Association of SNPs in ESR1 and ESR2 Genes with Egg Production in Anand Synthetic White Leghorn and Anand Bantamised White Leghorn Chicken
DOI:
https://doi.org/10.48165/ijvsbt.20.5.05Keywords:
Amplicon sequencing, Anand Bantamised White Leghorn, Anand Synthetic White Leghorn, ESR1, ESR2, Single Nucleotide Polymorphisms.Abstract
The objective of the present study was to find Single Nucleotide Polymorphisms (SNPs) in ESR1 and ESR2 genes and examine their association with egg production in chickens up to 64 weeks of age (EN64). Blood samples were taken from 48 Anand Synthetic White Leghorn (ASWLH) and 48 Anand Bantamised White Leghorn (ABWLH) chickens. Amplicon sequencing was carried out using the IlluminaMiseq platform, and a custom panel was developed to cover the exon regions of these genes. Total 91 SNPs, 59 previously reported and 32 novel SNPs were identified from 96 samples. In conclusion, the genetic variants g.52944897 T>C and rs3181386 inside the ESR2 gene exhibit potential as selection markers linked to EN64 in chickens.
Downloads
References
Drummond, A.E., & Fuller, P.J. (2012). Ovarian actions of estrogen receptor-β: An update. In: Seminars in Reproductive Medicine, 30(1), 32-38. Thieme Medical Publishers.
Emmen, J.M., Couse, J.F., Elmore, S.A., Yates, M.M., Kissling, G.E., & Korach, K.S. (2005). In vitro growth and ovulation of follicles from ovaries of estrogen receptor (ER) α and ERβ null mice indicate a role for ERβ in follicular maturation. Endocrinology, 146(6), 2817-2826.
Gonzalez-Moran, M.G. (2014). Changes in the cellular localization of estrogen receptor alpha in the growing and regressing ovaries of Gallus domesticus during development. Biochemical and Biophysical Research Communications, 447(1), 197-204.
Gonzalez-Moran, M.G., González-Arenas, A., Germán-Castelán, L., & Camacho-Arroyo, I. (2013). Changes in the content of sex steroid hormone receptors in the growing and regressing ovaries of Gallus domesticus during development. General and Comparative Endocrinology, 189, 51-58.
Guo, C., McDowell, I.C., Nodzenski, M., Scholtens, D.M., Allen, A.S., Lowe, W.L., & Reddy, T.E. (2017). Transversions have larger regulatory effects than transitions. BMC Genomics, 18, 1-9.
Kachchhi, A.V., Parmar, G.S., Patel, A.C., Patel, D.V., Koringa, P.G., & Savaliya, F.P. (2024a). SNPs detection in PRLHR, GHSR and SALL3 genes and their association analysis with egg production in
chicken. International Journal of Veterinary Sciences and Animal Husbandry, 9(2), 210-215.
Kachchhi, A.V., Patel, A.C., Parmar, G.S., Patel, D.V., Koringa, P.G., & Savaliya, F.P. (2024b). Screening of SNPs associated with egg production in two strains of White Leghorn. Indian Journal of Veterinary Sciences and Biotechnology, 20(3), 158-162.
Kang, B., Guo, J.R., Yang, H.M., Zhou, R.J., Liu, J.X., Li, S.Z., & Dong, C.Y. (2009). Differential expression profiling of ovarian genes in prelaying and laying geese. Poultry Science, 88(9), 1975-1983.
Kolluri, G., Tyagi, J.S., & Sasidhar, P.V.K. (2021). Research note: Indian poultry industry vis-a-vis coronavirus disease 2019: A situation analysis report. Poultry Science, 100(3), 100-108.
Lu, Q., Pallas, D.C., Surks, H.K., Baur, W.E., Mendelsohn, M.E., & Karas, R.H. (2004). Striatin assembles a membrane signaling complex necessary for rapid, nongenomic activation of endothelial NO synthase by estrogen receptor α. Proceedings of the National Academy of Sciences, 101(49), 17126-17131.
Lucinda, Fulton A., Mardis Elaine, R., & Wilson Richard, K. (2004). Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution. Nature, 432(7018), 695-716.
Moriarty, K., Kim, K.H., & Bender, J.R. (2006). Estrogen receptor mediated rapid signaling. Endocrinology, 147(12), 5557-5563. Ni, Y., Zhou, Y., Lu, L., Grossmann, R., & Zhao, R. (2007a). Developmental changes of FSH-R, LH-R, ER-β and GnRH-I expression in the ovary of prepubertal ducks (Anas platyrhynchos). Animal Reproduction Science, 100(3), 318-328.
Ni, Y., Zhu, Q., Zhou, Z., Grossmann, R., Chen, J., & Zhao, R. (2007b). Effect of dietary daidzein on egg production, shell quality, and gene expression of ERα, GH-R, and IGF-IR in shell glands of laying hens. Journal of Agriculture and Food Chemistry, 55(17), 6997-7001.
Pal, S., Patel, A.C., Hinsu, A.T., Panchal, K. J., Koringa, P.G., & Rank, D.N. (2023). The identification of single nucleotide polymorphisms in GnRH-I, GnRH-II/MRPS26, GnRHR exons and their association with egg production in Anand Synthetic White Leghorn and Anand Bantamised White Leghorn chicken. Indian Journal of Veterinary Sciences and Biotechnology, 19(2), 94-98.
Tremblay, G.B., Tremblay, A., Labrie, F., & Giguère, V. (1998). Ligand independent activation of the estrogen receptors α and β by mutations of a conserved tyrosine can be abolished by antiestrogens. Cancer Research, 58(5), 877-881.
Vinh, N.T., Giang, N.T.P., Linh, N.V., Dang, P.K., Cahn, N.X., Giang, N.T.C., ... & Thinh, N.H. (2021). Single nucleotide polymorphisms of candidate genes related to egg production traits in Vietnamese indigenous chickens. Brazilian Journal of Poultry Science, 23,
eRBCA-2020.
Downloads
Published
Issue
Section
License
Copyright (c) 2024 Indian Journal of Veterinary Sciences and Biotechnology
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.