DNA sequence polymorphisms within the bovine guanine nucleotide-binding protein Gs subunit alpha (Gsα)-encoding (GNAS) genomic imprinting domain are associated with performance traits

BackgroundGenes which are epigenetically regulated via genomic imprinting can be potential targets for artificial selection during animal breeding. Indeed, imprinted loci have been shown to underlie some important quantitative traits in domestic mammals, most notably muscle mass and fat deposition. In this candidate gene study, we have identified novel associations between six validated single nucleotide polymorphisms (SNPs) spanning a 97.6 kb region within the bovine guanine nucleotide-binding protein Gs subunit alpha gene (GNAS) domain on bovine chromosome 13 and genetic merit for a range of performance traits in 848 progeny-tested Holstein-Friesian sires. The mammalian GNAS domain consists of a number of reciprocally-imprinted, alternatively-spliced genes which can play a major role in growth, development and disease in mice and humans. Based on the current annotation of the bovine GNAS domain, four of the SNPs analysed (rs43101491, rs43101493, rs43101485 and rs43101486) were located upstream of the GNAS gene, while one SNP (rs41694646) was located in the second intron of the GNAS gene. The final SNP (rs41694656) was located in the first exon of transcripts encoding the putative bovine neuroendocrine-specific protein NESP55, resulting in an aspartic acid-to-asparagine amino acid substitution at amino acid position 192.ResultsSNP genotype-phenotype association analyses indicate that the single intronic GNAS SNP (rs41694646) is associated (P ≤ 0.05) with a range of performance traits including milk yield, milk protein yield, the content of fat and protein in milk, culled cow carcass weight and progeny carcass conformation, measures of animal body size, direct calving difficulty (i.e. difficulty in calving due to the size of the calf) and gestation length. Association (P ≤ 0.01) with direct calving difficulty (i.e. due to calf size) and maternal calving difficulty (i.e. due to the maternal pelvic width size) was also observed at the rs43101491 SNP. Following adjustment for multiple-testing, significant association (q ≤ 0.05) remained between the rs41694646 SNP and four traits (animal stature, body depth, direct calving difficulty and milk yield) only. Notably, the single SNP in the bovine NESP55 gene (rs41694656) was associated (P ≤ 0.01) with somatic cell count--an often-cited indicator of resistance to mastitis and overall health status of the mammary system--and previous studies have demonstrated that the chromosomal region to where the GNAS domain maps underlies an important quantitative trait locus for this trait. This association, however, was not significant after adjustment for multiple testing. The three remaining SNPs assayed were not associated with any of the performance traits analysed in this study. Analysis of all pairwise linkage disequilibrium (r2) values suggests that most allele substitution effects for the assayed SNPs observed are independent. Finally, the polymorphic coding SNP in the putative bovine NESP55 gene was used to test the imprinting status of this gene across a range of foetal bovine tissues.ConclusionsPrevious studies in other mammalian species have shown that DNA sequence variation within the imprinted GNAS gene cluster contributes to several physiological and metabolic disorders, including obesity in humans and mice. Similarly, the results presented here indicate an important role for the imprinted GNAS cluster in underlying complex performance traits in cattle such as animal growth, calving, fertility and health. These findings suggest that GNAS domain-associated polymorphisms may serve as important genetic markers for future livestock breeding programs and support previous studies that candidate imprinted loci may act as molecular targets for the genetic improvement of agricultural populations. In addition, we present new evidence that the bovine NESP55 gene is epigenetically regulated as a maternally expressed imprinted gene in placental and intestinal tissues from 8-10 week old bovine foetuses.

[1]  D. Haig,et al.  Evolutionary conflicts in pregnancy and calcium metabolism--a review. , 2004, Placenta.

[2]  Daniel F. Gudbjartsson,et al.  Parental origin of sequence variants associated with complex diseases , 2009, Nature.

[3]  M. Georges,et al.  Indirect effect of IGF2 intron3 g.3072G>A mutation on prolificacy in sows. , 2010, Animal genetics.

[4]  Ingo Ruczinski,et al.  Hypothesis-driven candidate gene association studies: practical design and analytical considerations. , 2009, American journal of epidemiology.

