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

被引:25
|
作者
Leduc, Magalie S. [1 ]
Hageman, Rachael S. [1 ]
Meng, Qingying [1 ]
Verdugo, Ricardo A. [1 ]
Tsaih, Shirng-Wern [1 ]
Churchill, Gary A. [1 ]
Paigen, Beverly [1 ]
Yuan, Rong [1 ]
机构
[1] Jackson Lab, Bar Harbor, ME 04609 USA
来源
AGING CELL | 2010年 / 9卷 / 05期
关键词
haplotype analysis; IGF-1; longevity; mouse; QTL; GROWTH-FACTOR-I; QUANTITATIVE TRAIT LOCI; BIOINFORMATICS TOOLBOX; LABORATORY MOUSE; P-VALUES; MICE; QTL; VARIANCE; RECEPTOR; POLYMORPHISMS;
D O I
10.1111/j.1474-9726.2010.00612.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
P>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.
引用
收藏
页码:823 / 836
页数:14
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