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来自健康雄性狒狒多组织样本的全基因组等位基因特异性表达揭示了哺乳动物的转录复杂性。

Genome-wide allele-specific expression in multi-tissue samples from healthy male baboons reveals the transcriptional complexity of mammals.

作者信息

Ramasamy Ramesh, Raveendran Muthuswamy, Harris R Alan, Le Hiep D, Mure Ludovic S, Benegiamo Giorgia, Dkhissi-Benyahya Ouria, Cooper Howard, Rogers Jeffrey, Panda Satchidananda

机构信息

Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.

Human Genome Sequencing Center and Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Cell Genom. 2025 May 14;5(5):100823. doi: 10.1016/j.xgen.2025.100823. Epub 2025 Apr 4.

Abstract

Allele-specific expression (ASE) is pivotal in understanding the genetic underpinnings of phenotypic variation within species, differences in disease susceptibility, and responses to environmental factors. We processed 11 different tissue types collected from 12 age-matched healthy olive baboons (Papio anubis) for genome-wide ASE analysis. By sequencing their genomes at a minimum depth of 30×, we identified over 16 million single-nucleotide variants (SNVs). We also generated long-read sequencing data, enabling the phasing of all variants present within the coding regions of 96.5% of assayable protein-coding genes as a single haplotype block. Given the extensive heterozygosity of baboons relative to humans, we could quantify ASE across 72% of the total annotated protein-coding gene set. We identified genes that exhibit ASE and affect specific tissues and genotypes. We discovered ASE SNVs that also exist in human populations with identical alleles and that are designated as pathogenic by both the PrimateAI-3D and AlphaMissense models.

摘要

等位基因特异性表达(ASE)对于理解物种内表型变异的遗传基础、疾病易感性差异以及对环境因素的反应至关重要。我们对从12只年龄匹配的健康橄榄狒狒(埃及狒狒)收集的11种不同组织类型进行了全基因组ASE分析。通过对它们的基因组进行至少30倍深度的测序,我们鉴定出超过1600万个单核苷酸变异(SNV)。我们还生成了长读长测序数据,能够将96.5%的可检测蛋白质编码基因编码区域内存在的所有变异作为单个单倍型块进行定相。鉴于狒狒相对于人类具有广泛的杂合性,我们能够对总共72%的注释蛋白质编码基因集进行ASE定量分析。我们鉴定出表现出ASE并影响特定组织和基因型的基因。我们发现了在人类群体中也存在相同等位基因的ASE SNV,并且这些SNV在PrimateAI-3D和AlphaMissense模型中均被指定为致病基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8599/12143330/169fd1fece81/fx1.jpg

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