Mammalian Genome

, Volume 15, Issue 10, pp 759–767

Klotho gene variation and expression in 20 inbred mouse strains

  • Arsun Bektas
  • Shepherd H. Schurman
  • Alexei A. Sharov
  • Mark G. Carter
  • Harry C. Dietz
  • Clair A. Francomano
Original Contributions

DOI: 10.1007/s00335-004-2375-3

Cite this article as:
Bektas, A., Schurman, S.H., Sharov, A.A. et al. Mamm Genome (2004) 15: 759. doi:10.1007/s00335-004-2375-3

Abstract

A defect in klotho gene expression in the mouse results in a syndrome that resembles human aging, with greatly shortened lifespan, arteriosclerosis, and defective hearing. In an effort to find functional murine variants of klotho, we sequenced the gene and examined renal expression of the secreted and membrane-bound Klotho isoforms from 16 laboratory-derived and 4 wild-derived inbred strains. Among the laboratory-derived strains, no sequence variation was found in any of the exons or intron–exon boundaries. Among the wild-derived strains, we found 45 sequence variants with six resulting in amino acid substitutions. One wild-derived strain, SPRET/Ei, had four amino acid substitutions and higher levels of the membrane form and total klotho mRNA. In addition, the membrane to secreted klotho expression ratio was elevated in three wildderived strains with amino acid substitutions. Interestingly, SPRET/Ei mice have longer lifespans, decreased atherosclerosis risk factors, and better hearing than almost all other mouse strains.

Copyright information

© Springer-Verlag 2004

Authors and Affiliations

  • Arsun Bektas
    • 1
  • Shepherd H. Schurman
    • 1
  • Alexei A. Sharov
    • 1
  • Mark G. Carter
    • 1
  • Harry C. Dietz
    • 2
    • 3
  • Clair A. Francomano
    • 1
  1. 1.Laboratory of Genetics, National Institute on AgingNational Institutes of HealthBaltimoreUSA
  2. 2.McKusick-Nathans Institute of Genetic MedicineBaltimoreUSA
  3. 3.Howard Hughes Medical InstituteBaltimoreUSA