Polymorphism of Estrogen Receptor α (ESR1) and β (ESR2) Gene and Its Association Analysis with Egg Quality in Wumeng Black-bone Chicken (Gallus gallus)
LI Wei-Bo1, GUO Zhi-Li2, ZHANG Yong2, WANG Tian-Song2, ZENG Shan-Shan2, OU Mao-Jun1,*, ZHANG Xi-Ben1, YE Hong-Ying1, CHEN Ze-Lin1, ZHANG Lin-Da1, ZHANG Jian-Ying1, LI Xia1
1 Bijie Institute of Animal Husbandry and Veterinary Science, Bijie 551700, China; 2 Key Laboratory of Animal Genetics, Breeding and Reproduction in the Plateau Mountainous Region, College of Animal Science, Guizhou University, Guiyang 550025, China
Abstract:Wumeng black-bone chicken is a kind of local chicken breed which has been bred for more than 20 years in Bijie area of Guizhou province. Its eggs are rich in a variety of trace elements and have high research value. To explore the effect of SNP of estrogen receptor α (ESR1) and β (ESR2) genes on egg quality of Wumeng black-bone chicken, two strains of Wumeng black-bone chicken, white-shell layer hens and green-shell layer hens, were used as materials to screen SNPs of ESR1 and ESR2 genes by direct sequencing of PCR products, and their correlation with egg quality were analyzed. The results showed that SNPs were not found in the ESR1 gene. There were 4 SNPs on exon 8 and its near introns of ESR2 gene, which were g.53223010 A>T mutation in intron 7, g.53223142 G>A mutation, g.5322338 C>T mutation in exon 8, causing threonine to be a methionine, which belonged to missense mutation, and g.53223404 G>A in intron 8. The mutation of g.53223338 C>T in white-shell layer hens was low polymorphism, and the other sites were moderate polymorphism, and all sites didn't deviate from Hardy-Weinberg equilibrium. The results of linkage disequilibrium analysis showed that the SNPs g.53223010 A>T and g.53223404 G>A of ESR2 gene in 2 chicken strains were completely balanced; There were linkage disequilibrium among SNPs sites g.53223142 G>A, g.53223404 G>A and g.53223010 A>T in white-shell layer hens, but there was no linkage disequilibrium in green-shell layer hens. There was no linkage imbalance among other sites. Five identical haplotypes were detected in both strains, 8 haplotypes were detected in white-shell layer hens, and 11 haplotypes were detected in green-shell layer hens. The results of egg quality correlation analysis showed that SNPs g.53223010 A>T, g.53223404 G>A and g.5322338 C>T might be the marker sites affecting egg-type index and yolk relative quality of white-shell eggs, while SNPs g.53223142 G>A might be the marker site affecting yolk weight of green-shell laying hens. White-shell layer hens H5H5 and H1H4 diploid had significant advantages in the egg-type index and eggshell thickness (P<0.05), respectively, while green-shell layer hens H3H4 diploid had significant advantages in egg yolk weight (P<0.05). When other diploids had significant advantages in one egg quality index, this diploid had significant disadvantages in another, but they could all be used as potential genetic markers affecting egg quality. This experiment provides a new genetic marker for molecular breeding of Wumeng black bone chicken.
