2. Academic Validation
  3. Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling

Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling

  • Cell. 2012 Aug 3;150(3):533-48. doi: 10.1016/j.cell.2012.06.028.
Moumita Chaki 1,  Rannar Airik,  Amiya K Ghosh,  Rachel H Giles,  Rui Chen,  Gisela G Slaats,  Hui Wang,  Toby W Hurd,  Weibin Zhou,  Andrew Cluckey,  Heon Yung Gee,  Gokul Ramaswami,  Chen-Jei Hong,  Bruce A Hamilton,  Igor Cervenka,  Ranjani Sri Ganji,  Vitezslav Bryja,  Heleen H Arts,  Jeroen van Reeuwijk,  Machteld M Oud,  Stef J F Letteboer,  Ronald Roepman,  Hervé Husson,  Oxana Ibraghimov-Beskrovnaya,  Takayuki Yasunaga,  Gerd Walz,  Lorraine Eley,  John A Sayer,  Bernhard Schermer,  Max C Liebau,  Thomas Benzing,  Stephanie Le Corre,  Iain Drummond,  Sabine Janssen,  Susan J Allen,  Sivakumar Natarajan,  John F O'Toole,  Massimo Attanasio,  Sophie Saunier,  Corinne Antignac,  Robert K Koenekoop,  Huanan Ren,  Irma Lopez,  Ahmet Nayir,  Corinne Stoetzel,  Helene Dollfus,  Rustin Massoudi,  Joseph G Gleeson,  Sharon P Andreoli,  Dan G Doherty,  Anna Lindstrad,  Christelle Golzio,  Nicholas Katsanis,  Lars Pape,  Emad B Abboud,  Ali A Al-Rajhi,  Richard A Lewis,  Heymut Omran,  Eva Y-H P Lee,  Shaohui Wang,  Joann M Sekiguchi,  Rudel Saunders,  Colin A Johnson,  Elizabeth Garner,  Katja Vanselow,  Jens S Andersen,  Joseph Shlomai,  Gudrun Nurnberg,  Peter Nurnberg,  Shawn Levy,  Agata Smogorzewska,  Edgar A Otto,  Friedhelm Hildebrandt
Affiliations

Affiliation

  • 1 Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, MI 48109, USA.
PMID: 22863007 DOI: 10.1016/j.cell.2012.06.028
Abstract

Nephronophthisis-related ciliopathies (NPHP-RC) are degenerative recessive diseases that affect kidney, retina, and brain. Genetic defects in NPHP gene products that localize to cilia and centrosomes defined them as "ciliopathies." However, disease mechanisms remain poorly understood. Here, we identify by whole-exome resequencing, mutations of MRE11, ZNF423, and CEP164 as causing NPHP-RC. All three genes function within the DNA damage response (DDR) pathway. We demonstrate that, upon induced DNA damage, the NPHP-RC proteins ZNF423, CEP164, and NPHP10 colocalize to nuclear foci positive for TIP60, known to activate ATM at sites of DNA damage. We show that knockdown of CEP164 or ZNF423 causes sensitivity to DNA damaging agents and that cep164 knockdown in zebrafish results in dysregulated DDR and an NPHP-RC phenotype. Our findings link degenerative diseases of the kidney and retina, disorders of increasing prevalence, to mechanisms of DDR.

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