QTL for several metabolic traits map to loci controlling growth and body composition in an F2 intercross between high- and low-growth chicken lines.

Quantitative trait loci (QTL) for metabolic and body composition traits were mapped at 7 and 9 wk, respectively, in an F(2) intercross between high-growth and low-growth chicken lines. These lines also diverged for abdominal fat percentage (AFP) and plasma insulin-like growth factor-I (IGF-I), insulin, and glucose levels. Genotypings were performed with 129 microsatellite markers covering 21 chromosomes. A total of 21 QTL with genomewide level of significance were detected by single-trait analyses for body weight (BW), breast muscle weight (BMW) and percentage (BMP), AF weight (AFW) and percentage (AFP), shank length (ShL) and diameter (ShD), fasting plasma glucose level (Gluc), and body temperature (T(b)). Other suggestive QTL were identified for these parameters and for plasma IGF-I and nonesterified fatty acid levels. QTL controlling adiposity and Gluc were colocalized on GGA3 and GGA5 and QTL for BW, ShL and ShD, adiposity, and T(b) on GGA4. Multitrait analyses revealed two QTL controlling Gluc and AFP on GGA5 and Gluc and T(b) on GGA26. Significant effects of the reciprocal cross were observed on BW, ShD, BMW, and Gluc, which may result from mtDNA and/or maternal effects. Most QTL regions for Gluc and adiposity harbor genes for which alleles have been associated with increased susceptibility to diabetes and/or obesity in humans. Identification of genes responsible for these metabolic QTL will increase our understanding of the constitutive "hyperglycemia" found in chickens. Furthermore, a comparative approach could provide new information on the genetic causes of diabetes and obesity in humans.

[1]  C. Thorns,et al.  Maternally-inherited diabetes and deafness: report of two affected German families with the A3243G mitochondrial DNA mutation. , 2009, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

[2]  F. Dulout,et al.  Gene frequencies of DRB3.2 locus of Argentine Creole cattle. , 2009, Animal genetics.

[3]  S Lagarrigue,et al.  A comprehensive analysis of QTL for abdominal fat and breast muscle weights on chicken chromosome 5 using a multivariate approach. , 2009, Animal genetics.

[4]  S. Panserat,et al.  Induction of glucokinase in chicken liver by dietary carbohydrates. , 2008, General and comparative endocrinology.

[5]  S. Tesseraud,et al.  Insulin immuno-neutralization in chicken: effects on insulin signaling and gene expression in liver and muscle. , 2008, The Journal of endocrinology.

[6]  A. Dehghan,et al.  An RBP4 promoter polymorphism increases risk of type 2 diabetes , 2008, Diabetologia.

[7]  J. Hirschhorn,et al.  The ENPP1 K121Q Polymorphism Is Associated With Type 2 Diabetes in European Populations , 2008, Diabetes.

[8]  F. Luft,et al.  Association of SGK1 Gene Polymorphisms with Type 2 Diabetes , 2008, Cellular Physiology and Biochemistry.

[9]  P. Froguel,et al.  Variations in the HHEX gene are associated with increased risk of type 2 diabetes in the Japanese population , 2007, Diabetologia.

[10]  J. Noguera,et al.  Association of CA repeat polymorphism at intron 1 of insulin-like growth factor (IGF-I) gene with circulating IGF-I concentration, growth, and fatness in swine. , 2007, Physiological genomics.

[11]  Hans H. Cheng,et al.  Functional genomics of the chicken--a model organism. , 2007, Poultry science.

[12]  Donald W. Bowden,et al.  Association of the Estrogen Receptor-α Gene With the Metabolic Syndrome and Its Component Traits in African-American Families , 2007, Diabetes.

[13]  A. Vignal,et al.  Identification of QTL controlling meat quality traits in an F2 cross between two chicken lines selected for either low or high growth rate , 2007, BMC Genomics.

[14]  T. Hudson,et al.  A genome-wide association study identifies novel risk loci for type 2 diabetes , 2007, Nature.

[15]  C. Ashwell,et al.  Genome-wide linkage analysis to identify chromosomal regions affecting phenotypic traits in the chicken. IV. Metabolic traits. , 2007, Poultry science.

[16]  C. Ashwell,et al.  Genome-wide linkage analysis to identify chromosomal regions affecting phenotypic traits in the chicken. III. Skeletal integrity. , 2007, Poultry science.

[17]  S. Lamont,et al.  Review of quantitative trait loci identified in the chicken. , 2006, Poultry science.

[18]  C. Bogardus,et al.  CHRM3 Gene Variation Is Associated With Decreased Acute Insulin Secretion and Increased Risk for Early-Onset Type 2 Diabetes in Pima Indians , 2006, Diabetes.

[19]  C. Evock-Clover,et al.  Genome-wide linkage analysis to identify chromosomal regions affecting phenotypic traits in the chicken. I. Growth and average daily gain. , 2006, Poultry science.

[20]  L. Andersson,et al.  QTL analysis of body composition and metabolic traits in an intercross between chicken lines divergently selected for growth. , 2006, Physiological genomics.

[21]  W. Hsueh,et al.  Obesity, Peroxisome Proliferator-Activated Receptor, and Atherosclerosis in Type 2 Diabetes , 2006, Arteriosclerosis, thrombosis, and vascular biology.

