Genetic structure, selective characterization and specific molecular identity cards of high-yielding Houdan chickens based on genome-wide SNP

被引:1
|
作者
Liu, Cong [1 ]
Liu, Pingquan [2 ]
Liu, Shuangxing [2 ]
Guo, Haishan [2 ]
Zhu, Tingqi [2 ]
Li, Wenting [1 ]
Wang, Kejun [1 ]
Kang, Xiangtao [1 ]
Sun, Guirong [1 ,2 ]
机构
[1] Henan Agr Univ, Shennong Lab, Zhengzhou 450046, Peoples R China
[2] Henan Agr Univ, Key Lab Livestock & Poultry Resources Poultry Eval, Minist Agr & Rural Affairs, Zhengzhou 310058, Peoples R China
关键词
high-yielding Houdan chicken; genetic diversity; population structure; selective signature; molecular identity card; POSITIVE SELECTION; DOMESTICATION; BREEDS; TOOL;
D O I
10.1016/j.psj.2024.104325
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The high-yielding Houdan chicken (GGF) is characterized by high egg production and disease resistance. This study conducted whole genome resequencing of the GGF population and compared it to data from other breeds. Genetic diversity analysis revealed higher observed heterozygosity (Ho), Polymorphism information content (PIC), number of runs of homozygosity (ROH), and inbreeding coefficient (F-ROH) in GGF. Linkage disequilibrium (LD) decay was slowest in GGF, indicating intensive inbreeding and strong selection. These findings suggest a need for appropriate strategies to enhance genetic diversity conservation in this breed. Population structure analysis demonstrated that GGF was genetically distinct from both the red jungle fowl (RJF) and Chinese indigenous chicken (CIC) populations, highlighting GGF as a unique genetic resource warranting intensive protection and utilization. Selective sweep analysis identified genes under selection in GGF, primarily enriched in signaling pathways related to oocyte meiosis and progesterone-mediated oocyte maturation. Key candidate genes included: CCNE1, SKP1, CDC20, CDK2, ADCY8, RPS6KA6, PPP3CB, PDE3B, HSP90AB1, and AKT3. These findings provide a theoretical foundation for their potential application in poultry breeding. Additionally, this study combined bioinformatics analysis with PCR amplification and Sanger sequencing to identify 4 SNPs that can serve as a molecular identity card (ID) for GGF: SNP1 (Chr2: 136130976), SNP3 (Chr4:11705164), SNP4 (Chr4: 63255588), and SNP5 (Chr24: 3271008). This study provides a scientific basis for effective management and conservation of GGF genetic resources, and establishes a simple, economical, and accurate set of molecular IDs to combat the proliferation of inferior breeds and protect genetic resources.
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页数:15
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