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基于全基因组CNV阵列和TSPY基因拷贝数估计公牛的体细胞镶嵌现象。

Somatic Mosaicism in Bulls Estimated from Genome-Wide CNV Array and TSPY Gene Copy Numbers.

作者信息

Oluwole Olutobi A, Revay Tamas, Mahboubi Kiana, Favetta Laura A, King W Allan

机构信息

Department of Biomedical Sciences, University of Guelph, Guelph, Ont., Canada.

出版信息

Cytogenet Genome Res. 2016;149(3):176-181. doi: 10.1159/000448368. Epub 2016 Aug 18.

Abstract

Somatic mosaicism has become a focus in human research due to the implications of individual genetic variability in disease. Here, we assessed somatic copy number variations (CNVs) in Holstein bulls in 2 respects. We estimated genome-wide CNVs and assayed CNVs of the TSPY gene, the most variable bovine gene from the Y chromosome. Somatic tissues (blood, lung, heart, muscle, testis, and brain) of 4 bulls were arrayed on the Illumina Bovine SNP50k chip and qPCR tested for TSPY copy numbers. Our results showed extensive copy number divergence in tissues within the same animal as well as significant copy number alterations of TSPY. We detected a mean of 31 CNVs per animal among which 14 were of germline origin, as they were constantly present in all investigated tissues of the animal, while 18 were specific to 1 tissue. Thus, 57% of the total number of detected CNVs was the result of de novo somatic events. Further, TSPY copy number was found to vary significantly among tissues as well as among the same tissue type from different animals in a wide range from 7 to 224% of the calibrator. Our study shows significant autosomal and Y-chromosomal de novo somatic CNV in bulls.

摘要

由于个体基因变异在疾病中的影响,体细胞嵌合体已成为人类研究的一个焦点。在此,我们从两个方面评估了荷斯坦公牛的体细胞拷贝数变异(CNV)。我们估计了全基因组CNV,并检测了Y染色体上变异最大的牛基因TSPY的CNV。将4头公牛的体细胞组织(血液、肺、心脏、肌肉、睾丸和大脑)排列在Illumina牛SNP50k芯片上,并通过qPCR检测TSPY拷贝数。我们的结果显示,同一动物体内不同组织间存在广泛的拷贝数差异,以及TSPY的显著拷贝数改变。我们检测到每头动物平均有31个CNV,其中14个起源于生殖系,因为它们在该动物所有被研究的组织中都持续存在,而18个是特定于某一组织的。因此,检测到的CNV总数中有57%是新生体细胞事件的结果。此外,发现TSPY拷贝数在不同组织之间以及来自不同动物的同一组织类型之间有显著差异,范围在对照的7%至224%之间。我们的研究表明,公牛中存在显著的常染色体和Y染色体新生体细胞CNV。

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