RECENT BIOCHEMICAL AND GENETIC ADVANCES IN OUR UNDERSTANDING OF BATTEN DISEASE (CEROID-LIPOFUSCINOSIS)

被引:13
作者
HALL, NA [1 ]
LAKE, BD [1 ]
PATRICK, AD [1 ]
机构
[1] UNIV LONDON,INST CHILD HLTH,LONDON,ENGLAND
关键词
BATTEN DISEASE; CEROID-LIPOFUSCINOSIS; ATP SYNTHASE; SUBUNIT-C; DOLICHOL; MITOCHONDRION; LYSOSOME; STORAGE DISEASE;
D O I
10.1159/000112183
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Protein is the major component of the intra-lysosomal storage material which characteristically accumulates in Batten's disease. In the late-infantile, juvenile and adult forms of the disease, and in a form affecting sheep, this protein is principally composed of a single polypeptide, subunit c of mitochondrial ATP synthase. Subunit c is not stored in the infantile form of Batten's disease, supporting recent genetic data which suggest this is a distinct disease. Nor is subunit c found in storage material within other lysosomal storage diseases or in lipofuscin of old age. Subunit c storage, therefore, is specific for the later-onset forms of Batten's disease and indeed may be central to their aetiology.
引用
收藏
页码:339 / 344
页数:6
相关论文
共 25 条
[1]  
Andermann E, 1988, Am J Med Genet Suppl, V5, P111
[2]  
Batten F. E., 1915, P ROY SOC MED, V8, P70
[3]  
Batten F.E., 1903, T OPHTHAL SOC UK, V23, P386
[4]   KUFS DISEASE - A CRITICAL REAPPRAISAL [J].
BERKOVIC, SF ;
CARPENTER, S ;
ANDERMANN, F ;
ANDERMANN, E ;
WOLFE, LS .
BRAIN, 1988, 111 :27-62
[5]  
CLAUSSEN M, IN PRESS AM J MED GE
[6]   THE SEQUENCE OF THE MAJOR PROTEIN STORED IN OVINE CEROID LIPOFUSCINOSIS IS IDENTICAL WITH THAT OF THE DICYCLOHEXYLCARBODIIMIDE-REACTIVE PROTEOLIPID OF MITOCHONDRIAL ATP SYNTHASE [J].
FEARNLEY, IM ;
WALKER, JE ;
MARTINUS, RD ;
JOLLY, RD ;
KIRKLAND, KB ;
SHAW, GJ ;
PALMER, DN .
BIOCHEMICAL JOURNAL, 1990, 268 (03) :751-758
[7]   BATTEN DISEASE (SPIELMEYER-VOGT DISEASE, JUVENILE ONSET NEURONAL CEROID-LIPOFUSCINOSIS) GENE (CLN3) MAPS TO HUMAN CHROMOSOME-16 [J].
GARDINER, M ;
SANDFORD, A ;
DEADMAN, M ;
POULTON, J ;
COOKSON, W ;
REEDERS, S ;
JOKIAHO, I ;
PELTONEN, L ;
EIBERG, H ;
JULIER, C .
GENOMICS, 1990, 8 (02) :387-390
[8]   ULTRASTRUCTURAL DIVERSITY AND ESSENCE OF RESIDUAL BODIES IN NEURONAL CEROID-LIPOFUSCINOSIS [J].
GOEBEL, HH ;
ZEMAN, W ;
PATEL, VK ;
PULLARKAT, R ;
LENARD, HG .
MECHANISMS OF AGEING AND DEVELOPMENT, 1979, 10 (1-2) :53-70
[9]  
Hall N A, 1988, Am J Med Genet Suppl, V5, P221
[10]   HIGH-MANNOSE DOLICHOL-LINKED OLIGOSACCHARIDES IN INFANTILE CEROID-LIPOFUSCINOSIS [J].
HALL, NA ;
HALTIA, M ;
PATRICK, AD .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1989, 17 (06) :1032-1033