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Joint multiple quantitative trait loci mapping for allometries of body compositions and metabolic traits to body weights in broiler

Published online by Cambridge University Press:  09 January 2020

X. Zhou
Affiliation:
Department of Information and Computing Science, Heilongjiang Bayi Agricultural University, No.5 Xinfeng Road, Gaoxin District, Daqing 163319, People’s Republic of China Bioinformatics Research Laboratory, Heilongjiang Bayi Agricultural University, No.5 Xinfeng Road, Gaoxin District, Daqing 163319, People’s Republic of China
Y. Zhang
Affiliation:
College of Animal Science and Veterinary Medicine, Heilongjiang Bayi Agricultural University, No. 5 Xinfeng Road, Gaoxin District, Daqing 163319, People’s Republic of China
H. Zhang
Affiliation:
Department of Information and Computing Science, Heilongjiang Bayi Agricultural University, No.5 Xinfeng Road, Gaoxin District, Daqing 163319, People’s Republic of China
J. Du
Affiliation:
Research Centre for Aquatic Biotechnology, Chinese Academy of Fishery Sciences, No. 150 Qingta west Road, Fengtai District, Beijing 100141, People’s Republic of China
J. Ye
Affiliation:
Department of Information and Computing Science, Heilongjiang Bayi Agricultural University, No.5 Xinfeng Road, Gaoxin District, Daqing 163319, People’s Republic of China Bioinformatics Research Laboratory, Heilongjiang Bayi Agricultural University, No.5 Xinfeng Road, Gaoxin District, Daqing 163319, People’s Republic of China
Y. Xu
Affiliation:
Department of Information and Computing Science, Heilongjiang Bayi Agricultural University, No.5 Xinfeng Road, Gaoxin District, Daqing 163319, People’s Republic of China Bioinformatics Research Laboratory, Heilongjiang Bayi Agricultural University, No.5 Xinfeng Road, Gaoxin District, Daqing 163319, People’s Republic of China
R. Yang*
Affiliation:
Research Centre for Aquatic Biotechnology, Chinese Academy of Fishery Sciences, No. 150 Qingta west Road, Fengtai District, Beijing 100141, People’s Republic of China
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Abstract

In order to map quantitative trait loci (QTLs) for allometries of body compositions and metabolic traits in chicken, we phenotypically characterize the allometric growths of multiple body components and metabolic traits relative to BWs using joint allometric scaling models and then establish random regression models (RRMs) to fit genetic effects of markers and minor polygenes derived from the pedigree on the allometric scalings. Prior to statistically inferring the QTLs for the allometric scalings by solving the RRMs, the LASSO technique is adopted to rapidly shrink most of marker genetic effects to zero. Computer simulation analysis confirms the reliability and adaptability of the so-called LASSO-RRM mapping method. In the F2 population constructed by multiple families, we formulate two joint allometric scaling models of body compositions and metabolic traits, in which six of nine body compositions are tested as significant, while six of eight metabolic traits are as significant. For body compositions, a total of 14 QTLs, of which 9 dominant, were detected to be associated with the allometric scalings of drumstick, fat, heart, shank, liver and spleen to BWs; while for metabolic traits, a total of 19 QTLs also including 9 dominant be responsible for the allometries of T4, IGFI, IGFII, GLC, INS, IGR to BWs. The detectable QTLs or highly linked markers can be used to regulate relative growths of the body components and metabolic traits to BWs in marker-assisted breeding of chickens.

