Literature DB >> 9288097

A mouse model for Zellweger syndrome.

M Baes1, P Gressens, E Baumgart, P Carmeliet, M Casteels, M Fransen, P Evrard, D Fahimi, P E Declercq, D Collen, P P van Veldhoven, G P Mannaerts.   

Abstract

The cerebro-hepato-renal syndrome of Zellweger is a fatal inherited disease caused by deficient import of peroxisomal matrix proteins. The pathogenic mechanisms leading to extreme hypotonia, severe mental retardation and early death are unknown. We generated a Zellweger animal model through inactivation of the murine Pxr1 gene (formally known as Pex5) that encodes the import receptor for most peroxisomal matrix proteins. Pxr1-/- mice lacked morphologically identifiable peroxisomes and exhibited the typical biochemical abnormalities of Zellweger patients. They displayed intrauterine growth retardation, were severely hypotonic at birth and died within 72 hours. Analysis of the neocortex revealed impaired neuronal migration and maturation and extensive apoptotic death of neurons.

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Year:  1997        PMID: 9288097     DOI: 10.1038/ng0997-49

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  74 in total

1.  Isolation and biochemical characterization of peroxisomes from cultured rat glial cells.

Authors:  I Singh; O Carillo; A Namboodiri
Journal:  Neurochem Res       Date:  2000-02       Impact factor: 3.996

2.  Functional studies on human Pex7p: subcellular localization and interaction with proteins containing a peroxisome-targeting signal type 2 and other peroxins.

Authors:  Karen Ghys; Marc Fransen; Guy P Mannaerts; Paul P Van Veldhoven
Journal:  Biochem J       Date:  2002-07-01       Impact factor: 3.857

3.  Tetratricopeptide repeat domain of Yarrowia lipolytica Pex5p is essential for recognition of the type 1 peroxisomal targeting signal but does not confer full biological activity on Pex5p.

Authors:  R K Szilard; R A Rachubinski
Journal:  Biochem J       Date:  2000-02-15       Impact factor: 3.857

Review 4.  Peroxisomes: 40 years of histochemical staining, personal reminiscences.

Authors:  H Dariush Fahimi
Journal:  Histochem Cell Biol       Date:  2009-02-14       Impact factor: 4.304

5.  A peroxisome deficiency-induced reductive cytosol state up-regulates the brain-derived neurotrophic factor pathway.

Authors:  Yuichi Abe; Masanori Honsho; Ryoko Kawaguchi; Takashi Matsuzaki; Yayoi Ichiki; Masashi Fujitani; Kazushirou Fujiwara; Masaaki Hirokane; Masahide Oku; Yasuyoshi Sakai; Toshihide Yamashita; Yukio Fujiki
Journal:  J Biol Chem       Date:  2020-03-12       Impact factor: 5.157

Review 6.  The surprising complexity of peroxisome biogenesis.

Authors:  L J Olsen
Journal:  Plant Mol Biol       Date:  1998-09       Impact factor: 4.076

Review 7.  Genetic-dependency of peroxisomal cell functions - emerging aspects.

Authors:  N Latruffe; J Vamecq; M Cherkaoui Malki
Journal:  J Cell Mol Med       Date:  2003 Jul-Sep       Impact factor: 5.310

8.  C-terminal tripeptide Ser-Asn-Leu (SNL) of human D-aspartate oxidase is a functional peroxisome-targeting signal.

Authors:  L Amery; C Brees; M Baes; C Setoyama; R Miura; G P Mannaerts; P P Van Veldhoven
Journal:  Biochem J       Date:  1998-12-01       Impact factor: 3.857

Review 9.  Mammalian peroxisomes and reactive oxygen species.

Authors:  Michael Schrader; H Dariush Fahimi
Journal:  Histochem Cell Biol       Date:  2004-07-08       Impact factor: 4.304

10.  alpha-Synuclein abnormalities in mouse models of peroxisome biogenesis disorders.

Authors:  Eugenia Yakunin; Ann Moser; Virginie Loeb; Ann Saada; Phyllis Faust; Denis I Crane; Myriam Baes; Ronit Sharon
Journal:  J Neurosci Res       Date:  2010-03       Impact factor: 4.164

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