Xiao-Ran Zhou, Andrea Schnepf, Jan Vanderborght, Daniel Leitner, Harry Vereecken, Guillaume Lobet
{"title":"韧皮部解剖限制根系结构的发展:来自硅实验的理论线索","authors":"Xiao-Ran Zhou, Andrea Schnepf, Jan Vanderborght, Daniel Leitner, Harry Vereecken, Guillaume Lobet","doi":"10.1093/insilicoplants/diad012","DOIUrl":null,"url":null,"abstract":"Abstract Plant growth and development involve the integration of numerous processes, influenced by both endogenous and exogenous factors. At any given time during a plant’s life cycle, the plant architecture is a readout of this continuous integration. However, untangling the individual factors and processes involved in the plant development and quantifying their influence on the plant developmental process is experimentally challenging. Here we used a combination of computational plant models (CPlantBox and PiafMunch) to help understand experimental findings about how local phloem anatomical features influence the root system architecture. Our hypothesis was that strong local phloem resistance would restrict local carbon flow and locally modify root growth patterns. To test this hypothesis, we simulated the mutual interplay between the root system architecture development and the carbohydrate distribution to provide a plausible mechanistic explanation for several experimental results. Our in silico experiments highlighted the strong influence of local phloem hydraulics on the root growth rates, growth duration and final length. The model result showed that a higher phloem resistivity leads to shorter roots due to the reduced flow of carbon within the root system. This effect was due to local properties of individual roots, and not linked to any of the pleiotropic effects at the root system level. Our results open a door to a better representation of growth processes in a plant computational model.","PeriodicalId":36138,"journal":{"name":"in silico Plants","volume":"54 1","pages":"0"},"PeriodicalIF":2.6000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phloem anatomy restricts root system architecture development: theoretical clues from <i>in silico</i> experiments\",\"authors\":\"Xiao-Ran Zhou, Andrea Schnepf, Jan Vanderborght, Daniel Leitner, Harry Vereecken, Guillaume Lobet\",\"doi\":\"10.1093/insilicoplants/diad012\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract Plant growth and development involve the integration of numerous processes, influenced by both endogenous and exogenous factors. At any given time during a plant’s life cycle, the plant architecture is a readout of this continuous integration. However, untangling the individual factors and processes involved in the plant development and quantifying their influence on the plant developmental process is experimentally challenging. Here we used a combination of computational plant models (CPlantBox and PiafMunch) to help understand experimental findings about how local phloem anatomical features influence the root system architecture. Our hypothesis was that strong local phloem resistance would restrict local carbon flow and locally modify root growth patterns. To test this hypothesis, we simulated the mutual interplay between the root system architecture development and the carbohydrate distribution to provide a plausible mechanistic explanation for several experimental results. Our in silico experiments highlighted the strong influence of local phloem hydraulics on the root growth rates, growth duration and final length. The model result showed that a higher phloem resistivity leads to shorter roots due to the reduced flow of carbon within the root system. This effect was due to local properties of individual roots, and not linked to any of the pleiotropic effects at the root system level. Our results open a door to a better representation of growth processes in a plant computational model.\",\"PeriodicalId\":36138,\"journal\":{\"name\":\"in silico Plants\",\"volume\":\"54 1\",\"pages\":\"0\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2023-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"in silico Plants\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/insilicoplants/diad012\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"AGRONOMY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"in silico Plants","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/insilicoplants/diad012","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRONOMY","Score":null,"Total":0}
Phloem anatomy restricts root system architecture development: theoretical clues from in silico experiments
Abstract Plant growth and development involve the integration of numerous processes, influenced by both endogenous and exogenous factors. At any given time during a plant’s life cycle, the plant architecture is a readout of this continuous integration. However, untangling the individual factors and processes involved in the plant development and quantifying their influence on the plant developmental process is experimentally challenging. Here we used a combination of computational plant models (CPlantBox and PiafMunch) to help understand experimental findings about how local phloem anatomical features influence the root system architecture. Our hypothesis was that strong local phloem resistance would restrict local carbon flow and locally modify root growth patterns. To test this hypothesis, we simulated the mutual interplay between the root system architecture development and the carbohydrate distribution to provide a plausible mechanistic explanation for several experimental results. Our in silico experiments highlighted the strong influence of local phloem hydraulics on the root growth rates, growth duration and final length. The model result showed that a higher phloem resistivity leads to shorter roots due to the reduced flow of carbon within the root system. This effect was due to local properties of individual roots, and not linked to any of the pleiotropic effects at the root system level. Our results open a door to a better representation of growth processes in a plant computational model.