Literature DB >> 23243086

Mutation of HERC2 causes developmental delay with Angelman-like features.

Gaurav V Harlalka1, Emma L Baple, Harold Cross, Simone Kühnle, Monica Cubillos-Rojas, Konstantin Matentzoglu, Michael A Patton, Karin Wagner, Roselyn Coblentz, Debra L Ford, Deborah J G Mackay, Barry A Chioza, Martin Scheffner, Jose Luis Rosa, Andrew H Crosby.   

Abstract

BACKGROUND: Deregulation of the activity of the ubiquitin ligase E6AP (UBE3A) is well recognised to contribute to the development of Angelman syndrome (AS). The ubiquitin ligase HERC2, encoded by the HERC2 gene is thought to be a key regulator of E6AP. METHODS AND
RESULTS: Using a combination of autozygosity mapping and linkage analysis, we studied an autosomal-recessive neurodevelopmental disorder with some phenotypic similarities to AS, found among the Old Order Amish. Our molecular investigation identified a mutation in HERC2 associated with the disease phenotype. We establish that the encoded mutant HERC2 protein has a reduced half-life compared with its wild-type counterpart, which is associated with a significant reduction in HERC2 levels in affected individuals.
CONCLUSIONS: Our data implicate a model in which disruption of HERC2 function relates to a reduction in E6AP activity resulting in neurodevelopmental delay, suggesting a previously unrecognised role of HERC2 in the pathogenesis of AS.

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Year:  2012        PMID: 23243086     DOI: 10.1136/jmedgenet-2012-101367

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


  34 in total

1.  Degradation of the deubiquitinating enzyme USP33 is mediated by p97 and the ubiquitin ligase HERC2.

Authors:  Nickie C Chan; Willem den Besten; Michael J Sweredoski; Sonja Hess; Raymond J Deshaies; David C Chan
Journal:  J Biol Chem       Date:  2014-05-22       Impact factor: 5.157

2.  The E3 ubiquitin protein ligase HERC2 modulates the activity of tumor protein p53 by regulating its oligomerization.

Authors:  Monica Cubillos-Rojas; Fabiola Amair-Pinedo; Roser Peiró-Jordán; Ramon Bartrons; Francesc Ventura; Jose Luis Rosa
Journal:  J Biol Chem       Date:  2014-04-09       Impact factor: 5.157

3.  Network Analysis of UBE3A/E6AP-Associated Proteins Provides Connections to Several Distinct Cellular Processes.

Authors:  Gustavo Martínez-Noël; Katja Luck; Simone Kühnle; Alice Desbuleux; Patricia Szajner; Jeffrey T Galligan; Diana Rodriguez; Leon Zheng; Kathleen Boyland; Flavian Leclere; Quan Zhong; David E Hill; Marc Vidal; Peter M Howley
Journal:  J Mol Biol       Date:  2018-02-06       Impact factor: 5.469

4.  High diagnostic yield of clinical exome sequencing in Middle Eastern patients with Mendelian disorders.

Authors:  Tarunashree Yavarna; Nader Al-Dewik; Mariam Al-Mureikhi; Rehab Ali; Fatma Al-Mesaifri; Laila Mahmoud; Noora Shahbeck; Shenela Lakhani; Mariam AlMulla; Zafar Nawaz; Patrik Vitazka; Fowzan S Alkuraya; Tawfeg Ben-Omran
Journal:  Hum Genet       Date:  2015-06-16       Impact factor: 4.132

5.  Fanconi anemia gene editing by the CRISPR/Cas9 system.

Authors:  Mark J Osborn; Richard Gabriel; Beau R Webber; Anthony P DeFeo; Amber N McElroy; Jordan Jarjour; Colby G Starker; John E Wagner; J Keith Joung; Daniel F Voytas; Christof von Kalle; Manfred Schmidt; Bruce R Blazar; Jakub Tolar
Journal:  Hum Gene Ther       Date:  2015-02       Impact factor: 5.695

Review 6.  Enzyme-substrate relationships in the ubiquitin system: approaches for identifying substrates of ubiquitin ligases.

Authors:  Hazel F O'Connor; Jon M Huibregtse
Journal:  Cell Mol Life Sci       Date:  2017-04-28       Impact factor: 9.261

7.  Complete loss of function of the ubiquitin ligase HERC2 causes a severe neurodevelopmental phenotype.

Authors:  Fanny Morice-Picard; Giovanni Benard; Hamid R Rezvani; Eulalie Lasseaux; Delphine Simon; Sébastien Moutton; Caroline Rooryck; Didier Lacombe; Clarisse Baumann; Benoit Arveiler
Journal:  Eur J Hum Genet       Date:  2016-10-19       Impact factor: 4.246

8.  Role of ubiquitin and the HPV E6 oncoprotein in E6AP-mediated ubiquitination.

Authors:  Franziska Mortensen; Daniel Schneider; Tanja Barbic; Anna Sladewska-Marquardt; Simone Kühnle; Andreas Marx; Martin Scheffner
Journal:  Proc Natl Acad Sci U S A       Date:  2015-07-27       Impact factor: 11.205

Review 9.  Functional and pathological relevance of HERC family proteins: a decade later.

Authors:  Susana Sánchez-Tena; Monica Cubillos-Rojas; Taiane Schneider; Jose Luis Rosa
Journal:  Cell Mol Life Sci       Date:  2016-01-22       Impact factor: 9.261

10.  Angelman syndrome-associated point mutations in the Zn2+-binding N-terminal (AZUL) domain of UBE3A ubiquitin ligase inhibit binding to the proteasome.

Authors:  Simone Kühnle; Gustavo Martínez-Noël; Flavien Leclere; Sebastian D Hayes; J Wade Harper; Peter M Howley
Journal:  J Biol Chem       Date:  2018-09-26       Impact factor: 5.157

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