Cellular and molecular aspects of Zellweger syndrome and other peroxisome biogenesis disorders

被引:37
作者
Brosius, U [1 ]
Gärtner, J [1 ]
机构
[1] Univ Dusseldorf, Dept Pediat, D-40225 Dusseldorf, Germany
关键词
peroxin; PEX gene; peroxisome; peroxisome biogenesis; peroxisome biogenesis disorder; Zellweger syndrome;
D O I
10.1007/s00018-002-8486-7
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
Peroxisomes are single-membrane-bound organelles present in virtually all eukaryotic cells. They are involved in numerous metabolic processes, both catabolic and anabolic, including beta-oxidation of very long chain fatty acids, metabolism of hydrogen peroxide, plasmalogen biosynthesis and bile acid synthesis. In several genetic diseases, there is either isolated deficiency of a specific peroxisomal protein (single-protein deficiencies) or a defect in the formation of the organelle with loss of multiple peroxisomal functions (peroxisome biogenesis disorders). X-linked adrenoleukodystrophy is an example of the former, and the Zellweger spectrum of the latter. Peroxisome biogenesis disorders are inherited in an autosomal recessive manner and result from mutations in any of at least 12 PEX genes that encode peroxins. This article reviews the peroxisomal system, the clinical, biochemical and molecular aspects of peroxisomal disorders, and discusses recent scientific advances in the understanding of peroxisome biogenesis.
引用
收藏
页码:1058 / 1069
页数:12
相关论文
共 105 条
[1]   Clofibrate-inducible, 2X-kDa peroxisomal integral membrane protein is encoded by PEX11 [J].
Abe, I ;
Okumoto, K ;
Tamura, S ;
Fujiki, Y .
FEBS LETTERS, 1998, 431 (03) :468-472
[2]   Pex14p, a peroxisomal membrane protein binding both receptors of the two PTS-dependent import pathways [J].
Albertini, M ;
Rehling, P ;
Erdmann, R ;
Girzalsky, W ;
Kiel, JAKW ;
Veenhuis, M ;
Kunau, WH .
CELL, 1997, 89 (01) :83-92
[3]   The Hansenula polymorpha PER9 gene encodes a peroxisomal membrane protein essential for peroxisome assembly and integrity [J].
Baerends, RJS ;
Rasmussen, SW ;
Hilbrands, RE ;
vanderHeide, M ;
Faber, KN ;
Reuvekamp, PTW ;
Kiel, JAKW ;
Cregg, JM ;
vanderKlei, IJ ;
Veenhuis, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (15) :8887-8894
[4]   Targeting elements in the amino-terminal part direct the human 70-kDa peroxisomal integral membrane protein (PMP70) to peroxisomes [J].
Biermanns, M ;
Gärtner, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 285 (03) :649-655
[5]   Saccharomyces cerevisiae PTS1 receptor Pex5p interacts with the SH3 domain of the peroxisomal membrane protein Pex13p in an unconventional, non-PXXP-related manner [J].
Bottger, G ;
Barnett, P ;
Klein, ATJ ;
Kragt, A ;
Tabak, HF ;
Distel, B .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (11) :3963-3976
[6]   DISORDERS OF PEROXISOME BIOGENESIS [J].
BRAVERMAN, N ;
DODT, G ;
GOULD, SJ ;
VALLE, D .
HUMAN MOLECULAR GENETICS, 1995, 4 :1791-1798
[7]   Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata [J].
Braverman, N ;
Steel, G ;
Obie, C ;
Moser, A ;
Moser, H ;
Gould, SJ ;
Valle, D .
NATURE GENETICS, 1997, 15 (04) :369-376
[8]  
Braverman NE, 1999, AM J HUM GENET, V65, pA286
[9]   THE TETRATRICOPEPTIDE REPEAT-DOMAIN OF THE PAS10 PROTEIN OF SACCHAROMYCES-CEREVISIAE IS ESSENTIAL FOR BINDING THE PEROXISOMAL TARGETING SIGNAL-SKL [J].
BROCARD, C ;
KRAGLER, F ;
SIMON, MM ;
SCHUSTER, T ;
HARTIG, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 204 (03) :1016-1022
[10]   Pex14p is a member of the protein linkage map of Pex5p [J].
Brocard, C ;
Lametschwandtner, G ;
Koudelka, R ;
Hartig, A .
EMBO JOURNAL, 1997, 16 (18) :5491-5500