Literature DB >> 7693762

Presence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders.

M Wendland1, S Subramani.   

Abstract

Cells from patients with peroxisome-deficient disorders contain membrane ghosts devoid of most matrix contents instead of normal peroxisomes indicating that the underlying molecular defects impair the import of matrix proteins into these peroxisome ghosts. Genetic heterogeneity for the molecular defects was inferred from the assignment of patients with peroxisome-deficient disorders into nine complementation groups. The aim of our studies was to analyze cell lines from six different complementation groups in a systematic manner for the presence of peroxisome ghosts, the ability to import Ser-Lys-Leu-containing proteins into peroxisome ghosts and for the presence of cytosolic factors required for peroxisomal protein import. We show that each of the cell lines analyzed contains peroxisome ghosts, but is unable to import matrix proteins as judged by a peroxisomal import assay using permeabilized cells. The addition of wild type cytosol did not restore the capacity to import matrix proteins but cytosol prepared from these cell lines was functional in stimulation of peroxisomal protein import in a heterologous system. These results implicate organelle-associated molecular defects in each of the six cell lines analyzed.

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Year:  1993        PMID: 7693762      PMCID: PMC288431          DOI: 10.1172/JCI116854

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  30 in total

1.  Peroxisomal integral membrane proteins in control and Zellweger fibroblasts.

Authors:  M J Santos; T Imanaka; H Shio; P B Lazarow
Journal:  J Biol Chem       Date:  1988-07-25       Impact factor: 5.157

2.  Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly.

Authors:  M J Santos; T Imanaka; H Shio; G M Small; P B Lazarow
Journal:  Science       Date:  1988-03-25       Impact factor: 47.728

3.  Genetic and phenotypic heterogeneity in disorders of peroxisome biogenesis--a complementation study involving cell lines from 19 patients.

Authors:  A A Roscher; S Hoefler; G Hoefler; E Paschke; F Paltauf; A Moser; H Moser
Journal:  Pediatr Res       Date:  1989-07       Impact factor: 3.756

4.  The 22-kD peroxisomal integral membrane protein in Zellweger syndrome--presence, abundance, and association with a peroxisomal thiolase precursor protein.

Authors:  J Gärtner; W W Chen; R I Kelley; S J Mihalik; H W Moser
Journal:  Pediatr Res       Date:  1991-02       Impact factor: 3.756

5.  Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata.

Authors:  A Balfe; G Hoefler; W W Chen; P A Watkins
Journal:  Pediatr Res       Date:  1990-03       Impact factor: 3.756

6.  Presence of peroxisomal membrane proteins in liver and fibroblasts from patients with the Zellweger syndrome and related disorders: evidence for the existence of peroxisomal ghosts.

Authors:  E A Wiemer; S Brul; W W Just; R Van Driel; E Brouwer-Kelder; M Van Den Berg; P J Weijers; R B Schutgens; H Van Den Bosch; A Schram
Journal:  Eur J Cell Biol       Date:  1989-12       Impact factor: 4.492

7.  Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophies.

Authors:  S Goldfischer; J Collins; I Rapin; B Coltoff-Schiller; C H Chang; M Nigro; V H Black; N B Javitt; H W Moser; P B Lazarow
Journal:  Science       Date:  1985-01-04       Impact factor: 47.728

8.  Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?

Authors:  A Poulos; P Sharp; M Whiting
Journal:  Clin Genet       Date:  1984-12       Impact factor: 4.438

9.  The 70-kDa peroxisomal membrane protein is a member of the Mdr (P-glycoprotein)-related ATP-binding protein superfamily.

Authors:  K Kamijo; S Taketani; S Yokota; T Osumi; T Hashimoto
Journal:  J Biol Chem       Date:  1990-03-15       Impact factor: 5.157

10.  A conserved tripeptide sorts proteins to peroxisomes.

Authors:  S J Gould; G A Keller; N Hosken; J Wilkinson; S Subramani
Journal:  J Cell Biol       Date:  1989-05       Impact factor: 10.539

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  14 in total

1.  Targeting and translocation of proteins into the hydrogenosome of the protist Trichomonas: similarities with mitochondrial protein import.

Authors:  P J Bradley; C J Lahti; E Plümper; P J Johnson
Journal:  EMBO J       Date:  1997-06-16       Impact factor: 11.598

2.  Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.

Authors:  Y Matsuzono; N Kinoshita; S Tamura; N Shimozawa; M Hamasaki; K Ghaedi; R J Wanders; Y Suzuki; N Kondo; Y Fujiki
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

3.  Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants.

Authors:  H Otera; K Okumoto; K Tateishi; Y Ikoma; E Matsuda; M Nishimura; T Tsukamoto; T Osumi; K Ohashi; O Higuchi; Y Fujiki
Journal:  Mol Cell Biol       Date:  1998-01       Impact factor: 4.272

4.  The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor.

Authors:  T Yahraus; N Braverman; G Dodt; J E Kalish; J C Morrell; H W Moser; D Valle; S J Gould
Journal:  EMBO J       Date:  1996-06-17       Impact factor: 11.598

5.  The peroxin pex3p initiates membrane assembly in peroxisome biogenesis.

Authors:  K Ghaedi; S Tamura; K Okumoto; Y Matsuzono; Y Fujiki
Journal:  Mol Biol Cell       Date:  2000-06       Impact factor: 4.138

6.  PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.

Authors:  K Ghaedi; M Honsho; N Shimozawa; Y Suzuki; N Kondo; Y Fujiki
Journal:  Am J Hum Genet       Date:  2000-08-31       Impact factor: 11.025

7.  Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.

Authors:  S Tamura; K Okumoto; R Toyama; N Shimozawa; T Tsukamoto; Y Suzuki; T Osumi; N Kondo; Y Fujiki
Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-14       Impact factor: 11.205

8.  Identification and characterization of the type-IVA cyclic AMP-specific phosphodiesterase RD1 as a membrane-bound protein expressed in cerebellum.

Authors:  Y Shakur; M Wilson; L Pooley; M Lobban; S L Griffiths; A M Campbell; J Beattie; C Daly; M D Houslay
Journal:  Biochem J       Date:  1995-03-15       Impact factor: 3.857

9.  Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

Authors:  M Honsho; S Tamura; N Shimozawa; Y Suzuki; N Kondo; Y Fujiki
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025

10.  PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p.

Authors:  K Okumoto; N Shimozawa; A Kawai; S Tamura; T Tsukamoto; T Osumi; H Moser; R J Wanders; Y Suzuki; N Kondo; Y Fujiki
Journal:  Mol Cell Biol       Date:  1998-07       Impact factor: 4.272

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