Type
Research Article
Copyright
© The Animal Consortium 2020

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References

Amos, CI 1994. Robust variance-components approach for assessing genetic linkage in pedigrees. American Journal of Human Genetics 54, 535543.Google ScholarPubMed
Calder, WA 1984. Size, function and life history. Harvard University Press, Cambridge, MA, USA.Google Scholar
Churchill, GA and Doerge, RW 1994. Empirical threshold values for quantitative trait mapping. Genetics 138, 963971.Google ScholarPubMed
Enquist, BJ and Niklas, KJ 2002. Global allocation rules for patterns of biomass partitioning in seed plants. Science 295, 15171520.CrossRefGoogle ScholarPubMed
Fang, M, Jiang, D, Gao, HJ, Sun, DX, Yang, RQ and Zhang, Q 2009. A new Bayesian automatic model selection approach for mapping quantitative trait loci under variance component model. Genetica 135, 429437.CrossRefGoogle ScholarPubMed
Friedman, J, Hastie, T and Tibshirani, R 2010. Regularization paths for generalized linear models via coordinate descent. Journal of Statistical Software 33, 122.CrossRefGoogle ScholarPubMed
Gao, HJ, Liu, YX, Zhang, TT, Yang, RQ and Yang, HM 2013. Statistical models for jointly analyzing multiple allometries. Journal of Theoretical Biology 318, 205209.CrossRefGoogle ScholarPubMed
Haseman, JK and Elston, RC 1972. The investigation of linkage between a quantitative trait and a marker locus. Behavior Genetics 2, 319.CrossRefGoogle Scholar
He, J, Zhao, YF, Zhao, JL, Gao, J, Xu, P and Yang, RQ 2018. Random regression analysis for body weights and main morphological traits in GIFT Tilapia (Oreochromis niloticus). Journal of Applied Genetics 59, 99107.CrossRefGoogle Scholar
Huxley, JS 1932. Problems of relative growth. Lincoln MacVeagh–The Dial Press, New York, NY, USA.Google Scholar
Kang, HM, Sul, JH, Service, SK, Zaitlen, NA, Kong, SY, Freimer, NB, Sabatti, C and Eskin, E 2010. Variance component model to account for sample structure in genome-wide association studies. Nature Genetics 42, 348354.CrossRefGoogle ScholarPubMed
Kang, HM, Zaitlen, NA, Wade, CM, Kirby, A, Heckerman, D, Daly, MJ and Eskin, E 2008. Efficient control of population structure in model organism association mapping. Genetics 178, 17091723.CrossRefGoogle ScholarPubMed
Lande, R 1977. On comparing coefficients of variation. Systematic Zoology 26, 214217.CrossRefGoogle Scholar
Li, HY, Huang, ZW, Gai, JY, Wu, S, Zeng, YR, Li, Q and Wu, RL 2007. A conceptual framework for mapping quantitative trait loci regulating ontogenetic allometry. PLoS ONE 2, e1245.CrossRefGoogle ScholarPubMed
Lippert, C, Listgarten, J, Liu, Y, Kadie, CM, Davidson, RI and Heckerman, D 2011. FaST linear mixed models for genome-wide association studies. Nature Methods 8, 833835.CrossRefGoogle ScholarPubMed
Liu, YX, Yang, TF, Li, HW and Yang, RQ 2014. Iteratively reweighted LASSO for mapping multiple quantitative trait loci. Briefings in Bioinformatics 15, 2029.CrossRefGoogle ScholarPubMed
Mcguigan, K, Nishimura, N, Currey, M, Hurwit, D and Cresko, WA 2010. Quantitative genetic variation in static allometry in the threespine stickleback. Integrative and Comparative Biology 50, 10671080.CrossRefGoogle ScholarPubMed
Niklas, KJ 1994. Size-dependent variations in plant growth rates and the “3/4-power rule”. American Journal of Botany 81, 134144.CrossRefGoogle Scholar
Niklas, KJ 2006. A phyletic perspective on the allometry of plant biomass partitioning patterns and functionally equivalent organ-categories. New Phytologist 171, 2740.CrossRefGoogle ScholarPubMed
