Overexpression of LaGRAS enhances phosphorus acquisition via increased root growth of phosphorus‐deficient white lupin

Author:

Aslam Mehtab Muhammad1234ORCID,Fritschi Felix B.4,Di Zhang23,Wang Guanqun23ORCID,Li Haoxuan23ORCID,Lam Hon‐Ming23ORCID,Waseem Muhammad56ORCID,Weifeng Xu17ORCID,Zhang Jianhua23ORCID

Affiliation:

1. College of Agriculture Yangzhou University Yangzhou China

2. Department of Biology Hong Kong Baptist University Kowloon Tong Hong Kong

3. State Key Laboratory of Agrobiotechnology The Chinese University of Hong Kong Shatin Hong Kong

4. College of Agriculture, Food and Natural Resources (CAFNR), Division of Plant Sciences & Technology University of Missouri Columbia Missouri USA

5. College of Horticulture Hainan University Haikou China

6. Department of Botany University of Narowal Narowal Pakistan

7. Center for Plant Water‐Use and Nutrition Regulation and College of Resource and Environment, College of Life Sciences Fujian Agriculture and Forestry University Fuzhou China

Abstract

AbstractThe GRAS transcription factors play an indispensable role in plant growth and responses to environmental stresses. The GRAS gene family has extensively been explored in various plant species; however, the comprehensive investigation of GRAS genes in white lupin remains insufficient. In this study, bioinformatics analysis of white lupin genome revealed 51 LaGRAS genes distributed into 10 distinct phylogenetic clades. Gene structure analyses revealed that LaGRAS proteins were considerably conserved among the same subfamilies. Notably, 25 segmental duplications and a single tandem duplication showed that segmental duplication was the major driving force for the expansion of GRAS genes in white lupin. Moreover, LaGRAS genes exhibited preferential expression in young cluster root and mature cluster roots and may play key roles in nutrient acquisition, particularly phosphorus (P). To validate this, RT‐qPCR analysis of white lupin plants grown under +P (normal P) and −P (P deficiency) conditions elucidated significant differences in the transcript level of GRAS genes. Among them, LaGRAS38 and LaGRAS39 were identified as potential candidates with induced expression in MCR under −P. Additionally, white lupin transgenic hairy root overexpressing OE‐LaGRAS38 and OE‐LaGRAS39 showed increased root growth, and P concentration in root and leaf compared to those with empty vector control, suggesting their role in P acquisition. We believe this comprehensive analysis of GRAS members in white lupin is a first step in exploring their role in the regulation of root growth, tissue development, and ultimately improving P use efficiency in legume crops under natural environments.

Publisher

Wiley

Subject

Cell Biology,Plant Science,Genetics,General Medicine,Physiology

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