Molecular cloning of a second human stanniocalcin homologue (STC2)

被引:108
作者
Ishibashi, K [1 ]
Miyamoto, K
Taketani, Y
Morita, K
Takeda, E
Sasaki, S
Imai, I
机构
[1] Jichi Med Sch, Dept Pharmacol, Tochigi 3290498, Japan
[2] Univ Tokushima, Sch Med, Dept Clin Nutr, Tokushima 7708503, Japan
[3] Tokyo Med & Dent Univ, Dept Internal Med 2, Tokyo 1138519, Japan
关键词
stanniocalcin; Na-phosphate cotransporter; HYP mice; phosphatonin;
D O I
10.1006/bbrc.1998.9300
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
Stanniocalcin (STC) is a Ca- and phosphate-regulating hormone produced by the corpuscles of Stannius in bony fishes. The mammalian homologue of STC has recently been reported (STC1), which stimulates the phosphate uptake of kidney. Here we report the cloning of a second mammalian stanniocalcin (STC2) from the human osteosarcoma cDNA library. STC2 has 302 amino acid residues with 34% identity with STC1 and eel STC. STC2 has a conserved N-glycosylation site and is rich in cysteines as is the case with other stanniocalcins. STC2 has the same exon-intron boundaries as STC1. The culture medium of STC2-transfected CHO cells inhibited the promoter activity of Na-phosphate cotransporter (NaPi-3) and also inhibited the phosphate uptake of a kidney cell line (OK cells). Therefore, the function of STC2 seems to be opposite to that of STC1 on Na-phosphate cotransporter. Northern blot analysis revealed multiple transcripts in number of human tissues with high levels being present in skeletal muscle and heart. STC2 was also expressed in mice widely and its expression was lower in hypophosphatemic mice (Hyp mice) in many organs. We have cloned a widely expressed new human stanniocalcin homologue which suppressed the expression of renal Na-phosphate cotransporter. (C) 1998 Academic Press.
引用
收藏
页码:252 / 258
页数:7
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