[1] 白俊艳, 樊红灯, 曹恒, 等. 2019. 鹌鹑ESR1基因的多态性与蛋品质的关联分析[J]. 浙江农业学报, 31(10): 1608-1614. (Bai J Y, Fan H D, Cao H, et al.2019. Association analysis between polymorphism of ESR1 gene and egg quality in quail[J]. Acta Agriculturae Zhejiangensis, 31(10): 1608-1614.) [2] 陈祥, 韦雄, 许厚强, 等. 2012. 鸡早期产蛋性能与ESR1基因内含子1多态性相关分析[J]. 畜牧与兽医, 44(05): 6-9. (Chen X, Wei X, Xu H Q, et al.2012. Analysis on the association of intron 1 of ESR1 gene with early egg production performance in chicken[J]. Animal Husbandry & Veterinary Medicine, 44(05): 6-9.) [3] 李杰章, 谭光辉, 吴磊, 等. 2020. 三穗鸭ITPR1基因SNPs鉴定及其与蛋壳品质性状的关联性[J]. 农业生物技术学报, 28(03): 455-464. (Li J Z, Tan G H, Wu L, et al.2020. SNPs Identification of ITPR1 gene and its correlation with eggshell quality traits in Sansui ducks (Anas platyrhyncha domestica)[J]. Journal of Agricultural Biotechnology, 28(03): 455-464.) [4] 李未博, 陈泽林, 张习本, 等. 2019. 乌蒙乌骨鸡绿壳蛋与白壳蛋的品质及营养成分分析[J]. 贵州畜牧兽医, 43(01): 11-14. (Li W B, Chen Z L, Zhang X B.2019. Comparative qnalysis of quality and nutrient composition of green and white shell eggs at Wumeng black-bone chickens[J]. Guizhou Journal of Animal Husbandry & Veterinary Medicine, 43(01): 11-14.) [5] 刘镜, 罗治华, 龚俞, 等. 2013. 贵州地方鸡种遗传资源特点及品种评价[J]. 饲料广角, 2013(22): 34-36. (Liu J, Luo Z H, Gong Y, et al.2013. Genetic resource characteristics and breed evaluation of Guizhou local chicken breeds[J]. Feed China, 2013(22): 34-36.) [6] 秦玉梅, 任嵩, 李佳玉, 等. 2017. 鸡FSHβ、ESRα基因多态性及其合并基因型与产蛋性能的关联性分析[J]. 江苏农业学报, 33(04): 854-862. (Qin Y M, Ren S, Li J Y, et al.2017. Effects of single and combined genotypes of FSHβ and ESRα genes on laying performance in chicken[J]. Jiangsu Journal of Agricultural Sciences, 33(04): 854-862.) [7] 孙杰, 任嵩, 张蕾, 等. 2020. 鸡FSHβ、ESRα、IGF-1、OVR基因多态性和聚合基因型与经济性状的关联性分析[J]. 中国畜牧杂志, 56(07): 109-114. (Sun J, Ren S, Zhang L, et al.2020. Association analysis of FSH β, ESR α, IGF-1, OVR gene polymorphisms and aggregation genotypes with economic traits in chickens[J]. Chinese Journal of Animal Science, 56(07): 109-114.) [8] 陶争荣, 徐小钦, 董丽艳, 等. 2016. 蛋鸽雌激素受体基因多态性与产蛋量关联分析[J].农业生物技术学报. 24(03): 373-379. (Tao Z R, Xu X Q, Dong L Y, et al.2016. Association analysis between the single nucleotide polymorphism of ESR genes and egg production in laying pigeon (Columba livia)[J]. Journal of Agricultural Biotechnology, 24(03): 373-379.) [9] 王文涛,李冬光,朱丽莉. 2015.黔东南小香鸡ESR1基因多态性及其与产蛋性状的相关性[J].贵州农业科学, 43(02): 100-103. (Wang W T, Li D G, Zhu L L.2015. Correlation between ESR1 gene's polymorphism and egg laying in Qiandongnan xiaoxiang hens[J]. Guizhou Agricultural Sciences, 43(02): 100-103.) [10] 韦雄, 邹成松, 张勇, 等. 2012. 长顺绿壳蛋鸡雌激素受体1基因SNP与蛋品质性状的相关性研究[J]. 中国畜牧兽医, 39(01): 142-145. (Wei X, Zou C S, Zhang Y, et al.2012. Study on association of ESR1 gene with egg quality of Changshun blue-shell chickens[J]. China Animal Husbandry & Veterinary Medicine, 39(01): 142-145.) [11] 文禹粱, 王翔宇, 郭晓飞, 等. 2019. 不同产羔数小尾寒羊BMP4基因表达及其错义突变与产羔数关联分析[J]. 