CSIR-Institute of Himalayan Bioresource Technology, Palampur, 176061, India.
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
Mol Biol Rep. 2024 May 3;51(1):605. doi: 10.1007/s11033-024-09574-7.
Cultivation of Crocus sativus (saffron) faces challenges due to inconsistent flowering patterns and variations in yield. Flowering takes place in a graded way with smaller corms unable to produce flowers. Enhancing the productivity requires a comprehensive understanding of the underlying genetic mechanisms that govern this size-based flowering initiation and commitment. Therefore, samples enriched with non-flowering and flowering apical buds from small (< 6 g) and large (> 14 g) corms were sequenced.
Apical bud enriched samples from small and large corms were collected immediately after dormancy break in July. RNA sequencing was performed using Illumina Novaseq 6000 to access the gene expression profiles associated with size dependent flowering. De novo transcriptome assembly and analysis using flowering committed buds from large corms at post-dormancy and their comparison with vegetative shoot primordia from small corms pointed out the major role of starch and sucrose metabolism, Auxin and ABA hormonal regulation. Many genes with known dual responses in flowering development and circadian rhythm like Flowering locus T and Cryptochrome 1 along with a transcript showing homology with small auxin upregulated RNA (SAUR) exhibited induced expression in flowering buds. Thorough prediction of Crocus sativus non-coding RNA repertoire has been carried out for the first time. Enolase was found to be acting as a major hub with protein-protein interaction analysis using Arabidopsis counterparts.
Transcripts belong to key pathways including phenylpropanoid biosynthesis, hormone signaling and carbon metabolism were found significantly modulated. KEGG assessment and protein-protein interaction analysis confirm the expression data. Findings unravel the genetic determinants driving the size dependent flowering in Crocus sativus.
由于开花模式不一致和产量变化,藏红花(番红花)的栽培面临挑战。开花是分阶段进行的,较小的球茎无法开花。提高生产力需要全面了解控制这种基于大小的开花启动和承诺的潜在遗传机制。因此,从小(<6 克)和大(>14 克)球茎中富集有非开花和开花顶芽的样品进行了测序。
在 7 月休眠期结束后立即从小和大球茎中采集顶芽富集样品。使用 Illumina Novaseq 6000 进行 RNA 测序,以获取与大小相关的开花相关的基因表达谱。使用大球茎休眠后开花的顶芽进行从头转录组组装和分析,并将其与小球茎的营养芽进行比较,指出淀粉和蔗糖代谢、生长素和 ABA 激素调节的主要作用。许多在开花发育和生物钟中具有双重反应的基因,如 Flowering locus T 和 Cryptochrome 1,以及一个与小生长素上调 RNA(SAUR)同源的转录本,在开花芽中表现出诱导表达。首次对番红花非编码 RNA 库进行了全面预测。发现烯醇酶作为一个主要的枢纽,使用拟南芥对应物进行蛋白质-蛋白质相互作用分析。
属于苯丙烷生物合成、激素信号和碳代谢等关键途径的转录本被发现显著调节。KEGG 评估和蛋白质-蛋白质相互作用分析证实了表达数据。研究结果揭示了驱动番红花大小相关开花的遗传决定因素。