Literature DB >> 26092869

Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity.

R Bachmann-Gagescu1, J C Dempsey2, I G Phelps2, B J O'Roak3, D M Knutzen4, T C Rue5, G E Ishak6, C R Isabella2, N Gorden7, J Adkins8, E A Boyle9, N de Lacy10, D O'Day2, A Alswaid11, Radha Ramadevi A12, L Lingappa13, C Lourenço14, L Martorell15, À Garcia-Cazorla16, H Ozyürek17, G Haliloğlu18, B Tuysuz19, M Topçu18, P Chance2, M A Parisi20, I A Glass21, J Shendure9, D Doherty21.   

Abstract

BACKGROUND: Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterised by hypotonia, ataxia, cognitive impairment, abnormal eye movements, respiratory control disturbances and a distinctive mid-hindbrain malformation. JS demonstrates substantial phenotypic variability and genetic heterogeneity. This study provides a comprehensive view of the current genetic basis, phenotypic range and gene-phenotype associations in JS.
METHODS: We sequenced 27 JS-associated genes in 440 affected individuals (375 families) from a cohort of 532 individuals (440 families) with JS, using molecular inversion probe-based targeted capture and next-generation sequencing. Variant pathogenicity was defined using the Combined Annotation Dependent Depletion algorithm with an optimised score cut-off.
RESULTS: We identified presumed causal variants in 62% of pedigrees, including the first B9D2 mutations associated with JS. 253 different mutations in 23 genes highlight the extreme genetic heterogeneity of JS. Phenotypic analysis revealed that only 34% of individuals have a 'pure JS' phenotype. Retinal disease is present in 30% of individuals, renal disease in 25%, coloboma in 17%, polydactyly in 15%, liver fibrosis in 14% and encephalocele in 8%. Loss of CEP290 function is associated with retinal dystrophy, while loss of TMEM67 function is associated with liver fibrosis and coloboma, but we observe no clear-cut distinction between JS subtypes.
CONCLUSIONS: This work illustrates how combining advanced sequencing techniques with phenotypic data addresses extreme genetic heterogeneity to provide diagnostic and carrier testing, guide medical monitoring for progressive complications, facilitate interpretation of genome-wide sequencing results in individuals with a variety of phenotypes and enable gene-specific treatments in the future. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Joubert syndrome; ciliopathy; genetic heterogeneity; genotype-phenotype; next generation sequencing

Mesh:

Year:  2015        PMID: 26092869      PMCID: PMC5082428          DOI: 10.1136/jmedgenet-2015-103087

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  52 in total

1.  Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population.

Authors:  Myriam Srour; Jeremy Schwartzentruber; Fadi F Hamdan; Luis H Ospina; Lysanne Patry; Damian Labuda; Christine Massicotte; Sylvia Dobrzeniecka; José-Mario Capo-Chichi; Simon Papillon-Cavanagh; Mark E Samuels; Kym M Boycott; Michael I Shevell; Rachel Laframboise; Valérie Désilets; Bruno Maranda; Guy A Rouleau; Jacek Majewski; Jacques L Michaud
Journal:  Am J Hum Genet       Date:  2012-03-15       Impact factor: 11.025

2.  Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients.

Authors:  A Poretti; T A G M Huisman; I Scheer; E Boltshauser
Journal:  AJNR Am J Neuroradiol       Date:  2011-06-16       Impact factor: 3.825

3.  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

4.  Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways.

Authors:  Liyun Sang; Julie J Miller; Kevin C Corbit; Rachel H Giles; Matthew J Brauer; Edgar A Otto; Lisa M Baye; Xiaohui Wen; Suzie J Scales; Mandy Kwong; Erik G Huntzicker; Mindan K Sfakianos; Wendy Sandoval; J Fernando Bazan; Priya Kulkarni; Francesc R Garcia-Gonzalo; Allen D Seol; John F O'Toole; Susanne Held; Heiko M Reutter; William S Lane; Muhammad Arshad Rafiq; Abdul Noor; Muhammad Ansar; Akella Radha Rama Devi; Val C Sheffield; Diane C Slusarski; John B Vincent; Daniel A Doherty; Friedhelm Hildebrandt; Jeremy F Reiter; Peter K Jackson
Journal:  Cell       Date:  2011-05-13       Impact factor: 41.582

5.  Joubert syndrome: episodic hyperpnea, abnormal eye movements, retardation and ataxia, associated with dysplasia of the cerebellar vermis.

Authors:  E Boltshauser; W Isler
Journal:  Neuropadiatrie       Date:  1977-02

6.  Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes.

