Cited by 57Metabolism and Genetic DisordersCellular transport and secretionDrug Transport and Resistance Mechanisms

Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p

Gloeckner, Christian J., Mayerhofer, Peter U., Landgraf, Pablo, Muntau, Ania C., Holzinger, Andreas, Gerber, Josef-Karl, Kammerer, Stefan, Adamski, Jerzy +1 more·2000·Biochemical and Biophysical Research Communications

Abstract

Four ABC half transporters (ALDP, ALDRP, PMP70, and PMP69) have been identified in the mammalian peroxisomal membrane but no function has been unambiguously assigned to any of them. To date X-linked adrenoleukodystrophy (X-ALD) is the only human disease known to result from a defect of one of these ABC transporters, ALDP. Using the yeast two-hybrid system and in vitro GST pull-down assays, we identified the peroxin PEX19p as a novel interactor of ALDP, ALDRP, and PMP70. The cytosolic farnesylated protein PEX19p was previously shown to be involved in an early step of the peroxisomal biogenesis. The PEX19p interaction occurs in an internal N-terminal region of ALDP which we verified to be important for proper peroxisomal targeting of this protein. Farnesylated wild-type PEX19p and a farnesylation-deficient mutant PEX19p did not differ in their ability to bind to ALDP. Our data provide evidence that PEX19p is a cytosolic acceptor protein for the peroxisomal ABC transporters ALDP, PMP70, and ALDRP and might be involved in the intracellular sorting and trafficking of these proteins to the peroxisomal membrane.

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Crossref · 10.1006/bbrc.2000.2572

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  • ALDP is synthesized on free cytosolic ribosomes then targeted to peroxisomes via a Pex19p-dependent pathway, then inserted post-translationally into the peroxisomal membrane.

    “ALDP is synthesized on free cytosolic ribosomes then targeted to peroxisomes via a peroxisomal biogenesis factor-19 (Pex19p)-dependent pathway, then inserted post-translationally into the peroxisomal membrane [141].”

    From Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy (2025) · cites this paper as [141]

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Authors
Gloeckner, C. J., Mayerhofer, P. U., Landgraf, P., Muntau, A. C., Holzinger, A., Gerber, J.-K., Kammerer, S., Adamski, J., & Roscher, A. A.
Affiliations
  • Helmholtz Munich (DE)
  • Ludwig-Maximilians-Universität München (DE)
  • Sequenom (United States) (US)
Corresponding author
  • Adamski, Jerzy
  • Roscher, Adelbert A.
Venue
Biochemical and Biophysical Research Communications
Publisher
Elsevier BV
Published
2000-04
Volume
271
Issue
1
Pages
144-150
ISSN
0006-291X (ISSN-L)
OpenAlex
W1972446643
Cited by
57
References
4
Citations by year
2026: 1 · 2025: 1 · 2023: 2 · 2022: 1 · 2021: 1 · 2019: 1 · 2017: 3 · 2015: 1 · 2014: 1 · 2013: 1 · 2012: 1
FWCI
3.01
Type
journal article
Language
en
Open access
closed
Locations
  • Biochemical and Biophysical Research Communications (publishedVersion)
  • PubMed (publishedVersion)
  • Open Research (University of Surrey) (submittedVersion)
  • Surrey Research Insight Open Access (The University of Surrey) (submittedVersion)
  • Site cant be reached (submittedVersion)
Funders
Deutsche Forschungsgemeinschaft
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
  • Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
Keywords
PEX19, ABC transporters, ALDP, PMP70, peroxisome biogenesis, peroxisomal membrane, protein-protein interaction, farnesylation, peroxisomal targeting, intracellular trafficking, X-linked adrenoleukodystrophy
MeSH terms
ATP Binding Cassette Transporter, Subfamily D, ATP Binding Cassette Transporter, Subfamily D, Member 1, Adrenoleukodystrophy, Animals, Brain, Glutathione Transferase, Humans, Membrane Proteins, Plasmids, Protein Binding, Proteins, Recombinant Fusion Proteins, Transfection, Gene Library, Protein Prenylation, Protein Structure, Tertiary, DNA, Complementary, ATP-Binding Cassette Transporters, COS Cells, Peroxisomes, Two-Hybrid System Techniques

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