比较转录组学精确定位了对磷限制的保守和特异性转录反应。

IF 5.6 2区 生物学 Q1 PLANT SCIENCES
Pooja Pant, Hui Duan, Nick Krom, Raul Huertas, Wolf-Rüdiger Scheible
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引用次数: 0

摘要

在面临肥料资源减少以及生物和非生物压力的情况下,将拟南芥的生物学知识转化为作物物种对于推进农业和确保粮食生产至关重要。然而,鉴定作物中拟南芥基因的功能同源性往往不是一件容易的事情。结合序列和表达数据可以提高对同源物的正确预测。在这里,我们对拟南芥、Medicago、Brachypodium和Setaria在磷(P)充足和磷限制条件下并排生长进行了大规模的RNA测序转录组学研究,以产生可比的转录组学数据集。对拟南芥中前200个磷限制诱导基因的比较表明,这些基因中约80%在其他3个物种中具有可识别的同源基因,而在豆科植物和禾草中仅约50%保留其磷限制反应。大多数磷饥饿反应的标志基因在所有四个物种中都是保守的。这项研究揭示了许多已知的、新颖的、未注释的、保守的和物种特异性的转录p饥饿反应的调节形式。利用独立的RT-qPCR技术对李树p限制标记基因的表达体进行鉴定和实验验证,表明比较转录组学在确定不同作物物种的功能同源物方面是有用的。这项研究为功能基因组学和转化研究提供了前所未有的资源,以创造高效磷作物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative transcriptomics pinpoints conserved and specific transcriptional responses to phosphorus limitation.

Translating biological knowledge from Arabidopsis to crop species is important to advance agriculture and secure food production in the face of dwindling fertilizer resources and biotic and abiotic stresses. However, it is often not trivial to identify functional homologs (orthologs) of Arabidopsis genes in crops. Combining sequence and expression data can improve the correct prediction of orthologs. Here, we conducted a large-scale RNA sequencing based transcriptomics study of Arabidopsis, Medicago, Brachypodium, and Setaria grown side-by-side in phosphorus (P)-sufficient and P-limited conditions to generate comparable transcriptomics datasets. Comparison of top 200 P-limitation-induced genes in Arabidopsis revealed that ~80% of these genes have identifiable close homologs in the other three species but only ~50% retain their P-limitation response in the legume and grasses. Most of the hallmark genes of the P-starvation response were found conserved in all four species. This study reveals many known, novel, unannotated, conserved, and species-specific forms of regulation of the transcriptional P-starvation response. Identification and experimental verification of expressologs by independent RT-qPCR for P-limitation marker genes in Prunus showed the usefulness of comparative transcriptomics in pinpointing the functional orthologs in diverse crop species. This study provides an unprecedented resource for functional genomics and translational research to create P-efficient crops.

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来源期刊
Journal of Experimental Botany
Journal of Experimental Botany 生物-植物科学
CiteScore
12.30
自引率
4.30%
发文量
450
审稿时长
1.9 months
期刊介绍: The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology. Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.
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