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诺福克岛人群线粒体基因组全序列种系来源突变率。

Pedigree derived mutation rate across the entire mitochondrial genome of the Norfolk Island population.

机构信息

Centre for Genomics and Personalised Health, Genomics Research Centre, School of Biomedical Sciences, Queensland University of Technology (QUT), 60 Musk Ave., Kelvin Grove, QLD, 4059, Australia.

Human Genomics, Kenepuru Science Centre, Institute of Environmental Science and Research, Wellington, New Zealand.

出版信息

Sci Rep. 2022 Apr 26;12(1):6827. doi: 10.1038/s41598-022-10530-3.

Abstract

Estimates of mutation rates for various regions of the human mitochondrial genome (mtGenome) vary widely, depending on whether they are inferred using a phylogenetic approach or obtained directly from pedigrees. Traditionally, only the control region, or small portions of the coding region have been targeted for analysis due to the cost and effort required to produce whole mtGenome Sanger profiles. Here, we report one of the first pedigree derived mutation rates for the entire human mtGenome. The entire mtGenome from 225 individuals originating from Norfolk Island was analysed to estimate the pedigree derived mutation rate and compared against published mutation rates. These individuals were from 45 maternal lineages spanning 345 generational events. Mutation rates for various portions of the mtGenome were calculated. Nine mutations (including two transitions and seven cases of heteroplasmy) were observed, resulting in a rate of 0.058 mutations/site/million years (95% CI 0.031-0.108). These mutation rates are approximately 16 times higher than estimates derived from phylogenetic analysis with heteroplasmy detected in 13 samples (n = 225, 5.8% individuals). Providing one of the first pedigree derived estimates for the entire mtGenome, this study provides a better understanding of human mtGenome evolution and has relevance to many research fields, including medicine, anthropology and forensics.

摘要

人类线粒体基因组(mtGenome)各区域的突变率估计值差异很大,具体取决于它们是通过系统发育方法推断得出的,还是直接从家系中获得的。传统上,由于产生整个 mtGenome Sanger 图谱所需的成本和工作量,仅对控制区或编码区的小部分进行了分析。在这里,我们报告了第一个全人类 mtGenome 家系衍生突变率之一。对来自诺福克岛的 225 个人的整个 mtGenome 进行了分析,以估计家系衍生的突变率,并与已发表的突变率进行了比较。这些个体来自跨越 345 代事件的 45 个母系谱系。计算了 mtGenome 各个部分的突变率。观察到 9 个突变(包括 2 个转换和 7 个异质性病例),导致 0.058 个突变/位点/百万年(95%CI 0.031-0.108)的速率。这些突变率比通过系统发育分析得出的估计值高约 16 倍,在 13 个样本(n=225,5.8%个体)中检测到异质性。该研究提供了第一个全 mtGenome 的家系衍生估计值之一,它为人类 mtGenome 进化提供了更好的理解,并与医学、人类学和法医学等许多研究领域相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d866/9042960/d0d1777c36e1/41598_2022_10530_Fig1_HTML.jpg

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