Quantitative Trait Loci Mapping for Growth Curve Variables in Ghezel Sheep
Subject Areas : CamelS. Hosseinzadeh 1 , A. Azartash 2 , S. Nikbin 3 , A. Javanmard 4 , M. Ali Abbasi 5 , S.A. Rafat 6 , M. Ghafari 7 , N. Hedayat-Evrigh 8 , S. Alijani 9
1 - Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran
2 - Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran
3 - Department of Animal Science, Faculty of Agriculture, University of Mohaghegh Ardabili, Ardabil, Iran
4 - Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran
5 - Animal Science Research Institute of Iran (ASRI), Agricultural Research Education and Extension Organization (AREEO), Karaj, Iran
6 - Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran
7 - Department of Animal Science, Faculty of Agriculture, Urmia University, Urmia, Iran
8 - Department of Animal Science, Faculty of Agriculture, University of Mohaghegh Ardabili, Ardabil, Iran
9 - Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran
Keywords: microsatellites, QTL mapping, Ghezel sheep, Half-sib,
Abstract :
Understanding the genomics aspect of curve variable allows for the combination of genomic regions of such model-based variables from multiple measurements into a few biologically meaningful variables. With this motivation, the aim of the current study was a model-based quantitative trait loci (QTL) detection for growth curve variables in Ghezel fat-tailed sheep. We tested the following items during research: 1) Determining the best nonlinear growth models using six nonlinear equations (Von Bertalanffy, Gompertz, Logistic, Richards, Weibull and Brody) according to 24905 obtained data sets collected from the Ghezel Sheep Breeding Center, Iran, during the 1994-2013 period; 2) Conducted partial genome scan to identify significant QTl controlling best growth model parameters in Ghezel sheep using three half-sib families (Family size=25-50) and 8 microsatellite markers distributed on ovine chromosome 1. In addition, QTL effects for two paternal half-sibs using two models, individual families and across families were calculated. Molecular data were analyzed using SAS and GridQTL programs. Observed results demonstrated the Brody model was the best growth model for growth data according to the lower values of RMSE, AIC and BIC and generally greater values of R2adj than other models. Thus, Brody model parameters (A, B, and C) were subjected to further QTL analysis. Also, our observation identified one significant QTL between the markers INRA11-CSSM004 associated with Brody model A variable (maturity) located in 123 CM in chromosome 1 (P<0.01). Analyses using more families and advance massive genotyping tools will be useful to confirm or to reject these findings.
Churchill G.A. and Doerge R.W. (1994). Empirical threshold values for quantitative trait mapping. Genetics. 138, 963-971.
Duan X., An B., Du L., Chang T., Liang M., Yang B.G., Xu L., Zhang L., Li J., Guangxin E. and Gao H. (2021). Genome-wide association analysis of growth curve parameters in chinesesimmental beef cattle. Animals. 11, 1-15.
Gautam L., Kumar V. and Nagda H. (2018). Estimation of growth curve parameters using non-linear growth curve models in Sonadi sheep. Int. J. Livest. Res. 8, 1-10.
Gebreselassie G., Berihulay H., Jiang L. and Ma Y. (2020). Review on genomic regions and candidate genes associated with economically important production and reproduction traits in sheep (Oviesaries). Animals. 10(1), 33-38.
Ghasemi M., Zamani P., Vatankhah M. and Abdoli R. (2019). Genome-wide association study of birth weight in sheep. Animal. 13(9), 1797-1803.
Ghavi Hossein-Zadeh N. (2015a). Estimation of genetic relationships between growth curve parameters in Guilan sheep. J. Anim. Sci. Technol. 57, 1-6.
Ghavi Hossein-Zadeh N. (2015b). Modeling the growth curve of Iranian Shall sheep using non-linear growth models. Small Rumin. Res. 130, 60-66.
Haldar A., French M.C., Brauning R., Edwards S.J., O'Connell A.R., Farquhar P.A. and Juengel J.L. (2014). Single-nucleotide polymorphisms in the LEPR gene are associated with divergent phenotypes for age at onset of puberty in Davisdale ewes. Biol. Reprod. 90(2), 33-41.
Hojjati F. and Hossein-Zadeh N.G. (2018). Comparison of non-linear growth models to describe the growth curve of Mehraban sheep. J. Appl. Anim. Res. 46, 499-504.
