School of Life Sciences and Center for Soybean Research of the State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Guangdong Provincial Key Laboratory for Plant Epigenetics, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518055, China.
Genes (Basel). 2021 Apr 25;12(5):640. doi: 10.3390/genes12050640.
Transcription activation is tightly associated with the openness of chromatin, which allows direct contact between transcriptional regulators, such as transcription factors, and their targeted DNA for downstream gene activation. However, the annotation of open chromatin regions (OCRs) in the wild soybean () genome is limited. We performed assay for transposase-accessible chromatin using sequencing (ATAC-seq) and successfully identified 22,333 OCRs in the leaf of W05 (a wild soybean accession). These OCRs were enriched in gene transcription start sites (TSS) and were positively correlated with downstream gene expression. Several known transcription factor (TF)-binding motifs were also enriched at the OCRs. A potential regulatory network was constructed using these transcription factors and the OCR-marked genes. Furthermore, by overlapping the OCR distribution with those of histone modifications from chromatin immunoprecipitation followed by sequencing (ChIP-seq), we found that the distribution of the activation histone mark, H3K4me3, but not that of the repressive H3K27me3 mark, was closely associated with OCRs for gene activation. Several putative enhancer-like distal OCRs were also found to overlap with LincRNA-encoding loci. Moreover, our data suggest that homologous OCRs could potentially influence homologous gene expression. Hence, the duplication of OCRs might be essential for plant genome architecture as well as for regulating gene expression.
转录激活与染色质的开放性密切相关,这使得转录调节剂(如转录因子)与其靶向 DNA 直接接触,从而激活下游基因。然而,野生大豆基因组中开放染色质区域 (OCR) 的注释有限。我们进行了转座酶可及染色质的测定 (ATAC-seq),成功鉴定了 W05 叶片中的 22333 个 OCR。这些 OCR 在基因转录起始位点 (TSS) 处富集,并且与下游基因表达呈正相关。一些已知的转录因子 (TF) 结合基序也在 OCR 处富集。使用这些转录因子和 OCR 标记的基因构建了一个潜在的调控网络。此外,通过将 OCR 分布与染色质免疫沉淀测序 (ChIP-seq) 中的组蛋白修饰分布重叠,我们发现激活组蛋白标记 H3K4me3 的分布与 OCR 密切相关,而抑制性 H3K27me3 标记的分布则与基因激活无关。还发现几个假定的增强子样远端 OCR 与 LincRNA 编码基因座重叠。此外,我们的数据表明,同源 OCR 可能潜在地影响同源基因的表达。因此,OCR 的复制可能对植物基因组结构以及基因表达的调控至关重要。