Tyagi Wricha, Rai Mayank
School of Crop Improvement, College of Post-Graduate Studies, Central Agricultural University (Imphal), Umroi Road, Umiam, Meghalaya, 793103, India.
Protoplasma. 2017 Mar;254(2):725-736. doi: 10.1007/s00709-016-0986-7. Epub 2016 May 26.
Low phosphorus (P) tolerance in rice is a biologically and agronomically important character. Low P tolerant Indica-type rice genotypes, Sahbhagi Dhan (SD) and Chakhao Poreiton (CP), are adapted to acidic soils and show variable response to low P levels. Using RNAseq approach, transcriptome data was generated from roots of SD and CP after 15 days of low P treatment to understand differences and similarities at molecular level. In response to low P, number of genes up-regulated (1318) was more when compared with down-regulated genes (761). Eight hundred twenty-one genes found to be significantly regulated between SD and CP in response to low P. De novo assembly using plant database led to further identification of 1535 novel transcripts. Functional annotation of significantly expressed genes suggests two distinct methods of low P tolerance. While root system architecture in SD works through serine-threonine kinase PSTOL1, suberin-mediated cell wall modification seems to be key in CP. The transcription data indicated that CP relies more on releasing its internally bound Pi and coping with low P levels by transcriptional and translational modifications and using dehydration response-based signals. Role of P transporters seems to be vital in response to low P in CP while sugar- and auxin-mediated pathway seems to be preferred in SD. At least six small RNA clusters overlap with transcripts highly expressed under low P, suggesting role of RNA super clusters in nutrient response in plants. These results help us to understand and thereby devise better strategy to enhance low P tolerance in Indica-type rice.
水稻的低磷耐受性是一个在生物学和农学上都很重要的性状。耐低磷的籼稻基因型品种萨巴吉丹(SD)和查考波雷顿(CP)适应酸性土壤,并且对低磷水平表现出不同的反应。采用RNA测序方法,在低磷处理15天后从SD和CP的根部生成转录组数据,以了解分子水平上的差异和相似性。响应低磷时,上调基因(1318个)的数量比下调基因(761个)更多。发现821个基因在SD和CP对低磷的响应中受到显著调控。利用植物数据库进行从头组装进一步鉴定出1535个新转录本。对显著表达基因的功能注释表明了两种不同的耐低磷方法。虽然SD的根系结构通过丝氨酸 - 苏氨酸激酶PSTOL1起作用,但在CP中,木栓质介导的细胞壁修饰似乎是关键。转录数据表明,CP更多地依赖于释放其内部结合的磷,并通过转录和翻译修饰以及利用基于脱水反应的信号来应对低磷水平。磷转运蛋白在CP对低磷的响应中似乎起着至关重要的作用,而糖和生长素介导的途径在SD中似乎更受青睐。至少有六个小RNA簇与在低磷条件下高度表达的转录本重叠,表明RNA超级簇在植物营养响应中的作用。这些结果有助于我们理解并从而制定更好的策略来提高籼稻的耐低磷性。