Attenuated down-regulation of PHOSPHATE TRANSPORTER1 genes as a mechanism for phosphorus sensitivity in phosphorus-efficient Hakea prostrata (Proteaceae)

Author:

Bird TobyORCID,Nestor Benjamin J.ORCID,Liu Shu TongORCID,Shen QiORCID,Ranathunge KosalaORCID,Lambers HansORCID,Finnegan Patrick M.ORCID

Abstract

Abstract Background and aims Phosphorus (P) is an essential plant nutrient and integral for crop yield. However, plants adapted to P-impoverished environments, such as Hakea prostrata (Proteaceae), are often sensitive to P supplies that would be beneficial to other plants. The strategies for phosphate uptake and transport in P-sensitive species have received little attention. Methods Using a recently-assembled transcriptome of H. prostrata, we identified 10 putative members of the PHOSPHATE TRANSPORTER1 (PHT1) gene family, which is responsible for inorganic phosphate (Pi) uptake and transport in plants. We examined plant growth, organ P concentrations and the transcript levels for the eight PHT1 members that were expressed in roots of H. prostrata at Pi supplies ranging from P-impoverished to P-excess. Key results Hakea prostrata plants suppressed cluster root growth above ecologically-relevant Pi supplies, whilst non-cluster root mass ratios were constant. Root P concentrations increased with increasing Pi supply. Of the eight H. prostrata PHT1 genes tested, four had relatively high transcript amounts in young roots suggesting important roles in Pi uptake; however, a maximum five-fold difference in expression between P-impoverished and P-excess conditions indicated a low P-responsiveness for these genes. The HpPHT1;8 and HpPHT1;9 genes were paralogous to Pi-responsive Arabidopsis thaliana PHT1;8 and PHT1;9 orthologues involved in root-to-shoot translocation of P, but only HpPHT1;9 was P responsive. Conclusions An attenuated ability of H. prostrata to regulate PHT1 expression in response to Pi supply is likely responsible for its low capacity to control P uptake and contributes to its high P sensitivity.

Funder

Australian Research Council

Research Training Fund Fee Stipend

University of Western Australia Co-funded Postgraduate Award

China Scholarship Council

Kwongan Foundation Top-up Scholarship

University of Western Australia

Publisher

Springer Science and Business Media LLC

Reference71 articles.

1. Ai P, Sun S, Zhao J, Fan X, Xin W, Guo Q, Yu L, Shen Q, Wu P, Miller AJ, Xu G (2009) Two rice phosphate transporters, OsPht1; 2 and OsPht1; 6, have different functions and kinetic properties in uptake and translocation. Plant J 57:798–809. https://doi.org/10.1111/j.1365-313X.2008.03726.x

2. Barragán-Rosillo AC, Peralta-Alvarez CA, Ojeda-Rivera JO, Arzate-Mejía RG, Recillas-Targa F, Herrera-Estrella L (2021) Genome accessibility dynamics in response to phosphate limitation is controlled by the PHR1 family of transcription factors in Arabidopsis. Proc Natl Acad Sci 118:e2107558118. https://doi.org/10.1073/pnas.2107558118

3. Bayle V, Arrighi J-F, Creff A, Nespoulous C, Vialaret J, Rossignol M, Gonzalez E, Paz-Ares J, Nussaume L (2011) Arabidopsis thaliana high-affinity phosphate transporters exhibit multiple levels of posttranslational regulation. Plant Cell 23:1523–1535. https://doi.org/10.1105/tpc.110.081067

4. Berardini TZ, Reiser L, Li D, Mezheritsky Y, Muller R, Strait E, Huala E (2015) The Arabidopsis information resource: making and mining the gold standard annotated reference plant genome. Genesis 53:474–485. https://doi.org/10.1002/dvg.22877

5. Bird T, Nestor BJ, Bayer PE, Wang G, Ilyasova A, Gille CE, Soraru BEH, Ranathunge K, Severn-Ellis AA, Jost R, Scheible W-R, Dassanayake M, Bately J, Edwards D, Lambers H, Finnegan PM (2024) Delayed leaf greening involves a major shift in the expression of cytosolic and mitochondrial ribosomes to plastid ribosomes in the highly phosphorus-use-efficient Hakea prostrata (Proteaceae). Plant Soil. https://doi.org/10.1007/s11104-023-06275-1

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3