Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteins

被引:84
作者
Braiterman, LT
Zheng, SQ
Watkins, PA
Geraghty, MT
Johnson, G
McGuinness, MC
Moser, AB
Smith, KD
机构
[1] Kennedy Krieger Res Inst, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
[4] San Diego State Univ, Dept Biol & Mol Biol, San Diego, CA 92182 USA
关键词
D O I
10.1093/hmg/7.2.239
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
X-Linked adrenoleukodystrophy (X-ALD) is a neurodegenerative disorder characterized by reduced peroxisomal very long chain fatty acid (VLCFA) beta-oxidation. The X-ALD gene product (ALDP) is a peroxisomal transmembrane protein with an ATP binding cassette (ABC), ALDP and three other ABC proteins (PMP70, ALDR, P70R) localize to the peroxisomal membrane, The function of this family of peroxisomal membrane proteins is unknown, We used complementation studies to begin analysis of their role in VLCFA beta-oxidation and on the peroxisomal membrane. Expression of either ALDP or PMP70 restores VLCFA beta-oxidation in X-ALD fibroblasts, indicating overlapping functions, Their expression also restores peroxisome biogenesis in cells that are deficient in the peroxisomal membrane protein Pex2p, Thus it is likely that complex protein interactions are involved in the function and biogenesis of peroxisomal membranes that may contribute to disease heterogeneity.
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页码:239 / 247
页数:9
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