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单分子实时转录测序鉴定藏红花开花调控基因。

Single-molecule real-time transcript sequencing identified flowering regulatory genes in Crocus sativus.

机构信息

Huzhou Central Hospital, Huzhou Hospital affiliated with Zhejiang University, Huzhou, 31300, Zhejiang, China.

Department of Plant, Soil and Climate, Utah State University, Logan, 84322, USA.

出版信息

BMC Genomics. 2019 Nov 14;20(1):857. doi: 10.1186/s12864-019-6200-5.

Abstract

BACKGROUND

Saffron crocus (Crocus sativus) is a valuable spice with medicinal uses in gynaecopathia and nervous system diseases. Identify flowering regulatory genes plays a vital role in increasing flower numbers, thereby resulting in high saffron yield.

RESULTS

Two full length transcriptome gene sets of flowering and non-flowering saffron crocus were established separately using the single-molecule real-time (SMRT) sequencing method. A total of sixteen SMRT cells generated 22.85 GB data and 75,351 full-length saffron crocus unigenes on the PacBio RS II panel and further obtained 79,028 SSRs, 72,603 lncRNAs and 25,400 alternative splicing (AS) events. Using an Illumina RNA-seq platform, an additional fifteen corms with different flower numbers were sequenced. Many differential expression unigenes (DEGs) were screened separately between flowering and matched non-flowering top buds with cold treatment (1677), flowering top buds of 20 g corms and non-flowering top buds of 6 g corms (1086), and flowering and matched non-flowering lateral buds (267). A total of 62 putative flower-related genes that played important roles in vernalization (VRNs), gibberellins (G3OX, G2OX), photoperiod (PHYB, TEM1, PIF4), autonomous (FCA) and age (SPLs) pathways were identified and a schematic representation of the flowering gene regulatory network in saffron crocus was reported for the first time. After validation by real-time qPCR in 30 samples, two novel genes, PB.20221.2 (p = 0.004, r = 0.52) and PB.38952.1 (p = 0.023, r = 0.41), showed significantly higher expression levels in flowering plants. Tissue distribution showed specifically high expression in flower organs and time course expression analysis suggested that the transcripts increasingly accumulated during the flower development period.

CONCLUSIONS

Full-length transcriptomes of flowering and non-flowering saffron crocus were obtained using a combined NGS short-read and SMRT long-read sequencing approach. This report is the first to describe the flowering gene regulatory network of saffron crocus and establishes a reference full-length transcriptome for future studies on saffron crocus and other Iridaceae plants.

摘要

背景

藏红花(Crocus sativus)是一种具有药用价值的香料,可用于妇科疾病和神经系统疾病。鉴定开花调节基因在增加花数方面起着至关重要的作用,从而导致藏红花产量高。

结果

使用单分子实时(SMRT)测序方法分别建立了开花和不开花藏红花的全长转录组基因集。总共 16 个 SMRT 细胞在 PacBio RS II 面板上生成了 22.85GB 的数据和 75351 个全长藏红花 unigenes,并进一步获得了 79028 个 SSRs、72603 个 lncRNAs 和 25400 个选择性剪接(AS)事件。使用 Illumina RNA-seq 平台,对另外 15 个具有不同花数的球茎进行了测序。在冷处理(1677)、20g 球茎的开花顶芽和 6g 球茎的不开花顶芽(1086)以及开花和匹配的不开花侧芽(267)之间,分别筛选了许多差异表达的 unigenes(DEGs)。总共鉴定了 62 个与春化(VRNs)、赤霉素(G3OX、G2OX)、光周期(PHYB、TEM1、PIF4)、自主(FCA)和年龄(SPLs)途径有关的假定花相关基因,并首次报道了藏红花开花基因调控网络的示意图。在 30 个样本中通过实时 qPCR 验证后,两个新基因 PB.20221.2(p=0.004,r=0.52)和 PB.38952.1(p=0.023,r=0.41)在开花植物中的表达水平显著升高。组织分布显示在花器官中特异性高表达,时间过程表达分析表明在花发育期间转录本逐渐积累。

结论

使用 NGS 短读和 SMRT 长读测序组合方法获得了开花和不开花藏红花的全长转录组。本报告首次描述了藏红花的开花基因调控网络,并为藏红花和其他鸢尾科植物的进一步研究建立了全长转录组参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aaef/6854690/61853584b5e6/12864_2019_6200_Fig1_HTML.jpg

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