Literature DB >> 20169535

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

Dai Shiba1, Danielle K Manning, Hisashi Koga, David R Beier, Takahiko Yokoyama.   

Abstract

A primary cilium is an antenna-like structure extending from the surface of most vertebrate cells. It is structurally divided along its vertical axis into sub-compartments that include the ciliary tip, the shaft, the ciliary necklace segment, the transitional zone and the basal body. We recently discovered that the shaft of the primary cilia has a distinct molecular compartment, termed the "Inv compartment", which is characterized by the accumulation of Inv at the base of primary cilia. Inv was discovered as a causative gene in inv mutant mice. It was later found to be responsible for the infantile type of nephronophthisis (NPHP2). Nephronophthisis (NPHP) is an autosomal recessive kidney disease. Nine causative genes have been identified, with all examined products thought to function in cilia, basal body and/or centrioles. However, their exact intra-ciliary localization and relationship have not been clear. Here, we report that products of Nphp3 and Nek8 (the mouse orthologs of the causative genes for NPHP3 and NPHP9, respectively) localize to the Inv compartment. We also show that Inv is essential for the compartmental localization of Nphp3 and Nek8, whereas localization of Inv does not require Nphp3 or Nek8. Nphp1 and Nphp4 also localize at the proximal region of the cilium, but not in Inv compartment. Our results indicate that Inv acts as an anchor for Nphp3 and Nek8 in the Inv compartment, and suggest that Inv compartment is a candidate site for intra-ciliary interaction of Inv, Nphp3 and Nek8. 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20169535      PMCID: PMC9134828          DOI: 10.1002/cm.20428

Source DB:  PubMed          Journal:  Cytoskeleton (Hoboken)        ISSN: 1949-3592


  29 in total

1.  Nek8, a NIMA family kinase member, is overexpressed in primary human breast tumors.

Authors:  Alex J Bowers; John F Boylan
Journal:  Gene       Date:  2004-03-17       Impact factor: 3.688

Review 2.  Primary cilia in normal and pathological tissues.

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3.  Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia.

Authors:  Manfred Fliegauf; Judit Horvath; Christian von Schnakenburg; Heike Olbrich; Dominik Müller; Julia Thumfart; Bernhard Schermer; Gregory J Pazour; Hartmut P H Neumann; Hanswalter Zentgraf; Thomas Benzing; Heymut Omran
Journal:  J Am Soc Nephrol       Date:  2006-08-02       Impact factor: 10.121

4.  Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents.

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Journal:  Nature       Date:  2000 Dec 21-28       Impact factor: 49.962

5.  The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin.

Authors:  Géraldine Mollet; Rémi Salomon; Olivier Gribouval; Flora Silbermann; Delphine Bacq; Gilbert Landthaler; David Milford; Ahmet Nayir; Gianfranco Rizzoni; Corinne Antignac; Sophie Saunier
Journal:  Nat Genet       Date:  2002-09-09       Impact factor: 38.330

6.  Localization of Inv in a distinctive intraciliary compartment requires the C-terminal ninein-homolog-containing region.

Authors:  Dai Shiba; Yoshihisa Yamaoka; Haruo Hagiwara; Tetsuro Takamatsu; Hiroshi Hamada; Takahiko Yokoyama
Journal:  J Cell Sci       Date:  2008-12-02       Impact factor: 5.285

7.  Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells.

Authors:  Surya M Nauli; Francis J Alenghat; Ying Luo; Eric Williams; Peter Vassilev; Xiaogang Li; Andrew E H Elia; Weining Lu; Edward M Brown; Stephen J Quinn; Donald E Ingber; Jing Zhou
Journal:  Nat Genet       Date:  2003-01-06       Impact factor: 38.330

8.  The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.

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Journal:  Nat Genet       Date:  2007-06-10       Impact factor: 38.330

9.  Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia.

Authors:  Carsten Bergmann; Manfred Fliegauf; Nadina Ortiz Brüchle; Valeska Frank; Heike Olbrich; Jan Kirschner; Bernhard Schermer; Ingolf Schmedding; Andreas Kispert; Bettina Kränzlin; Gudrun Nürnberg; Christian Becker; Tiemo Grimm; Gundula Girschick; Sally A Lynch; Peter Kelehan; Jan Senderek; Thomas J Neuhaus; Thomas Stallmach; Hanswalter Zentgraf; Peter Nürnberg; Norbert Gretz; Cecilia Lo; Soeren Lienkamp; Tobias Schäfer; Gerd Walz; Thomas Benzing; Klaus Zerres; Heymut Omran
Journal:  Am J Hum Genet       Date:  2008-03-27       Impact factor: 11.025

10.  NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis.

Authors:  Edgar A Otto; Melissa L Trapp; Ulla T Schultheiss; Juliana Helou; Lynne M Quarmby; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2008-01-16       Impact factor: 10.121

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  49 in total

Review 1.  Ciliary diffusion barrier: the gatekeeper for the primary cilium compartment.

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

Review 2.  The ciliary transition zone: from morphology and molecules to medicine.

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

Review 3.  The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization.

Authors:  Jeremy F Reiter; Oliver E Blacque; Michel R Leroux
Journal:  EMBO Rep       Date:  2012-06-29       Impact factor: 8.807

Review 4.  Mechanisms of nephronophthisis and related ciliopathies.

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

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

Review 6.  Cilia and coordination of signaling networks during heart development.

Authors:  Karen Koefoed; Iben Rønn Veland; Lotte Bang Pedersen; Lars Allan Larsen; Søren Tvorup Christensen
Journal:  Organogenesis       Date:  2013-12-17       Impact factor: 2.500

Review 7.  Senior-Løken syndrome: a syndromic form of retinal dystrophy associated with nephronophthisis.

Authors:  C C Ronquillo; P S Bernstein; W Baehr
Journal:  Vision Res       Date:  2012-07-20       Impact factor: 1.886

Review 8.  Compartments within a compartment: what C. elegans can tell us about ciliary subdomain composition, biogenesis, function, and disease.

Authors:  Oliver E Blacque; Anna A W M Sanders
Journal:  Organogenesis       Date:  2014-04-14       Impact factor: 2.500

9.  Novel Biochemical and Structural Insights into the Interaction of Myristoylated Cargo with Unc119 Protein and Their Release by Arl2/3.

Authors:  Mamta Jaiswal; Eyad K Fansa; Stefanie K Kösling; Tom Mejuch; Herbert Waldmann; Alfred Wittinghofer
Journal:  J Biol Chem       Date:  2016-08-01       Impact factor: 5.157

10.  Conserved Ankyrin Repeat Proteins and Their NIMA Kinase Partners Regulate Extracellular Matrix Remodeling and Intracellular Trafficking in Caenorhabditis elegans.

Authors:  Vladimir Lažetić; David S Fay
Journal:  Genetics       Date:  2016-10-31       Impact factor: 4.562

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