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Identification of genetic determinants of IGF-1 levels and longevity among mouse inbred strains

  • Magalie S. Leduc
  • , Rachael S. Hageman
  • , Qingying Meng
  • , Ricardo A. Verdugo
  • , Shirng Wern Tsaih
  • , Gary A. Churchill
  • , Beverly Paigen
  • , Rong Yuan
  • Jackson Laboratory

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

The IGF-1 signaling pathway plays an important role in regulating longevity. To identify the genetic loci and genes that regulate plasma IGF-1 levels, we intercrossed MRL/MpJ and SM/J, inbred mouse strains that differ in IGF-1 levels. Quantitative trait loci (QTL) analysis of IGF-1 levels of these F2 mice detected four QTL on chromosomes (Chrs) 9 (48 Mb), 10 (86 Mb), 15 (18 Mb), and 17 (85 Mb). Haplotype association mapping of IGF-1 levels in 28 domesticated inbred strains identified three suggestive loci in females on Chrs 2 (13 Mb), 10 (88 Mb), and 17 (28 Mb) and in four males on Chrs 1 (159 Mb), 3 (52 and 58 Mb), and 16 (74 Mb). Except for the QTL on Chr 9 and 16, all loci co-localized with IGF-1 QTL previously identified in other mouse crosses. The most significant locus was the QTL on Chr 10, which contains the Igf1 gene and which had a LOD score of 31.8. Haplotype analysis among 28 domesticated inbred strains revealed a major QTL on Chr 10 overlapping with the QTL identified in the F2 mice. This locus showed three major haplotypes; strains with haplotype 1 had significantly lower plasma IGF-1 and extended longevity (P < 0.05) than strains with haplotype 2 or 3. Bioinformatic analysis, combined with sequencing and expression studies, showed that Igf1 is the most likely QTL gene, but that other genes may also play a role in this strong QTL.

Original languageEnglish
Pages (from-to)823-836
Number of pages14
JournalAging Cell
Volume9
Issue number5
DOIs
StatePublished - Oct 2010

Keywords

  • Haplotype analysis
  • IGF-1
  • Longevity
  • Mouse
  • QTL

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