Mapping quantitative trait loci for serum insulin-like growth factor-1 levels in mice

Citation
Cj. Rosen et al., Mapping quantitative trait loci for serum insulin-like growth factor-1 levels in mice, BONE, 27(4), 2000, pp. 521-528
Citations number
18
Language
INGLESE
art.tipo
Article
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","da verificare
Journal title
BONE
ISSN journal
8756-3282 → ACNP
Volume
27
Issue
4
Year of publication
2000
Pages
521 - 528
Database
ISI
SICI code
8756-3282(200010)27:4<521:MQTLFS>2.0.ZU;2-N
Abstract
Serum insulin-like growth factor-1 (IGF-1) and femoral bone mineral density (BMD) differ between two inbred strains of mice, C3H/HeJ (C3H) and C57BL/6 J (B6), by approximately 30% and 50%, respectively. Similarly, skeletal IGF -1 content, bone formation, mineral apposition, and marrow stromal cell num bers are higher in C3H than in B6 mice, Because IGF-1 and several bone para meters cosegregate, we hypothesize that the serum IGF-1 phenotype has a str ong heritable component and that genetic determinants for serum IGF-1 are i nvolved in the regulation of bone mass. We intercrossed (B6 x C3H)F1 hybrid s and analyzed 682 F2 female offspring at 4 months of age for serum IGF-1 b y radioimmunoassay and femoral BMD by peripheral quantitative computerized tomography (pQCT), Genomic DNA was assayed by polymerase chain reaction (PC R) to determine alleles for 114 Mit markers inherited in F2 mice at average distances of 14 centimorgans (cM) along each chromosome (Chr), Serum IGF-1 levels in the F2 progeny were relatively normal in distribution, but showe d a greater range than either progenitor, indicating that serum IGF-1 level is a polygenic trait with an estimated heritability of 52%, Serum IGF-1 co rrelated with femoral length (r = 0.266, p < 0.0001) and femoral BMD (r = 0 .267, p < 0.0001), Whole genome scans for main effects associated with seru m IGF-1 levels revealed three significant QTLs (in order of significance) o n mouse Chrs 6, 15, and 10, The QTL on Chr 6 showed a significant reduction in IGF-1 associated with increasing C3H allele number, whereas the Chr 15 and Chr 10 loci showed additive effects with increasing C3H allele number. A genome-wide search for interacting marker pairs identified a significant interaction between the Chr 6 QTL and a locus on Chr 11, This interactive e ffect suggested that when the Chr 11 locus was homozygous for C3H, there wa s no effect of the Chr 6 locus on serum IGF-1; however, the combination of C3H alleles on Chr 6 with B6 alleles on Chr 11 was associated with reduced serum IGF-1 concentrations. To test this in vivo, we tested congenic mice c arrying the Chr 6 QTL region from C3H on a B6 background (B6.C3H-6). Both s erum IGF-1 and femoral BMD were significantly lower in female congenic than progenitor B6 mice. In summary, we identified three major QTLs on mouse Ch rs 6, 10, and 15, and noted a major locus-locus interaction between Chrs 6 and 11, We named these QTLs IGF-1 serum levels (Igf1sl1 to Igf1sl4), Functi onal isolation of the Igf1sl1 QTL on Chr 6 for IGF-1 in B6.C3H-6 congenic m ice demonstrated effects on both the IGF-1 and BMD phenotypes, The genetic determinants of these Igf1sl QTLs will provide much insight into the regula tion of IGF-1 and the subsequent acquisition of peak bone mass. (Bone 27:52 1-528; 2000) (C) 2000 by Elsevier Science Inc. All rights reserved.