Fibrate induction of the adrenoleukodystrophy‐related gene (ABCD2): Promoter analysis and role of the peroxisome proliferator‐activated receptor PPARα
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X‐linked adrenoleukodystrophy (X‐ALD) is a neurodegenerative disease due to a defect in the ABCD1 (ALD) gene. ABCD1, and the two close homologues ABCD2 (ALDR) and ABCD3 (PMP70), are genes encoding ATP‐binding cassette half‐transporters of the peroxisomal membrane. As overexpression of the ABCD2 or ABCD3 gene can reverse the biochemical phenotype of X‐ALD (reduced β‐oxidation of very‐long‐chain fatty acids), pharmacological induction of these partially redundant genes may represent a therapeutic approach to X‐ALD. We previously reported that the ABCD2 and ABCD3 genes could be strongly induced by fibrates, which are hypolipidaemic drugs and peroxisome‐proliferators in rodents. We provide evidence that the induction is dependent on peroxisome proliferator‐activated receptor (PPARα) as both genes were not induced in fenofibrate‐treated PPARα–/– knock‐out mice. To further characterize the PPARα pathway, we cloned and analysed the promoter of the ABCD2 gene, the closest homologue of the ABCD1 gene. The proximal region (2 kb) of the rat promoter displayed a high conservation with the human and mouse cognate sequences suggesting an important role of the region in regulation of the ABCD2 gene. Classically, fibrate‐induction involves interaction of PPARα with a response element (PPRE) characterized by a direct repeat of the AGGTCA‐like motif. Putative PPRE motifs of the rat ABCD2 promoter were studied in the isolated form or in their promoter context by gel‐shift assay and transfection of COS‐7 cells. We failed to characterize a functional PPRE, suggesting a different mechanism for the PPARα‐dependent regulation of the ABCD2 gene.
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ALDR/ABCD2 is the closest paralogue of ALD and a target of PPARa and SREBP transcription factors.
“its closest paralogue and a target of PPARa and SREBP transcription factors.”
From Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophy (2004) · cites this paper as [25]
Pharmacological induction of ABCD2 was shown to compensate for ABCD1 defect in vitro and in rare cases in vivo.
“Pharmacological induction of ABCD2 was indeed shown to compensate for ABCD1 defect in vitro and in rare cases, in vivo, opening the way for clinical trials [ 43 , 44 , 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 , 54 , 55 , 56 , 57 , 58 ].”
From Peroxisomal ABC Transporters: An Update (2021) · cites this paper as [46]
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- Authors
- Fourcade, S., Savary, S., Albet, S., Gauthé, D., Gondcaille, C., Pineau, T., Bellenger, J., Bentejac, M., Holzinger, A., Berger, J., & Bugaut, M.
- Affiliations
- University of Vienna (AT)
- Venue
- European Journal of Biochemistry
- Publisher
- Wiley
- Published
- 2001-06
- Volume
- 268
- Issue
- 12
- Pages
- 3490-3500
- ISSN
- 0014-2956 (ISSN-L)
- 1432-1033
- OpenAlex
- W1499068934
- Cited by
- 70
- References
- 55
- Citations by year
- 2023: 1 · 2022: 2 · 2021: 2 · 2018: 2 · 2016: 1 · 2015: 3 · 2014: 5 · 2013: 6 · 2012: 1
- FWCI
- 1.98
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- European Journal of Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Keywords
- X-linked adrenoleukodystrophy, ABCD2, ABCD1, ABCD3, peroxisomal ABC transporters, fibrates, fenofibrate, PPARα, gene induction, promoter analysis, peroxisome proliferator response element, very long chain fatty acid beta-oxidation, PPARα knockout mice, peroxisome proliferators
- MeSH terms
- ATP Binding Cassette Transporter, Subfamily D, Adrenoleukodystrophy, Animals, Hypolipidemic Agents, Base Sequence, DNA, Gene Expression Regulation, Humans, Male, Molecular Sequence Data, Fenofibrate, Promoter Regions, Genetic, Sequence Homology, Nucleic Acid, Transcription Factors, Transcription, Genetic, Rats, Wistar, Receptors, Cytoplasmic and Nuclear, Mice, Knockout, ATP-Binding Cassette Transporters, Mice, Rats
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