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超微结构和分子分析揭示了过表达该基因的细胞中核仁活性增强。

Ultrastructural and Molecular Analyses Reveal Enhanced Nucleolar Activity in Cells Overexpressing the Gene.

作者信息

Macovei Anca, Faè Matteo, Biggiogera Marco, de Sousa Araújo Susana, Carbonera Daniela, Balestrazzi Alma

机构信息

Department of Biology and Biotechnology 'L. Spallanzani', Pavia, Italy.

Instituto de Technologia Quìmica e Biologica António Xavier, Universidade Nova de Lisboa, Lisbon, Portugal.

出版信息

Front Plant Sci. 2018 May 11;9:596. doi: 10.3389/fpls.2018.00596. eCollection 2018.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c562/5958304/98fb2b4d7ed0/fpls-09-00596-g001.jpg

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