Literature DB >> 9016792

Isolation of a new peroxisome-deficient CHO cell mutant defective in peroxisome targeting signal-1 receptor.

T Tsukamoto1, A Bogaki, K Okumoto, K Tateishi, Y Fujiki, N Shimozawa, Y Suzuki, N Kondo, T Osumi.   

Abstract

For the study of mechanism of peroxisome biogenesis, we attempted to isolate CHO cell mutants deficient in peroxisome biogenesis. We used as the parent strain a stable CHO transformant of rat PEX2 (formerly named peroxisome assembly factor-1) cDNA, to avoid unusually frequent isolation of Pex2 mutants. Among the three peroxisome-deficient mutants obtained, ZP102 was a new CHO mutant of complementation group 2, and was restored for peroxisome assembly by the transfection of human PEX5 (formerly called PXR1 or PTS1R) cDNA. This approach would facilitate the isolation of new complementation gorups of peroxisome-deficient CHO mutants and the identification of essential genes for peroxisome biogenesis.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9016792     DOI: 10.1006/bbrc.1996.5971

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  8 in total

1.  Metabolic conversion of C20 polymethylene-interrupted polyunsaturated fatty acids to essential fatty acids.

Authors:  Tamotsu Tanaka; Sachika Uozumi; Katsuya Morito; Takashi Osumi; Akira Tokumura
Journal:  Lipids       Date:  2014-05       Impact factor: 1.880

2.  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

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.  Peroxisomes are formed from complex membrane structures in PEX6-deficient CHO cells upon genetic complementation.

Authors:  Noriyo Hashiguchi; Tomoko Kojidani; Tsuneo Imanaka; Tokuko Haraguchi; Yasushi Hiraoka; Eveline Baumgart; Sadaki Yokota; Toshiro Tsukamoto; Takashi Osumi
Journal:  Mol Biol Cell       Date:  2002-02       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.  Alterations of fatty acid metabolism and membrane fluidity in peroxisome-defective mutant ZP102 cells.

Authors:  Michiaki Nagura; Makiko Saito; Masao Iwamori; Yoichi Sakakihara; Takashi Igarashi
Journal:  Lipids       Date:  2004-01       Impact factor: 1.880

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

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.