Literature DB >> 16648254

Deficiency of the zinc finger protein ZPR1 causes neurodegeneration.

Beth Doran1, Norberto Gherbesi, Gregory Hendricks, Richard A Flavell, Roger J Davis, Laxman Gangwani.   

Abstract

Mutations that cause reduced expression of the full-length Survival Motor Neurons (SMN) protein are a major cause of spinal muscular atrophy (SMA), a disease characterized by degeneration of the alpha-motor neurons in the anterior horn of the spinal cord. The severity of SMA may be influenced by the actions of modifier genes. One potential modifier gene is represented by ZPR1, which is down-regulated in patients with SMA and encodes a zinc finger protein that interacts with complexes formed by SMN. To test the functional significance of ZPR1 gene down-regulation, we examined a mouse model with targeted ablation of the Zpr1 gene. We report that ZPR1-deficient mice exhibit axonal pathology and neurodegeneration. These data identify ZPR1 deficiency as a contributing factor in neurodegenerative disorders.

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Year:  2006        PMID: 16648254      PMCID: PMC1464363          DOI: 10.1073/pnas.0602057103

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  28 in total

1.  Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7.

Authors:  C F Rochette; L C Surh; P N Ray; P E McAndrew; T W Prior; A H Burghes; M Vanasse; L R Simard
Journal:  Neurogenetics       Date:  1997-09       Impact factor: 2.660

2.  Motor proteins regulate force interactions between microtubules and microfilaments in the axon.

Authors:  F J Ahmad; J Hughey; T Wittmann; A Hyman; M Greaser; P W Baas
Journal:  Nat Cell Biol       Date:  2000-05       Impact factor: 28.824

Review 3.  Neurodegenerative tauopathies.

Authors:  V M Lee; M Goedert; J Q Trojanowski
Journal:  Annu Rev Neurosci       Date:  2001       Impact factor: 12.449

4.  Reduced survival motor neuron (Smn) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III.

Authors:  S Jablonka; B Schrank; M Kralewski; W Rossoll; M Sendtner
Journal:  Hum Mol Genet       Date:  2000-02-12       Impact factor: 6.150

Review 5.  Axonal pathology in myelin disorders.

Authors:  C Bjartmar; X Yin; B D Trapp
Journal:  J Neurocytol       Date:  1999 Apr-May

Review 6.  Overview of hereditary neuropathy with liability to pressure palsies.

Authors:  P F Chance
Journal:  Ann N Y Acad Sci       Date:  1999-09-14       Impact factor: 5.691

Review 7.  Spinal muscular atrophy: a delayed development hypothesis.

Authors:  Irena Hausmanowa-Petrusewicz; Gerta Vrbová
Journal:  Neuroreport       Date:  2005-05-12       Impact factor: 1.837

8.  Late onset neurological phenotype of the X-ALD gene inactivation in mice: a mouse model for adrenomyeloneuropathy.

Authors:  Aurora Pujol; Colette Hindelang; Noëlle Callizot; Udo Bartsch; Melitta Schachner; Jean Louis Mandel
Journal:  Hum Mol Genet       Date:  2002-03-01       Impact factor: 6.150

9.  Spinal muscular atrophy disrupts the interaction of ZPR1 with the SMN protein.

Authors:  L Gangwani; M Mikrut; S Theroux; M Sharma; R J Davis
Journal:  Nat Cell Biol       Date:  2001-04       Impact factor: 28.824

10.  Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy.

Authors:  S Rudnik-Schöneborn; H H Goebel; W Schlote; S Molaian; H Omran; U Ketelsen; R Korinthenberg; D Wenzel; H Lauffer; M Kreiss-Nachtsheim; B Wirth; K Zerres
Journal:  Neurology       Date:  2003-03-25       Impact factor: 9.910

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  24 in total

1.  The zinc finger protein ZPR1 is a potential modifier of spinal muscular atrophy.

Authors:  Saif Ahmad; Yi Wang; Gouse M Shaik; Arthur H Burghes; Laxman Gangwani
Journal:  Hum Mol Genet       Date:  2012-03-14       Impact factor: 6.150

2.  Genetic inhibition of JNK3 ameliorates spinal muscular atrophy.

Authors:  Naresh K Genabai; Saif Ahmad; Zhanying Zhang; Xiaoting Jiang; Cynthia A Gabaldon; Laxman Gangwani
Journal:  Hum Mol Genet       Date:  2015-09-30       Impact factor: 6.150

3.  Associations of genetic variants for adult lipid levels with lipid levels in children. The Generation R Study.

Authors:  Ardashel Latsuzbaia; Vincent W V Jaddoe; Albert Hofman; Oscar H Franco; Janine F Felix
Journal:  J Lipid Res       Date:  2016-10-24       Impact factor: 5.922

4.  Nuclear factor 45 (NF45) is a regulatory subunit of complexes with NF90/110 involved in mitotic control.

Authors:  Deyu Guan; Nihal Altan-Bonnet; Andrew M Parrott; Cindy J Arrigo; Quan Li; Mohammed Khaleduzzaman; Hong Li; Chee-Gun Lee; Tsafi Pe'ery; Michael B Mathews
Journal:  Mol Cell Biol       Date:  2008-05-05       Impact factor: 4.272

Review 5.  Spinal muscular atrophy and the antiapoptotic role of survival of motor neuron (SMN) protein.

Authors:  Ryan S Anderton; Bruno P Meloni; Frank L Mastaglia; Sherif Boulos
Journal:  Mol Neurobiol       Date:  2013-01-13       Impact factor: 5.590

6.  Loss of translation elongation factor (eEF1A2) expression in vivo differentiates between Wallerian degeneration and dying-back neuronal pathology.

Authors:  Lyndsay M Murray; Derek Thomson; Annalijn Conklin; Thomas M Wishart; Thomas H Gillingwater
Journal:  J Anat       Date:  2008-12       Impact factor: 2.610

7.  SMN complex localizes to the sarcomeric Z-disc and is a proteolytic target of calpain.

Authors:  Michael P Walker; T K Rajendra; Luciano Saieva; Jennifer L Fuentes; Livio Pellizzoni; A Gregory Matera
Journal:  Hum Mol Genet       Date:  2008-08-08       Impact factor: 6.150

8.  Survival motor neuron protein regulates apoptosis in an in vitro model of spinal muscular atrophy.

Authors:  Graham C Parker; Xingli Li; Roumen A Anguelov; Gabor Toth; Adam Cristescu; Gyula Acsadi
Journal:  Neurotox Res       Date:  2008-01       Impact factor: 3.911

9.  Structural insights into the interaction of the evolutionarily conserved ZPR1 domain tandem with eukaryotic EF1A, receptors, and SMN complexes.

Authors:  Ashwini K Mishra; Laxman Gangwani; Roger J Davis; David G Lambright
Journal:  Proc Natl Acad Sci U S A       Date:  2007-08-17       Impact factor: 11.205

10.  A short antisense oligonucleotide masking a unique intronic motif prevents skipping of a critical exon in spinal muscular atrophy.

Authors:  Natalia N Singh; Maria Shishimorova; Lu Cheng Cao; Laxman Gangwani; Ravindra N Singh
Journal:  RNA Biol       Date:  2009-07-14       Impact factor: 4.652

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