Demir Eymen, Argun Karsli Bahar, Özdemir Demir, Bilginer Umit, Doğru Huriye, Kaya Sarp, Atmaca Veli, Tufan Nimet, Demir Ebru, Karsli Taki
Department of Animal Science, Faculty of Agriculture, Akdeniz University, Antalya, 07070, Republic of Türkiye.
Department of Agricultural Biotechnology, Faculty of Agriculture, Eskişehir Osmangazi University, Eskişehir, 26160, Republic of Türkiye.
Poult Sci. 2025 Jul;104(7):105193. doi: 10.1016/j.psj.2025.105193. Epub 2025 Apr 19.
Next-generation sequencing (NGS) technologies have revolutionized livestock genomics by enabling rapid, high-resolution genotyping of local populations with thousands of single nucleotide polymorphisms (SNPs), offering unprecedented accuracy and cost efficiency. This study presents the first comprehensive genomic assessment of the Denizli (DNZ) and Gerze (GRZ) chicken breeds, comparing them to commercial broiler and layer hybrid lines using the double digest restriction-site associated DNA sequencing (ddRADseq) technique. A total of 94,208 bi-allelic SNPs were common between DNZ and GRZ, while 33,284 SNPs were retained among all populations after the quality filtering process. Genetic diversity parameters were higher in native Turkish chicken breeds compared to hybrid lines in which minor allele frequency (MAF) was higher than 0.3 in DNZ and GRZ while it was lower than this value in commercial hybrid lines. Notably, DNZ displayed the highest observed (0.386) and expected (0.375) heterozygosity, whereas the broiler hybrid line showed the lowest heterozygosity (0.254), suggesting inbreeding depression (FIS = 0.241). The negative inbreeding coefficient values occurring due to random mating were observed in DNZ and GRZ chicken breeds, while this value was estimated at 0.118 in the layer hybrid line. Population structure analyses such as principal component analyses (PCA), genetic distance-based neighbor-joining (NJ) tree, ADMIXTURE, and TreeMix algorithm revealed that DNZ and GRZ were genetically distinct from both each other and commercial hybrid lines. The results of this study confirm that comprehensive conservation strategies are efficient approaches to keeping genetic variability at an optimal level without inbreeding. Moreover, this study demonstrates the efficacy of ddRADseq in generating high-throughput genotypic data, providing a cost-effective framework for genomic diversity and population structure studies in indigenous chicken breeds.
下一代测序(NGS)技术通过对当地群体进行快速、高分辨率的数千个单核苷酸多态性(SNP)基因分型,彻底改变了家畜基因组学,提供了前所未有的准确性和成本效益。本研究首次对代尼兹利(DNZ)和盖尔泽(GRZ)鸡品种进行了全面的基因组评估,并使用双酶切限制性位点关联DNA测序(ddRADseq)技术将它们与商业肉鸡和蛋鸡杂交系进行了比较。DNZ和GRZ之间共有94,208个双等位基因SNP,而在质量过滤过程后,所有群体中保留了33,284个SNP。与杂交系相比,土耳其本土鸡品种的遗传多样性参数更高,其中DNZ和GRZ的次要等位基因频率(MAF)高于0.3,而商业杂交系中的MAF低于该值。值得注意的是,DNZ显示出最高的观察杂合度(0.386)和期望杂合度(0.375),而肉鸡杂交系显示出最低的杂合度(0.254),表明存在近交衰退(FIS = 0.241)。在DNZ和GRZ鸡品种中观察到由于随机交配导致的负近交系数值,而在蛋鸡杂交系中该值估计为0.118。主成分分析(PCA)、基于遗传距离的邻接法(NJ)树、ADMIXTURE和TreeMix算法等群体结构分析表明,DNZ和GRZ在遗传上彼此不同,也与商业杂交系不同。本研究结果证实,全面的保护策略是在不发生近亲繁殖的情况下将遗传变异性保持在最佳水平的有效方法。此外,本研究证明了ddRADseq在生成高通量基因型数据方面的有效性,为本土鸡品种的基因组多样性和群体结构研究提供了一个具有成本效益的框架。