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作 者:陶勇[1] 王金玉[1] 李国辉[1] 胡玉萍[1]
机构地区:[1]扬州大学动物科学与技术学院
出 处:《安徽农业科学》2008年第11期4528-4529,4531,共3页Journal of Anhui Agricultural Sciences
基 金:江苏省高新技术项目(BG2004316);江苏省"青蓝工程"培养基金资助项目
摘 要:[目的]为深入研究鸡MC4R基因和分子育种提供参考。[方法]采用饱和酚/氯仿法从鸡血中提取DNA,利用PCR-SSCP和DNA测序的方法,对京海黄鸡MC4R基因的单核苷酸多态性进行分析。[结果]对PCR产物进行SSCP分析,2对引物均表现出多态性。引物A得到2种基因型(AA型和AB型)。引物Z也得到2种基因型(CC型和CD型)。将测序结果与发表的鸡MC4R基因序列的比较结果进行比较,发现2个单核苷酸多态位点,其中A引物扩增序列中的多态位点为662 bp处G→C的点突变造成的,而Z引物扩增序列中的多态位点是由于在733~734 bp插入了一个C碱基引起的。[结论]该研究中未检测到BB和DD纯合基因型,这可能与在京海黄鸡培育过程中采用分子标记方法进行选择有关。[Objective] The research aimed to provide reference for further study on chicken MC4R gene and its molecular breeding. [Method] DNA was extracted from chicken blood by using saturated hydroxybenzene/chloroform method. And the single nucleotide polymorphism of MC4R gene in Jinghai yellow chicken was analyzed by using the methods of PCR-SSCP and DNA sequencing. [Result] The PCR products were analyzed by SSCP and 2 pairs of primers showed the polymorphism. Two kinds of genotypes (AA type and AB type) were obtained frmn primer A and 2 kinds of genotypes (CC type and CD type) were obtained from primer Z. The comparison results between the sequencing results and the reported MC4R gene sequences showed that 2 single nueleotide polymorphic loci were found. The polymorphic loci in the amplified sequences of primer A was caused by point mutation from G to C at 662 bp and that in the amplified sequences of primer was caused by inserting one C base at 733-734 bp. [Conclusion] In this study, pure genotypes BB and DD were not detected, which was probably related with the molecular marker method used in the breeding of Jinghai yellow chicken.
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