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玉米雄配子减数分裂过程中精确双链断裂修复所必需。

Is Required for Accurate Double-Strand Break Repair During Maize Male Meiosis.

作者信息

Zhang Ting, Jing Ju-Li, Liu Lei, He Yan

机构信息

Ministry of Education Key Laboratory of Crop Heterosis and Utilization, National Maize Improvement Center of China, College of Agronomy and Biotechnology, China Agricultural University, Beijing, China.

Beijing Key Lab of Plant Resource Research and Development, Beijing Technology and Business University, Beijing, China.

出版信息

Front Plant Sci. 2021 Feb 26;12:626528. doi: 10.3389/fpls.2021.626528. eCollection 2021.

Abstract

RAD17, a replication factor C (RFC)-like DNA damage sensor protein, is involved in DNA checkpoint control and required for both meiosis and mitosis in yeast and mammals. In plant, the meiotic function of was only reported in rice so far. Here, we identified and characterized the homolog in maize. The mutants exhibited normal vegetative growth but male was partially sterile. In pollen mother cells, non-homologous chromosome entanglement and chromosome fragmentation were frequently observed. Immunofluorescence analysis manifested that DSB formation occurred as normal and the loading pattern of RAD51 signals was similar to wild-type at the early stage of prophase I in the mutants. The localization of the axial element ASY1 was normal, while the assembly of the central element ZYP1 was severely disrupted in meiocytes. Surprisingly, no obvious defect in female sterility was observed in mutants. Taken together, our results suggest that is involved in DSB repair likely by promoting synaptonemal complex assembly in maize male meiosis. These phenomena highlight a high extent of divergence from its counterpart in rice, indicating that the dysfunction can result in a drastic dissimilarity in meiotic outcome in different plant species.

摘要

RAD17是一种类复制因子C(RFC)的DNA损伤传感蛋白,参与DNA检查点控制,是酵母和哺乳动物减数分裂和有丝分裂所必需的。在植物中,到目前为止,其减数分裂功能仅在水稻中有报道。在此,我们鉴定并表征了玉米中的该同源物。该突变体营养生长正常,但雄性部分不育。在该突变体的花粉母细胞中,经常观察到非同源染色体缠结和染色体片段化。免疫荧光分析表明,在突变体减数第一次分裂前期早期,双链断裂(DSB)正常形成,且RAD51信号的加载模式与野生型相似。轴向元件ASY1的定位正常,而在该突变体的减数分裂细胞中,中央元件ZYP1的组装严重受损。令人惊讶的是,在该突变体中未观察到明显的雌性不育缺陷。综上所述,我们的结果表明,该基因可能通过促进玉米雄性减数分裂中联会复合体的组装参与DSB修复。这些现象凸显了其与水稻中对应物的高度差异,表明该基因功能障碍可导致不同植物物种减数分裂结果的巨大差异。

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