[5]  Xiaoxiang Hu,et al.  Advanced technologies for genomic analysis in farm animals and its application for QTL mapping , 2009, Genetica.

[6]  Michel Georges,et al.  On the Detection of Imprinted Quantitative Trait Loci in Line Crosses: Effect of Linkage Disequilibrium , 2008, Genetics.

[7]  L. Weinstein,et al.  The role of GNAS and other imprinted genes in the development of obesity , 2010, International Journal of Obesity.

[8]  C. Haley,et al.  Genome-wide QTL mapping for three traits related to teat number in a White Duroc × Erhualian pig resource population , 2009, BMC Genetics.

[9]  A. Nekrutenko,et al.  Wheels within wheels: clues to the evolution of the Gnas and Gnal loci. , 2008, Molecular biology and evolution.

[10]  B. Żelazowska,et al.  Association of polymorphisms in exons 2 and 10 of the insulin-like growth factor 2 (IGF2) gene with milk production traits in Polish Holstein-Friesian cattle , 2009, Journal of Dairy Research.

[11]  Eden R Martin,et al.  A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms , 2008, Genetic epidemiology.

[12]  O. Gavrilova,et al.  Alternative Gnas gene products have opposite effects on glucose and lipid metabolism. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[13]  D. A. Magee,et al.  Single nucleotide polymorphisms at the imprinted bovine insulin-like growth factor 2 (IGF2) locus are associated with dairy performance in Irish Holstein-Friesian cattle. , 2011, The Journal of dairy research.

[14]  J. Weller,et al.  From QTL to QTN identification in livestock--winning by points rather than knock-out: a review. , 2007, Animal genetics.

[15]  R. Stöger Epigenetics and obesity. , 2008, Pharmacogenomics.

[16]  D. Haig Huddling: Brown Fat, Genomic Imprinting and the Warm Inner Glow , 2008, Current Biology.

[17]  M. Province,et al.  Avoiding the high Bonferroni penalty in genome‐wide association studies , 2009, Genetic epidemiology.

[18]  M. Surani,et al.  Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis , 1984, Nature.

[19]  R. Veerkamp,et al.  Genetic parameters for EUROP carcass traits within different groups of cattle in Ireland. , 2007, Journal of animal science.

[20]  Y. le Maho,et al.  Role of huddling on the energetic of growth in a newborn altricial mammal. , 2007, American journal of physiology. Regulatory, integrative and comparative physiology.

[21]  A. Laslop,et al.  Secretion and Molecular Forms of NESP55, a Novel Genomically Imprinted Neuroendocrine-Specific Protein from AtT-20 Cells , 2004, Neurosignals.

[22]  M. Groenen,et al.  Genome-wide scan for body composition in pigs reveals important role of imprinting. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[23]  Y. Kaziro,et al.  Isolation and characterization of the human Gs alpha gene. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[24]  R. Randel,et al.  Brown adipose tissue development and metabolism in ruminants. , 2004, Journal of animal science.

[25]  S. Vigneau,et al.  Genomic imprinting mechanisms in mammals. , 2008, Mutation research.

[26]  R. Lewontin The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models. , 1964, Genetics.

[27]  H. Jüppner,et al.  GNAS Locus and Pseudohypoparathyroidism , 2005, Hormone Research in Paediatrics.

[28]  C. Spillane,et al.  A phylogenetic approach to test for evidence of parental conflict or gene duplications associated with protein-encoding imprinted orthologous genes in placental mammals , 2010, Mammalian Genome.

[29]  T. Ito,et al.  Lessons from comparative analysis of species-specific imprinted genes , 2006, Cytogenetic and Genome Research.

[30]  J. Mee,et al.  Prevalence of, and risk factors associated with, perinatal calf mortality in pasture-based Holstein-Friesian cows. , 2008, Animal : an international journal of animal bioscience.

[31]  Min Chen,et al.  Studies of the regulation and function of the Gsα gene Gnas using gene targeting technology , 2007 .

[32]  R. Feil Epigenetic asymmetry in the zygote and mammalian development. , 2009, The International journal of developmental biology.

