Hyphal editing of the conserved premature stop codon in CHE1 is stimulated by oxidative stress in Fusarium graminearum

被引:0
|
作者
Zou, Jingwen [1 ,2 ]
Du, Yanfei [1 ,2 ]
Xing, Xiaoxing [1 ,2 ]
Huang, Panpan [1 ,2 ]
Wang, Zeyi [3 ]
Liu, Huiquan [1 ,2 ]
Wang, Qinhu [1 ,2 ]
Xu, Jinrong [1 ,2 ,3 ]
机构
[1] Northwest A&F Univ, Coll Plant Protect, State Key Lab Crop Stress Biol Arid Areas, Yangling 712100, Shaanxi, Peoples R China
[2] Northwest A&F Univ, Coll Plant Protect, NWAFU Purdue Joint Res Ctr, Yangling 712100, Shaanxi, Peoples R China
[3] Purdue Univ, Dept Bot & Plant Pathol, W Lafayette, IN 47907 USA
来源
STRESS BIOLOGY | 2024年 / 4卷 / 01期
关键词
Editing during asexual reproduction; mRNA editing; Hyphal editing; ADAT-mediated mRNA editing; CHE1; Tad2 and Tad3; RNA; PROTEINS;
D O I
10.1007/s44154-024-00174-w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although genome-wide A-to-I editing mediated by adenosine-deaminase-acting-on-tRNA (ADAT) occurs during sexual reproduction in the presence of stage-specific cofactors, RNA editing is not known to occur during vegetative growth in filamentous fungi. Here we identified 33 A-to-I RNA editing events in vegetative hyphae of Fusarium graminearum and functionally characterized one conserved hyphal-editing site. Similar to ADAT-mediated editing during sexual reproduction, majority of hyphal-editing sites are in coding sequences and nonsynonymous, and have strong preference for U at -1 position and hairpin loops. Editing at TA(437)G, one of the hyphal-specific editing sites, is a premature stop codon correction (PSC) event that enables CHE1 gene to encode a full-length zinc fingertranscription factor. Manual annotations showed that this PSC site is conserved in CHE1 orthologs from closely-related Fusarium species. Whereas the che1 deletion and CHE1(TAA) (G(438) to A) mutants had no detectable phenotype, the CHE1(TGG) (A(437) to G) mutant was defective in hyphal growth, conidiation, sexual reproduction, and plant infection. However, the CHE1(TGG) mutant was increased in tolerance against oxidative stress and editing of TA(437)G in CHE1 was stimulated by H2O2 treatment in F. graminearum. These results indicate that fixation of the premature stop codon in CHE1 has a fitness cost on normal hyphal growth and reproduction but provides a benefit to tolerance against oxidative stress. Taken together, A-to-I editing events, although rare (not genome-wide), occur during vegetative growth and editing in CHE1 plays a role in response to oxidative stress in F. graminearum and likely in other fungal pathogens.
引用
收藏
页数:13
相关论文
共 5 条
  • [1] The FgHOG1 Pathway Regulates Hyphal Growth, Stress Responses, and Plant Infection in Fusarium graminearum
    Zheng, Dawei
    Zhang, Shijie
    Zhou, Xiaoying
    Wang, Chenfang
    Xiang, Ping
    Zheng, Qian
    Xu, Jin-Rong
    PLOS ONE, 2012, 7 (11):
  • [2] Is the Fgap1 mediated response to oxidative stress chemotype dependent in Fusarium graminearum?
    Montibus, Mathilde
    Khosravi, Claire
    Zehraoui, Enric
    Verdal-Bonnin, Marie-Noeelle
    Richard-Forget, Florence
    Barreau, Christian
    FEMS MICROBIOLOGY LETTERS, 2016, 363 (02)
  • [3] The bZIP Transcription Factor Fgap1 Mediates Oxidative Stress Response and Trichothecene Biosynthesis But Not Virulence in Fusarium graminearum
    Montibus, Mathilde
    Ducos, Christine
    Bonnin-Verdal, Marie-Noelle
    Bormann, Jorg
    Ponts, Nadia
    Richard-Forget, Florence
    Barreau, Christian
    PLOS ONE, 2013, 8 (12):
  • [4] A MADS-box transcription factor FoRlm1 regulates aerial hyphal growth, oxidative stress, cell wall biosynthesis and virulence in Fusarium oxysporum f. sp. cubense
    Ding, Zhaojian
    Xu, Tianwei
    Zhu, Weiju
    Li, Lijie
    Fu, Qiyan
    FUNGAL BIOLOGY, 2020, 124 (3-4) : 183 - 193
  • [5] Familial hypercholesterolemia.: Acceptor splice site (G → C) mutation in intron 7 of the LDL-R gene:: alternate RNA editing causes exon 8 skipping or a premature stop codon in exon 8.: LDL-RHonduras-1 [LDL-R1061(-1) G→C]
    Yu, L
    Heere-Ress, E
    Boucher, B
    Defesche, JC
    Kastelein, J
    Lavoie, MA
    Genest, J
    ATHEROSCLEROSIS, 1999, 146 (01) : 125 - 131