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从全基因组序列中恢复线粒体基因组,以推断 1883 年现代瘤牛和印度牛的母系多样性。

Recovery of mitogenomes from whole genome sequences to infer maternal diversity in 1883 modern taurine and indicine cattle.

机构信息

School of Applied Systems Biology, La Trobe University, Bundoora, VIC, 3083, Australia.

Agriculture Victoria, AgriBio, Centre for AgriBioscience, Bundoora, VIC, 3083, Australia.

出版信息

Sci Rep. 2022 Apr 4;12(1):5582. doi: 10.1038/s41598-022-09427-y.

DOI:10.1038/s41598-022-09427-y
PMID:35379858
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8980051/
Abstract

Maternal diversity based on a sub-region of mitochondrial genome or variants were commonly used to understand past demographic events in livestock. Additionally, there is growing evidence of direct association of mitochondrial genetic variants with a range of phenotypes. Therefore, this study used complete bovine mitogenomes from a large sequence database to explore the full spectrum of maternal diversity. Mitogenome diversity was evaluated among 1883 animals representing 156 globally important cattle breeds. Overall, the mitogenomes were diverse: presenting 11 major haplogroups, expanding to 1309 unique haplotypes, with nucleotide diversity 0.011 and haplotype diversity 0.999. A small proportion of African taurine (3.5%) and indicine (1.3%) haplogroups were found among the European taurine breeds and composites. The haplogrouping was largely consistent with the population structure derived from alternate clustering methods (e.g. PCA and hierarchical clustering). Further, we present evidence confirming a new indicine subgroup (I1a, 64 animals) mainly consisting of breeds originating from China and characterised by two private mutations within the I1 haplogroup. The total genetic variation was attributed mainly to within-breed variance (96.9%). The accuracy of the imputation of missing genotypes was high (99.8%) except for the relatively rare heteroplasmic genotypes, suggesting the potential for trait association studies within a breed.

摘要

基于线粒体基因组的亚区或变体的母系多样性通常用于了解家畜过去的人口事件。此外,越来越多的证据表明线粒体遗传变异与一系列表型直接相关。因此,本研究使用来自大型序列数据库的完整牛线粒体基因组来探索母系多样性的全貌。在代表 156 个全球重要牛品种的 1883 只动物中评估了线粒体基因组的多样性。总体而言,线粒体基因组具有多样性:呈现 11 个主要的单倍群,扩展到 1309 个独特的单倍型,核苷酸多样性为 0.011,单倍型多样性为 0.999。在欧洲牛品种和复合品种中发现了一小部分非洲牛(3.5%)和印度牛(1.3%)单倍群。单倍群分组与来自替代聚类方法(例如 PCA 和层次聚类)得出的种群结构基本一致。此外,我们提供了证据证实了一个新的印度牛亚群(I1a,64 只动物),主要由起源于中国的品种组成,其特点是 I1 单倍群内有两个私有突变。总遗传变异主要归因于品种内的方差(96.9%)。缺失基因型的推断准确性很高(99.8%),除了相对罕见的异质合子基因型外,这表明在一个品种内进行性状关联研究的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/8980051/05337892a55c/41598_2022_9427_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/8980051/046ef9118e4d/41598_2022_9427_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/8980051/0bd8438e7cd4/41598_2022_9427_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/8980051/02de682cc0e6/41598_2022_9427_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/8980051/654b812b73be/41598_2022_9427_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/8980051/05337892a55c/41598_2022_9427_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/8980051/046ef9118e4d/41598_2022_9427_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/8980051/0bd8438e7cd4/41598_2022_9427_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/8980051/02de682cc0e6/41598_2022_9427_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/8980051/654b812b73be/41598_2022_9427_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a9/8980051/05337892a55c/41598_2022_9427_Fig5_HTML.jpg

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