Peters, RH 1983. The ecological implications of body size. Cambridge University Press, Cambridge, UK.CrossRefGoogle Scholar
Rakitsch, B, Lippert, C, Stegle, O and Borgwardt, K 2013. A Lasso multi-marker mixed model for association mapping with population structure correction. Bioinformatics 29, 206214.CrossRefGoogle ScholarPubMed
Schaeffer, LR 2004. Application of random regression models in animal breeding. Livestock Production Science 86, 3545.CrossRefGoogle Scholar
Segura, V, Vilhjálmsson, BJ, Platt, A, Korte, A, Seren, Ü, Long, Q and Nordborg, M 2013. An efficient multi-locus mixed-model approach for genome-wide association studies in structured populations. Nature Genetics 44, 825830.CrossRefGoogle Scholar
Woods, LCS 2014. QTL mapping in outbred populations: successes and challenges. Physiological Genomics 46, 8190.CrossRefGoogle Scholar
West, GB and Brown, JH 2005. The origin of allometric scaling laws in biology from genomes to ecosystems: towards a quantitative unifying theory of biological structure and organization. Journal of Experimental Biology 208, 15751592.CrossRefGoogle ScholarPubMed
Wu, RL and Hou, W 2006. A hyperspace model to decipher the genetic architecture of developmental processes: allometry meets ontogeny. Genetics 172, 627637.CrossRefGoogle ScholarPubMed
Wu, RL, Ma, CX, Lou, YX and Casella, G 2009. Molecular dissection of allometry, ontogeny, and plasticity: a genomic view of developmental biology. Bioscience 53, 10411047.CrossRefGoogle Scholar
Wu, TT, Chen, YF, Hastie, T, Sobel, E and Lange, K 2009. Genome-wide association analysis by lasso penalized logistic regression. Bioinformatics 25, 714721.CrossRefGoogle ScholarPubMed
Xu, SZ 1998. Mapping quantitative trait loci using multiple families of line cross. Genetics 148, 517524.Google Scholar
Xu, SZ and Atchley, WR 1995. A random model approach to interval mapping of quantitative trait loci. Genetics 141, 11891197.Google ScholarPubMed
Yi, NJ and Xu, SZ 2001. Bayesian mapping of quantitative trait loci under complicated mating designs. Genetics 157, 17591771.Google ScholarPubMed
Yu, JM, Pressoir, G, Briggs, WH, Vroh Bi, I, Yamasaki, M, Doebley, JF, McMullen, MD, Gaut, BS, Nielsen, DM, Holland, JB, Kresovich, S and Buckler, ES 2006. A unified mixed-model method for association mapping that accounts for multiple levels of relatedness. Nature Genetics 38, 203208.CrossRefGoogle ScholarPubMed
Zhang, ZW, Ersoz, E, Lai, CQ, Todhunter, RJ, Tiwari, HK, Gore, MA, Bradbury, PJ, Yu, JM, Arnett, KD, Ordovas, JM and Buckler, ES 2010. Mixed linear model approach adapted for genome-wide association studies. Nature Genetics 42, 355360.CrossRefGoogle ScholarPubMed
Zhao, JL, Li, SL, Wang, LJ, Jiang, L, Yang, RQ and Cui, YH 2017. Genome-wide random regression analysis for parent-of-origin effects of body composition allometries in mouse. Scientific Reports 7, 45191.CrossRefGoogle Scholar
Zhao, JL, Zhao, YF, Song, ZC, Liu, HM, Liu, YX and Yang, RQ 2018. Genetic analysis of the main growth traits using random regression models in Japanese flounder (Paralichthys olivaceus). Aquaculture Research 29, 15041511.CrossRefGoogle Scholar
Zhou, H, Deeb, N, Evock-Clover, CM, Ashwell, CM and Lamont, SJ 2006. Genome-wide linkage analysis to identify chromosomal regions affecting phenotypic traits in the chicken. II. Body composition. Poultry Science 85, 17121721.CrossRefGoogle ScholarPubMed
Zhou, H, Evock-Clover, CM, McMurtry, JP, Ashwell, CM and Lamont, SJ 2007. Genome-wide linkage analysis to identify chromosomal regions affecting phenotypic traits in the chicken. IV. Metabolic traits. Poultry Science 86, 267276.CrossRefGoogle ScholarPubMed