Lin Tao , Xinyi Luo , Junhuan Lv , Zhishan Guo , Yibo Yang , Hui Wang , Luping Gu , Yang Yang , Yanshan Lu , Jiayi Wu , Hu Zhu , Ján Jásik , Yalin Li , Min Yu
{"title":"PIN7和AUX1对亚砷酸盐抑制拟南芥根系生长的响应","authors":"Lin Tao , Xinyi Luo , Junhuan Lv , Zhishan Guo , Yibo Yang , Hui Wang , Luping Gu , Yang Yang , Yanshan Lu , Jiayi Wu , Hu Zhu , Ján Jásik , Yalin Li , Min Yu","doi":"10.1016/j.envexpbot.2025.106147","DOIUrl":null,"url":null,"abstract":"<div><div>Arsenite (As<sup>III</sup>), regarded as a hazard to human health and food safety, restrains root growth. This event has received little attention, and the mechanism underlying how As<sup>III</sup> affects auxin dynamics to repress root growth remains unknown. Here, our results have suggested that As<sup>III</sup>-inhibited root growth possibly involved an elevated auxin level in roots, as supported in multiple experiments such as (1) transgenic <em>DII-VENUS</em> and <em>DR5rev::GFP</em>; (2) IAA determination by enzyme-linked immunosorbent assay; (3) phenotype analysis of <em>taa1</em> (defective in auxin biosynthesis) mutant; and (4) the external application of 1-naphthylphthalamic acid (NPA) to manipulate auxin transport. This consequence could be explained through up-regulated transcriptional levels of auxin biosynthesis-related genes in whole plants. Phenotypes of auxin transport-related carriers have displayed that loss of PIN7 and AUX1, but not PIN1/2/3 transporters, ameliorated the extent of As<sup>III</sup>-induced root growth inhibition. Moreover, As<sup>III</sup> specifically enhanced the abundance of PM-localized PIN7 and AUX1 involved in transcriptional but not post-transcriptional regulation. A real-time <em>in vitro</em> observation of PM-localized PIN2 using the transgenic <em>pPIN2::PIN2-Dendra2</em> line has revealed that As<sup>III</sup> did not influence the endocytosis of PM-localized PIN2 carriers in root apices. Overall, our results propose that As<sup>III</sup> stress-elevated auxin level in the root apex possibly involves up-regulation transcriptional levels of auxin biosynthesis- and auxin transport-related genes but does not target PIN2 dynamics, finally, leading to auxin accumulation in root apices and root growth inhibition.</div></div>","PeriodicalId":11758,"journal":{"name":"Environmental and Experimental Botany","volume":"234 ","pages":"Article 106147"},"PeriodicalIF":4.5000,"publicationDate":"2025-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Coordinated PIN7 and AUX1 responses to arsenite-restrained root growth in Arabidopsis\",\"authors\":\"Lin Tao , Xinyi Luo , Junhuan Lv , Zhishan Guo , Yibo Yang , Hui Wang , Luping Gu , Yang Yang , Yanshan Lu , Jiayi Wu , Hu Zhu , Ján Jásik , Yalin Li , Min Yu\",\"doi\":\"10.1016/j.envexpbot.2025.106147\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Arsenite (As<sup>III</sup>), regarded as a hazard to human health and food safety, restrains root growth. This event has received little attention, and the mechanism underlying how As<sup>III</sup> affects auxin dynamics to repress root growth remains unknown. Here, our results have suggested that As<sup>III</sup>-inhibited root growth possibly involved an elevated auxin level in roots, as supported in multiple experiments such as (1) transgenic <em>DII-VENUS</em> and <em>DR5rev::GFP</em>; (2) IAA determination by enzyme-linked immunosorbent assay; (3) phenotype analysis of <em>taa1</em> (defective in auxin biosynthesis) mutant; and (4) the external application of 1-naphthylphthalamic acid (NPA) to manipulate auxin transport. This consequence could be explained through up-regulated transcriptional levels of auxin biosynthesis-related genes in whole plants. Phenotypes of auxin transport-related carriers have displayed that loss of PIN7 and AUX1, but not PIN1/2/3 transporters, ameliorated the extent of As<sup>III</sup>-induced root growth inhibition. Moreover, As<sup>III</sup> specifically enhanced the abundance of PM-localized PIN7 and AUX1 involved in transcriptional but not post-transcriptional regulation. A real-time <em>in vitro</em> observation of PM-localized PIN2 using the transgenic <em>pPIN2::PIN2-Dendra2</em> line has revealed that As<sup>III</sup> did not influence the endocytosis of PM-localized PIN2 carriers in root apices. Overall, our results propose that As<sup>III</sup> stress-elevated auxin level in the root apex possibly involves up-regulation transcriptional levels of auxin biosynthesis- and auxin transport-related genes but does not target PIN2 dynamics, finally, leading to auxin accumulation in root apices and root growth inhibition.</div></div>\",\"PeriodicalId\":11758,\"journal\":{\"name\":\"Environmental and Experimental Botany\",\"volume\":\"234 \",\"pages\":\"Article 106147\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2025-04-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental and Experimental Botany\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0098847225000644\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental and Experimental Botany","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0098847225000644","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
Coordinated PIN7 and AUX1 responses to arsenite-restrained root growth in Arabidopsis
Arsenite (AsIII), regarded as a hazard to human health and food safety, restrains root growth. This event has received little attention, and the mechanism underlying how AsIII affects auxin dynamics to repress root growth remains unknown. Here, our results have suggested that AsIII-inhibited root growth possibly involved an elevated auxin level in roots, as supported in multiple experiments such as (1) transgenic DII-VENUS and DR5rev::GFP; (2) IAA determination by enzyme-linked immunosorbent assay; (3) phenotype analysis of taa1 (defective in auxin biosynthesis) mutant; and (4) the external application of 1-naphthylphthalamic acid (NPA) to manipulate auxin transport. This consequence could be explained through up-regulated transcriptional levels of auxin biosynthesis-related genes in whole plants. Phenotypes of auxin transport-related carriers have displayed that loss of PIN7 and AUX1, but not PIN1/2/3 transporters, ameliorated the extent of AsIII-induced root growth inhibition. Moreover, AsIII specifically enhanced the abundance of PM-localized PIN7 and AUX1 involved in transcriptional but not post-transcriptional regulation. A real-time in vitro observation of PM-localized PIN2 using the transgenic pPIN2::PIN2-Dendra2 line has revealed that AsIII did not influence the endocytosis of PM-localized PIN2 carriers in root apices. Overall, our results propose that AsIII stress-elevated auxin level in the root apex possibly involves up-regulation transcriptional levels of auxin biosynthesis- and auxin transport-related genes but does not target PIN2 dynamics, finally, leading to auxin accumulation in root apices and root growth inhibition.
期刊介绍:
Environmental and Experimental Botany (EEB) publishes research papers on the physical, chemical, biological, molecular mechanisms and processes involved in the responses of plants to their environment.
In addition to research papers, the journal includes review articles. Submission is in agreement with the Editors-in-Chief.
The Journal also publishes special issues which are built by invited guest editors and are related to the main themes of EEB.
The areas covered by the Journal include:
(1) Responses of plants to heavy metals and pollutants
(2) Plant/water interactions (salinity, drought, flooding)
(3) Responses of plants to radiations ranging from UV-B to infrared
(4) Plant/atmosphere relations (ozone, CO2 , temperature)
(5) Global change impacts on plant ecophysiology
(6) Biotic interactions involving environmental factors.