CHAKI, Moumita, 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 ČERVENKA, Sri Ranjani GANJI, Vítězslav BRYJA, Heleen H. ARTS, Jeroen VAN REEUWIJK, Machteld M. OUD, Stef J.F. LETTEBOER, Ronald ROEPMAN, Hervé HUSSON, Oxana IBRAGHIMOV-BESKROVNAYA, Takayuky YSUNAGA, Gerd WALZ, Lorraine ELEY, Bernhard SCHERMER, John A. SYAER, 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 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 and Friedhelm HILDEBRANDT. Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling. Cell. United States of America: Cell Press, Cambridge, MA, USA, vol. 150, No 3, p. 533-548. ISSN 0092-8674. doi:10.1016/j.cell.2012.06.028. 2012.
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Basic information
Original name Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling
Authors CHAKI, Moumita (840 United States of America), Rannar AIRIK (840 United States of America), Amiya K. GHOSH (840 United States of America), Rachel H. GILES (840 United States of America), Rui CHEN (840 United States of America), Gisela G. SLAATS (840 United States of America), Hui WANG (840 United States of America), Toby W. HURD (840 United States of America), Weibin ZHOU (840 United States of America), Andrew CLUCKEY (840 United States of America), Heon-Yung GEE (840 United States of America), Gokul RAMASWAMI (826 United Kingdom of Great Britain and Northern Ireland), Chen-Jei HONG (840 United States of America), Bruce A. HAMILTON, (840 United States of America), Igor ČERVENKA (703 Slovakia, belonging to the institution), Sri Ranjani GANJI (356 India, belonging to the institution), Vítězslav BRYJA (203 Czech Republic, guarantor, belonging to the institution), Heleen H. ARTS (840 United States of America), Jeroen VAN REEUWIJK (840 United States of America), Machteld M. OUD (840 United States of America), Stef J.F. LETTEBOER (840 United States of America), Ronald ROEPMAN (840 United States of America), Hervé HUSSON (840 United States of America), Oxana IBRAGHIMOV-BESKROVNAYA (840 United States of America), Takayuky YSUNAGA (840 United States of America), Gerd WALZ (840 United States of America), Lorraine ELEY (840 United States of America), Bernhard SCHERMER (840 United States of America), John A. SYAER (840 United States of America), Max C. LIEBAU (840 United States of America), Thomas BENZING (840 United States of America), Stephanie LE CORRE (840 United States of America), Iain DRUMMOND (840 United States of America), Sabine JANSSEN (840 United States of America), Susan J. ALLEN (840 United States of America), Sivakumar NATARAJAN (840 United States of America), John F. O TOOLE (840 United States of America), Massimo ATTANASIO (840 United States of America), Sophie SAUNIER (840 United States of America), Corinne ANTIGNAC (840 United States of America), Robert K. KOENEKOOP (840 United States of America), Huanan REN (840 United States of America), Irma LOPEZ (840 United States of America), Ahmet NAYIR (840 United States of America), Corinne STOETZEL (826 United Kingdom of Great Britain and Northern Ireland), Helene DOLLFUS (840 United States of America), Rustin MASSOUDI (840 United States of America), Joseph G. GLEESON (840 United States of America), Sharon P. ANDREOLI (840 United States of America), Dan G. DOHERTY (840 United States of America), Anna LINDSTRAD (840 United States of America), Christelle GOLZIO (840 United States of America), Nicholas KATSANIS (840 United States of America), Lars PAPE (840 United States of America), Emad B. ABBOUD (840 United States of America), Ali A. AL-RAJHI (840 United States of America), Richard A. LEWIS (840 United States of America), Heymut OMRAN (840 United States of America), Eva LEE (840 United States of America), Shaohui WANG (840 United States of America), JoAnn M. SEKIGUCHI (840 United States of America), Rudel SAUNDERS (840 United States of America), Colin A. JOHNSON (840 United States of America), Elizabeth GARNER (840 United States of America), Katja VANSELOW (840 United States of America), Jens S. ANDERSEN (840 United States of America), Joseph SHLOMAI (840 United States of America), Gudrun NURNBERG (840 United States of America), Peter NURNBERG (840 United States of America), Shawn LEVY (840 United States of America), Agata SMOGORZEWSKA (840 United States of America), Edgar A. OTTO (840 United States of America) and Friedhelm HILDEBRANDT (840 United States of America).
Edition Cell, United States of America, Cell Press, Cambridge, MA, USA, 2012, 0092-8674.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30105 Physiology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 31.957
RIV identification code RIV/00216224:14310/12:00074681
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1016/j.cell.2012.06.028
UT WoS 000307301400013
Keywords in English NPHP; CEP 164; ZNF423; renal ciliopathies
Tags AKR, rivok
Changed by Changed by: prof. Ing. Petr Dvořák, CSc., učo 47260. Changed: 7/5/2014 08:39.
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.
Links
MSM0021622430, plan (intention)Name: Funkční a molekulární charakteristiky nádorových a normálních kmenových buněk - identifikace cílů pro nová terapeutika a terapeutické strategie
Investor: Ministry of Education, Youth and Sports of the CR, Functional and molecular characteristics of cancer and normal stem cells - identification of targets for novel therapeutics and therapeutic strategies
1658, interní kód MUName: EMBO Young Investigator Programme (Acronym: EMBO)
Investor: EMBO (European Molecular Biology Organization), EMBO Young Investigator Programme
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