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序列多样性分析提高恒河猴基因组的生物医学应用价值。

Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility.

机构信息

Department of Animal Sciences, Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.

Department of Surgery, School of Medicine, University of Missouri, Columbia, MO 65211, USA.

出版信息

Science. 2020 Dec 18;370(6523). doi: 10.1126/science.abc6617.

Abstract

The rhesus macaque () is the most widely studied nonhuman primate (NHP) in biomedical research. We present an updated reference genome assembly (Mmul_10, contig N50 = 46 Mbp) that increases the sequence contiguity 120-fold and annotate it using 6.5 million full-length transcripts, thus improving our understanding of gene content, isoform diversity, and repeat organization. With the improved assembly of segmental duplications, we discovered new lineage-specific genes and expanded gene families that are potentially informative in studies of evolution and disease susceptibility. Whole-genome sequencing (WGS) data from 853 rhesus macaques identified 85.7 million single-nucleotide variants (SNVs) and 10.5 million indel variants, including potentially damaging variants in genes associated with human autism and developmental delay, providing a framework for developing noninvasive NHP models of human disease.

摘要

恒河猴()是生物医学研究中应用最广泛的非人类灵长类动物(NHP)。我们呈现了一个更新的参考基因组组装(Mmul_10,N50 为 46 Mbp),其序列连续性提高了 120 倍,并使用 650 万个全长转录本进行注释,从而提高了我们对基因内容、异构体多样性和重复组织的理解。通过改进的片段重复序列组装,我们发现了新的谱系特异性基因和扩展的基因家族,这些基因在进化和疾病易感性研究中可能具有重要意义。对 853 只恒河猴的全基因组测序(WGS)数据进行分析,鉴定出 8570 万个单核苷酸变异(SNVs)和 1050 万个插入缺失变异,包括与人类自闭症和发育迟缓相关基因中的潜在致病变异,为开发非侵入性的人类疾病恒河猴模型提供了框架。

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