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DNA-based Determination of Ancestry in Cynomolgus Macaques (Macaca fascicularis)

机译:食蟹猕猴(Macaca fascicularis)中基于DNA的祖先测定。

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摘要

Interest in the genetic composition of cynomolgus macaques (Macaca fascicularis) has increased due to the rising demand for NHP models in human biomedical research. Significant genetic differences among regional populations of cynomolgus macaques can confound interpretations of research results because they do not solely reflect differences in experimental treatment effects. Therefore, the common origin of cynomolgus macaques used as research subjects should be verified by using region-specific genetic markers to minimize the influence of underlying genetic variation among animals selected as research subjects on phenotypes under study. We compared the effectiveness of 18 short tandem repeat (STR) markers with that of 83 single-nucleotide polymorphism (SNP) markers to differentiate the ancestry of cynomolgus macaques from 6 different populations (Cambodia, Sumatra, Mauritius, Singapore, and the islands of Luzon and Zamboanga in the Philippines). Genetic diversity indices such as allele numbers and expected heterozygosity based on SNP were lower and exhibited lower standard errors than those provided by STR, probably because, unlike STR, most SNP are biallelic and consequently exhibit maximal expected heterozygosity values of 0.50. However, the standard error of estimates of observed heterozygosity based on SNP was higher than that for STR, perhaps reflecting sampling errors. Only 27 SNP were required to match the resolving power of 17 STR to detect population structure, that is, 1.6 SNP:1 STR. Whereas STR only differentiated the Mauritian population from all other populations, SNP detected 4 genetically distinct groups (Cambodia, Singapore-Sumatra, Mauritius, and Zamboanga). SNP are poised to become as valuable as STR for understanding and detecting genetic structure among cynomolgus macaques. Although STR will remain an important tool for cynomolgus macaque population studies, SNP have the potential to become the mainstream marker type.
机译:由于人类生物医学研究对NHP模型的需求不断增加,因此对食蟹猕猴(Macaca fascicularis)的遗传组成的兴趣有所增加。食蟹猕猴的区域种群之间的显着遗传差异可能会混淆研究结果的解释,因为它们并不仅仅反映实验治疗效果的差异。因此,应通过使用区域特异性遗传标记来验证用作研究对象的食蟹猕猴的共同起源,以最大程度地减少被选作研究对象的动物之间潜在的遗传变异对所研究表型的影响。我们比较了18个短串联重复序列(STR)标记和83个单核苷酸多态性(SNP)标记的有效性,以区分来自6个不同种群(柬埔寨,苏门答腊,毛里求斯,新加坡和吕宋岛的猕猴)的血统。和菲律宾的三宝颜)。遗传多样性指数(如基于SNP的等位基因数和预期的杂合度)比STR提供的更低,并且表现出更低的标准误,这可能是因为,与STR不同,大多数SNP是双等位基因,因此预期的最大预期杂合度值为0.50。然而,基于SNP的观察到的杂合性估计的标准误差高于STR的标准误差,这可能反映了采样误差。仅需要27个SNP即可匹配17个STR的分辨能力来检测种群结构,即1.6 SNP:1 STR。 STR仅将毛里求斯人口与所有其他人群区分开,而SNP检测到4个遗传上不同的群体(柬埔寨,新加坡-苏门答​​腊,毛里求斯和三宝颜)。 SNP有望与STR一样,对于了解和检测猕猴的遗传结构具有重要的意义。尽管STR仍将是猕猴猕猴种群研究的重要工具,但SNP有可能成为主流标记类型。

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