Literature DB >> 22387013

Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFB.

Andreas Zankl1, Emma L Duncan, Paul J Leo, Graeme R Clark, Evgeny A Glazov, Marie-Claude Addor, Troels Herlin, Chong Ae Kim, Bruno P Leheup, Jim McGill, Steven McTaggart, Stephan Mittas, Anna L Mitchell, Geert R Mortier, Stephen P Robertson, Marie Schroeder, Paulien Terhal, Matthew A Brown.   

Abstract

Multicentric carpotarsal osteolysis (MCTO) is a rare skeletal dysplasia characterized by aggressive osteolysis, particularly affecting the carpal and tarsal bones, and is frequently associated with progressive renal failure. Using exome capture and next-generation sequencing in five unrelated simplex cases of MCTO, we identified previously unreported missense mutations clustering within a 51 base pair region of the single exon of MAFB, validated by Sanger sequencing. A further six unrelated simplex cases with MCTO were also heterozygous for previously unreported mutations within this same region, as were affected members of two families with autosomal-dominant MCTO. MAFB encodes a transcription factor that negatively regulates RANKL-induced osteoclastogenesis and is essential for normal renal development. Identification of this gene paves the way for development of novel therapeutic approaches for this crippling disease and provides insight into normal bone and kidney development. Copyright Â
© 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22387013      PMCID: PMC3309183          DOI: 10.1016/j.ajhg.2012.01.003

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  39 in total

1.  MafB is an inducer of monocytic differentiation.

Authors:  L M Kelly; U Englmeier; I Lafon; M H Sieweke; T Graf
Journal:  EMBO J       Date:  2000-05-02       Impact factor: 11.598

2.  The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.

Authors:  Aaron McKenna; Matthew Hanna; Eric Banks; Andrey Sivachenko; Kristian Cibulskis; Andrew Kernytsky; Kiran Garimella; David Altshuler; Stacey Gabriel; Mark Daly; Mark A DePristo
Journal:  Genome Res       Date:  2010-07-19       Impact factor: 9.043

3.  A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.

Authors:  Terri H Beaty; Jeffrey C Murray; Mary L Marazita; Ronald G Munger; Ingo Ruczinski; Jacqueline B Hetmanski; Kung Yee Liang; Tao Wu; Tanda Murray; M Daniele Fallin; Richard A Redett; Gerald Raymond; Holger Schwender; Sheng-Chih Jin; Margaret E Cooper; Martine Dunnwald; Maria A Mansilla; Elizabeth Leslie; Stephen Bullard; Andrew C Lidral; Lina M Moreno; Renato Menezes; Alexandre R Vieira; Aline Petrin; Allen J Wilcox; Rolv T Lie; Ethylin W Jabs; Yah Huei Wu-Chou; Philip K Chen; Hong Wang; Xiaoqian Ye; Shangzhi Huang; Vincent Yeow; Samuel S Chong; Sun Ha Jee; Bing Shi; Kaare Christensen; Mads Melbye; Kimberly F Doheny; Elizabeth W Pugh; Hua Ling; Eduardo E Castilla; Andrew E Czeizel; Lian Ma; L Leigh Field; Lawrence Brody; Faith Pangilinan; James L Mills; Anne M Molloy; Peadar N Kirke; John M Scott; James M Scott; Mauricio Arcos-Burgos; Alan F Scott
Journal:  Nat Genet       Date:  2010-05-02       Impact factor: 38.330

4.  Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss.

Authors:  Michael A Simpson; Melita D Irving; Esra Asilmaz; Mary J Gray; Dimitra Dafou; Frances V Elmslie; Sahar Mansour; Sue E Holder; Caroline E Brain; Barbara K Burton; Katherine H Kim; Richard M Pauli; Salim Aftimos; Helen Stewart; Chong Ae Kim; Muriel Holder-Espinasse; Stephen P Robertson; William M Drake; Richard C Trembath
Journal:  Nat Genet       Date:  2011-03-06       Impact factor: 38.330

5.  ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.

Authors:  Kai Wang; Mingyao Li; Hakon Hakonarson
Journal:  Nucleic Acids Res       Date:  2010-07-03       Impact factor: 16.971

6.  C/EBPbetaDeltauORF mice--a genetic model for uORF-mediated translational control in mammals.

Authors:  Klaus Wethmar; Valérie Bégay; Jeske J Smink; Katrin Zaragoza; Volker Wiesenthal; Bernd Dörken; Cornelis F Calkhoven; Achim Leutz
Journal:  Genes Dev       Date:  2010-01-01       Impact factor: 11.361

7.  Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia.

Authors:  Evgeny A Glazov; Andreas Zankl; Marina Donskoi; Tony J Kenna; Gethin P Thomas; Graeme R Clark; Emma L Duncan; Matthew A Brown
Journal:  PLoS Genet       Date:  2011-03-24       Impact factor: 5.917

8.  Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.