Authors:  Enza Maria Valente; Clare V Logan; Soumaya Mougou-Zerelli; Jeong Ho Lee; Jennifer L Silhavy; Francesco Brancati; Miriam Iannicelli; Lorena Travaglini; Sveva Romani; Barbara Illi; Matthew Adams; Katarzyna Szymanska; Annalisa Mazzotta; Ji Eun Lee; Jerlyn C Tolentino; Dominika Swistun; Carmelo D Salpietro; Carmelo Fede; Stacey Gabriel; Carsten Russ; Kristian Cibulskis; Carrie Sougnez; Friedhelm Hildebrandt; Edgar A Otto; Susanne Held; Bill H Diplas; Erica E Davis; Mario Mikula; Charles M Strom; Bruria Ben-Zeev; Dorit Lev; Tally Lerman Sagie; Marina Michelson; Yuval Yaron; Amanda Krause; Eugen Boltshauser; Nadia Elkhartoufi; Joelle Roume; Stavit Shalev; Arnold Munnich; Sophie Saunier; Chris Inglehearn; Ali Saad; Adila Alkindy; Sophie Thomas; Michel Vekemans; Bruno Dallapiccola; Nicholas Katsanis; Colin A Johnson; Tania Attié-Bitach; Joseph G Gleeson
Journal:  Nat Genet       Date:  2010-05-30       Impact factor: 38.330

Review 7.  Joubert syndrome: congenital cerebellar ataxia with the molar tooth.

Authors:  Marta Romani; Alessia Micalizzi; Enza Maria Valente
Journal:  Lancet Neurol       Date:  2013-07-17       Impact factor: 44.182

8.  Joubert syndrome 2 (JBTS2) in Ashkenazi Jews is associated with a TMEM216 mutation.

Authors:  Simon Edvardson; Avraham Shaag; Shamir Zenvirt; Yaniv Erlich; Gregory J Hannon; Alan L Shanske; John Moshe Gomori; Joseph Ekstein; Orly Elpeleg
Journal:  Am J Hum Genet       Date:  2009-12-31       Impact factor: 11.025

9.  Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.

Authors:  Brian J O'Roak; Laura Vives; Wenqing Fu; Jarrett D Egertson; Ian B Stanaway; Ian G Phelps; Gemma Carvill; Akash Kumar; Choli Lee; Katy Ankenman; Jeff Munson; Joseph B Hiatt; Emily H Turner; Roie Levy; Diana R O'Day; Niklas Krumm; Bradley P Coe; Beth K Martin; Elhanan Borenstein; Deborah A Nickerson; Heather C Mefford; Dan Doherty; Joshua M Akey; Raphael Bernier; Evan E Eichler; Jay Shendure
Journal:  Science       Date:  2012-11-15       Impact factor: 47.728

10.  TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.

Authors:  Erica E Davis; Qi Zhang; Qin Liu; Bill H Diplas; Lisa M Davey; Jane Hartley; Corinne Stoetzel; Katarzyna Szymanska; Gokul Ramaswami; Clare V Logan; Donna M Muzny; Alice C Young; David A Wheeler; Pedro Cruz; Margaret Morgan; Lora R Lewis; Praveen Cherukuri; Baishali Maskeri; Nancy F Hansen; James C Mullikin; Robert W Blakesley; Gerard G Bouffard; Gabor Gyapay; Susanne Rieger; Burkhard Tönshoff; Ilse Kern; Neveen A Soliman; Thomas J Neuhaus; Kathryn J Swoboda; Hulya Kayserili; Tomas E Gallagher; Richard A Lewis; Carsten Bergmann; Edgar A Otto; Sophie Saunier; Peter J Scambler; Philip L Beales; Joseph G Gleeson; Eamonn R Maher; Tania Attié-Bitach; Hélène Dollfus; Colin A Johnson; Eric D Green; Richard A Gibbs; Friedhelm Hildebrandt; Eric A Pierce; Nicholas Katsanis
Journal:  Nat Genet       Date:  2011-01-23       Impact factor: 38.330

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  89 in total

1.  Joubert Syndrome in French Canadians and Identification of Mutations in CEP104.

Authors:  Myriam Srour; Fadi F Hamdan; Dianalee McKnight; Erica Davis; Hanna Mandel; Jeremy Schwartzentruber; Brissa Martin; Lysanne Patry; Christina Nassif; Alexandre Dionne-Laporte; Luis H Ospina; Emmanuelle Lemyre; Christine Massicotte; Rachel Laframboise; Bruno Maranda; Damian Labuda; Jean-Claude Décarie; Françoise Rypens; Dorith Goldsher; Catherine Fallet-Bianco; Jean-François Soucy; Anne-Marie Laberge; Catalina Maftei; Kym Boycott; Bernard Brais; Renée-Myriam Boucher; Guy A Rouleau; Nicholas Katsanis; Jacek Majewski; Orly Elpeleg; Mary K Kukolich; Stavit Shalev; Jacques L Michaud
Journal:  Am J Hum Genet       Date:  2015-10-17       Impact factor: 11.025

