Cloning, expression pattern and essentiality of the high-affinity copper transporter 1 (ctr1) gene in zebrafish

被引:66
|
作者
Mackenzie, NC
Brito, M
Reyes, AE
Allende, ML
机构
[1] Univ Chile, Fac Ciencias, Dept Biol, Millennium Nucleus Dev Biol, Santiago, Chile
[2] Univ Diego Portales, Fac Ciencias Salud, Santiago, Chile
关键词
copper homeostasis; metal transport; morpholino; fish;
D O I
10.1016/j.gene.2003.11.019
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The high-affinity copper transporter 1 (Ctr1) is a highly conserved transmembrane protein that mediates the internalization of copper ions from the extracellular medium. In this study, we have isolated the zebrafish ctrl gene. The zebrafish ctr1 cDNA encodes a protein with 69% identity to the human orthologue and shows conservation of specific amino acid residues involved in copper transport. We find only a single ctrl gene in the zebrafish genome which maps to linkage group 5. The genomic structure of the zebrafish gene shows that it consists of five exons and that exon-intron boundaries are absolutely conserved with the mammalian ctr1 genes. Expression in embryos was analyzed by reverse transcription -polymerase chain reaction (RT-PCR) and by in situ hybridization. Zebrafish ctr1 is maternally loaded, and transcripts can be detected throughout development and in adult fish. Distribution of ctrl message appears ubiquitous during early stages becoming restricted to the brain and ventral tissues by 24 h post fertilization (hpf). Beginning at 3 days post fertilization (dpf), expression is found mainly in the developing intestine. Specific knockdown of ctrl by antisense morpholino oligonucleotides (MOs) causes early larval lethality. Defects include cell death in tissues where ctrl is most heavily expressed, a finding similar to that described for a mouse knockout of mCtr1. Despite the existence of at least one other copper transport mechanism in the fish, our studies show that zebrafish ctr1 is an essential gene for development. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:113 / 120
页数:8
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