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转录的复杂性。

IF 11.1 Q1 CELL BIOLOGY
Cell genomics Pub Date : 2025-05-14 Epub Date: 2025-04-04 DOI:10.1016/j.xgen.2025.100823
Ramesh Ramasamy, Muthuswamy Raveendran, R Alan Harris, Hiep D Le, Ludovic S Mure, Giorgia Benegiamo, Ouria Dkhissi-Benyahya, Howard Cooper, Jeffrey Rogers, Satchidananda Panda
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引用次数: 0

摘要

等位基因特异性表达(ASE)是理解物种内表型变异、疾病易感性差异和对环境因素反应的遗传基础的关键。我们从12只年龄匹配的健康橄榄狒狒(Papio anubis)中收集了11种不同的组织类型,用于全基因组ASE分析。通过对其基因组进行至少30倍深度的测序,我们确定了超过1600万个单核苷酸变异(snv)。我们还生成了长读测序数据,使96.5%的可测蛋白质编码基因编码区域内的所有变异都能作为单个单倍型块进行分相。考虑到狒狒相对于人类的广泛杂合性,我们可以对72%的总注释蛋白编码基因集进行ASE量化。我们确定了表现出ASE并影响特定组织和基因型的基因。我们发现ASE snv也存在于具有相同等位基因的人群中,并且被灵长类ai - 3d和AlphaMissense模型指定为致病性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genome-wide allele-specific expression in multi-tissue samples from healthy male baboons reveals the transcriptional complexity of mammals.

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.

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