Authors:  Emma L Duncan; Patrick Danoy; John P Kemp; Paul J Leo; Eugene McCloskey; Geoffrey C Nicholson; Richard Eastell; Richard L Prince; John A Eisman; Graeme Jones; Philip N Sambrook; Ian R Reid; Elaine M Dennison; John Wark; J Brent Richards; Andre G Uitterlinden; Tim D Spector; Chris Esapa; Roger D Cox; Steve D M Brown; Rajesh V Thakker; Kathryn A Addison; Linda A Bradbury; Jacqueline R Center; Cyrus Cooper; Catherine Cremin; Karol Estrada; Dieter Felsenberg; Claus-C Glüer; Johanna Hadler; Margaret J Henry; Albert Hofman; Mark A Kotowicz; Joanna Makovey; Sing C Nguyen; Tuan V Nguyen; Julie A Pasco; Karena Pryce; David M Reid; Fernando Rivadeneira; Christian Roux; Kari Stefansson; Unnur Styrkarsdottir; Gudmar Thorleifsson; Rumbidzai Tichawangana; David M Evans; Matthew A Brown
Journal:  PLoS Genet       Date:  2011-04-21       Impact factor: 5.917

9.  Targeted capture and massively parallel sequencing of 12 human exomes.

Authors:  Sarah B Ng; Emily H Turner; Peggy D Robertson; Steven D Flygare; Abigail W Bigham; Choli Lee; Tristan Shaffer; Michelle Wong; Arindam Bhattacharjee; Evan E Eichler; Michael Bamshad; Deborah A Nickerson; Jay Shendure
Journal:  Nature       Date:  2009-08-16       Impact factor: 49.962

10.  Exome sequencing identifies the cause of a mendelian disorder.

Authors:  Sarah B Ng; Kati J Buckingham; Choli Lee; Abigail W Bigham; Holly K Tabor; Karin M Dent; Chad D Huff; Paul T Shannon; Ethylin Wang Jabs; Deborah A Nickerson; Jay Shendure; Michael J Bamshad
Journal:  Nat Genet       Date:  2009-11-13       Impact factor: 38.330

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  35 in total

Review 1.  Genetics of cleft lip and cleft palate.

Authors:  Elizabeth J Leslie; Mary L Marazita
Journal:  Am J Med Genet C Semin Med Genet       Date:  2013-10-04       Impact factor: 3.908

2.  A Familial Case of Multicentric Carpotarsal Osteolysis Syndrome and Treatment Outcome.

Authors:  Jariya Upadia; Alicia Gomes; Peter Weiser; Maria Descartes
Journal:  J Pediatr Genet       Date:  2018-06-16

3.  Multicentric carpotarsal osteolysis syndrome is caused by only a few domain-specific mutations in MAFB, a negative regulator of RANKL-induced osteoclastogenesis.

Authors:  Steven Mumm; Margaret Huskey; Shenghui Duan; Deborah Wenkert; Katherine L Madson; Gary S Gottesman; Angela R Nenninger; Ronald M Laxer; William H McAlister; Michael P Whyte
Journal:  Am J Med Genet A       Date:  2014-07-02       Impact factor: 2.802

4.  Total Hip Arthroplasty in a Patient with Multicentric Carpotarsal Osteolysis: a Case Report.

Authors:  Kai Sun; Brian Barlow; Fardina Malik; Allan Inglis; Mark Figgie; Susan Goodman
Journal:  HSS J       Date:  2016-01-22

Review 5.  Exome sequencing greatly expedites the progressive research of Mendelian diseases.

Authors:  Xuejun Zhang
Journal:  Front Med       Date:  2014-01-03       Impact factor: 4.592

Review 6.  Next-generation sequencing: a frameshift in skeletal dysplasia gene discovery.

Authors:  S Lazarus; A Zankl; E L Duncan
Journal:  Osteoporos Int       Date:  2013-08-01       Impact factor: 4.507

7.  Integration of Cistromic and Transcriptomic Analyses Identifies Nphs2, Mafb, and Magi2 as Wilms' Tumor 1 Target Genes in Podocyte Differentiation and Maintenance.

Authors:  Lihua Dong; Stefan Pietsch; Zenglai Tan; Birgit Perner; Ralph Sierig; Dagmar Kruspe; Marco Groth; Ralph Witzgall; Hermann-Josef Gröne; Matthias Platzer; Christoph Englert
Journal:  J Am Soc Nephrol       Date:  2015-01-02       Impact factor: 10.121

8.  Multicentric carpotarsal osteolysis syndrome: long-term follow-up of three patients.

Authors:  Céline Klein; Jonathan Bellity; Georges Finidori; Christophe Glorion; Stéphanie Pannier
Journal:  Skeletal Radiol       Date:  2018-02-03       Impact factor: 2.199

9.  Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects.

Authors:  Jong G Park; Max A Tischfield; Alicia A Nugent; Long Cheng; Silvio Alessandro Di Gioia; Wai-Man Chan; Gail Maconachie; Thomas M Bosley; C Gail Summers; David G Hunter; Caroline D Robson; Irene Gottlob; Elizabeth C Engle
Journal:  Am J Hum Genet       Date:  2016-05-12       Impact factor: 11.025

Review 10.  Osteopetrosis: genetics, treatment and new insights into osteoclast function.

Authors:  Cristina Sobacchi; Ansgar Schulz; Fraser P Coxon; Anna Villa; Miep H Helfrich
Journal:  Nat Rev Endocrinol       Date:  2013-07-23       Impact factor: 43.330

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