解析与微生物组相关的代谢性疾病的全基因组研究。
Dissecting genome-wide studies for microbiome-related metabolic diseases.
机构信息
Division of Human Genetics, Department of Pathology, University of Cape Town, Observatory 7925, Cape Town, South Africa.
Laboratory of Human Pathologies Biology, Department of Biology, Faculty of Sciences, and Genomic Center of Human Pathologies, Faculty of Medicine and Pharmacy, Mohammed V University, Agdal Rabat, B.P, 8007 N.U, Morocco.
出版信息
Hum Mol Genet. 2020 Sep 30;29(R1):R73-R80. doi: 10.1093/hmg/ddaa105.
Despite the meteoric rise in genome-wide association studies for metabolic diseases (MetD) over the last few years, our understanding of the pathogenesis of these diseases is still far from complete. Recent developments have established that MetD arises from complex interactions between host genetics, the gut microbiome and the environment. However, our knowledge of the genetic and microbiome components involved and the underlying molecular mechanisms remains limited. Here, we review and summarize recent studies investigating the genetic and microbiome basis of MetD. Then, given the critical importance of study-individual's ancestry in these studies, we leverage 4932 whole-genome sequence samples from 18 worldwide ethnic groups to examine genetic diversity in currently reported variants associated with MetD. The analyses show marked differences in gene-specific proportion of pathogenic single-nucleotide polymorphisms (SNPs) and gene-specific SNPs MAFs across ethnic groups, highlighting the importance of population- and ethnic-specific investigations in pinpointing the causative factors for MetD. We conclude with a discussion of research areas where further investigation on interactions between host genetics, microbiome and the environment is needed.
尽管近年来代谢疾病(MetD)的全基因组关联研究迅速发展,但我们对这些疾病发病机制的理解仍远远不够。最近的研究结果表明,MetD 是由宿主遗传学、肠道微生物组和环境之间的复杂相互作用引起的。然而,我们对所涉及的遗传和微生物组成分以及潜在的分子机制的了解仍然有限。在这里,我们回顾和总结了最近关于 MetD 的遗传和微生物组基础的研究。然后,鉴于在这些研究中个体的祖先对研究的重要性,我们利用来自 18 个全球种族的 4932 个全基因组序列样本,来检测与 MetD 相关的已报道变异中与致病性单核苷酸多态性(SNP)和特定基因 SNP 等位基因频率(MAF)相关的遗传多样性。分析结果显示,不同种族之间基因特异性致病性 SNP 比例和基因特异性 SNP MAF 存在显著差异,突出了在确定 MetD 致病因素方面进行基于人群和种族的特定研究的重要性。最后,我们讨论了需要进一步研究宿主遗传学、微生物组和环境之间相互作用的研究领域。