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BayFish: Bayesian inference of transcription dynamics from population snapshots of single-molecule RNA FISH in single cells

机译:BayFish:单细胞中单分子RNA FISH种群快照的转录动力学的贝叶斯推断

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Background: The organisation of vertebrate genomes into topologically associating domains (TADs) is believed to facilitate the regulation of the genes located within them. A remaining question is whether TAD organisation is achieved through the interactions of the regulatory elements within them or if these interactions are favoured by the pre-existence of TADs. If the latter is true, the fusion of two independent TADs should result in the rewiring of the transcriptional landscape and the generation of ectopic contacts. Results: We show that interactions within the PAX3 and FOXO1 domains are restricted to their respective TADs in normal conditions, while in a patient-derived alveolar rhabdomyosarcoma cell line, harbouring the diagnostic t(2;13) (q35;q14) translocation that brings together the PAX3 and FOXO1 genes, the PAX3 promoter interacts ectopically with FOXO1 sequences. Using a combination of 4C-seq datasets, we have modelled the three-dimensional organisation of the fused landscape in alveolar rhabdomyosarcoma. Conclusions: The chromosomal translocation that leads to alveolar rhabdomyosarcoma development generates a novel TAD that is likely to favour ectopic PAX3:FOXO1 oncogene activation in non-PAX3 territories. Rhabdomyosarcomas may therefore arise from cells which do not normally express PAX3. The borders of this novel TAD correspond to the original 5'- and 3'- borders of the PAX3 and FOXO1 TADs, respectively, suggesting that TAD organisation precedes the formation of regulatory long-range interactions. Our results demonstrate that, upon translocation, novel regulatory landscapes are formed allowing new intra-TAD interactions between the original loci involved.
机译:背景:脊椎动物基因组组织成拓扑关联域(TADs)被认为有助于调节位于其内的基因。剩下的问题是,TAD组织是通过其内部的监管要素之间的相互作用来实现还是由TAD的存在促进这些相互作用。如果后者是正确的,则两个独立的TAD的融合应导致转录环境的重新连接和异位接触的产生。结果:我们显示,在正常情况下,PAX3和FOXO1域内的相互作用仅限于其各自的TAD,而在患者来源的肺泡横纹肌肉瘤细胞系中,则具有诊断性t(2; 13)(q35; q14)易位结合PAX3和FOXO1基因,PAX3启动子与FOXO1序列异位相互作用。使用4C-seq数据集的组合,我们对肺泡横纹肌肉瘤中融合景观的三维组织进行了建模。结论:导致肺泡横纹肌肉瘤发展的染色体易位产生了一种新颖的TAD,该TAD可能会促进非PAX3区域中异位PAX3:FOXO1癌基因的激活。因此,横纹肌肉瘤可能源于通常不表达PAX3的细胞。该新型TAD的边界分别对应于PAX3和FOXO1 TAD的原始5'-和3'-边界,这表明TAD组织先于监管性远程相互作用的形成。我们的研究结果表明,易位后,形成了新的监管格局,允许在所涉及的原始基因座之间进行新的TAD内相互作用。

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