Jiang J., Cao Y., Shan H., Wu J., Song X. and Jiang Y. (2021). The GWAS analysis of body size and population verification of related SNPs in Hu sheep. Front. Genet. 12, 642552.
Knott S.A. and Haley C.S. (1992). A simple regression method for mapping quantitative trait loci in line crosses using flanking markers. Heredity. 69, 315-324.
Knott S.A., Elsen J.M. and Haley C.S. (1996). Methods for multiple-marker mapping of quantitative trait loci in half- sib populations. Theor. Appl. Genet. 93, 71-80.
Lander E. and Kruglyak L. (1995). Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results. Nat. Genet. 11, 241-247.
Lien S., Karlsen A., Klemetsdal G., Våge D.I., Olsaker I., Klungland H., Aasland M., Heringstad B., Ruane J. and Gomez-Raya L. (2000). A primary screen of the bovine genome for quantitative trait loci affecting twinning rate. Mamm. Genome. 11, 877-882.
López B., Lupi T.M., León J.M., López F., Agudo B. and Delgado J.V. (2018). Characterization of the commercial growth curves of Spanish Merino, Fleischschaf, and crossbred lambs in an associative economy context. Small Rumin. Res. 164, 8-14.
Malau-Aduli A.E.O., Niibayashi T., Kojima T., Oshima K., Mizoguchi Y. and Komatsu M. (2005). Mapping the quantitative trait loci (QTL) for body shape and conformation measurements on BTA1 in Japanese Black cattle. Anim. Sci. J. 76, 19-27.
McRae A.F., Bishop S.C., Walling G.A., Wilson A.D. and Visscher P.M. (2005). Mapping of multiple quantitative trait loci for growth and carcass traits in a complex commercial sheep pedigree. Anim. Sci. 80(2), 135-141.
Mokhtari M.S., Borzi N.K., Fozi M.A. and Behzadi M.R.B. (2019). Evaluation of non-linear models for genetic parameters estimation of growth curve traits in Kermani sheep. Trop. Anim. Health Prod. 51, 2203-2212.
Nimase R., Bangar Y., Nimbalkar C., Shinde O. and Lawar V. (2017). Genetic parameter estimates for growth curve characteristics of deccani sheep. Int. J. Livest. Res. 7(5), 1-8.
Raadsma H.W., Thomson P.C., Zenger K.R., Cavanagh C., Lam M.K., Jonas E., Jones M., Attard G., Palmer D. and Nicholas F.W. (2009). Mapping quantitative trait loci (QTL) in sheep. I. A new male framework linkage map and QTL for growth rate and body weight. Genet. Sel. Evol. 41, 1-17.
Seyedsharifi R., Badbarin S., Seifdavati J., Hedayat-Evrigh N., Mariezcurrena-Berasain M.A. and Salem A.Z.M. (2021). Influence of quantitative trait loci on growth traits of chromosome 1 in Sanjabi lambs during the first year of growth. Small Rumin. Res. 194, 1-4.
Shams S.S., Vahed S.Z., Soltanzad F., Kafil V., Barzegari A., Atashpaz S. and Barar J. (2011). Highly effective DNA extraction method from fresh, frozen, dried and clotted blood samples. BioImpacts. 1, 183-187.
Soller M. and Genizi A. (1978). The efficiency of experimental designs for the detection of linkage between a marker locus and a locus affecting a quantitative trait in segregating populations. Biometrics. 34, 47-55.
Visser C., Van Marle-Köster E., Snyman M.A., Bovenhuis H. and Crooijmans R.P.M.A. (2013). Quantitative trait loci associated with pre-weaning growth in South African Angora goats. Small Rumin. Res. 112, 15-20.
Walling G.A., Visscher P.M., Wilson A.D., McTeir B.L., Simm G. and Bishop S.C. (2004). Mapping of quantitative trait loci for growth and carcass traits in commercial sheep populations. J. Anim. Sci. 82, 2234-2245.
Woollard J., Tuggle C.K. and Ponce de León F.A. (2000). Rapid communication: Localization of POU1F1 to bovine, ovine, and caprine 1q21-22. J. Anim. Sci. 78, 242-252.