PEROXISOMAL DISORDERS - COMPLEMENTATION ANALYSIS USING BETA-OXIDATION OF VERY LONG-CHAIN FATTY-ACIDS

被引:25
作者
MCGUINNESS, MC [1 ]
MOSER, AB [1 ]
MOSER, HW [1 ]
WATKINS, PA [1 ]
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21205
关键词
D O I
10.1016/S0006-291X(05)80218-9
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
Complementation studies, using fused cell lines from patients with peroxisomal disorders, have shown correction of defective plasmalogen synthesis and phytanic acid oxidation as wll as an increase in the number of peroxisomes. At least six complementation groups have been reported. We demostrate here that complementing cell lines also acquire the ability to oxidize very long chain fatty acids (VLCFA), and that complementation groups defined with this technique are identical to those reported previously when plasmalogen synthesis was used as the criterion for complementation. This VLCFA complementation technique is of particular value in the study of patients in whom defective VLCFA is the only or major enzymatic defect, and we show complementation between cell lines from two patients each with an isolated defect in one of the peroxisomal fatty acid beta-oxidation enzymes. © 1990 Academic Press, Inc.
引用
收藏
页码:364 / 369
页数:6
相关论文
共 13 条
  • [1] GENETIC-HETEROGENEITY IN THE CEREBROHEPATORENAL (ZELLWEGER) SYNDROME AND OTHER INHERITED DISORDERS WITH A GENERALIZED IMPAIRMENT OF PEROXISOMAL FUNCTIONS - A STUDY USING COMPLEMENTATION ANALYSIS
    BRUL, S
    WESTERVELD, A
    STRIJLAND, A
    WANDERS, RJA
    SCHRAM, AW
    HEYMANS, HSA
    SCHUTGENS, RBH
    VANDENBOSCH, H
    TAGER, JM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (06) : 1710 - 1715
  • [2] GENETIC COMPLEMENTATION IN HETEROKARYONS OF HUMAN FIBROBLASTS DEFECTIVE IN COBALAMIN METABOLISM
    GRAVEL, RA
    MAHONEY, MJ
    RUDDLE, FH
    ROSENBERG, LE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (08) : 3181 - 3185
  • [3] BIOCHEMICAL-ABNORMALITIES IN RHIZOMELIC CHONDRODYSPLASIA PUNCTATA
    HOEFLER, G
    HOEFLER, S
    WATKINS, PA
    CHEN, WW
    MOSER, A
    BALDWIN, V
    MCGILLIVARY, B
    CHARROW, J
    FRIEDMAN, JM
    RUTLEDGE, L
    HASHIMOTO, T
    MOSER, HW
    [J]. JOURNAL OF PEDIATRICS, 1988, 112 (05) : 726 - 733
  • [4] TRANSLOCATION OF ACYL-COA OXIDASE INTO PEROXISOMES REQUIRES ATP HYDROLYSIS BUT NOT A MEMBRANE-POTENTIAL
    IMANAKA, T
    SMALL, GM
    LAZAROW, PB
    [J]. JOURNAL OF CELL BIOLOGY, 1987, 105 (06) : 2915 - 2922
  • [5] NEONATAL SEIZURES AND RETARDATION IN A GIRL WITH BIOCHEMICAL FEATURES OF X-LINKED ADRENOLEUKODYSTROPHY - A POSSIBLE NEW PEROXISOMAL DISEASE ENTITY
    NAIDU, S
    HOEFLER, G
    WATKINS, PA
    CHEN, WW
    MOSER, AB
    HOEFLER, S
    RANCE, NE
    POWERS, JM
    BEARD, M
    GREEN, WR
    HASHIMOTO, T
    MOSER, HW
    [J]. NEUROLOGY, 1988, 38 (07) : 1100 - 1107
  • [6] POLLTHE BT, 1989, HUM GENET, V81, P175
  • [7] POLLTHE BT, 1988, AM J HUM GENET, V42, P422
  • [8] GENETIC AND PHENOTYPIC HETEROGENEITY IN DISORDERS OF PEROXISOME BIOGENESIS - A COMPLEMENTATION STUDY INVOLVING CELL-LINES FROM 19 PATIENTS
    ROSCHER, AA
    HOEFLER, S
    HOEFLER, G
    PASCHKE, E
    PALTAUF, F
    MOSER, A
    MOSER, H
    [J]. PEDIATRIC RESEARCH, 1989, 26 (01) : 67 - 72
  • [9] HUMAN PEROXISOMAL 3-OXOACYL-COENZYME-A THIOLASE DEFICIENCY
    SCHRAM, AW
    GOLDFISCHER, S
    VANROERMUND, CWT
    BROUWERKELDER, EM
    COLLINS, J
    HASHIMOTO, T
    HEYMANS, HSA
    VANDENBOSCH, H
    SCHUTGENS, RBH
    TAGER, JM
    WANDERS, RJA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (08) : 2494 - 2496
  • [10] INSITU GENETIC COMPLEMENTATION ANALYSIS OF CELLS WITH GENERALIZED PEROXISOMAL DYSFUNCTION
    SINGH, AK
    KULVATUNYOU, N
    SINGH, I
    STANLEY, WS
    [J]. HUMAN HEREDITY, 1989, 39 (05) : 298 - 301