: 10.1159/000320888

Source DB:  PubMed          Journal:  Nephron Exp Nephrol        ISSN: 1660-2129


  35 in total

1.  Crk-associated substrate p130(Cas) interacts with nephrocystin and both proteins localize to cell-cell contacts of polarized epithelial cells.

Authors:  J C Donaldson; P J Dempsey; S Reddy; A H Bouton; R J Coffey; S K Hanks
Journal:  Exp Cell Res       Date:  2000-04-10       Impact factor: 3.905

2.  Nephrocystin-conserved domains involved in targeting to epithelial cell-cell junctions, interaction with filamins, and establishing cell polarity.

Authors:  John C Donaldson; Rebecca S Dise; Marylyn D Ritchie; Steven K Hanks
Journal:  J Biol Chem       Date:  2002-05-10       Impact factor: 5.157

3.  Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy.

Authors:  John F O'Toole; Yangjian Liu; Erica E Davis; Christopher J Westlake; Massimo Attanasio; Edgar A Otto; Dominik Seelow; Gudrun Nurnberg; Christian Becker; Matti Nuutinen; Mikko Kärppä; Jaakko Ignatius; Johanna Uusimaa; Salla Pakanen; Elisa Jaakkola; Lambertus P van den Heuvel; Henry Fehrenbach; Roger Wiggins; Meera Goyal; Weibin Zhou; Matthias T F Wolf; Eric Wise; Juliana Helou; Susan J Allen; Carlos A Murga-Zamalloa; Shazia Ashraf; Moumita Chaki; Saskia Heeringa; Gil Chernin; Bethan E Hoskins; Hassan Chaib; Joseph Gleeson; Takehiro Kusakabe; Takako Suzuki; R Elwyn Isaac; Lynne M Quarmby; Bryan Tennant; Hisashi Fujioka; Hannu Tuominen; Ilmo Hassinen; Hellevi Lohi; Judith L van Houten; Agnes Rotig; John A Sayer; Boris Rolinski; Peter Freisinger; Sethu M Madhavan; Martina Herzer; Florence Madignier; Holger Prokisch; Peter Nurnberg; Peter K Jackson; Peter Jackson; Hemant Khanna; Nicholas Katsanis; Friedhelm Hildebrandt
Journal:  J Clin Invest       Date:  2010-02-22       Impact factor: 14.808

4.  Mutations of NPHP2 and NPHP3 in infantile nephronophthisis.

Authors:  Kálmán Tory; Caroline Rousset-Rouvière; Marie-Claire Gubler; Vincent Morinière; Audrey Pawtowski; Céline Becker; Claude Guyot; Sophie Gié; Yaacov Frishberg; Hubert Nivet; Georges Deschênes; Pierre Cochat; Marie-France Gagnadoux; Sophie Saunier; Corinne Antignac; Rémi Salomon
Journal:  Kidney Int       Date:  2009-01-28       Impact factor: 10.612

5.  A mitotic transcriptional switch in polycystic kidney disease.

Authors:  Francisco Verdeguer; Stephanie Le Corre; Evelyne Fischer; Celine Callens; Serge Garbay; Antonia Doyen; Peter Igarashi; Fabiola Terzi; Marco Pontoglio
Journal:  Nat Med       Date:  2009-12-06       Impact factor: 53.440

6.  Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy.

Authors:  Edgar A Otto; Toby W Hurd; Rannar Airik; Moumita Chaki; Weibin Zhou; Corinne Stoetzel; Suresh B Patil; Shawn Levy; Amiya K Ghosh; Carlos A Murga-Zamalloa; Jeroen van Reeuwijk; Stef J F Letteboer; Liyun Sang; Rachel H Giles; Qin Liu; Karlien L M Coene; Alejandro Estrada-Cuzcano; Rob W J Collin; Heather M McLaughlin; Susanne Held; Jennifer M Kasanuki; Gokul Ramaswami; Jinny Conte; Irma Lopez; Joseph Washburn; James Macdonald; Jinghua Hu; Yukiko Yamashita; Eamonn R Maher; Lisa M Guay-Woodford; Hartmut P H Neumann; Nicholas Obermüller; Robert K Koenekoop; Carsten Bergmann; Xiaoshu Bei; Richard A Lewis; Nicholas Katsanis; Vanda Lopes; David S Williams; Robert H Lyons; Chi V Dang; Daniela A Brito; Mónica Bettencourt Dias; Xinmin Zhang; James D Cavalcoli; Gudrun Nürnberg; Peter Nürnberg; Eric A Pierce; Peter K Jackson; Corinne Antignac; Sophie Saunier; Ronald Roepman; Helene Dollfus; Hemant Khanna; Friedhelm Hildebrandt
Journal:  Nat Genet       Date:  2010-09-12       Impact factor: 38.330

7.  Cyclic nucleotide signaling in polycystic kidney disease.

Authors:  Xiaofang Wang; Christopher J Ward; Peter C Harris; Vicente E Torres
Journal:  Kidney Int       Date:  2009-11-18       Impact factor: 10.612

8.  Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia.

