Zhou M, Lei M, Rao Y, Nie Q, Zeng H, Xia M, Liang F, Zhang D, Zhang X
Department of Animal Genetics, Breeding and Reproduction, College of Animal Science, South China Agricultural University, Guangzhou 510642, Guangdong, China.
Poult Sci. 2008 May;87(5):893-903. doi: 10.3382/ps.2007-00495.
Broodiness is a polygenic trait controlled by a small number of autosomal genes. Vasoactive intestinal peptide receptor-1 (VIPR-1) gene could be a candidate of chicken broodiness, and its genomic variations and genetic effects on chicken broodiness traits were analyzed in this study. The partial cloning and sequencing of the VIPR-1 gene showed that the average nucleotide diversity was 0.00669 +/- 0.00093 in Red Jungle Fowls (RJF), and 0.00582 +/- 0.00026 in domestic chickens. One hundred twenty-eight variation sites were identified in the 11,136-bp region of the chicken VIPR-1 gene. Twenty variation sites were genotyped using PCR-RFLP or PCR method to analyze average diversity, linkage-disequilibrium pattern, and haplotype structure in RJF, Xinghua chickens, Ningdu Sanhuang chickens, Baier Huang chickens, and Leghorn Layers. The RJF, Xinghua, Ningdu Sanhuang, and Baier Huang exhibited distinct characteristic of decreasing r(2) value over physical distance. Haplotype analyses showed that some variation sites of the 27-kb region from exon 6 to exon 11 could be associated with broodiness. The distribution of genotypic and allelic frequencies, and heterozygosities in the above 5 populations showed that A-284G, A+457G, C+598T, D+19820I, C+37454T, C+42913T, and C+53327T might be associated with broodiness. The 7 sites and the other 4 sites were genotyped in 644 NDH individuals under cage condition and were used for association analyses between each site and chicken broodiness traits. A significant association (P < 0.05) was found between C+598T in intron 2 and broody frequency (%). Another significant association (P < 0.05) was found between C+53327T and duration of broodiness, in which allele C was positive for DB.
抱窝是一种由少数常染色体基因控制的多基因性状。血管活性肠肽受体-1(VIPR-1)基因可能是鸡抱窝性的一个候选基因,本研究对其基因组变异及对鸡抱窝性状的遗传效应进行了分析。VIPR-1基因的部分克隆和测序表明,原鸡(RJF)的平均核苷酸多样性为0.00669±0.00093,家鸡为0.00582±0.00026。在鸡VIPR-1基因11136 bp区域内鉴定出128个变异位点。利用PCR-RFLP或PCR方法对20个变异位点进行基因分型,以分析原鸡、杏花鸡、宁都三黄鸡、白耳黄鸡和来航蛋鸡的平均多样性、连锁不平衡模式和单倍型结构。原鸡、杏花鸡、宁都三黄鸡和白耳黄鸡表现出r(2)值随物理距离降低的明显特征。单倍型分析表明,外显子6至外显子11的27 kb区域的一些变异位点可能与抱窝性有关。上述5个群体的基因型和等位基因频率分布以及杂合度表明,A-284G、A+457G、C+598T、D+19820I、C+37454T、C+42913T和C+53327T可能与抱窝性有关。在笼养条件下,对644只宁都黄鸡个体的这7个位点和另外4个位点进行基因分型,并用于每个位点与鸡抱窝性状之间的关联分析。发现内含子2中的C+598T与抱窝频率(%)之间存在显著关联(P<0.05)。还发现C+53327T与抱窝持续时间之间存在另一个显著关联(P<0.05),其中等位基因C对抱窝持续时间有正向作用。