Literature DB >> 22307522

The E3 ubiquitin ligase TRIM11 mediates the degradation of congenital central hypoventilation syndrome-associated polyalanine-expanded PHOX2B.

Sara Parodi1, Eleonora Di Zanni, Simona Di Lascio, Paola Bocca, Ignazia Prigione, Diego Fornasari, Maria Pennuto, Tiziana Bachetti, Isabella Ceccherini.   

Abstract

Expansions of a polyalanine (polyA) stretch in the coding region of the PHOX2B gene cause congenital central hypoventilation syndrome (CCHS), a neurocristopathy characterized by the absence of adequate control of autonomic breathing. Expansion of polyA in PHOX2B leads to protein misfolding and accumulation into inclusions. The mechanisms that regulate mutant protein degradation and turnover have been poorly elucidated. Here, we investigate the regulation of degradation of wild-type and polyA-expanded PHOX2B. We show that expanded PHOX2B is targeted for degradation through the ubiquitin-proteasome system, resulting in lowered levels of the mutant protein relative to its wild-type counterpart. Moreover, we show that mutant PHOX2B forms ubiquitin-positive inclusions, which sequester wild-type PHOX2B. This sequestration correlates with reduced transcriptional activity of endogenous wild-type protein in neuroblastoma cells. Finally, we show that the E3 ubiquitin ligase TRIM11 plays a critical role in the clearance of mutant PHOX2B through the proteasome. Importantly, clearance of mutant PHOX2B by TRIM11 correlates with a rescue of PHOX2B transcriptional activity. We propose that CCHS is partially caused by a dominant-negative effect of expanded PHOX2B due to the retention of the wild-type protein in pathogenic aggregates. Our results demonstrate that TRIM11 is a novel modifier of mutant PHOX2B toxicity and represents a potential therapeutic target for CCHS.

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Year:  2012        PMID: 22307522     DOI: 10.1007/s00109-012-0868-1

Source DB:  PubMed          Journal:  J Mol Med (Berl)        ISSN: 0946-2716            Impact factor:   4.599


  35 in total

1.  A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation.

Authors:  S Caburet; A Demarez; L Moumné; M Fellous; E De Baere; R A Veitia
Journal:  J Med Genet       Date:  2004-12       Impact factor: 6.318

2.  Sleep-disordered breathing in newborn mice heterozygous for the transcription factor Phox2b.

Authors:  Estelle Durand; Stéphane Dauger; Alexandre Pattyn; Claude Gaultier; Christo Goridis; Jorge Gallego
Journal:  Am J Respir Crit Care Med       Date:  2005-04-28       Impact factor: 21.405

Review 3.  The other trinucleotide repeat: polyalanine expansion disorders.

Authors:  Andrea Albrecht; Stefan Mundlos
Journal:  Curr Opin Genet Dev       Date:  2005-06       Impact factor: 5.578

4.  Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.

Authors:  Jeanne Amiel; Béatrice Laudier; Tania Attié-Bitach; Ha Trang; Loïc de Pontual; Blanca Gener; Delphine Trochet; Heather Etchevers; Pierre Ray; Michel Simonneau; Michel Vekemans; Arnold Munnich; Claude Gaultier; Stanislas Lyonnet
Journal:  Nat Genet       Date:  2003-03-17       Impact factor: 38.330

5.  A molecular pathogenesis for transcription factor associated poly-alanine tract expansions.

Authors:  Andrea N Albrecht; Uwe Kornak; Annett Böddrich; Kathrin Süring; Peter N Robinson; Asita C Stiege; Rudi Lurz; Sigmar Stricker; Erich E Wanker; Stefan Mundlos
Journal:  Hum Mol Genet       Date:  2004-08-27       Impact factor: 6.150

6.  Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development.

Authors:  Lara Moumné; Aurélie Dipietromaria; Frank Batista; Ayhan Kocer; Marc Fellous; Eric Pailhoux; Reiner A Veitia
Journal:  Hum Mol Genet       Date:  2007-12-24       Impact factor: 6.150

7.  Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity.

Authors:  Jun-Ichi Niwa; Shinsuke Ishigaki; Nozomi Hishikawa; Masahiko Yamamoto; Manabu Doyu; Shigeo Murata; Keiji Tanaka; Naoyuki Taniguchi; Gen Sobue
Journal:  J Biol Chem       Date:  2002-07-26       Impact factor: 5.157

8.  Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.

Authors:  Debra E Weese-Mayer; Elizabeth M Berry-Kravis; Lili Zhou; Brion S Maher; Jean M Silvestri; Mark E Curran; Mary L Marazita
Journal:  Am J Med Genet A       Date:  2003-12-15       Impact factor: 2.802

9.  A human mutation in Phox2b causes lack of CO2 chemosensitivity, fatal central apnea, and specific loss of parafacial neurons.

