Center for Evolution and Medicine, School of Life Sciences, Arizona State University, Tempe, Arizona, United States of America.
The Translational Genomics Research Institute, Phoenix, Arizona, United States of America.
PLoS Genet. 2020 May 26;16(5):e1008749. doi: 10.1371/journal.pgen.1008749. eCollection 2020 May.
Indonesia is the world's fourth most populous country, host to striking levels of human diversity, regional patterns of admixture, and varying degrees of introgression from both Neanderthals and Denisovans. However, it has been largely excluded from the human genomics sequencing boom of the last decade. To serve as a benchmark dataset of molecular phenotypes across the region, we generated genome-wide CpG methylation and gene expression measurements in over 100 individuals from three locations that capture the major genomic and geographical axes of diversity across the Indonesian archipelago. Investigating between- and within-island differences, we find up to 10.55% of tested genes are differentially expressed between the islands of Sumba and New Guinea. Variation in gene expression is closely associated with DNA methylation, with expression levels of 9.80% of genes correlating with nearby promoter CpG methylation, and many of these genes being differentially expressed between islands. Genes identified in our differential expression and methylation analyses are enriched in pathways involved in immunity, highlighting Indonesia's tropical role as a source of infectious disease diversity and the strong selective pressures these diseases have exerted on humans. Finally, we identify robust within-island variation in DNA methylation and gene expression, likely driven by fine-scale environmental differences across sampling sites. Together, these results strongly suggest complex relationships between DNA methylation, transcription, archaic hominin introgression and immunity, all jointly shaped by the environment. This has implications for the application of genomic medicine, both in critically understudied Indonesia and globally, and will allow a better understanding of the interacting roles of genomic and environmental factors shaping molecular and complex phenotypes.
印度尼西亚是世界上第四大人口大国,拥有引人注目的人类多样性、区域混合模式以及来自尼安德特人和丹尼索瓦人的不同程度的基因渗入。然而,它在过去十年的人类基因组测序热潮中基本上被排除在外。为了成为该地区分子表型的基准数据集,我们在来自三个地点的 100 多个人中生成了全基因组 CpG 甲基化和基因表达测量值,这些地点涵盖了印度尼西亚群岛的主要基因组和地理多样性轴。在研究岛屿之间和岛屿内部的差异时,我们发现,在所测试的基因中,有高达 10.55%的基因在松巴哇岛和新几内亚岛之间表达不同。基因表达的变化与 DNA 甲基化密切相关,有 9.80%的基因的表达水平与附近启动子 CpG 甲基化相关,并且这些基因中的许多在岛屿之间表达不同。在我们的差异表达和甲基化分析中鉴定出的基因富集在参与免疫的途径中,突出了印度尼西亚作为传染病多样性的热带来源及其对人类施加的强烈选择压力。最后,我们确定了 DNA 甲基化和基因表达在岛内的强烈变化,这可能是由采样点之间的细微环境差异驱动的。总的来说,这些结果强烈表明 DNA 甲基化、转录、古人类基因渗入和免疫之间存在复杂的关系,所有这些都受到环境的共同塑造。这对基因组医学的应用具有重要意义,不仅在研究严重不足的印度尼西亚,而且在全球范围内,并且将有助于更好地理解塑造分子和复杂表型的基因组和环境因素的相互作用作用。