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

Identification of genetic determinants of IGF-1 levels and longevity among mouse inbred strains.
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DOI:
10.1111/j.1474-9726.2010.00612.x
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发表时间:
2010-10
期刊:
影响因子:
7.8
通讯作者:
Yuan R
Yuan R
中科院分区:
生物学1区
文献类型:
--
作者:
Leduc MS;Hageman RS;Meng Q;Verdugo RA;Tsaih SW;Churchill GA;Paigen B;Yuan R

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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 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.
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