School of Medicine, Tsinghua University, Beijing, China.
School of Medicine and the Tsinghua-Peking Center for Life science, Tsinghua University, Beijing, China.
Brief Bioinform. 2021 Nov 5;22(6). doi: 10.1093/bib/bbab181.
Hi-C is a genome-wide assay based on Chromosome Conformation Capture and high-throughput sequencing to decipher 3D chromatin organization in the nucleus. However, computational methods to detect functional interactions utilizing Hi-C data face challenges including the correction for various sources of biases and the identification of functional interactions with low counts of interacting fragments. We present Chrom-Lasso, a lasso linear regression model that removes complex biases assumption-free and identifies functional interacting loci with increased power by combining information of local reads distribution surrounding the area of interest. We showed that interacting regions identified by Chrom-Lasso are more enriched for 5C validated interactions and functional GWAS hits than that of GOTHiC and Fit-Hi-C. To further demonstrate the ability of Chrom-Lasso to detect interactions of functional importance, we performed time-series Hi-C and RNA-seq during T cell activation and exhaustion. We showed that the dynamic changes in gene expression and chromatin interactions identified by Chrom-Lasso were largely concordant with each other. Finally, we experimentally confirmed Chrom-Lasso's finding that Erbb3 was co-regulated with distinct neighboring genes at different states during T cell activation. Our results highlight Chrom-Lasso's utility in detecting weak functional interaction between cis-regulatory elements, such as promoters and enhancers.
Hi-C 是一种基于染色体构象捕获和高通量测序的全基因组检测方法,用于破译细胞核内的 3D 染色质结构。然而,利用 Hi-C 数据检测功能相互作用的计算方法面临着各种挑战,包括对各种来源的偏差进行校正,以及识别具有低相互作用片段计数的功能相互作用。我们提出了 Chrom-Lasso,这是一种套索线性回归模型,它可以在不假设复杂偏差的情况下进行校正,并通过整合感兴趣区域周围局部读取分布的信息,以提高功率来识别功能相互作用的位点。我们表明,与 GOTHiC 和 Fit-Hi-C 相比,Chrom-Lasso 识别的相互作用区域在 5C 验证的相互作用和功能 GWAS 命中方面更为丰富。为了进一步证明 Chrom-Lasso 检测功能重要性相互作用的能力,我们在 T 细胞激活和耗竭期间进行了时间序列 Hi-C 和 RNA-seq 实验。我们表明,Chrom-Lasso 识别的基因表达和染色质相互作用的动态变化在很大程度上是相互一致的。最后,我们通过实验证实了 Chrom-Lasso 的发现,即在 T 细胞激活过程中,Erbb3 与不同的邻近基因在不同状态下共同受到调控。我们的结果强调了 Chrom-Lasso 在检测顺式调控元件(如启动子和增强子)之间的弱功能相互作用方面的实用性。