Zaidi Syed Shan-E-Ali, Shakir Sara, De Kort Hanne, Mehta Devang, Nguyen Vu, Gutzat Ruben, Vanderschuren Hervé
Plant Genetics and Rhizospheric Processes Laboratory, TERRA Teaching and Research Center, Gembloux Agro-Bio Tech, University of Liège, Gembloux, Belgium.
UMR Biologie du Fruit et Pathologie, INRAE, Université de Bordeaux, Villenave d'Ornon, France.
PLoS Biol. 2025 Jul 15;23(7):e3003275. doi: 10.1371/journal.pbio.3003275. eCollection 2025 Jul.
Extrachromosomal circular DNA (eccDNA) has been described in several eukaryotic species and has been shown to impact phenomena as diverse as cancer and herbicide tolerance. EccDNA is thought to arise mainly through transposable element (TE) mobilization. Because studies based on short-read sequencing cannot efficiently identify full-length eccDNA forms generated from TEs, we employed the CIDER-Seq pipeline based on long-read sequencing, to obtain full-length eccDNAs from Arabidopsis. The generated eccDNA datasets identified centromeric/pericentromeric regions as hotspots of eccDNAs with several eccDNA molecules originating from Helitron and LTR TEs. To investigate the role of epigenetic marks on TE-derived eccDNA biogenesis, we studied Arabidopsis methylation mutants dcl3, rdr6, ros1, and ddm1. Contrasting the TE-suppression previously reported in the hypermethylated ros1 mutants, we identified activation of TEs in ros1, specifically of LTR/Gypsy TEs. An enrichment of LTR/Copia elements was identified in actively dividing calli and the shoot apical meristem (SAM). Uncharacterized "variable TEs" with high eccDNA and expression were identified in the SAM, including ATCOPIA58. Together, our study reveals the genomic origins of eccDNAs and delineates the link between epigenetic regulation, transposon mobilization, and eccDNA biogenesis.
染色体外环状DNA(eccDNA)已在多种真核生物中被描述,并已被证明会影响癌症和除草剂耐受性等多种现象。人们认为eccDNA主要通过转座元件(TE)的移动产生。由于基于短读长测序的研究无法有效识别由TE产生的全长eccDNA形式,我们采用了基于长读长测序的CIDER-Seq流程,从拟南芥中获得全长eccDNA。生成的eccDNA数据集将着丝粒/近着丝粒区域确定为eccDNA的热点,有几个eccDNA分子起源于Helitron和LTR TE。为了研究表观遗传标记在TE衍生的eccDNA生物发生中的作用,我们研究了拟南芥甲基化突变体dcl3、rdr6、ros1和ddm1。与之前在高甲基化ros1突变体中报道的TE抑制相反,我们在ros1中发现了TE的激活,特别是LTR/Gypsy TE的激活。在活跃分裂的愈伤组织和茎尖分生组织(SAM)中发现了LTR/Copia元件的富集。在SAM中鉴定出具有高eccDNA和表达的未表征“可变TE”,包括ATCOPIA58。总之,我们的研究揭示了eccDNA的基因组起源,并描绘了表观遗传调控、转座子移动和eccDNA生物发生之间的联系。