Authors:  Véronique Dubreuil; Nélina Ramanantsoa; Delphine Trochet; Vanessa Vaubourg; Jeanne Amiel; Jorge Gallego; Jean-François Brunet; Christo Goridis
Journal:  Proc Natl Acad Sci U S A       Date:  2008-01-15       Impact factor: 11.205

10.  Geldanamycin promotes nuclear localisation and clearance of PHOX2B misfolded proteins containing polyalanine expansions.

Authors:  Tiziana Bachetti; Paola Bocca; Silvia Borghini; Ivana Matera; Ignazia Prigione; Roberto Ravazzolo; Isabella Ceccherini
Journal:  Int J Biochem Cell Biol       Date:  2006-09-14       Impact factor: 5.085

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  11 in total

1.  Expanding the phenotype of congenital central hypoventilation syndrome impacts management decisions.

Authors:  Heather M Byers; Maida Chen; Andrew S Gelfand; Bruce Ong; Marisa Jendras; Ian A Glass
Journal:  Am J Med Genet A       Date:  2018-04-25       Impact factor: 2.802

2.  Transcription Factors Phox2a/2b Upregulate Expression of Noradrenergic and Dopaminergic Phenotypes in Aged Rat Brains.

Authors:  Yan Fan; Fei Zeng; Russell W Brown; Jennifer B Price; Thomas C Jones; Meng-Yang Zhu
Journal:  Neurotox Res       Date:  2020-07-02       Impact factor: 3.911

Review 3.  Proceedings of the fourth international conference on central hypoventilation.

Authors:  Ha Trang; Jean-François Brunet; Hermann Rohrer; Jorge Gallego; Jeanne Amiel; Tiziana Bachetti; Kenneth H Fischbeck; Thomas Similowski; Christian Straus; Isabella Ceccherini; Debra E Weese-Mayer; Matthias Frerick; Katarzyna Bieganowska; Linda Middleton; Francesco Morandi; Giancarlo Ottonello
Journal:  Orphanet J Rare Dis       Date:  2014-12-05       Impact factor: 4.123

4.  Structural and functional differences in PHOX2B frameshift mutations underlie isolated or syndromic congenital central hypoventilation syndrome.

Authors:  Simona Di Lascio; Roberta Benfante; Eleonora Di Zanni; Silvia Cardani; Annalisa Adamo; Diego Fornasari; Isabella Ceccherini; Tiziana Bachetti
Journal:  Hum Mutat       Date:  2017-11-21       Impact factor: 4.878

5.  TRIM11 facilitates chemoresistance in nasopharyngeal carcinoma by activating the β-catenin/ABCC9 axis via p62-selective autophagic degradation of Daple.

Authors:  Runa Zhang; Si-Wei Li; Lijuan Liu; Jun Yang; Guofu Huang; Yi Sang
Journal:  Oncogenesis       Date:  2020-05-07       Impact factor: 7.485

Review 6.  Research Advances on Therapeutic Approaches to Congenital Central Hypoventilation Syndrome (CCHS).

Authors:  Simona Di Lascio; Roberta Benfante; Silvia Cardani; Diego Fornasari
Journal:  Front Neurosci       Date:  2021-01-12       Impact factor: 4.677

7.  TRIM11 negatively regulates IFNβ production and antiviral activity by targeting TBK1.

Authors:  Younglang Lee; Byeongwoon Song; Chankyu Park; Ki-Sun Kwon
Journal:  PLoS One       Date:  2013-05-13       Impact factor: 3.240

8.  The human antiviral factor TRIM11 is under the regulation of HIV-1 Vpr.

Authors:  Ting Yuan; Weitong Yao; Fang Huang; Binlian Sun; Rongge Yang
Journal:  PLoS One       Date:  2014-08-08       Impact factor: 3.240

9.  Alanine Expansions Associated with Congenital Central Hypoventilation Syndrome Impair PHOX2B Homeodomain-mediated Dimerization and Nuclear Import.

Authors:  Simona Di Lascio; Debora Belperio; Roberta Benfante; Diego Fornasari
Journal:  J Biol Chem       Date:  2016-04-27       Impact factor: 5.157

Review 10.  Guidelines for diagnosis and management of congenital central hypoventilation syndrome.

Authors:  Ha Trang; Martin Samuels; Isabella Ceccherini; Matthias Frerick; Maria Angeles Garcia-Teresa; Jochen Peters; Johannes Schoeber; Marek Migdal; Agneta Markstrom; Giancarlo Ottonello; Raffaele Piumelli; Maria Helena Estevao; Irena Senecic-Cala; Barbara Gnidovec-Strazisar; Andreas Pfleger; Raquel Porto-Abal; Miriam Katz-Salamon
Journal:  Orphanet J Rare Dis       Date:  2020-09-21       Impact factor: 4.123

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