Alternative RNA splicing generates a glycosylphosphatidylinositol-anchored form of ceruloplasmin in mammalian brain

被引:167
作者
Patel, BN
Dunn, RJ
David, S
机构
[1] Montreal Gen Hosp, Res Inst, Ctr Res Neurosci, Montreal, PQ H3G 1A4, Canada
[2] McGill Univ, Montreal, PQ H3G 1A4, Canada
关键词
D O I
10.1074/jbc.275.6.4305
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
Ceruloplasmin is a copper containing ferroxidase that is essential for normal iron homeostasis. Whereas ceruloplasmin in plasma is produced and secreted by hepatocytes, in the brain a glycosylphosphatidylinositol (GPI)-anchored form of ceruloplasmin is expressed on the surface of astrocytes, By using a cDNA cloning approach, we have now determined that the GPI-anchored form of ceruloplasmin is generated by alternative RNA splicing. The splicing occurs downstream of exon 18 and replaces the C-terminal 5 amino acids of the secreted form with an alternative 30 amino acids that signal GPI anchor addition. RNase protection analysis demonstrates that the GPI-anchored form is the major form in the brain, whereas the secreted form predominates in the liver. Individuals with aceruloplasminemia, a hereditary deficiency of ceruloplasmin, have severe iron deposition in a number of organs, including the brain where it results-in neurodegeneration. Therefore, this novel GPI-anchored form of ceruloplasmin is likely to play an important role in iron metabolism in the central nervous system.
引用
收藏
页码:4305 / 4310
页数:6
相关论文
共 39 条
[1]   THE FET3 GENE OF SACCHAROMYCES-CEREVISIAE ENCODES A MULTICOPPER OXIDASE REQUIRED FOR FERROUS IRON UPTAKE [J].
ASKWITH, C ;
EIDE, D ;
VANHO, A ;
BERNARD, PS ;
LI, LT ;
DAVISKAPLAN, S ;
SIPE, DM ;
KAPLAN, J .
CELL, 1994, 76 (02) :403-410
[2]   DEVELOPMENTAL PROFILE OF PLASMA-PROTEINS IN HUMAN FETAL CEREBROSPINAL-FLUID AND BLOOD [J].
BELL, JE ;
FRYER, AA ;
COLLINS, M ;
MARSHALL, T ;
JONES, PW ;
STRANGE, R ;
HUME, R .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1991, 17 (06) :441-456
[3]  
Bothwell TH, 1998, SEMIN HEMATOL, V35, P55
[4]  
Bottai D, 1997, J COMP NEUROL, V389, P65, DOI 10.1002/(SICI)1096-9861(19971208)389:1<65::AID-CNE5>3.0.CO
[5]  
2-C
[6]   FINE-STRUCTURE OF THE HUMAN CERULOPLASMIN GENE [J].
DAIMON, M ;
YAMATANI, K ;
IGARASHI, M ;
FUKASE, N ;
KAWANAMI, T ;
KATO, T ;
TOMINAGA, M ;
SASAKI, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 208 (03) :1028-1035
[7]   Molecular mechanisms of iron uptake in eukaryotes [J].
DeSilva, DM ;
Askwith, CC ;
Kaplan, J .
PHYSIOLOGICAL REVIEWS, 1996, 76 (01) :31-47
[8]  
FLEMING RE, 1990, J BIOL CHEM, V265, P7701
[9]  
GAITSKHOKI V S, 1990, Biokhimiya, V55, P927
[10]   ALTERED BRAIN METABOLISM OF IRON AS A CAUSE OF NEURODEGENERATIVE DISEASES [J].
GERLACH, M ;
BENSHACHAR, D ;
RIEDERER, P ;
YOUDIM, MBH .
JOURNAL OF NEUROCHEMISTRY, 1994, 63 (03) :793-807