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基因组编辑内含子增强子揭示了它们在拟南芥组织特异性基因表达精细调控中的作用。

Genomic editing of intronic enhancers unveils their role in fine-tuning tissue-specific gene expression in Arabidopsis thaliana.

机构信息

Key Laboratory of Soybean Biology in Chinese Ministry of Education, Northeast Agricultural University, Harbin 150030, China.

Department of Plant Biology, Michigan State University, East Lansing, MI 48824, USA.

出版信息

Plant Cell. 2021 Jul 19;33(6):1997-2014. doi: 10.1093/plcell/koab093.

Abstract

Enhancers located in introns are abundant and play a major role in the regulation of gene expression in mammalian species. By contrast, the functions of intronic enhancers in plants have largely been unexplored and only a handful of plant intronic enhancers have been reported. We performed a genome-wide prediction of intronic enhancers in Arabidopsis thaliana using open chromatin signatures based on DNase I sequencing. We identified 941 candidate intronic enhancers associated with 806 genes in seedling tissue and 1,271 intronic enhancers associated with 1,069 genes in floral tissue. We validated the function of 15 of 21 (71%) of the predicted intronic enhancers in transgenic assays using a reporter gene. We also created deletion lines of three intronic enhancers associated with two different genes using CRISPR/Cas. Deletion of these enhancers, which span key transcription factor binding sites, did not abolish gene expression but caused varying levels of transcriptional repression of their cognate genes. Remarkably, the transcriptional repression of the deletion lines occurred at specific developmental stages and resulted in distinct phenotypic effects on plant morphology and development. Clearly, these three intronic enhancers are important in fine-tuning tissue- and development-specific expression of their cognate genes.

摘要

内含子中的增强子数量丰富,在哺乳动物物种的基因表达调控中发挥着重要作用。相比之下,植物内含子增强子的功能在很大程度上尚未被探索,仅报道了少数几种植物内含子增强子。我们使用基于 DNase I 测序的染色质开放性特征,在拟南芥中进行了全基因组内含子增强子预测。我们在幼苗组织中鉴定出了 941 个与 806 个基因相关的候选内含子增强子,在花组织中鉴定出了 1271 个与 1069 个基因相关的内含子增强子。我们使用报告基因在转基因实验中验证了 21 个预测的内含子增强子中的 15 个(71%)的功能。我们还使用 CRISPR/Cas 技术创建了与两个不同基因相关的三个内含子增强子的缺失系。这些增强子缺失并没有消除基因表达,而是导致其同源基因的转录抑制程度不同,这些增强子缺失跨越了关键转录因子结合位点。值得注意的是,缺失系的转录抑制发生在特定的发育阶段,并导致植物形态和发育的独特表型效应。显然,这三个内含子增强子在精细调节其同源基因的组织特异性和发育特异性表达方面非常重要。

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