Table_5_Full-length transcriptome sequencing provides insights into alternative splicing under cold stress in peanut.xlsx

IntroductionPeanut (Arachis hypogaea L.), also called groundnut is an important oil and cash crop grown widely in the world. The annual global production of groundnuts has increased to approximately 50 million tons, which provides a rich source of vegetable oils and proteins for humans. Low temperature (non-freezing) is one of the major factors restricting peanut growth, yield, and geographic distribution. Since the complexity of cold-resistance trait, the molecular mechanism of cold tolerance and related gene networks were largely unknown in peanut.
MethodsIn this study, comparative transcriptomic analysis of two peanut cultivars (SLH vs. ZH12) with differential cold tolerance under low temperature (10°C) was performed using Oxford Nanopore Technology (ONT) platform.
Results and discussionAs a result, we identified 8,949 novel gene loci and 95,291 new/novel isoforms compared with the reference database. More differentially expressed genes (DEGs) were discovered in cold-sensitive cultivar (ZH12) than cold-tolerant cultivar (SLH), while more alternative splicing events were found in SLH compared to ZH12. Gene Ontology (GO) analyses of the common DEGs showed that the “response to stress”, “chloroplast part”, and “transcription factor activity” were the most enriched GO terms, indicating that photosynthesis process and transcription factors play crucial roles in cold stress response in peanut. We also detected a total of 708 differential alternative splicing genes (DASGs) under cold stress compared to normal condition. Intron retention (IR) and exon skipping (ES) were the most prevalent alternative splicing (AS) events. In total, 4,993 transcription factors and 292 splicing factors were detected, many of them had differential expression levels and/or underwent AS events in response to cold stress. Overexpression of two candidate genes (encoding trehalose-6-phosphatephosphatases, AhTPPs) in yeast improves cold tolerance. This study not only provides valuable resources for the study of cold resistance in peanut but also lay a foundation for genetic modification of cold regulators to enhance stress tolerance in crops

【引言】花生（Arachis hypogaea L.），又名落花生（groundnut），是全球广泛种植的重要油料与经济作物。当前全球花生年总产量已增至约5000万吨，可为人类提供丰富的植物油与蛋白质来源。非冻害低温是限制花生生长、产量及地理分布的主要因素之一。由于抗寒性状的复杂性，花生的耐冷分子机制及相关基因网络目前仍不完全明确。
【材料与方法】本研究采用牛津纳米孔测序技术（Oxford Nanopore Technology, ONT）平台，对两个耐冷性存在差异的花生栽培品种（SLH与ZH12）在10℃低温处理条件下的样本开展比较转录组分析。
【结果与讨论】本研究比对参考数据库后，共鉴定得到8949个新基因位点以及95291个新转录本亚型。相较于耐冷品种SLH，冷敏感品种ZH12中鉴定到的差异表达基因（differentially expressed genes, DEGs）数量更多；而SLH中的可变剪接事件数则多于ZH12。对共同差异表达基因进行基因本体（Gene Ontology, GO）富集分析结果显示，"胁迫响应""叶绿体组分"及"转录因子活性"为最显著富集的GO条目，表明光合作用过程与转录因子在花生冷胁迫响应中发挥关键作用。此外，相较于正常培养条件，低温处理下共鉴定得到708个差异可变剪接基因（differential alternative splicing genes, DASGs）。内含子保留（intron retention, IR）与外显子跳跃（exon skipping, ES）为最主要的可变剪接（alternative splicing, AS）事件类型。本研究共检测到4993个转录因子与292个剪接因子，其中众多基因在冷胁迫响应过程中存在差异表达，或发生了可变剪接事件。在酵母中过表达两个候选基因（编码海藻糖-6-磷酸磷酸酶，AhTPPs）可显著提升其耐冷性。本研究不仅为花生抗寒研究提供了宝贵的组学资源，同时也为通过遗传改造冷调控因子以提升作物抗逆性奠定了理论基础。