{"title":"在禾谷镰刀菌中,CHE1 中保守的过早终止密码子的头状花序编辑受到氧化胁迫的刺激。","authors":"Jingwen Zou, Yanfei Du, Xiaoxing Xing, Panpan Huang, Zeyi Wang, Huiquan Liu, Qinhu Wang, JinRong Xu","doi":"10.1007/s44154-024-00174-w","DOIUrl":null,"url":null,"abstract":"<p><p>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<sup>437</sup>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<sup>TAA</sup> (G<sup>438</sup> to A) mutants had no detectable phenotype, the CHE1<sup>TGG</sup> (A<sup>437</sup> to G) mutant was defective in hyphal growth, conidiation, sexual reproduction, and plant infection. However, the CHE1<sup>TGG</sup> mutant was increased in tolerance against oxidative stress and editing of TA<sup>437</sup>G in CHE1 was stimulated by H<sub>2</sub>O<sub>2</sub> 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.</p>","PeriodicalId":74874,"journal":{"name":"Stress biology","volume":"4 1","pages":"30"},"PeriodicalIF":0.0000,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11169179/pdf/","citationCount":"0","resultStr":"{\"title\":\"Hyphal editing of the conserved premature stop codon in CHE1 is stimulated by oxidative stress in Fusarium graminearum.\",\"authors\":\"Jingwen Zou, Yanfei Du, Xiaoxing Xing, Panpan Huang, Zeyi Wang, Huiquan Liu, Qinhu Wang, JinRong Xu\",\"doi\":\"10.1007/s44154-024-00174-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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<sup>437</sup>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<sup>TAA</sup> (G<sup>438</sup> to A) mutants had no detectable phenotype, the CHE1<sup>TGG</sup> (A<sup>437</sup> to G) mutant was defective in hyphal growth, conidiation, sexual reproduction, and plant infection. However, the CHE1<sup>TGG</sup> mutant was increased in tolerance against oxidative stress and editing of TA<sup>437</sup>G in CHE1 was stimulated by H<sub>2</sub>O<sub>2</sub> 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.</p>\",\"PeriodicalId\":74874,\"journal\":{\"name\":\"Stress biology\",\"volume\":\"4 1\",\"pages\":\"30\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-06-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11169179/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Stress biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s44154-024-00174-w\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Stress biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s44154-024-00174-w","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
虽然在有性生殖过程中会出现由腺苷脱氨酶作用于 tRNA(ADAT)介导的全基因组 A 到 I 的编辑,但在丝状真菌的无性生殖过程中还没有发现 RNA 编辑。在这里,我们发现了禾谷镰刀菌无性菌丝中的 33 个 A 到 I RNA 编辑事件,并从功能上鉴定了一个保守的菌丝编辑位点。与有性生殖过程中ADAT介导的编辑相似,大多数透明质酸编辑位点位于编码序列中,并且是非同义的,对-1位的U和发夹环有强烈的偏好。TA437G是全长锌指转录因子的一个特异性编辑位点,它的编辑是一个过早终止密码子校正(PSC)事件,使CHE1基因能够编码一个全长的锌指转录因子。人工注释表明,这个 PSC 位点在近缘镰刀菌的 CHE1 同源物中是保守的。che1 缺失突变体和 CHE1TAA(G438 至 A)突变体没有可检测到的表型,而 CHE1TGG(A437 至 G)突变体在菌丝生长、分生孢子、有性生殖和植物感染方面存在缺陷。然而,CHE1TGG 突变体对氧化胁迫的耐受性增强,在禾谷镰孢中,H2O2 处理会刺激 CHE1 中 TA437G 的编辑。这些结果表明,CHE1 中过早终止密码子的固定对正常的茎叶生长和繁殖有一定的影响,但对氧化胁迫的耐受性却有好处。综上所述,A-I 编辑事件虽然罕见(并非全基因组),但会在禾谷镰刀菌(F. graminearum)以及其他真菌病原体的无性生长过程中发生,CHE1 中的编辑在应对氧化胁迫方面发挥了作用。
Hyphal editing of the conserved premature stop codon in CHE1 is stimulated by oxidative stress in Fusarium graminearum.
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 TA437G, 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 CHE1TAA (G438 to A) mutants had no detectable phenotype, the CHE1TGG (A437 to G) mutant was defective in hyphal growth, conidiation, sexual reproduction, and plant infection. However, the CHE1TGG mutant was increased in tolerance against oxidative stress and editing of TA437G 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.