Literature DB >> 7685346

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

R Thieringer1, C R Raetz.   

Abstract

Chinese hamster ovary (CHO) mutant cells deficient in peroxisome biogenesis regain peroxisomes after transfection with a cDNA coding for peroxisome assembly factor (PAF)-1 from rat liver. Reconstitution of the transfected mutant cells with wild-type cytoplasm was not required, demonstrating that expression of the PAF-1 gene alone was sufficient for the restoration of peroxisome biogenesis. Plasmalogen biosynthesis in the transfected mutants was also restored to approximately wild-type levels. The nucleotide sequence of the cDNA encoding the open reading frame for PAF-1 from CHO-K1 cells was determined. This allowed us to identify point mutations of PAF-1 in two peroxisomal mutant cell lines. The mutation in ZR-78 cells changed a cysteine to a tyrosine codon in a region located at the carboxyl terminus of the protein, which resembles the zinc finger motif of DNA-binding proteins. A point mutation in the PAF-1 gene of ZR-82 leads to premature termination.

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Year:  1993        PMID: 7685346

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  8 in total

1.  Restoration of peroxisome biogenesis in a peroxisome-deficient mammalian cell line by expression of either the 35 kDa or the 70 kDa peroxisomal membrane proteins.

Authors:  J Gärtner; C Obie; P Watkins; D Valle
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

2.  A new complementation assay for peroxisome-deficient cell lines.

Authors:  D R FitzPatrick; D Valle
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

3.  Nonsense suppressor therapies rescue peroxisome lipid metabolism and assembly in cells from patients with specific PEX gene mutations.

Authors:  Patricia K Dranchak; Erminia Di Pietro; Ann Snowden; Nathan Oesch; Nancy E Braverman; Steven J Steinberg; Joseph G Hacia
Journal:  J Cell Biochem       Date:  2011-05       Impact factor: 4.429

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

Authors:  T Tsukamoto; N Shimozawa; Y Fujiki
Journal:  Mol Cell Biol       Date:  1994-08       Impact factor: 4.272

5.  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

6.  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

7.  Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder.

Authors:  P L Faust; M E Hatten
Journal:  J Cell Biol       Date:  1997-12-01       Impact factor: 10.539

8.  Functional Peroxisomes Are Essential for Efficient Cholesterol Sensing and Synthesis.

Authors:  Khanichi N Charles; Janis E Shackelford; Phyllis L Faust; Steven J Fliesler; Herbert Stangl; Werner J Kovacs
Journal:  Front Cell Dev Biol       Date:  2020-11-06
  8 in total

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