[33]  Gregory D. Schuler,et al.  Database resources of the National Center for Biotechnology Information: update , 2004, Nucleic acids research.

[34]  A. Plagge,et al.  Physiological dysfunctions associated with mutations of the imprinted Gnas locus. , 2008, Physiology.

[35]  J. Peters,et al.  Two imprinted gene mutations: three phenotypes. , 2000, Human molecular genetics.

[36]  B. Guldbrandtsen,et al.  Detection of quantitative trait loci in Danish Holstein cattle affecting clinical mastitis, somatic cell score, udder conformation traits, and assessment of associated effects on milk yield. , 2008, Journal of dairy science.

[37]  S. Sato,et al.  The effects of single and epistatic quantitative trait loci for fatty acid composition in a Meishan x Duroc crossbred population. , 2009, Journal of animal science.

[38]  D. Bonthron,et al.  The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[39]  H. Spencer Effects of genomic imprinting on quantitative traits , 2009, Genetica.

[40]  Min Chen,et al.  Genetic diseases associated with heterotrimeric G proteins. , 2006, Trends in pharmacological sciences.

[41]  G. Rogers,et al.  Relationships among severity and duration of clinical mastitis and sire transmitting abilities for somatic cell score, udder type traits, productive life, and protein yield. , 2002, Journal of dairy science.

[42]  G. Kelsey,et al.  Physiological functions of the imprinted Gnas locus and its protein variants Galpha(s) and XLalpha(s) in human and mouse. , 2008, The Journal of endocrinology.

[43]  D. Berry,et al.  Genomic selection in Ireland , 2009 .

[44]  L. Wilkinson,et al.  Imprinted Nesp55 Influences Behavioral Reactivity to Novel Environments , 2005, Molecular and Cellular Biology.

[45]  Jan Nedergaard,et al.  Brown adipose tissue: function and physiological significance. , 2004, Physiological reviews.

[46]  G. Kelsey Epigenetics and Imprinted Genes: Insights from the Imprinted Gnas Locus , 2009, Hormone Research in Paediatrics.

[47]  J. Peters,et al.  Control of imprinting at the Gnas cluster. , 2007, Advances in experimental medicine and biology.

[48]  B. Horsthemke,et al.  Genomic imprinting and imprinting defects in humans. , 2008, Advances in genetics.

[49]  D. Haig Genomic imprinting and kinship: how good is the evidence? , 2004, Annual review of genetics.

[50]  M. Nei,et al.  MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. , 2007, Molecular biology and evolution.

[51]  R. Veerkamp,et al.  Combining somatic cell count traits for optimal selection against mastitis. , 2010, Journal of dairy science.

[52]  D. A. Magee,et al.  Single nucleotide polymorphisms within the bovine DLK1-DIO3 imprinted domain are associated with economically important production traits in cattle. , 2011, The Journal of heredity.

[53]  S. Tsai,et al.  Characterization of Conserved and Nonconserved Imprinted Genes in Swine1 , 2009, Biology of reproduction.

[54]  D. A. Magee,et al.  A catalogue of validated single nucleotide polymorphisms in bovine orthologs of mammalian imprinted genes and associations with beef production traits. , 2010, Animal : an international journal of animal bioscience.

[55]  G. Simm,et al.  Genomic scan for quantitative trait loci of chemical and physical body composition and deposition on pig chromosome X including the pseudoautosomal region of males , 2009, Genetics Selection Evolution.

[56]  H. Khatib Imprinting of Nesp55 gene in cattle , 2004, Mammalian Genome.

[57]  M. Bartolomei,et al.  Genomic imprinting: intricacies of epigenetic regulation in clusters. , 2003, Annual review of cell and developmental biology.

[58]  Mark Daly,et al.  Haploview: analysis and visualization of LD and haplotype maps , 2005, Bioinform..

[59]  M. Schutz,et al.  Selection on somatic cell score to improve resistance to mastitis in the United States. , 1994, Journal of dairy science.

[60]  D. A. Magee,et al.  High Concordance of Bovine Single Nucleotide Polymorphism Genotypes Generated Using Two Independent Genotyping Strategies , 2010, Animal biotechnology.

