ANAC050 confers aluminium resistance by cooperating with secretion of organic acids and accumulation of cell wall hemicelluloses in plants

被引：0

作者：

Tao, Ye ^{[1
,2
,3
]}

Li, Su ^{[1
,2
]}

Liu, Yusong ^{[1
]}

Guo, Rui ^{[4
]}

Chen, Changzhao ^{[5
]}

Huang, Jiu ^{[5
]}

Zhang, Qiang ^{[4
]}

Shen, Renfang ^{[1
,2
]}

Zhu, Xiaofang ^{[1
,2
]}

机构：

[1] Chinese Acad Sci, Inst Soil Sci, State Key Lab Soil & Sustainable Agr, Nanjing 210008, Peoples R China

[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China

[3] Jiangsu Acad Agr Sci, Inst Food Crops, Nanjing 210014, Peoples R China

[4] China Natl Rice Res Inst, State Key Lab Rice Biol & Breeding, Hangzhou 311400, Peoples R China

[5] China Univ Min & Technol, Xuzhou 221116, Peoples R China

来源：

PEDOSPHERE | 2025年 / 35卷 / 02期

基金：

中国国家自然科学基金;

关键词：

Al accumulation; Al toxicity; Arabidopsis; cell wall fixation; sensitive phenotype; transcription factor; transgenic line; TRANSCRIPTION FACTOR FAMILY; MALATE TRANSPORTERS; ACTIVATED CITRATE; BINDING-CAPACITY; ROOT-GROWTH; ARABIDOPSIS; TOLERANCE; GENE; SENSITIVITY; XYLOGLUCAN;

D O I：

10.1016/j.pedsph.2024.02.001

中图分类号：

S15 [土壤学];

学科分类号：

0903 ; 090301 ;

摘要：

Aluminium (Al) toxicity is one of the key factors limiting crop output in acidic soils, but until now little has been known about how Al is regulated transcriptionally in plants. This study identified Arabidopsis NAC transcription factor ANAC050 in the regulation of Al tolerance. ANAC050 was located in the nucleus and displayed constitutive expression in the silique, flower, leaf, stem, and root, despite the fact that Al stress decreased its expression and protein accumulation. When compared with the Columbia ecotype wild-type, anac050 mutants that lacked function of ANAC050 exhibited Al sensitivity phenotype, while transgenic lines that overexpressed ANAC050 showed an Al-resistant phenotype, indicating the favorable influence of ANAC050 on preserving Al tolerance in plants. Further analysis indicated that anac050 mutants accumulated more Al in roots, implying that ANAC050 may confer a potential operation of an Al exclusion mechanism. Interestingly, anac050 mutants had down-regulated the expression of the genes encoding MULTIDRUG AND TOXIC COMPOUND EXTRUSION (MATE) and AL-ACTIVATED MALATE TRANSPORTER (ALMT1), which were involved in the secretion of citrate and malate, even though there was no evidence of a direct interaction between them, suggesting ANAC050 may mediate the secretion of citrate and malate indirectly. Together with the decreased hemicellulose content, lower Al content was also discovered in root cell walls and hemicelluloses of anac050 mutants, pointing to a potential interaction between ANAC017 and XYLOGLUCAN ENDOTRANSGLUCOSYLASE/HYDROLASE (XTH). Although there was no evidence of a direct interaction between ANAC050 and XTH31, it is worth mentioning that the expression of XTH31, which is essential for xyloglucan modification, was down-regulated in anac050 mutants irrespective of the amount of Al given. In conclusion, our findings showed that ANAC050 contributed to Al resistance by indirect control of the release of organic acids and the accumulation of cell wall hemicelluloses.

引用

页码：338 / 351

页数：14