[22]  M. Schreiweis,et al.  Identification of quantitative trait loci associated with bone traits and body weight in an F2 resource population of chickens* , 2005, Genetics Selection Evolution.

[23]  L. Fajas,et al.  Cyclin D3 Promotes Adipogenesis through Activation of Peroxisome Proliferator-Activated Receptor γ , 2005, Molecular and Cellular Biology.

[24]  L. Andersson,et al.  Many QTLs with minor additive effects are associated with a large difference in growth between two selection lines in chickens. , 2005, Genetical research.

[25]  A. Vignal,et al.  Microsatellite mapping of QTL affecting growth, feed consumption, egg production, tonic immobility and body temperature of Japanese quail , 2005, BMC Genomics.

[26]  J. E. Silva,et al.  Thyroid Hormone and the Energetic Cost of Keeping Body Temperature , 2005, Bioscience reports.

[27]  M. Taouis,et al.  Glucokinase in chicken (Gallus gallus). Partial cDNA cloning, immunodetection and activity determination. , 2005, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.

[28]  R. F. Furlong Insights into vertebrate evolution from the chicken genome sequence , 2005, Genome Biology.

[29]  Colin N. Dewey,et al.  Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution , 2004, Nature.

[30]  Paul E. Boardman,et al.  A genetic variation map for chicken with 2.8 million single-nucleotide polymorphisms , 2004, Nature.

[31]  H. Gilbert,et al.  Comparison of three multitrait methods for QTL detection , 2003, Genetics Selection Evolution.

[32]  M. McCarthy,et al.  Association and haplotype analysis of the insulin-degrading enzyme (IDE) gene, a strong positional and biological candidate for type 2 diabetes susceptibility. , 2003, Diabetes.

[33]  J. Woolliams,et al.  Quantitative trait loci affecting fatness in the chicken. , 2002, Animal genetics.

[34]  George Seaton,et al.  QTL Express: mapping quantitative trait loci in simple and complex pedigrees , 2002, Bioinform..

[35]  C. Beaumont,et al.  Genetic analysis of a selection experiment on the growth curve of chickens. , 2001, Poultry science.

[36]  E. Van Obberghen,et al.  The Matricellular Protein SPARC/Osteonectin as a Newly Identified Factor Up-regulated in Obesity* , 2001, The Journal of Biological Chemistry.

[37]  J. Simon,et al.  Insulin-like growth factors and body growth in chickens divergently selected for high or low growth rate. , 2001, The Journal of endocrinology.

[38]  M. Schartl,et al.  First report on chicken genes and chromosomes 2000 , 2000, Cytogenetic and Genome Research.

[39]  N. Rideau Peculiarities of Insulin Secretion in Chickens , 1998, Annals of the New York Academy of Sciences.

[40]  B. Mangin,et al.  Comparison of several confidence intervals for QTL location , 1997, Heredity.

[41]  E. Lander,et al.  Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results , 1995, Nature Genetics.

[42]  S. Zinn,et al.  Effects of infusions of various doses of bovine growth hormone-releasing factor on blood hormones and metabolites in lactating Holstein cows. , 1989, The Journal of endocrinology.

[43]  J. Simon,et al.  Effects of selection for high and low plasma glucose concentration in chickens. , 1987, British poultry science.

[44]  Frank E. Harrell,et al.  A new distribution-free quantile estimator , 1982 .

[45]  F. Ricard,et al.  Essai de sélection sur la forme de la courbe de croissance chez le poulet. Dispositif expérimental et premiers résultats d'ensemble , 1975, Annales de génétique et de sélection animale.

[46]  Frank Russell,et al.  The Pima Indians , 1975 .

[47]  Ricard Fh Growth rate and carcass characteristics of chicken broilers obtained from normal or dwarf (dw) dams. , 1971 .

[48]  Hans H. Cheng,et al.  A high-density SNP-based linkage map of the chicken genome reveals sequence features correlated with recombination rate. , 2009, Genome research.

[49]  T. Sanke,et al.  Polymorphisms in the IDE-KIF11-HHEX gene locus are reproducibly associated with type 2 diabetes in a Japanese population. , 2008, The Journal of clinical endocrinology and metabolism.

[50]  C. Langefeld,et al.  Association of the estrogen receptor-alpha gene with the metabolic syndrome and its component traits in African-American families: the Insulin Resistance Atherosclerosis Family Study. , 2007, Diabetes.

[51]  Yuan Zhang,et al.  Renal expression and localization of the facilitative glucose transporters GLUT1 and GLUT12 in animal models of hypertension and diabetic nephropathy. , 2006, American journal of physiology. Renal physiology.

[52]  Hans H. Cheng,et al.  A consensus linkage map of the chicken genome. , 2000, Genome research.

[53]  C. Mathews,et al.  Inheritance of a mitochondrial DNA defect and impaired glucose tolerance in BHE/Cdb rats , 1999, Diabetologia.

[54]  J. Simon Chicken as a useful species for the comprehension of insulin action , 1989 .

[55]  F. H. Ricard Growth rate and carcass characteristics of chicken broilers obtained from normal or dwarf (dw) dams. , 1971, World's poultry science journal.

[56]  F. Ricard,et al.  RELATION ENTRE LES DÉPÔTS ADIPEUX VISCÉRAUX ET LES LIPIDES CORPORELS CHEZ LE POULET , 1965 .