Shelley A. Cole, Martha M. Lyke, Clinton Christensen, Deborah Newman, Alec Bagwell, Samuel Galindo, Jeremy Glenn, Donna G. Layne-Colon, Ken Sayers, Suzette Tardif, Laura A. Cox, Corinna Ross, Ian H. Cheeseman
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引用次数: 0
摘要
狨猴是研究衰老、神经生物学和许多其他课题的基本非人灵长类动物模型。由于血液和其他组织中经常出现嵌合体,缺乏对变异进行经济有效的全基因组检测的工具,以及动物在群落间的历史性合并和迁移,圈养狨猴群落的遗传管理变得十分复杂。我们对西南国家灵长类研究中心(SNPRC)饲养的 82 只狨猴的毛囊 DNA(一种嵌合度极低的 DNA 来源)进行了基因型测序(GBS)。我们的主要目标是确定狨猴种群的遗传特征,以便进行血统验证和种群管理,并向科学界介绍这一宝贵资源的功能基因构成。我们利用 GBS 数据重建了近期群落间合并的遗传遗产,确定了以前由于血统信息不完整而不知道其关系的遗传相关动物,并表明 SNPRC 群落中的动物似乎表现出较低的近亲繁殖水平。在我们鉴定的超过 99,000 个单核苷酸变异(SNVs)中,超过 9800 个位于已知存在对人类有临床意义的致病变异的基因区域内。总之,我们利用毛囊 DNA 进行低分辨率(稀疏)基因分型是圈养狨猴群遗传管理和鉴定潜在 SNVs 以开发生物医学研究模型的有力策略。
Genetic characterization of a captive marmoset (Callithrix jacchus) colony using genotype-by-sequencing
The marmoset is a fundamental nonhuman primate model for the study of aging, neurobiology, and many other topics. Genetic management of captive marmoset colonies is complicated by frequent chimerism in the blood and other tissues, a lack of tools to enable cost-effective, genome-wide interrogation of variation, and historic mergers and migrations of animals between colonies. We implemented genotype-by-sequencing (GBS) of hair follicle derived DNA (a minimally chimeric DNA source) of 82 marmosets housed at the Southwest National Primate Research Center (SNPRC). Our primary goals were the genetic characterization of our marmoset population for pedigree verification and colony management and to inform the scientific community of the functional genetic makeup of this valuable resource. We used the GBS data to reconstruct the genetic legacy of recent mergers between colonies, to identify genetically related animals whose relationships were previously unknown due to incomplete pedigree information, and to show that animals in the SNPRC colony appear to exhibit low levels of inbreeding. Of the >99,000 single-nucleotide variants (SNVs) that we characterized, >9800 are located within gene regions known to harbor pathogenic variants of clinical significance in humans. Overall, we show the combination of low-resolution (sparse) genotyping using hair follicle DNA is a powerful strategy for the genetic management of captive marmoset colonies and for identifying potential SNVs for the development of biomedical research models.