{"title":"An automated root phenotype platform enables nondestructive high-throughput root system architecture dissection in wheat","authors":"Zhen Zhang, Xiaolong Qiu, Guanghui Guo, Xiaojing Zhu, Jiawei Shi, Ning Zhang, Shenglong Ding, Nazhu Tang, Yunfeng Qu, Zhe Sun, Huilin Li, Feifei Ma, Shangyuan Xie, Qian Lv, Liming Fu, Ge Hu, Ying Cao, Haowei Ge, Hao Li, Jinling Huang, Weigang Xu, Wanneng Yang, Yun Zhou, Chun-Peng Song","doi":"10.1093/plphys/kiaf154","DOIUrl":null,"url":null,"abstract":"The root system architecture (RSA) determines plant growth and yield. The characterization of optimal RSA and discovery of genetic loci or candidate genes that control root traits are therefore important research goals. However, the hidden nature of the root system makes it difficult to perform nondestructive, rapid analyses of RSA. In this study, we developed an automated, nondestructive, high-throughput root phenotyping platform (Root-HTP) and a corresponding data processing pipeline for efficient, large-scale characterization of wheat (Triticum aestivum L.) RSA. This system is capable of tracking root growth dynamics and RSA variation across all wheat developmental stages. In situ phenotyping using Root-HTP extracted 47 RSA traits, including 33 novel traits in wheat and 23 novel traits in other crops. We used root trait data from the phenotyping system and yield trait data to conduct a genome-wide association study (GWAS) of 155 wheat accessions, which identified 2,650 SNPs and 233 quantitative trait loci (QTLs) associated with aspects of root architecture. The candidate gene TaMYB93 was detected in a QTL for root tortuosity, and EMS mutants confirmed its effect on RSA in wheat. We explored the relationship between root- and yield-related traits and identified 20 root-related QTLs that were also associated with yield traits. Furthermore, we have built a predictive model for wheat yield based on 18 RSA traits and propose a parsimonious RSA ideotype associated with high yields. The data generated from this study provide insight into the genetic architecture of wheat RSA and support for RSA ideotype-based wheat breeding and yield prediction.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"35 1","pages":""},"PeriodicalIF":6.5000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiaf154","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
The root system architecture (RSA) determines plant growth and yield. The characterization of optimal RSA and discovery of genetic loci or candidate genes that control root traits are therefore important research goals. However, the hidden nature of the root system makes it difficult to perform nondestructive, rapid analyses of RSA. In this study, we developed an automated, nondestructive, high-throughput root phenotyping platform (Root-HTP) and a corresponding data processing pipeline for efficient, large-scale characterization of wheat (Triticum aestivum L.) RSA. This system is capable of tracking root growth dynamics and RSA variation across all wheat developmental stages. In situ phenotyping using Root-HTP extracted 47 RSA traits, including 33 novel traits in wheat and 23 novel traits in other crops. We used root trait data from the phenotyping system and yield trait data to conduct a genome-wide association study (GWAS) of 155 wheat accessions, which identified 2,650 SNPs and 233 quantitative trait loci (QTLs) associated with aspects of root architecture. The candidate gene TaMYB93 was detected in a QTL for root tortuosity, and EMS mutants confirmed its effect on RSA in wheat. We explored the relationship between root- and yield-related traits and identified 20 root-related QTLs that were also associated with yield traits. Furthermore, we have built a predictive model for wheat yield based on 18 RSA traits and propose a parsimonious RSA ideotype associated with high yields. The data generated from this study provide insight into the genetic architecture of wheat RSA and support for RSA ideotype-based wheat breeding and yield prediction.
期刊介绍:
Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research.
As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.