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染色体结构变异对生物通路进化的影响。

Impact of constitutional copy number variants on biological pathway evolution.

机构信息

Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY, USA.

出版信息

BMC Evol Biol. 2013 Jan 23;13:19. doi: 10.1186/1471-2148-13-19.

DOI:10.1186/1471-2148-13-19
PMID:23342974
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3563492/
Abstract

BACKGROUND

Inherited Copy Number Variants (CNVs) can modulate the expression levels of individual genes. However, little is known about how CNVs alter biological pathways and how this varies across different populations. To trace potential evolutionary changes of well-described biological pathways, we jointly queried the genomes and the transcriptomes of a collection of individuals with Caucasian, Asian or Yoruban descent combining high-resolution array and sequencing data.

RESULTS

We implemented an enrichment analysis of pathways accounting for CNVs and genes sizes and detected significant enrichment not only in signal transduction and extracellular biological processes, but also in metabolism pathways. Upon the estimation of CNV population differentiation (CNVs with different polymorphism frequencies across populations), we evaluated that 22% of the pathways contain at least one gene that is proximal to a CNV (CNV-gene pair) that shows significant population differentiation. The majority of these CNV-gene pairs belong to signal transduction pathways and 6% of the CNV-gene pairs show statistical association between the copy number states and the transcript levels.

CONCLUSIONS

The analysis suggested possible examples of positive selection within individual populations including NF-kB, MAPK signaling pathways, and Alu/L1 retrotransposition factors. Altogether, our results suggest that constitutional CNVs may modulate subtle pathway changes through specific pathway enzymes, which may become fixed in some populations.

摘要

背景

遗传拷贝数变异 (CNVs) 可以调节个体基因的表达水平。然而,人们对于 CNVs 如何改变生物途径以及这种改变在不同人群中如何变化知之甚少。为了追踪描述良好的生物途径的潜在进化变化,我们结合高分辨率阵列和测序数据,共同查询了具有高加索人、亚洲人或约鲁巴人血统的个体的基因组和转录组。

结果

我们对考虑 CNVs 和基因大小的途径进行了富集分析,并不仅在信号转导和细胞外生物过程中检测到了显著的富集,而且在代谢途径中也检测到了显著的富集。在估计 CNV 群体分化(不同人群中具有不同多态性频率的 CNVs)时,我们评估了 22%的途径至少包含一个基因,该基因靠近 CNV(CNV-基因对),该基因显示出显著的群体分化。这些 CNV-基因对中的大多数属于信号转导途径,6%的 CNV-基因对显示出拷贝数状态和转录水平之间的统计关联。

结论

分析表明,包括 NF-kB、MAPK 信号通路和 Alu/L1 反转录因子在内的个体群体中可能存在正选择的例子。总的来说,我们的结果表明,构成性 CNVs 可能通过特定的途径酶来调节微妙的途径变化,这些变化可能在某些人群中固定下来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80fe/3563492/4d72786f3f96/1471-2148-13-19-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80fe/3563492/5fd1098aa270/1471-2148-13-19-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80fe/3563492/b53315e061b9/1471-2148-13-19-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80fe/3563492/f197a65620c4/1471-2148-13-19-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80fe/3563492/4d72786f3f96/1471-2148-13-19-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80fe/3563492/5fd1098aa270/1471-2148-13-19-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80fe/3563492/b53315e061b9/1471-2148-13-19-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80fe/3563492/f197a65620c4/1471-2148-13-19-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80fe/3563492/4d72786f3f96/1471-2148-13-19-4.jpg

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