Cloning and expression analysis of rainbow trout Oncorhynchus mykiss tumour necrosis factor-α

被引:218
|
作者
Laing, KJ
Wang, TH
Zou, J
Holland, J
Hong, SH
Bols, N
Hirono, I
Aoki, T
Secombes, CJ
机构
[1] Univ Aberdeen, Dept Zool, Aberdeen AB24 2TZ, Scotland
[2] Univ Waterloo, Dept Biol, Waterloo, ON N2L 3G1, Canada
[3] Tokyo Univ Fisheries, Dept Aquat Biosci, Tokyo 108, Japan
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2001年 / 268卷 / 05期
关键词
gene structure; mRNA expression; rainbow trout; tumour necrosis factor;
D O I
10.1046/j.1432-1327.2001.01996.x
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
A rainbow trout (Oncorhynchus mykiss) gene for tumor necrosis factor (TNF) has been cloned and sequenced. The cDNA contains an open reading frame of 738 nucleotides that translate into a 246 amino-acid putative peptide, with a 5' untranslated region (UTR) of 140 bp and a 3' UTR of 506 bp. Two potential N-linked glycosylation sites exist in the translation. The genomic sequence measures 2007 bp and contains three introns that intercept four coding exons. Expression studies using RT-PCR have shown that the trout TNF gene is constitutively expressed in the gill and kidney of unstimulated fish. Trout TNF expression could be up-regulated by stimulation of isolated head kidney leucocytes with lipopolysaccharide (LPS). Similarly, stimulation of a trout macrophage cell line (RTS11) with LPS resulted in an increased transcript level, as did incubation with recombinant trout interleukin (IL)-1 beta. The optimal timing for induction of TNF expression in trout macrophages was determined using recombinant trout IL-1 beta, where a clear induction was apparent by 2 h and peaked at 4 h. Evidence that this TNF gene is equivalent to mammalian TNF-alpha is discussed.
引用
收藏
页码:1315 / 1322
页数:8
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