Southwest National Primate Research Center, San Antonio, Texas, USA.
Texas Biomedical Research Institute, San Antonio, Texas, USA.
Am J Primatol. 2024 Jul;86(7):e23630. doi: 10.1002/ajp.23630. Epub 2024 Apr 24.
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.
狨猴是研究衰老、神经生物学和许多其他课题的基本非人类灵长类动物模型。由于血液和其他组织中经常存在嵌合体、缺乏能够进行经济高效的全基因组变异检测的工具,以及动物在群体之间的历史合并和迁移,圈养狨猴群体的遗传管理变得复杂。我们对西南国家灵长类动物研究中心(SNPRC)饲养的 82 只狨猴的毛囊衍生 DNA(一种最小程度嵌合的 DNA 来源)进行了基因型测序(GBS)。我们的主要目标是对我们的狨猴群体进行遗传特征分析,以验证系谱并进行群体管理,并向科学界介绍这一宝贵资源的功能遗传构成。我们使用 GBS 数据重建了最近群体间合并的遗传遗产,鉴定了由于不完全系谱信息而以前未知的遗传相关动物,并表明 SNPRC 群体中的动物似乎表现出低水平的近亲繁殖。在所鉴定的 >99000 个单核苷酸变异(SNV)中,>9800 个位于已知在人类中携带临床意义致病性变异的基因区域内。总体而言,我们表明使用毛囊 DNA 进行低分辨率(稀疏)基因分型的组合是圈养狨猴群体遗传管理的有力策略,并可用于鉴定潜在的 SNV,以开发生物医学研究模型。