共 23 条
Identification of a parathyroid hormone in the fish Fugu rubripes
被引:41
作者:

Danks, JA
论文数: 0 引用数: 0
h-index: 0
机构: St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia

Ho, PMW
论文数: 0 引用数: 0
h-index: 0
机构: St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia

Notini, AJ
论文数: 0 引用数: 0
h-index: 0
机构: St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia

Katsis, F
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h-index: 0
机构: St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia

Hoffmann, P
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h-index: 0
机构: St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia

Kemp, BE
论文数: 0 引用数: 0
h-index: 0
机构: St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia

Martin, TJ
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h-index: 0
机构: St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia

Zajac, JD
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h-index: 0
机构: St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia
机构:
[1] St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia
[2] Univ Melbourne, Austin Repatriat Med Ctr, Dept Med, Heidelberg, Vic, Australia
关键词:
calcium regulation;
evolution;
gene duplication;
lower vertebrates;
parathyroid gland;
D O I:
10.1359/jbmr.2003.18.7.1326
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
A PTH gene has been isolated from the fish Fugu rubripes. The encoded protein of 80 amino acid has the lowest homology with any of the PTH family members. Fugu PTH(1-34) had 5-fold lower potency than human PTH(1-34) in a mammalian cell system. Introduction: Parathyroid hormone (PTH) is the major hypercalcemic hormone in higher vertebrates. Fish lack parathyroid glands, but there have numerous attempts to identify and isolate PTH from fish. Materials and Methods: Polymerase chain reaction (PCR) was performed with primers based on preliminary data from the Joint Genome Institute database. PCR amplification was performed on genomic DNA isolated from Fugu rubripes. PCR products were purified and DNA was sequenced. All sequence was confirmed from more than one independently amplified PCR product. Multiple sequence alignments were carried out, and the percentage of identities and similarities were calculated. An unrooted phylogenetic tree, using all the known PTH and PTH-related protein (PTHrP) amino acid sequences, was determined. Synthetic peptides were tested in a biological assay that measured cyclic adenosine 3',5'-monophosphate formation in UMR106.1 cells. Rabbit polyclonal antisera specific for N-terminal human PTHrP and one rabbit polyclonal antiserum specific for N terminus hPTH were used to test the cross-reactivity with fPTH(1-34) in immunoblots.
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页码:1326 / 1331
页数:6
相关论文
共 23 条
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