[61]  L. Hansen,et al.  Heritability of clinical mastitis incidence and relationships with sire transmitting abilities for somatic cell score, udder type traits, productive life, and protein yield. , 2000, Journal of dairy science.

[62]  A. Laslop,et al.  The new chromogranin-like protein NESP55 is preferentially localized in adrenaline-synthesizing cells of the bovine and rat adrenal medulla , 1999, Neuroscience Letters.

[63]  J. T. Napel,et al.  Alternative somatic cell count traits as mastitis indicators for genetic selection. , 2008, Journal of dairy science.

[64]  M. Quon,et al.  Paternal versus maternal transmission of a stimulatory G-protein alpha subunit knockout produces opposite effects on energy metabolism. , 2000, The Journal of clinical investigation.

[65]  M. Georges,et al.  The callipyge locus: evidence for the trans interaction of reciprocally imprinted genes. , 2003, Trends in genetics : TIG.

[66]  Michel Georges,et al.  The callipyge mutation and other genes that affect muscle hypertrophy in sheep , 2005, Genetics Selection Evolution.

[67]  Florentia M. Smith,et al.  Maternally-inherited Grb10 reduces placental size and efficiency. , 2010, Developmental biology.

[68]  W. G. Hill,et al.  Linkage disequilibrium in finite populations , 1968, Theoretical and Applied Genetics.

[69]  D. Accili,et al.  Variable and tissue-specific hormone resistance in heterotrimeric Gs protein α-subunit (Gsα) knockout mice is due to tissue-specific imprinting of the Gsα gene , 1998 .

[70]  S. Schmutz,et al.  IGF2 gene characterization and association with rib eye area in beef cattle. , 2007, Animal genetics.

[71]  H. Khatib,et al.  Comparative analysis of sequence characteristics of imprinted genes in human, mouse, and cattle , 2007, Mammalian Genome.

[72]  T. Moore,et al.  Genomic imprinting in mammalian development: a parental tug-of-war. , 1991, Trends in genetics : TIG.

[73]  R. T. Tecirlioglu,et al.  Analysis of Imprinted Messenger RNA Expression During Bovine Preimplantation Development1 , 2004, Biology of reproduction.

[74]  S. Eder,et al.  Neuroendocrine Secretory Protein 55 (NESP55): Alternative Splicing onto Transcripts of the GNAS Gene and Posttranslational Processing of a Maternally Expressed Protein , 2000, Neuroendocrinology.

[75]  J. Dekkers,et al.  A calcitonin receptor (CALCR) single nucleotide polymorphism is associated with growth performance and bone integrity in response to dietary phosphorus deficiency. , 2010, Journal of animal science.

[76]  I M Morison,et al.  The imprinted gene and parent-of-origin effect database , 2001, Nucleic Acids Res..

[77]  P. Tveden-Nyborg,et al.  Analysis of the expression of putatively imprinted genes in bovine peri-implantation embryos. , 2008, Theriogenology.

[78]  H. Spencer,et al.  A census of mammalian imprinting. , 2005, Trends in genetics : TIG.

[79]  R. Fischer‐Colbrie,et al.  Molecular Cloning and Characterization of NESP55, a Novel Chromogranin-like Precursor of a Peptide with 5-HT1B Receptor Antagonist Activity* , 1997, The Journal of Biological Chemistry.

[80]  P. Arnaud,et al.  Genome-wide identification of new imprinted genes. , 2010, Briefings in functional genomics.

[81]  Pascal Leroy,et al.  An imprinted QTL with major effect on muscle mass and fat deposition maps to the IGF2 locus in pigs , 1999, Nature Genetics.

[82]  Leif Andersson,et al.  A regulatory mutation in IGF2 causes a major QTL effect on muscle growth in the pig , 2003, Nature.

[83]  Min Chen,et al.  Studies of the regulation and function of the Gs alpha gene Gnas using gene targeting technology. , 2007, Pharmacology & therapeutics.

[84]  D. Solter,et al.  Completion of mouse embryogenesis requires both the maternal and paternal genomes , 1984, Cell.

[85]  A. Ferguson-Smith,et al.  Mechanisms regulating imprinted genes in clusters. , 2007, Current opinion in cell biology.