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Ultrastructural and Molecular Analyses Reveal Enhanced Nucleolar Activity in Medicago truncatula Cells Overexpressing the MtTdp2α Gene

机译:超微结构和分子分析揭示了过表达MtTdp2α基因的紫花苜蓿细胞中增强的核仁活性。

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摘要

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, Medicago truncatula suspension cultures overexpressing the MtTdp2α 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 MtTdp2α-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. MtTdp2α-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 MtTdp2α-overexpression enhances nucleolar activity in plant cells.
机译:酪氨酸-DNA磷酸二酯酶2(Tdp2)参与修复5'-末端封闭的DNA损伤的作用仍然很少在植物中探索。为了获得新的见解,研究了过表达MtTdp2α基因(分别为Tdp2α-13C和Tdp2α-28系)的紫花苜蓿悬浮培养物和携带空载体的对照(CTRL)系。透射电子显微镜(TEM)显示核仁增大(与CTRL相比,扩大了44%),核仁液泡的存在,多核酸盐细胞的频率增加(与CTRL相比,高达4.3倍)和环数减少Tdp2α-13C和Tdp2α-28品系的核仁。暗示在MtTdp2α过表达细胞系中核仁活性增强的超微结构数据与溴尿苷掺入的结果整合在一起。后者揭示了在核仁内和核仁外区域的Tdp2α-13C和Tdp2α-28细胞中标记转录物的增加。 MtTdp2α过表达的细胞显示出对依托泊苷的耐受性,依托泊苷是DNA拓扑异构酶II的选择性抑制剂,通过DNA扩散分析证明。 TEM分析显示依托泊苷在核仁内引起的重排,类似于在转录损伤下在动物细胞中观察到的核仁帽。基于这些发现,很明显,MtTdp2α过度表达增强了植物细胞中的核仁活性。

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