Literature DB >> 8035823

Peroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis.

T Tsukamoto1, N Shimozawa, Y Fujiki.   

Abstract

A cDNA encoding 35-kDa peroxisome assembly factor 1 (PAF-1), a peroxisomal integral membrane protein, was cloned from Chinese hamster ovary (CHO) cells and sequenced. The CHO PAF-1 comprised 304 amino acids, one residue shorter than rat or human PAF-1, and showed high homology to rat and human PAF-1: 90 and 86% at the nucleotide sequence level and 92 and 90% in amino acid sequence, respectively. PAF-1 from these three species contains a conserved cysteine-rich sequence at the C-terminal region which is exactly the same as that of a novel cysteine-rich RING finger motif family. PAF-1 cDNA from a peroxisome-deficient CHO cell mutant, Z65 (T. Tsukamoto, S. Yokota, and Y. Fujiki, J. Cell Biol. 110:651-660, 1990), contained a nonsense mutation at the codon for Trp-114, resulting in premature termination. Truncation in PAF-1 of either 19 amino acids from the N terminus or 92 residues from the C terminus maintained the peroxisome assembly-restoring activity when tested in both the Z65 mutant and the fibroblasts from a Zellweger patient. In contrast, deletion of 27 or 102 residues from the N or C terminus eliminated the activity. PAF-1 is encoded by free polysomal RNA, consistent with a general rule for biogenesis of peroxisomal proteins, including membrane polypeptides, implying the posttranslational transport and integration of PAF-1 into peroxisomal membrane.

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Year:  1994        PMID: 8035823      PMCID: PMC359065          DOI: 10.1128/mcb.14.8.5458-5465.1994

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  37 in total

1.  Rapid and efficient site-specific mutagenesis without phenotypic selection.

Authors:  T A Kunkel
Journal:  Proc Natl Acad Sci U S A       Date:  1985-01       Impact factor: 11.205

2.  Absence of DNA in peroxisomes of Candida tropicalis.

Authors:  T Kamiryo; M Abe; K Okazaki; S Kato; N Shimamoto
Journal:  J Bacteriol       Date:  1982-10       Impact factor: 3.490

3.  Synthesis of a major integral membrane polypeptide of rat liver peroxisomes on free polysomes.

Authors:  Y Fujiki; R A Rachubinski; P B Lazarow
Journal:  Proc Natl Acad Sci U S A       Date:  1984-11       Impact factor: 11.205

4.  Peroxisome-deficient Chinese hamster ovary cells with point mutations in peroxisome assembly factor-1.

Authors:  R Thieringer; C R Raetz
Journal:  J Biol Chem       Date:  1993-06-15       Impact factor: 5.157

5.  Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.

Authors:  N Shimozawa; T Tsukamoto; Y Suzuki; T Orii; Y Fujiki
Journal:  J Clin Invest       Date:  1992-11       Impact factor: 14.808

6.  Synthesis of 3-ketoacyl-CoA thiolase of rat liver peroxisomes on free polyribosomes as a larger precursor. Induction of thiolase mRNA activity by clofibrate.

Authors:  Y Fujiki; R A Rachubinski; R M Mortensen; P B Lazarow
Journal:  Biochem J       Date:  1985-03-15       Impact factor: 3.857

7.  Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome.

Authors:  J Gärtner; H Moser; D Valle
Journal:  Nat Genet       Date:  1992-04       Impact factor: 38.330

8.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

9.  Development of the yeast Pichia pastoris as a model organism for a genetic and molecular analysis of peroxisome assembly.

Authors:  S J Gould; D McCollum; A P Spong; J A Heyman; S Subramani
Journal:  Yeast       Date:  1992-08       Impact factor: 3.239

10.  Acyl-Coa oxidase and hydratase-dehydrogenase, two enzymes of the peroxisomal beta-oxidation system, are synthesized on free polysomes of clofibrate-treated rat liver.

Authors:  R A Rachubinski; Y Fujiki; R M Mortensen; P B Lazarow
Journal:  J Cell Biol       Date:  1984-12       Impact factor: 10.539

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  9 in total

Review 1.  The surprising complexity of peroxisome biogenesis.

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

2.  Functional identification of a Leishmania gene related to the peroxin 2 gene reveals common ancestry of glycosomes and peroxisomes.

Authors:  J A Flaspohler; W L Rickoll; S M Beverley; M Parsons
Journal:  Mol Cell Biol       Date:  1997-03       Impact factor: 4.272

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 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

5.  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

6.  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

7.  The Pichia pastoris PER6 gene product is a peroxisomal integral membrane protein essential for peroxisome biogenesis and has sequence similarity to the Zellweger syndrome protein PAF-1.

Authors:  H R Waterham; Y de Vries; K A Russel; W Xie; M Veenhuis; J M Cregg
Journal:  Mol Cell Biol       Date:  1996-05       Impact factor: 4.272

8.  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

9.  Formation of the peroxisome lumen is abolished by loss of Pichia pastoris Pas7p, a zinc-binding integral membrane protein of the peroxisome.

Authors:  J E Kalish; C Theda; J C Morrell; J M Berg; S J Gould
Journal:  Mol Cell Biol       Date:  1995-11       Impact factor: 4.272

  9 in total

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