OsS40-14 参与水稻暗诱衰老的 ROS 和质粒组织相关调控网络

Habiba Habiba, Chunlan Fan, Wuqiang Hong, Ximiao Shi, Xiaowei Wang, Weiqi Wang, Wenfang Lin, Yanyun Li, Noor ul Ain, Ying Miao, Xiangzi Zheng
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摘要

黑暗诱导的衰老会引发显著的新陈代谢变化,从而回收资源并确保植物存活。在这项研究中,我们在水稻中发现了一种转录因子 OsS40-14,它能形成同源寡聚体。osS40-14基因敲除突变体在黑暗诱导条件下表现出主叶和旗叶的留绿表型,叶绿素和光合能力显著保留,活性氧(ROS)明显减少,而OsS40-14过表达转基因株系(oeOsS40-14)在黑暗诱导叶片衰老条件下表现出加速衰老表型。转录组分析表明,当oss40-14 和 WT 的分离叶片在黑暗条件下处理 72 小时后,oss40-14 相对于 WT 有 1585 个 DEGs(|Log2FC| >|=1,P 值<0.05)被重新编程。原生质体瞬时表达 OsS40-14 系统的 CUT&Tag-seq 分析表明,OsS40-14 在基因组转录起始位点(TSS)富集了 40.95%。序列聚类分析显示,OsS40-14蛋白主要富集并结合在TACCCACAAGACAC保守元件上。通过单核苷酸突变 EMSA,确定了 OsS40 蛋白的种子区 "ACCCA"。通过对转录组和CUT&Tag-seq数据集的整合分析,发现了153个OsS40-14靶向的DEGs,与WT相比,它们主要富集在oss40-14暗诱导条件下的质体组织和光合作用过程中。其中,经ChIP-PCR和RT-qPCR证实,有11个OsS40-14的候选靶标,如葡萄糖6-磷酸/磷酸转运体、Na+/H+反转运体、过氧化氢酶、几丁质酶2、磷酸转运体19、OsWAK32和OsRLCK319被直接靶向并上调。这证明了在黑暗诱导的叶片衰老过程中,OsS40-14介导大分子代谢和养分循环控制质体组织的新模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Involvement of OsS40-14 in ROS and plastid organization related regulatory networks of dark-induced senescence in rice
Dark-induced senescence triggers significant metabolic changes that recycle resources and ensure plant survival. In this study, we identified a transcription factor OsS40-14 in rice, which can form homo-oligomers. The oss40-14 knockout mutants exhibited stay-green phenotype of primary leaf and flag leaf during dark-induced condition, with substantial retention of chlorophylls and photosynthetic capacity as well as remarkably reduced reactive oxygen species (ROS), while OsS40-14 overexpressing transgenic lines (oeOsS40-14) showed an accelerated senescence phenotype under dark-induced leaf senescence conditions. Transcriptome analysis revealed that when the detached leaves of oss40-14 and WT were treated in darkness condition for 72 hours, 1585 DEGs (|Log2FC| >=1, P value<0.05) were reprogrammed in oss40-14 relative to WT. CUT&Tag-seq analysis in protoplast transient expression of OsS40-14 system showed that OsS40-14 was 40.95% enriched in the transcription start site (TSS) of the genome. Sequence clustering analysis showed that OsS40-14 protein was mainly enriched and bound to TACCCACAAGACAC conserved elements. The seed region "ACCCA" of OsS40 proteins was identified by single nucleotide mutagenesis EMSA. The integrative analysis of transcriptome and CUT&Tag-seq datasets showed 153 OsS40-14-targeted DEGs, they mainly enriched in plastid organization and photosynthesis process at dark-induced condition in oss40-14 relative to WT. Among them, eleven candidate targets of OsS40-14 such as Glucose 6-phosphate/phosphate translocator, Na+/H+ antiporter, Catalase, Chitinase 2, Phosphate transporter 19, OsWAK32, and OsRLCK319 were directly targeted and upregulated confirmed by ChIP-PCR and RT-qPCR. It demonstrates a novel model of OsS40-14 mediating macromolecule metabolism and nutrient recycling controls the plastid organization during dark-induced leaf senescence.
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