Genome-wide search for loci controlling serum IGF binding protein levels of mice

被引:14
作者
Brockmann, GA
Haley, CS
Wolf, E
Karle, S
Kratzsch, J
Renne, U
Schwerin, M
Hoeflich, A
机构
[1] Res Inst Biol Farm Anim, Dept Biol Mol, D-18196 Dummerstorf, Germany
[2] Roslin Inst, Roslin EH25 9PS, Midlothian, Scotland
[3] Univ Munich, Dept Mol Anim Breeding, D-81377 Munich, Germany
[4] Univ Leipzig, Dept Clin Chem, D-04103 Leipzig, Germany
[5] Univ Leipzig, Dept Pathobiochem, D-04103 Leipzig, Germany
关键词
IGFBP-2; IGFBP-3; IGFBP-4; linkage;
D O I
10.1096/fj.00-0391com
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A segregating F-2 pedigree based on two mouse Lines (DU6i and DBA/2) with extremely different growth characteristics was generated to search for loci affecting serum levels of insulin-like growth factor (IGF) binding proteins (IGFBPs) and to estimate their effects on growth and body composition. DU6i is characterized by high body mass and obesity associated with hyperinsulinemia, hyperleptinemia, and elevated serum IGF-I concentrations. Furthermore, significantly elevated serum levels of IGFBP-2, IGFBP-3, and IGFBP-4 were found in DU6i vs. DBA/2 mice. Linkage analysis identified loci with major effects on the serum level of IGFBP-3 on Chromosome 5 at 58 cM (Igfbp3q1; F = 9.9) and on Chromosome 10 at 46 cM (Igfbp3q2; F = 33.8). A locus significantly influencing serum IGFBP-2 levels in males was found on Chromosome 7. Additional linkage was detected in males and females for IGFBP-2 on Chromosomes 8, 11, 14, 17, and X, and for ICFBP-4 on Chromosome 4. Additional loci affecting IGFBPs acted in a sex-specific manner. The identified loci coincide in part with chromosomal regions controlling growth and obesity. Thus, multiple genes or pleiotropic gene effects may be assumed for these chromosomal regions. The identification of quantitative trait loci for IGFBPs as subcomponents of growth regulation and differentiation will further improve the understanding of complex trait regulation.
引用
收藏
页码:978 / 987
页数:10
相关论文
共 53 条
[41]   Gigantism in mice lacking suppressor of cytokine signalling-2 [J].
Metcalf, D ;
Greenhalgh, CJ ;
Viney, E ;
Willson, TA ;
Starr, R ;
Nicola, NA ;
Hilton, DJ ;
Alexander, WS .
NATURE, 2000, 405 (6790) :1069-1073
[42]  
Mitsui S, 1997, BRIT J DERMATOL, V137, P693
[43]   EXPRESSION OF HUMAN INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN-3 IN TRANSGENIC MICE [J].
MURPHY, LJ ;
MOLNAR, P ;
LU, X ;
HUANG, H .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 1995, 15 (03) :293-303
[44]   Insulin-like growth factor-binding proteins in serum and other biological fluids: Regulation and functions [J].
Rajaram, S ;
Baylink, DJ ;
Mohan, S .
ENDOCRINE REVIEWS, 1997, 18 (06) :801-831
[45]  
Richardson RL, 1998, GROWTH DEVELOP AGING, V62, P3
[46]   TEMPERATURE-GRADIENT GEL-ELECTROPHORESIS OF NUCLEIC-ACIDS - ANALYSIS OF CONFORMATIONAL TRANSITIONS, SEQUENCE VARIATIONS, AND PROTEIN-NUCLEIC ACID INTERACTIONS [J].
RIESNER, D ;
STEGER, G ;
ZIMMAT, R ;
OWENS, RA ;
WAGENHOFER, M ;
HILLEN, W ;
VOLLBACH, S ;
HENCO, K .
ELECTROPHORESIS, 1989, 10 (5-6) :377-389
[47]  
SCHULER L, 1985, ARCH TIERZUCHT, V28, P357
[48]   Signal transduction by β1 integrin receptors in human chondrocytes in vitro:: collaboration with the insulin-like growth factor-1 receptor [J].
Shakibaei, M ;
John, T ;
de Souza, P ;
Rahmanzadeh, R ;
Merker, HJ .
BIOCHEMICAL JOURNAL, 1999, 342 :615-623
[49]   ADAM 12, a disintegrin metalloprotease, interacts with insulin-like growth factor-binding protein-3 [J].
Shi, ZD ;
Xu, WZ ;
Loechel, F ;
Wewer, UM ;
Murphy, LJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (24) :18574-18580
[50]  
SHIMASAKI S, 1991, Progress in Growth Factor Research, V3, P243, DOI 10.1016/0955-2235(91)90003-M