The ferroxidase LPR5 functions in the maintenance of phosphate homeostasis and is required for normal growth and development of rice

Author:

Ai Hao1,Cao Yue2ORCID,Jain Ajay3ORCID,Wang Xiaowen14,Hu Zhi1,Zhao Gengmao1,Hu Siwen1,Shen Xing1,Yan Yan5,Liu Xiuli1,Sun Yafei16,Lan Xiaoxia1,Xu Guohua1ORCID,Sun Shubin1ORCID

Affiliation:

1. State Key Laboratory of Crop Genetics and Germplasm Enhancement, Key Laboratory of Plant Nutrition and Fertilization in Low-Middle Reaches of the Yangtze River, Ministry of Agriculture, Nanjing Agricultural University, China

2. School of Environmental Science and Engineering, Guangdong Provincial Key Lab for Environmental Pollution Control and Remediation Technology,Sun Yat-sen University, Guangzhou, China

3. Amity Institute of Biotechnology, Amity University Rajasthan, Jaipur, India

4. Landscape Architecture Department, College of Horticulture, Nanjing Agricultural University, China

5. Institute for Plant Genomics and Biotechnology, Texas A&M University, College Station, TX, USA

6. Institute of Eco-Environment and Plant Protection, Shanghai Academy of Agricultural Sciences, Shanghai, China

Abstract

Abstract Members of the Low Phosphate Root (LPR) family have been identified in rice (Oryza sativa) and expression analyses have been conducted. Here, we investigated the functions of one of the five members in rice, LPR5. qRT-PCR and promoter–GUS reporter analyses indicated that under Pi-sufficient conditions OsLPR5 was highly expressed in the roots, and specific expression occurred in the leaf collars and nodes, and its expression was increased under Pi-deficient conditions. In vitro analysis of the purified OsLPR5 protein showed that it exhibited ferroxidase activity. Overexpression of OsLPR5 triggered higher ferroxidase activity, and elevated concentrations of Fe(III) in the xylem sap and of total Fe in the roots and shoots. Transient expression of OsLPR5 in Nicotiana benthamiana provided evidence of its subcellular localization to the cell wall and endoplasmic reticulum. Knockout mutation in OsLPR5 by means of CRISPR-Cas9 resulted in adverse effects on Pi translocation, on the relative expression of Cis-NATOsPHO1;2, and on several morphological traits, including root development and yield potential. Our results indicate that ferroxidase-dependent OsLPR5 has both a broad-spectrum influence on growth and development in rice as well as affecting a subset of physiological and molecular traits that govern Pi homeostasis.

Funder

National Program on R&D of Transgenic Plants

National Natural Science Foundation of China

National Key Research and Development Program of China

International Workshop on the nexus of food-energy-water (FEWS) systems: US–China

Innovative Research Team Development Plan of the Ministry of Education

111 Project

Postgraduate Research & Practice Innovation Program of Jiangsu Province

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Physiology

Cited by 21 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