Ren Panrong, Meng Yaxiong, Li Baochun, Ma Xiaole, Si Erjing, Lai Yong, Wang Juncheng, Yao Lirong, Yang Ke, Shang Xunwu, Wang Huajun
Gansu Provincial Key Lab of Aridland Crop Science/Gansu Key Lab of Crop Improvement and Germplasm Enhancement, Gansu Agricultural University, Lanzhou, China.
College of Agronomy, Gansu Agricultural University, Lanzhou, China.
Front Plant Sci. 2018 Apr 18;9:500. doi: 10.3389/fpls.2018.00500. eCollection 2018.
A lack of phosphorus (P) in plants can severely constrain growth and development. Barley, one of the earliest domesticated crops, is extensively planted in poor soil around the world. To date, the molecular mechanisms of enduring low phosphorus, at the transcriptional level, in barley are still unclear. In the present study, two different barley genotypes (GN121 and GN42)-with contrasting phosphorus efficiency-were used to reveal adaptations to low phosphorus stress, at three time points, at the morphological, physiological, biochemical, and transcriptome level. GN121 growth was less affected by phosphorus starvation and recovery than that of GN42. The biomass and inorganic phosphorus concentration of GN121 and GN42 declined under the low phosphorus-induced stress and increased after recovery with normal phosphorus. However, the range of these parameters was higher in GN42 than in GN121. Subsequently, a more complete genome annotation was obtained by correcting with the data sequenced on Illumina HiSeq X 10 and PacBio RSII SMRT platform. A total of 6,182 and 5,270 differentially expressed genes (DEGs) were identified in GN121 and GN42, respectively. The majority of these DEGs were involved in phosphorus metabolism such as phospholipid degradation, hydrolysis of phosphoric enzymes, sucrose synthesis, phosphorylation/dephosphorylation and post-transcriptional regulation; expression of these genes was significantly different between GN121 and GN42. Specifically, six and seven DEGs were annotated as phosphorus transporters in roots and leaves, respectively. Furthermore, a putative model was constructed relying on key metabolic pathways related to phosphorus to illustrate the higher phosphorus efficiency of GN121 compared to GN42 under low phosphorus conditions. Results from this study provide a multi-transcriptome database and candidate genes for further study on phosphorus use efficiency (PUE).
植物中磷(P)的缺乏会严重限制其生长和发育。大麦是最早被驯化的作物之一,在世界各地的贫瘠土壤中广泛种植。迄今为止,大麦在转录水平上耐受低磷的分子机制仍不清楚。在本研究中,使用了两种不同的大麦基因型(GN121和GN42)——它们的磷效率不同——在三个时间点,从形态学、生理学、生物化学和转录组水平揭示对低磷胁迫的适应性。与GN42相比,GN121的生长受磷饥饿和恢复的影响较小。在低磷诱导的胁迫下,GN121和GN42的生物量和无机磷浓度下降,恢复正常磷供应后增加。然而,这些参数在GN42中的变化范围高于GN121。随后,通过用Illumina HiSeq X 10和PacBio RSII SMRT平台测序的数据进行校正,获得了更完整的基因组注释。在GN121和GN42中分别鉴定出6182个和5270个差异表达基因(DEG)。这些DEG中的大多数参与磷代谢,如磷脂降解、磷酸酶水解、蔗糖合成、磷酸化/去磷酸化和转录后调控;这些基因的表达在GN121和GN42之间存在显著差异。具体而言,分别有6个和7个DEG被注释为根和叶中的磷转运体。此外,基于与磷相关的关键代谢途径构建了一个推测模型,以说明在低磷条件下GN121比GN42具有更高的磷效率。本研究结果为进一步研究磷利用效率(PUE)提供了一个多转录组数据库和候选基因。