Peroxisome biogenesis disorders: Identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13

Nobuyuki Shimozawa, Yasuyuki Suzuki, Zhongyi Zhang, Atsushi Imamura, Toshiro Tsukamoto, Takashi Osumi, Keita Tateishi, Kanji Okumoto, Yukio Fujiki, Tadao Orii, Peter G. Barth, Ronald J.A. Wanders, Naomi Kondo

研究成果: ジャーナルへの寄稿記事

19 引用 (Scopus)

抄録

Ten complementation groups of generalized peroxisome biogenesis disorders (PBD), (excluding rhizomelic chondrodysplasia punctata) have been identified using complementation analysis. Four of the genes involved have been identified using two different methods of (1) genetic functional complementation of peroxisome deficient CHO cell mutants and (2) homology searches for human dbEST, based on yeast genes involved in peroxisome biogenesis (PEX genes). We report here the first identification of a new complementation group which is genetically different from peroxisome deficient CHO mutants. There were no complementations by the human PEX 13 gene. The nature of the related gene is being investigated.

元の言語英語
ページ(範囲)368-371
ページ数4
ジャーナルBiochemical and Biophysical Research Communications
243
発行部数2
DOI
出版物ステータス出版済み - 2 13 1998

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Peroxisomes
Genes
Rhizomelic Chondrodysplasia Punctata
CHO Cells
Yeast
Yeasts
Peroxisome biogenesis disorders

All Science Journal Classification (ASJC) codes

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

これを引用

Peroxisome biogenesis disorders : Identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13. / Shimozawa, Nobuyuki; Suzuki, Yasuyuki; Zhang, Zhongyi; Imamura, Atsushi; Tsukamoto, Toshiro; Osumi, Takashi; Tateishi, Keita; Okumoto, Kanji; Fujiki, Yukio; Orii, Tadao; Barth, Peter G.; Wanders, Ronald J.A.; Kondo, Naomi.

:: Biochemical and Biophysical Research Communications, 巻 243, 番号 2, 13.02.1998, p. 368-371.

研究成果: ジャーナルへの寄稿記事

Shimozawa, N, Suzuki, Y, Zhang, Z, Imamura, A, Tsukamoto, T, Osumi, T, Tateishi, K, Okumoto, K, Fujiki, Y, Orii, T, Barth, PG, Wanders, RJA & Kondo, N 1998, 'Peroxisome biogenesis disorders: Identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13', Biochemical and Biophysical Research Communications, 巻. 243, 番号 2, pp. 368-371. https://doi.org/10.1006/bbrc.1997.8067
Shimozawa, Nobuyuki ; Suzuki, Yasuyuki ; Zhang, Zhongyi ; Imamura, Atsushi ; Tsukamoto, Toshiro ; Osumi, Takashi ; Tateishi, Keita ; Okumoto, Kanji ; Fujiki, Yukio ; Orii, Tadao ; Barth, Peter G. ; Wanders, Ronald J.A. ; Kondo, Naomi. / Peroxisome biogenesis disorders : Identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13. :: Biochemical and Biophysical Research Communications. 1998 ; 巻 243, 番号 2. pp. 368-371.
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