Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiency

Yoshiharu Nishida, Ken Ichi Hirano, Kosuke Tsukamoto, Makoto Nagano, Chiaki Ikegami, Zhongyan Zhang, Ken ichi Tsujii, Akifumi Matsuyama, Tohru Ohama, Fumihiko Matsuura, Masato Ishigami, Naohiko Sakai, Hisatoyo Hiraoka, Shizuya Yamashita, Yuji Matsuzawa, Makoto Nagano, Mitsuaki Ishihara, Hiroaki Hattori, Toru Egashira, Naoki SakaneYoshihide Yoshida, Kirsten Roomp, Cheryl Wellington, Michael R. Hayden, Susumu Misugi

研究成果: Article

26 引用 (Scopus)

抄録

ATP-binding cassette transporter-1 (ABCA1) gene is mutated in patients with familial high-density lipoprotein deficiency (FHD). In order to know the molecular basis for FHD, we characterized three different ABCA1 mutations associated with FHD (G1158A/A255T, C5946T/R1851X, and A5226G/N1611D) with respect to their expression in the passaged fibroblasts from the patients and in the cells transfected with the mutated cDNAs. Fibroblasts from the all patients showed markedly decreased cholesterol efflux to apolipoprotein (apo)-Al. In the fibroblasts homozygous for G1158A/A255T, the immunoreactive mass of ABCA1 could not be detected, even when stimulated by 9-cis-retinoic acid and 22-R-hydroxycholesterol. In the fibroblasts homozygous for C5946T/R1851X, ABCA1 mRNA was comparable. Because the mutant ABCA1 protein (R1851X) was predicted to lack the epitope for the antibody used, we transfected FLAG-tagged truncated mutant (R1851X/ABCA1-FLAG) cDNA into Cos-7 cells, showing that the mutant protein expression was markedly reduced. The expression of N1611D ABCA1 protein was comparable in both fibroblasts and over-expressing cells, although cholesterol efflux from the cells was markedly reduced. These data indicated that, in the three patients investigated, the abnormalities and dysfunction of ABCA1 occurred at the different levels, providing important information about the expression, regulation, and function of ABCA1.

元の言語English
ページ(範囲)713-721
ページ数9
ジャーナルBiochemical and Biophysical Research Communications
290
発行部数2
DOI
出版物ステータスPublished - 01-01-2002

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ATP Binding Cassette Transporter 1
HDL Lipoproteins
Mutation
Fibroblasts
Complementary DNA
Cholesterol
Familial HDL deficiency
Apolipoproteins
Mutant Proteins
Epitopes
Proteins
Genes

All Science Journal Classification (ASJC) codes

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

これを引用

Nishida, Yoshiharu ; Hirano, Ken Ichi ; Tsukamoto, Kosuke ; Nagano, Makoto ; Ikegami, Chiaki ; Zhang, Zhongyan ; Tsujii, Ken ichi ; Matsuyama, Akifumi ; Ohama, Tohru ; Matsuura, Fumihiko ; Ishigami, Masato ; Sakai, Naohiko ; Hiraoka, Hisatoyo ; Yamashita, Shizuya ; Matsuzawa, Yuji ; Nagano, Makoto ; Ishihara, Mitsuaki ; Hattori, Hiroaki ; Egashira, Toru ; Sakane, Naoki ; Yoshida, Yoshihide ; Roomp, Kirsten ; Wellington, Cheryl ; Hayden, Michael R. ; Misugi, Susumu. / Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiency. :: Biochemical and Biophysical Research Communications. 2002 ; 巻 290, 番号 2. pp. 713-721.
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title = "Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiency",
abstract = "ATP-binding cassette transporter-1 (ABCA1) gene is mutated in patients with familial high-density lipoprotein deficiency (FHD). In order to know the molecular basis for FHD, we characterized three different ABCA1 mutations associated with FHD (G1158A/A255T, C5946T/R1851X, and A5226G/N1611D) with respect to their expression in the passaged fibroblasts from the patients and in the cells transfected with the mutated cDNAs. Fibroblasts from the all patients showed markedly decreased cholesterol efflux to apolipoprotein (apo)-Al. In the fibroblasts homozygous for G1158A/A255T, the immunoreactive mass of ABCA1 could not be detected, even when stimulated by 9-cis-retinoic acid and 22-R-hydroxycholesterol. In the fibroblasts homozygous for C5946T/R1851X, ABCA1 mRNA was comparable. Because the mutant ABCA1 protein (R1851X) was predicted to lack the epitope for the antibody used, we transfected FLAG-tagged truncated mutant (R1851X/ABCA1-FLAG) cDNA into Cos-7 cells, showing that the mutant protein expression was markedly reduced. The expression of N1611D ABCA1 protein was comparable in both fibroblasts and over-expressing cells, although cholesterol efflux from the cells was markedly reduced. These data indicated that, in the three patients investigated, the abnormalities and dysfunction of ABCA1 occurred at the different levels, providing important information about the expression, regulation, and function of ABCA1.",
author = "Yoshiharu Nishida and Hirano, {Ken Ichi} and Kosuke Tsukamoto and Makoto Nagano and Chiaki Ikegami and Zhongyan Zhang and Tsujii, {Ken ichi} and Akifumi Matsuyama and Tohru Ohama and Fumihiko Matsuura and Masato Ishigami and Naohiko Sakai and Hisatoyo Hiraoka and Shizuya Yamashita and Yuji Matsuzawa and Makoto Nagano and Mitsuaki Ishihara and Hiroaki Hattori and Toru Egashira and Naoki Sakane and Yoshihide Yoshida and Kirsten Roomp and Cheryl Wellington and Hayden, {Michael R.} and Susumu Misugi",
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Nishida, Y, Hirano, KI, Tsukamoto, K, Nagano, M, Ikegami, C, Zhang, Z, Tsujii, KI, Matsuyama, A, Ohama, T, Matsuura, F, Ishigami, M, Sakai, N, Hiraoka, H, Yamashita, S, Matsuzawa, Y, Nagano, M, Ishihara, M, Hattori, H, Egashira, T, Sakane, N, Yoshida, Y, Roomp, K, Wellington, C, Hayden, MR & Misugi, S 2002, 'Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiency', Biochemical and Biophysical Research Communications, 巻. 290, 番号 2, pp. 713-721. https://doi.org/10.1006/bbrc.2001.6219

Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiency. / Nishida, Yoshiharu; Hirano, Ken Ichi; Tsukamoto, Kosuke; Nagano, Makoto; Ikegami, Chiaki; Zhang, Zhongyan; Tsujii, Ken ichi; Matsuyama, Akifumi; Ohama, Tohru; Matsuura, Fumihiko; Ishigami, Masato; Sakai, Naohiko; Hiraoka, Hisatoyo; Yamashita, Shizuya; Matsuzawa, Yuji; Nagano, Makoto; Ishihara, Mitsuaki; Hattori, Hiroaki; Egashira, Toru; Sakane, Naoki; Yoshida, Yoshihide; Roomp, Kirsten; Wellington, Cheryl; Hayden, Michael R.; Misugi, Susumu.

:: Biochemical and Biophysical Research Communications, 巻 290, 番号 2, 01.01.2002, p. 713-721.

研究成果: Article

TY - JOUR

T1 - Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiency

AU - Nishida, Yoshiharu

AU - Hirano, Ken Ichi

AU - Tsukamoto, Kosuke

AU - Nagano, Makoto

AU - Ikegami, Chiaki

AU - Zhang, Zhongyan

AU - Tsujii, Ken ichi

AU - Matsuyama, Akifumi

AU - Ohama, Tohru

AU - Matsuura, Fumihiko

AU - Ishigami, Masato

AU - Sakai, Naohiko

AU - Hiraoka, Hisatoyo

AU - Yamashita, Shizuya

AU - Matsuzawa, Yuji

AU - Nagano, Makoto

AU - Ishihara, Mitsuaki

AU - Hattori, Hiroaki

AU - Egashira, Toru

AU - Sakane, Naoki

AU - Yoshida, Yoshihide

AU - Roomp, Kirsten

AU - Wellington, Cheryl

AU - Hayden, Michael R.

AU - Misugi, Susumu

PY - 2002/1/1

Y1 - 2002/1/1

N2 - ATP-binding cassette transporter-1 (ABCA1) gene is mutated in patients with familial high-density lipoprotein deficiency (FHD). In order to know the molecular basis for FHD, we characterized three different ABCA1 mutations associated with FHD (G1158A/A255T, C5946T/R1851X, and A5226G/N1611D) with respect to their expression in the passaged fibroblasts from the patients and in the cells transfected with the mutated cDNAs. Fibroblasts from the all patients showed markedly decreased cholesterol efflux to apolipoprotein (apo)-Al. In the fibroblasts homozygous for G1158A/A255T, the immunoreactive mass of ABCA1 could not be detected, even when stimulated by 9-cis-retinoic acid and 22-R-hydroxycholesterol. In the fibroblasts homozygous for C5946T/R1851X, ABCA1 mRNA was comparable. Because the mutant ABCA1 protein (R1851X) was predicted to lack the epitope for the antibody used, we transfected FLAG-tagged truncated mutant (R1851X/ABCA1-FLAG) cDNA into Cos-7 cells, showing that the mutant protein expression was markedly reduced. The expression of N1611D ABCA1 protein was comparable in both fibroblasts and over-expressing cells, although cholesterol efflux from the cells was markedly reduced. These data indicated that, in the three patients investigated, the abnormalities and dysfunction of ABCA1 occurred at the different levels, providing important information about the expression, regulation, and function of ABCA1.

AB - ATP-binding cassette transporter-1 (ABCA1) gene is mutated in patients with familial high-density lipoprotein deficiency (FHD). In order to know the molecular basis for FHD, we characterized three different ABCA1 mutations associated with FHD (G1158A/A255T, C5946T/R1851X, and A5226G/N1611D) with respect to their expression in the passaged fibroblasts from the patients and in the cells transfected with the mutated cDNAs. Fibroblasts from the all patients showed markedly decreased cholesterol efflux to apolipoprotein (apo)-Al. In the fibroblasts homozygous for G1158A/A255T, the immunoreactive mass of ABCA1 could not be detected, even when stimulated by 9-cis-retinoic acid and 22-R-hydroxycholesterol. In the fibroblasts homozygous for C5946T/R1851X, ABCA1 mRNA was comparable. Because the mutant ABCA1 protein (R1851X) was predicted to lack the epitope for the antibody used, we transfected FLAG-tagged truncated mutant (R1851X/ABCA1-FLAG) cDNA into Cos-7 cells, showing that the mutant protein expression was markedly reduced. The expression of N1611D ABCA1 protein was comparable in both fibroblasts and over-expressing cells, although cholesterol efflux from the cells was markedly reduced. These data indicated that, in the three patients investigated, the abnormalities and dysfunction of ABCA1 occurred at the different levels, providing important information about the expression, regulation, and function of ABCA1.

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U2 - 10.1006/bbrc.2001.6219

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