摘要
[目的]评价马鹿粪便DNA的微卫星基因型可靠性,为后续保护遗传学方面的研究提供参考。[方法]选择7个多态性较高的微卫星位点,扩增167份马鹿粪便DNA,通过3~4次的重复扩增统计等位基因丢失率和假等位基因出现率。[结果]7个位点的等位基因丢失率平均为0.034,假等位基因出现率平均为0.023。[结论]对于杂合体,3~4次的重复扩增可以满足基因型后续分析要求,而纯合体需要7次以上的重复扩增。
[Objective]The aim was to assess reliability of microsatellite genotypes from wapiti fecal DNA in order to offer researching reference for conservation genetics in the future.[Method]Using 7 high variable loci,167 fecal DNA were genotyped,the ratio of allele dropout and false allele by 3-4 times repeat amplification was estimeated.[Result]The average ratio for allele dropout was 0.034 in 7 loci,the false allele was 0.023.[Conclusion]The method of 3-4 times repeat amplification may be used to assess the genotypes of the heterozygote,while 7 times or more would be carried in the homozygote.
出处
《安徽农业科学》
CAS
北大核心
2010年第15期8279-8280,共2页
Journal of Anhui Agricultural Sciences
基金
国家自然科学基金项目(30870309)
黑龙江省自然科学基金重点项目(ZJN-0501)
美国老虎和犀牛基金资助项目(98210-2-G191)
牡丹江师范学院教改规划项目(10-XY01068)
关键词
马鹿
粪便样品
微卫星
基因型
Wapiti
Fecal sample
Microsatellite
Genotype