ArticleBMC plant biology2019
Root plasticity and Pi recycling within plants contribute to low-P tolerance in Tibetan wild barley.
Article in BMC plant biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Unlocking Barley's Phosphorus Efficiency: The Emerging Role of RNA Processing in Low-Phosphorus Adaptation.Plants (Basel, Switzerland) · 2026Review
- Divergent Successional Patterns ofMicroorganisms · 2026Article
- Effects of calcium phosphate and phosphorus-dissolving bacteria on microbial structure and function during Torreya Grandis branch waste composting.BMC microbiology · 2024Article
- Transcriptomics Insights into Phosphorus Stress Response ofInternational journal of molecular sciences · 2023Article
- Heritability of temperature-mediated flower size plasticity inQuantitative plant biology · 2023Article
- Starve to Sustain-An Ancient Syrian Landrace of Sorghum as Tool for Phosphorous Bio-Economy?International journal of molecular sciences · 2021Article
- Greater morphological and primary metabolic adaptations in roots contribute to phosphate-deficiency tolerance in the bread wheat cultivar Kenong199.BMC plant biology · 2021Article
- Cultivar-Dependent Responses in Plant Growth, Leaf Physiology, Phosphorus Use Efficiency, and Tuber Quality of Potatoes Under Limited Phosphorus Availability Conditions.Frontiers in plant science · 2021Article
- Article
- Wild Barley Exhibits Higher Phosphorus-Use Efficiency and Greater Rhizosheath Carboxylates Than Cultivated Barley Under Low-Phosphorus Conditions.Physiologia plantarumArticle
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Authors and funding
6 authors.
Funding
Abstract
backgroundBarley is a low phosphorus (P) demand cereal crop. Tibetan wild barley, as a progenitor of cultivated barley, has revealed outstanding ability of tolerance to low-P stress. However, the underlying mechanisms of low-P adaption and the relevant genetic controlling are still unclear.
resultsWe identified low-P tolerant barley lines in a doubled-haploid (DH) population derived from an elite Tibetan wild barley accession and a high-yield cultivar. The tolerant lines revealed greater root plasticity in the terms of lateral root length, compared to low-P sensitive lines, in response to low-P stress. By integrating the QTLs associated with root length and root transcriptomic profiling, candidate genes encoding isoflavone reductase, nitrate reductase, nitrate transporter and transcriptional factor MYB were identified. The differentially expressed genes (DEGs) involved the growth of lateral root, Pi transport within cells as well as from roots to shoots contributed to the differences between low-P tolerant line L138 and low-P sensitive lines L73 in their ability of P acquisition and utilization.
conclusionsThe plasticity of root system is an important trait for barley to tolerate low-P stress. The low-P tolerance in the elite DH line derived from a cross of Tibetan wild barley and cultivated barley is characterized by enhanced growth of lateral root and Pi recycling within plants under low-P stress.
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