Rat adrenoleukodystrophy-related (ALDR) gene: full-length cDNA sequence and new insight in expression
Abstract
X-linked adrenoleukodystrophy (X-ALD) is an inherited demyelinating disorder due to mutations in the ALD gene, which encodes a peroxisomal ABC half-transporter (ALDP). It has been suggested that ALDP assembles with ALDRP (adrenoleukodystrophy-related protein), a close homologous half-transporter, to form a functional heterodimer. For the first time full-length ALDRP cDNA (5.5 kb) was cloned, and 5' and 3' RACE analysis revealed that alternative usage of polyadenylation sites generates the two transcripts of 3.0 and 5.5 kb observed in the rat in Northern blot analysis. Southern blotting and chromosomal mapping demonstrated one ALDR locus in the rat genome. Characterisation of the 3' flanking region suggested that an ID sequence might be responsible for high expression of the 5.5 kb ALDRP transcript in rat brain. ALDR gene expression was found to be high in the liver of rats before weaning and very low in adult rats; the reverse developmental regulation was observed in the brain. Fenofibrate, which is a potent inducer of the ALDR gene in the liver of adult rats, could not induce the ALDR gene in suckling rats. The exact significance of this result with regard to development of an efficient pharmacological gene therapy for X-ALD is discussed.
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ALDRP has been identified in mouse, rat, and man.
“It has been identified in mouse [Lombard-Platet et al., 1996], rat [Albet et al., 2001], and man [Holzinger et al., 1997a].”
From ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations (2001) · cites this paper as Albet et al., 2001
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References 50 · Cited by 18
- Authors
- Albet, S., Bentejac, M., Savary, S., Gondcaille, C., Netik, A., Berger, J., Szpirer, C., Troffer-Charlier, N., & Bugaut, M.
- Affiliations
- Université de Bourgogne (FR)
- University of Vienna (AT)
- Université Libre de Bruxelles (BE)
- Institut de génétique et de biologie moléculaire et cellulaire (FR)
- Corresponding author
- Bugaut, Maurice
- Venue
- Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression
- Publisher
- Elsevier BV
- Published
- 2001-01
- Volume
- 1517
- Issue
- 2
- Pages
- 257-269
- ISSN
- 0167-4781 (ISSN-L)
- OpenAlex
- W1997047641
- Cited by
- 18
- References
- 50
- Citations by year
- 2014: 1 · 2013: 4
- FWCI
- 0.74
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression (publishedVersion)
- PubMed (publishedVersion)
- Dépôt institutionnel de l'Université libre de Bruxelles (Université Libre de Bruxelles) (submittedVersion)
- Funders
- Association Européenne contre les Leucodystrophies
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Health Sciences › Medicine › Physiology › Lysosomal Storage Disorders Research
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Keywords
- X-linked adrenoleukodystrophy, ALDP, rats, cDNA cloning, alternative polyadenylation, mRNA isoforms, gene expression regulation, liver development, brain expression, fenofibrate
- MeSH terms
- ATP Binding Cassette Transporter, Subfamily D, Adrenoleukodystrophy, Amino Acid Sequence, Animals, Base Sequence, Brain, Chromosome Mapping, Cloning, Molecular, Molecular Sequence Data, Fenofibrate, Proteins, Protein Biosynthesis, Gene Library, Rats, Wistar, DNA, Complementary, Gene Expression Regulation, Developmental, ATP-Binding Cassette Transporters, 5' Untranslated Regions, 3' Untranslated Regions, Mice, Rats
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