Cloning and expression analysis of the sheep ceruloplasmin cDNA

被引:15
作者
Lockhart, PJ
Mercer, JFB [1 ]
机构
[1] Deakin Univ, Ctr Cellular & Mol Biol, Burwood 3125, Australia
[2] Royal Childrens Hosp, Murdoch Inst, Parkville, Vic 3052, Australia
基金
英国医学研究理事会;
关键词
copper metabolism; gene expression; liver development; northern blot; nucleotide sequence;
D O I
10.1016/S0378-1119(99)00276-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The cDNA encoding sheep ceruloplasmin (sCP) was isolated from a sheep liver cDNA library. The cDNA contig was 3530 nucleotides in length and encoded a protein of 1048 amino acids. The deduced amino acid sequence showed a high degree of conservation (87%) when compared to the human ceruloplasmin (hCP) sequence. Northern blot analysis of sheep tissue revealed that the sheep ceruloplasmin gene (sCP) was expressed primarily in the liver, but low levels of mRNA were detected in the hypothalamus, spleen and uterus. No sCP mRNA was detected in the cortex, heart, intestine or kidney. Expression was not significantly affected by hepatic copper content. Northern blot analysis of sheep liver during development demonstrated little sCP expression during fetal life, but significant levels of mRNA were observed after birth. Significantly, the developmental expression pattern of sCP was closely correlated with that of the sheep Wilson disease gene (sATP7B), suggesting that the expression of the two genes may be coordinated to ensure that copper is supplied to apoceruloplasmin. Overall, the structure and expression of sCP appeared similar to other mammals, suggesting that abnormalities in CP were not responsible for the unusual sheep copper phenotype. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:251 / 257
页数:7
相关论文
共 39 条
[1]  
ALDRED AR, 1987, J BIOL CHEM, V262, P2875
[2]  
BALISTRERI WF, 1996, TXB PEDIAT, P1125
[3]   HEPATIC CERULOPLASMIN-GENE EXPRESSION DURING DEVELOPMENT IN THE GUINEA-PIG - CORRELATION WITH CHANGES IN HEPATIC COPPER-METABOLISM [J].
BINGLE, CD ;
EPSTEIN, O ;
SRAI, SKS ;
GITLIN, JD .
BIOCHEMICAL JOURNAL, 1991, 276 :771-775
[4]   MOLECULAR MECHANISMS OF PROTEIN SECRETION - THE ROLE OF THE SIGNAL SEQUENCE [J].
BRIGGS, MS ;
GIERASCH, LM .
ADVANCES IN PROTEIN CHEMISTRY, 1986, 38 :109-180
[5]   THE WILSON DISEASE GENE IS A PUTATIVE COPPER TRANSPORTING P-TYPE ATPASE SIMILAR TO THE MENKES GENE [J].
BULL, PC ;
THOMAS, GR ;
ROMMENS, JM ;
FORBES, JR ;
COX, DW .
NATURE GENETICS, 1993, 5 (04) :327-337
[7]  
Danks D.M., 1995, METABOLIC MOL BASIS, P2211
[8]   BLOOD COPPER VARIATION AMONG SPECIES [J].
EVANS, GW ;
WIEDERAN.RE .
AMERICAN JOURNAL OF PHYSIOLOGY, 1967, 213 (05) :1183-&
[9]  
FLEMING RE, 1990, J BIOL CHEM, V265, P7701
[10]   DEFECTIVE BILIARY-EXCRETION OF COPPER IN WILSONS DISEASE [J].
FROMMER, DJ .
GUT, 1974, 15 (02) :125-129