Macovei Anca, Faè Matteo, Biggiogera Marco, de Sousa Araújo Susana, Carbonera Daniela, Balestrazzi Alma
Department of Biology and Biotechnology 'L. Spallanzani', Pavia, Italy.
Instituto de Technologia Quìmica e Biologica António Xavier, Universidade Nova de Lisboa, Lisbon, Portugal.
Front Plant Sci. 2018 May 11;9:596. doi: 10.3389/fpls.2018.00596. eCollection 2018.
The role of tyrosyl-DNA phosphodiesterase 2 (Tdp2) involved in the repair of 5'-end-blocking DNA lesions is still poorly explored in plants. To gain novel insights, suspension cultures overexpressing the gene (Tdp2α-13C and Tdp2α-28 lines, respectively) and a control (CTRL) line carrying the empty vector were investigated. Transmission electron microscopy (TEM) revealed enlarged nucleoli (up to 44% expansion of the area, compared to CTRL), the presence of nucleolar vacuoles, increased frequency of multinucleolate cells (up to 4.3-fold compared to CTRL) and reduced number of ring-shaped nucleoli in Tdp2α-13C and Tdp2α-28 lines. Ultrastructural data suggesting for enhanced nucleolar activity in -overexpressing lines were integrated with results from bromouridine incorporation. The latter revealed an increase of labeled transcripts in both Tdp2α-13C and Tdp2α-28 cells, within the nucleolus and in the extra-nucleolar region. -overexpressing cells showed tolerance to etoposide, a selective inhibitor of DNA topoisomerase II, as evidenced by DNA diffusion assay. TEM analysis revealed etoposide-induced rearrangements within the nucleolus, resembling the nucleolar caps observed in animal cells under transcription impairment. Based on these findings it is evident that -overexpression enhances nucleolar activity in plant cells.
酪氨酰-DNA磷酸二酯酶2(Tdp2)在植物中参与5'-末端封闭DNA损伤修复的作用仍未得到充分研究。为了获得新的见解,研究了分别过表达该基因的悬浮培养物(Tdp2α-13C和Tdp2α-28系)以及携带空载体的对照(CTRL)系。透射电子显微镜(TEM)显示,Tdp2α-13C和Tdp2α-28系中核仁增大(与CTRL相比,面积扩大达44%)、存在核仁液泡、多核仁细胞频率增加(与CTRL相比高达4.3倍)且环形核仁数量减少。超微结构数据表明过表达系中核仁活性增强,并与溴尿苷掺入结果相结合。后者显示,在Tdp2α-13C和Tdp2α-28细胞的核仁内和核仁外区域,标记转录物均增加。DNA扩散试验证明,过表达细胞对拓扑异构酶II的选择性抑制剂依托泊苷具有耐受性。TEM分析显示依托泊苷诱导核仁内重排,类似于在转录受损的动物细胞中观察到的核仁帽。基于这些发现,很明显过表达增强了植物细胞中的核仁活性。