Review 2.  Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

Authors:  Mary Ella Pierpont; Martina Brueckner; Wendy K Chung; Vidu Garg; Ronald V Lacro; Amy L McGuire; Seema Mital; James R Priest; William T Pu; Amy Roberts; Stephanie M Ware; Bruce D Gelb; Mark W Russell
Journal:  Circulation       Date:  2018-11-20       Impact factor: 29.690

3.  Mutations in KIAA0753 cause Joubert syndrome associated with growth hormone deficiency.

Authors:  Joshi Stephen; Thierry Vilboux; Luhe Mian; Chulaluck Kuptanon; Courtney M Sinclair; Deniz Yildirimli; Dawn M Maynard; Joy Bryant; Roxanne Fischer; Meghana Vemulapalli; James C Mullikin; Marjan Huizing; William A Gahl; May Christine V Malicdan; Meral Gunay-Aygun
Journal:  Hum Genet       Date:  2017-02-20       Impact factor: 4.132

Review 4.  Ciliopathies: Genetics in Pediatric Medicine.

Authors:  Machteld M Oud; Ideke J C Lamers; Heleen H Arts
Journal:  J Pediatr Genet       Date:  2016-11-10

5.  TMEM67 mutations found in a case of Joubert syndrome with renal hypodysplasia.

Authors:  Yumiko Komatsu; Toshifumi Suzuki; Yoshinori Tsurusaki; Noriko Miyake; Naomichi Matsumoto; Kunimasa Yan
Journal:  CEN Case Rep       Date:  2016-01-21

Review 6.  The complexity of the cilium: spatiotemporal diversity of an ancient organelle.

Authors:  Westley Heydeck; Lorraine Fievet; Erica E Davis; Nicholas Katsanis
Journal:  Curr Opin Cell Biol       Date:  2018-08-20       Impact factor: 8.382

7.  Characterization of three ciliopathy pedigrees expands the phenotype associated with biallelic C2CD3 variants.

Authors:  Nicole J Boczek; Katharina Hopp; Lacey Benoit; Daniel Kraft; Margot A Cousin; Patrick R Blackburn; Charles D Madsen; Gavin R Oliver; Asha A Nair; Jie Na; Diana W Bianchi; Geoffrey Beek; Peter C Harris; Pavel Pichurin; Eric W Klee
Journal:  Eur J Hum Genet       Date:  2018-08-10       Impact factor: 4.246

8.  Prospective Evaluation of Kidney Disease in Joubert Syndrome.

Authors:  Leah R Fleming; Daniel A Doherty; Melissa A Parisi; Ian A Glass; Joy Bryant; Roxanne Fischer; Baris Turkbey; Peter Choyke; Kailash Daryanani; Meghana Vemulapalli; James C Mullikin; May Christine Malicdan; Thierry Vilboux; John A Sayer; William A Gahl; Meral Gunay-Aygun
Journal:  Clin J Am Soc Nephrol       Date:  2017-11-16       Impact factor: 8.237

9.  Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish.

Authors:  Julie C Van De Weghe; Tamara D S Rusterholz; Brooke Latour; Megan E Grout; Kimberly A Aldinger; Ranad Shaheen; Jennifer C Dempsey; Sateesh Maddirevula; Yong-Han H Cheng; Ian G Phelps; Matthias Gesemann; Himanshu Goel; Ohad S Birk; Talal Alanzi; Rifaat Rawashdeh; Arif O Khan; Michael J Bamshad; Deborah A Nickerson; Stephan C F Neuhauss; William B Dobyns; Fowzan S Alkuraya; Ronald Roepman; Ruxandra Bachmann-Gagescu; Dan Doherty
Journal:  Am J Hum Genet       Date:  2017-06-15       Impact factor: 11.025

10.  Characteristics of Liver Disease in 100 Individuals With Joubert Syndrome Prospectively Evaluated at a Single Center.

Authors:  Anna Strongin; Theo Heller; Dan Doherty; Ian A Glass; Melissa A Parisi; Joy Bryant; Peter Choyke; Baris Turkbey; Kailash Daryanani; Deniz Yildirimli; Meghana Vemulapalli; Jim C Mullikin; May C Malicdan; Thierry Vilboux; William A Gahl; Meral Gunay-Aygun
Journal:  J Pediatr Gastroenterol Nutr       Date:  2018-03       Impact factor: 2.839

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