农业生物技术学报, 27(01): 80-88. (Wen Y L, Wang X Y, Guo X F, et al.2019. BMP4 gene expression in Small tail han sheep (Ovis aries) with different litter[J]. Journal of Agricultural Biotechnology, 27(01): 80-88.) [12] 吴磊, 李杰章, 谭光辉, 等. 2020a. 长顺绿壳蛋鸡OCX-32基因SNPs鉴定及其与蛋壳品质的关联性[J]. 农业生物技术学报, 28(03): 465-474. (Wu L, Li J Z, Tan G H, et al.2020a. SNPs identification of OCX-32 gene and its correlation with eggshell quality in Changshun blue-eggshell chicken (Gallus gallus)[J]. Journal of Agricultural Biotechnology, 28(03): 465-474.) [13] 吴磊, 覃媛钰, 谭光辉, 等. 2020b. 贵州地方鸡IL8RB基因多态性及其对肉品质的影响[J]. 福建农林大学学报(自然科学版), 49(04): 512-518. (Wu L, Qin Y Y, Tan G H, et al.2020b. Polymorphism of the IL8RB gene in 3 Guizhou local chicken and its effect on meat quality[J]. Journal of Fujian Agriculture and Forestry University(Natural Science Edition), 49(04): 512-518.) [14] 武子寅. 2013. 邵伯鸡母系(S2) ESR和NCOA1基因多态性与产蛋性能关联分析及其表达规律研究[D]. 硕士学位论文, 扬州大学, 导师: 王杏龙, pp. 1-9. (Wu Z Y.2013. Analysis of Polymorphism with Egg-laying Performance and Expression on ESR and NCOA1 Gene in Shaobo hen (S2 line)[D]. Thesis for M.S., Yangzhou University, Suppervisor: Wang X L, pp. 1-9.) [15] 杨宁. 2010. 家禽生产学[M]. 第二版. 北京. 中国农业出版社, pp. 269-272 (Yang N.2010. Poultry production science[M]. Second Edition, China Agricultural Press, Beijing, China, pp. 269-272.) [16] Britt K L, Findlay J K.2002. Estrogen actions in the ovary revisited[J]. Journal of Endocrinology. 175(2): 269-276. [17] Drummond A E, Fuller P J.2012. Ovarian actions of estrogen receptor-β: An update[J]. Seminars in Reproductive Medicine, 30(1): 32-38. [18] Dunn I C, Joseph N T, Bain M, et al.2009. Polymorphisms in eggshell organic matrix genes are associated with eggshell quality measurements in pedigree Rhode Island Red hens[J]. Animal Genetics, 40(1): 110-114. [19] González-Morán M G.2019. Changes in the immunohistochemical localization of estrogen receptor alpha and in the stereological parameters of the testes of mature and aged chickens (Gallus domesticus)[J]. Biochemical and Biophysical Research Communications, 510(2): 309-314. [20] Li J, Leghari I H, He B, et al.2014. Estrogen stimulates expression of chicken hepatic vitellogenin Ⅱ and very low-density apolipoprotein Ⅱ through ER-α[J]. Theriogenology, 82(3): 517-524. [21] Niu X, Tyasi T L, Qin N, et al.2017. Sequence variations in estrogen receptor 1 and 2 genes and their association with egg production traits in Chinese Dagu chickens[J]. Journal of Veterinary Medical Science, 79(5): 927-934. [22] Richards J S.1980. Maturation of ovarian follicles: Actions and interactions of pituitary and ovarian hormones on follicular cell differentiation[J]. Physiological Reviews, 60(1): 51-89. [23] Zheng H, Li H, Tan W, et al.2018. Oestrogen regulates the expression of cathepsin E-A-like gene through ERΒ in liver of chicken (Gallus gallus)[J]. Journal of Genetics, 97(1): 145-155.