Transcriptome Analysis Reveals the Molecular Mechanisms for Mycorrhiza-Enhanced Drought Tolerance in Maize by Regulating the Ca2+ Signaling Pathway.

IF 4.2 2区 生物学 Q2 MICROBIOLOGY
Qiaoming Zhang, Wenjing Yang, Miaomiao Wang, Junwei Chen, Zhaoran Zhang, Yanan Wei, Qingshan Chang, Minggui Gong
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Abstract

With the continuous change of climate, drought stress has emerged as the primary constraint on crop growth, posing a significant threat to the stability of global grain reserves. Arbuscular mycorrhizal fungi (AMF), as a kind of widely distributed root endophytes, enhance the drought tolerance of maize (Zea mays L.) through regulating the physiological and molecular responses. However, comprehensive transcriptome analysis to reveal the molecular mechanism of drought tolerance in the symbiotic process between AMF and maize is still limited. In the potted plant experiment, maizes inoculated with and without arbuscular mycorrhizal fungus Funneliformis mosseae were grown under well-watered (WW) or drought-stressed (DS) conditions. By using RNA-Seq and transcriptome analysis on maize roots and leaves, this work aimed to investigate the differential expressed genes (DEGs) related to the Ca2+ signaling pathway induced by AMF symbiosis under drought stress. Our findings indicated that F. mosseae inoculation resulted in a decrease in the net fluxes of Ca2+, while simultaneously elevating Ca2+ contents in the maize roots and leaves under well-watered or drought-stressed conditions. Notably, 189 DEGs were regulated not only by AMF symbiosis and drought stress, but also exhibited preferential expression in either leaves or roots. The annotation and enrichment of Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) showed that most of the DEGs were significantly enriched in Ca2+ signaling pathway genes, related to signal transduction, cellular process, and defense response. A high number of DEGs with this function (including calcineurin B-like protein (CBL), CBL-interacting protein kinase (CIPK), mitogen-activated protein kinase (MAPK), and calcium-dependent protein kinase (CDPK) receptor kinases) were upregulated-DEGs or downregulated-DEGs in F. mosseae-inoculated maizes under drought stress. Furthermore, some DEGs belong to transcription factor (TF) families, including bHLH ERF, and, MYB, were speculated to play key roles in improving the drought tolerance of maize. Based on the expression data and co-expression analysis between TF and Ca2+ signaling pathway genes, Whirly1 with CBL11, and BRI1-EMS-SUPPRESSOR 1 (BES1) with CBL10, CIPK24, CDPK1, CDPK14, CDPK19, and MAPK9 genes showed significant positive correlations, while B3 domain-containing transcription factors (B3 TFs) with MAPK1 and both CBL9 genes showed significant negative correlations in response to both F. mosseae inoculation and drought stress. The regulation of Ca2+ signaling pathways by AMF symbiosis was an important response mechanism of maize to improve their drought resistance. This study provides insightful perspectives on how AMF-induced modulation of gene expression within the Ca2+ signaling pathway can enhance the drought tolerance of mycorrhizal maize in the future.

转录组分析揭示菌根调控Ca2+信号通路增强玉米抗旱性的分子机制
随着气候的不断变化,干旱胁迫已成为制约作物生长的首要因素,对全球粮食储备的稳定构成重大威胁。丛枝菌根真菌(AMF)是一种分布广泛的根系内生真菌,通过调节玉米的生理和分子反应来增强玉米的抗旱性。然而,综合转录组分析揭示AMF与玉米共生过程中抗旱的分子机制仍然有限。盆栽试验中,接种和不接种丛枝菌根真菌的玉米分别在水分充足(WW)和干旱胁迫(DS)条件下生长。通过对玉米根系和叶片进行RNA-Seq和转录组分析,探讨干旱胁迫下AMF共生诱导Ca2+信号通路的差异表达基因(DEGs)。结果表明,在水分充足或干旱胁迫条件下,接种mosseae导致玉米根系和叶片Ca2+净通量降低,同时Ca2+含量升高。值得注意的是,189℃不仅受到AMF共生和干旱胁迫的调控,而且在叶片和根中均表现出优先表达。基因本体(GO)和京都基因与基因组百科全书(KEGG)的注释和富集表明,大多数deg显著富集与信号转导、细胞过程和防御反应相关的Ca2+信号通路基因。在干旱胁迫下,接种F. mossee的玉米中,具有该功能的大量DEGs(包括钙调磷酸酶b样蛋白(CBL)、钙调磷酸酶相互作用蛋白激酶(CIPK)、丝裂原活化蛋白激酶(MAPK)和钙依赖性蛋白激酶(CDPK)受体激酶)的DEGs上调或下调。此外,一些转录因子(TF)家族的deg,包括bHLH、ERF和MYB,被推测在提高玉米抗旱性中起关键作用。基于TF与Ca2+信号通路基因的表达数据和共表达分析,发现whly1与CBL11、bri1 - mes - suppressor 1 (BES1)与CBL10、CIPK24、CDPK1、CDPK14、CDPK19和MAPK9基因在接种和干旱胁迫下均呈显著正相关,而B3结构域转录因子(B3 TFs)与MAPK1和CBL9基因在干旱胁迫下均呈显著负相关。AMF共生对Ca2+信号通路的调控是玉米抗旱性提高的重要响应机制。这项研究为amf诱导的Ca2+信号通路基因表达调控如何在未来增强菌根玉米的抗旱性提供了有见地的观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Fungi
Journal of Fungi Medicine-Microbiology (medical)
CiteScore
6.70
自引率
14.90%
发文量
1151
审稿时长
11 weeks
期刊介绍: Journal of Fungi (ISSN 2309-608X) is an international, peer-reviewed scientific open access journal that provides an advanced forum for studies related to pathogenic fungi, fungal biology, and all other aspects of fungal research. The journal publishes reviews, regular research papers, and communications in quarterly issues. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on paper length. Full experimental details must be provided so that the results can be reproduced.
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