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Jean Mosser, Yves Lutz, Marie Elisabeth Stoeckel, Claude Olivier Sarde, Christine Kretz, Anne Marie Douar, Jacqueline Lopez, Patrick Aubourg, Jean Louis Mandel, The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein, Human Molecular Genetics, Volume 3, Issue 2, February 1994, Pages 265–271, https://doi.org/10.1093/hmg/3.2.265
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Abstract
Adrenoleukodystrophy is a severe genetic demye-llnating disease associated with an impairment of β-oxidation of very long chain fatty acids (VLCFA) In peroxisomes. Earlier studies had suggested that a deficiency in VLCFA CoA synthetase was the primary defect. A candidate adrenoleukodystrophy gene has recently been cloned and was found unexpectedly to encode a putative ATP-binding cassette transporter. We have raised monoclonal antibodies against this protein, that detect a 75kDa band. This protein was absent in several patients with adrenoleukodystrophy. Immunofluorescence and Immunoelectron microscopy showed that the adrenoleukodystrophy protein (ALDP) is associated with the peroxisomal membrane. Distinct Immunofluorescence patterns were observed in cell lines from patients with Zellweger syndrome (a peroxisomal biogenesis disorder) belonging to different complementation groups.