Authors:  Dai Shiba; Danielle K Manning; Hisashi Koga; David R Beier; Takahiko Yokoyama
Journal:  Cytoskeleton (Hoboken)       Date:  2010-02

9.  Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella.

Authors:  G J Pazour; B L Dickert; Y Vucica; E S Seeley; J L Rosenbaum; G B Witman; D G Cole
Journal:  J Cell Biol       Date:  2000-10-30       Impact factor: 10.539

10.  Nephrocystin-1 and nephrocystin-4 are required for epithelial morphogenesis and associate with PALS1/PATJ and Par6.

Authors:  Marion Delous; Nathan E Hellman; Helori-Maël Gaudé; Flora Silbermann; André Le Bivic; Rémi Salomon; Corinne Antignac; Sophie Saunier
Journal:  Hum Mol Genet       Date:  2009-09-14       Impact factor: 6.150

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  38 in total

1.  Nephronophthisis 13: implications of its association with Caroli disease and altered intracellular localization of WDR19 in the kidney.

Authors:  Jiwon M Lee; Yo Han Ahn; Hee Gyung Kang; I I Soo Ha; Kyoungbun Lee; Kyung Chul Moon; Joo Hoon Lee; Young Seo Park; Yong Mee Cho; Jun-Seok Bae; Nayoung K D Kim; Woong-Yang Park; Hae I I Cheong
Journal:  Pediatr Nephrol       Date:  2015-03-01       Impact factor: 3.714

2.  Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19.

Authors:  Cecilie Bredrup; Sophie Saunier; Machteld M Oud; Torunn Fiskerstrand; Alexander Hoischen; Damien Brackman; Sabine M Leh; Marit Midtbø; Emilie Filhol; Christine Bole-Feysot; Patrick Nitschké; Christian Gilissen; Olav H Haugen; Jan-Stephan F Sanders; Irene Stolte-Dijkstra; Dorus A Mans; Eric J Steenbergen; Ben C J Hamel; Marie Matignon; Rolph Pfundt; Cécile Jeanpierre; Helge Boman; Eyvind Rødahl; Joris A Veltman; Per M Knappskog; Nine V A M Knoers; Ronald Roepman; Heleen H Arts
Journal:  Am J Hum Genet       Date:  2011-10-20       Impact factor: 11.025

3.  Juvenile nephronophthisis and dysthyroidism: a rare association.

Authors:  Fateme Shamekhi Amiri; Ariana Kariminejad
Journal:  CEN Case Rep       Date:  2017-03-13

Review 4.  Nephronophthisis and related syndromes.

Authors:  Matthias T F Wolf
Journal:  Curr Opin Pediatr       Date:  2015-04       Impact factor: 2.856

Review 5.  Cell polarity and cystic kidney disease.

Authors:  Sorin Fedeles; Anna Rachel Gallagher
Journal:  Pediatr Nephrol       Date:  2012-11-16       Impact factor: 3.714

6.  Primary cilia and the exocyst are linked to urinary extracellular vesicle production and content.

Authors:  Xiaofeng Zuo; Sang-Ho Kwon; Michael G Janech; Yujing Dang; Steven D Lauzon; Ben Fogelgren; Noemi Polgar; Joshua H Lipschutz
Journal:  J Biol Chem       Date:  2019-11-06       Impact factor: 5.157

7.  Gene mutation analysis in Iranian children with nephronophthisis: a two-center study.

Authors:  Alaleh Gheissari; Maryam Harandavar; Friedhelm Hildebrandt; Daniela A Braun; Maryam Sedghi; Nastaran Parsi; Alireza Merrikhi; Yahya Madihi; Farzaneh Aghamohammadi
Journal:  Iran J Kidney Dis       Date:  2015-03       Impact factor: 0.892

8.  Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD.

Authors:  Ekim Z Taskiran; Emine Korkmaz; Safak Gucer; Can Kosukcu; Figen Kaymaz; Cansu Koyunlar; Elizabeth C Bryda; Moumita Chaki; Dongmei Lu; Komal Vadnagara; Cengiz Candan; Rezan Topaloglu; Franz Schaefer; Massimo Attanasio; Carsten Bergmann; Fatih Ozaltin
Journal:  J Am Soc Nephrol       Date:  2014-03-07       Impact factor: 10.121

9.  Disruption of a ciliary B9 protein complex causes Meckel syndrome.

Authors:  William E Dowdle; Jon F Robinson; Andreas Kneist; M Salomé Sirerol-Piquer; Suzanna G M Frints; Kevin C Corbit; Norann A Zaghloul; Norran A Zaghloul; Gesina van Lijnschoten; Leon Mulders; Dideke E Verver; Klaus Zerres; Randall R Reed; Tania Attié-Bitach; Colin A Johnson; José Manuel García-Verdugo; Nicholas Katsanis; Carsten Bergmann; Jeremy F Reiter
Journal:  Am J Hum Genet       Date:  2011-07-15       Impact factor: 11.025

10.  SDCCAG8 regulates pericentriolar material recruitment and neuronal migration in the developing cortex.

Authors:  Ryan Insolera; Wei Shao; Rannar Airik; Friedhelm Hildebrandt; Song-Hai Shi
Journal:  Neuron       Date:  2014-07-31       Impact factor: 17.173

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