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Putative bovine topological association domains and CTCF binding motifs can reduce the search space for causative regulatory variants of complex traits

机译:推测的牛拓扑关联域和CTCF结合基序可以减少复杂性状的致病性调控变异的搜索空间

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Topological association domains (TADs) are chromosomal domains characterised by frequent internal DNA-DNA interactions. The transcription factor CTCF binds to conserved DNA sequence patterns called CTCF binding motifs to either prohibit or facilitate chromosomal interactions. TADs and CTCF binding motifs control gene expression, but they are not yet well defined in the bovine genome. In this paper, we sought to improve the annotation of bovine TADs and CTCF binding motifs, and assess whether the new annotation can reduce the search space for cis-regulatory variants. We used genomic synteny to map TADs and CTCF binding motifs from humans, mice, dogs and macaques to the bovine genome. We found that our mapped TADs exhibited the same hallmark properties of those sourced from experimental data, such as housekeeping genes, transfer RNA genes, CTCF binding motifs, short interspersed elements, H3K4me3 and H3K27ac. We showed that runs of genes with the same pattern of allele-specific expression (ASE) (either favouring paternal or maternal allele) were often located in the same TAD or between the same conserved CTCF binding motifs. Analyses of variance showed that when averaged across all bovine tissues tested, TADs explained 14% of ASE variation (standard deviation, SD: 0.056), while CTCF explained 27% (SD: 0.078). Furthermore, we showed that the quantitative trait loci (QTLs) associated with gene expression variation (eQTLs) or ASE variation (aseQTLs), which were identified from mRNA transcripts from 141 lactating cows’ white blood and milk cells, were highly enriched at putative bovine CTCF binding motifs. The linearly-furthermost, and most-significant aseQTL and eQTL for each genic target were located within the same TAD as the gene more often than expected (Chi-Squared test P-value
机译:拓扑关联域(TAD)是以频繁的内部DNA-DNA相互作用为特征的染色体域。转录因子CTCF与称为CTCF结合基序的保守DNA序列模式结合,以阻止或促进染色体相互作用。 TAD和CTCF结合基序控制基因表达,但在牛基因组中尚未明确定义。在本文中,我们试图改善牛TAD和CTCF结合基序的注释,并评估新注释是否可以减少顺式调节变体的搜索空间。我们使用基因组同义性将人,小鼠,狗和猕猴的TAD和CTCF结合基序映射到牛基因组。我们发现,我们绘制的TAD表现出与那些来自实验数据的特征相同的特征,例如管家基因,转移RNA基因,CTCF结合基序,短散布的元素,H3K4me3和H3K27ac。我们显示,具有相同等位基因特异性表达(ASE)模式(有利于父本或母本等位基因)的基因运行通常位于同一TAD或相同的保守CTCF结合基序之间。方差分析显示,在所有测试的牛组织中取平均值时,TAD解释了ASE变异的14%(标准偏差,SD:0.056),而CTCF解释了27%(SD:0.078)。此外,我们发现与基因表达变异(eQTL)或ASE变异(aseQTL)相关的定量性状位点(QTL)是从141头奶牛的白血和乳细胞的mRNA转录本中鉴定的,在假定的牛中高度富集CTCF结合基序。每个基因靶标中线性最远,最重要的aseQTL和eQTL与基因位于同一TAD的频率比预期的高(Chi-Squared测试P值<0.001)。我们的结果表明,基因组同构可用于在功能上注释保守的转录成分,并提供了一种减少牛基因组中致病性调控变异的搜索空间的工具。

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