Production and characterization of transgenic mice harboring mutant human UMOD gene

Yuichi Takiue, Makoto Hosoyamada, Takuya Yokoo, Masaki Kimura, Manami Ochiai, Kiyoko Kaneko, Kimiyoshi Ichida, Tatsuo Hosoya, Toshiaki Shibasaki

研究成果: Article査読

9 被引用数 (Scopus)

抄録

Familial juvenile hyperuricemic nephropathy is caused by mutations in the UMOD gene encoding uromodulin. A transgenic mouse model was developed by introducing a human mutant UMOD (C148W) cDNA under control of the mouse umod promoter. Uromodulin accumulation was observed in the thick ascending limb cells in the kidney of transgenic mice. However, the urinary excretion of uromodulin in transgenic mice did not decrease and LC-MS/MS analysis indicated it was of mouse origin. Moreover, the creatinine clearance was not different between wildtype and transgenic animals. Consequently, the onset of the disease was not observed in transgenic mice until 24 weeks of age.

本文言語English
ページ(範囲)596-600
ページ数5
ジャーナルNucleosides, Nucleotides and Nucleic Acids
27
6-7
DOI
出版ステータスPublished - 2008 6月

ASJC Scopus subject areas

  • 生化学
  • 分子医療
  • 遺伝学

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