Two sexually compatible monokaryons from a heterokaryotic Lentinula edodes strain respond differently to heat stress.

IF 4 2区 生物学 Q2 MICROBIOLOGY Frontiers in Microbiology Pub Date : 2025-02-12 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1522075
Yuan Guo, Wenyu Jiao, Yajie Zhang, Meiting Tan, Qi Gao, Yu Liu, Shouxian Wang
{"title":"Two sexually compatible monokaryons from a heterokaryotic <i>Lentinula edodes</i> strain respond differently to heat stress.","authors":"Yuan Guo, Wenyu Jiao, Yajie Zhang, Meiting Tan, Qi Gao, Yu Liu, Shouxian Wang","doi":"10.3389/fmicb.2025.1522075","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Despite the extensive research conducted on heat responses of <i>Lentinula edodes</i> heterokaryotic cells, the responses of the two sexually compatible monokaryons to heat stress (HS) remain largely unknown.</p><p><strong>Methods: </strong>To bridge this gap, we examined the nucleus-specific (SP3 and SP30) heat resistant mechanisms using an integrated physiological, metabolomic and transcriptomic approach.</p><p><strong>Results: </strong>The results showed that HS elicited the boost of ROS and hampered mycelium growth for both monokaryons. Metabolome and transcriptome analysis demonstrated that the two sexually compatible monokaryons responded differently to HS. For SP3, the differentially expressed genes (DEGs) were significantly enriched in Mitogen-Activated Protein Kinase (MAPK) signaling, cell cycle and sugar metabolism, whereas those DEGs for SP30 were enriched in glyoxylate and dicarboxylate metabolism, and protein processing. The differentially accumulated metabolites (DAMs) of both strains were enriched in the glycerophospholipid metabolism, alpha-linolenic acid metabolism, biosynthesis of cofactors, etc, but were regulated differently in each strain. The enriched KEGG pathways for SP3 tend to be downregulated, whereas those in SP30 exhibited a contrary trend. The genes in MAPK signaling pathway were associated with the glycerophospholipid metabolism in SP3, but not in SP30. Omics-integration analysis revealed distinguishing regulatory networks and identified completely different hub genes for the two strains.</p><p><strong>Discussion: </strong>Our findings revealed, for the first time, the different heat-resistance mechanisms of the two compatible nuclei and provided candidate metabolites, responsive genes and regulatory pathways for further experimental validation.</p>","PeriodicalId":12466,"journal":{"name":"Frontiers in Microbiology","volume":"16 ","pages":"1522075"},"PeriodicalIF":4.0000,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11861359/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fmicb.2025.1522075","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Despite the extensive research conducted on heat responses of Lentinula edodes heterokaryotic cells, the responses of the two sexually compatible monokaryons to heat stress (HS) remain largely unknown.

Methods: To bridge this gap, we examined the nucleus-specific (SP3 and SP30) heat resistant mechanisms using an integrated physiological, metabolomic and transcriptomic approach.

Results: The results showed that HS elicited the boost of ROS and hampered mycelium growth for both monokaryons. Metabolome and transcriptome analysis demonstrated that the two sexually compatible monokaryons responded differently to HS. For SP3, the differentially expressed genes (DEGs) were significantly enriched in Mitogen-Activated Protein Kinase (MAPK) signaling, cell cycle and sugar metabolism, whereas those DEGs for SP30 were enriched in glyoxylate and dicarboxylate metabolism, and protein processing. The differentially accumulated metabolites (DAMs) of both strains were enriched in the glycerophospholipid metabolism, alpha-linolenic acid metabolism, biosynthesis of cofactors, etc, but were regulated differently in each strain. The enriched KEGG pathways for SP3 tend to be downregulated, whereas those in SP30 exhibited a contrary trend. The genes in MAPK signaling pathway were associated with the glycerophospholipid metabolism in SP3, but not in SP30. Omics-integration analysis revealed distinguishing regulatory networks and identified completely different hub genes for the two strains.

Discussion: Our findings revealed, for the first time, the different heat-resistance mechanisms of the two compatible nuclei and provided candidate metabolites, responsive genes and regulatory pathways for further experimental validation.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
来自异核香菇菌株的两个性相容的单核细胞对热应激的反应不同。
背景:尽管对香菇异核细胞的热反应进行了广泛的研究,但两种性相容的单核细胞对热应激(HS)的反应在很大程度上仍然未知。方法:为了弥补这一空白,我们使用综合生理学,代谢组学和转录组学方法研究了核特异性(SP3和SP30)耐热机制。结果:HS对两种单核细胞均有促进ROS的作用,抑制菌丝生长。代谢组和转录组分析表明,两种性相容的单核细胞对HS的反应不同。对于SP3,差异表达基因(DEGs)在丝裂原活化蛋白激酶(MAPK)信号、细胞周期和糖代谢中显著富集,而SP30的差异表达基因(DEGs)在乙醛酸盐和二羧酸盐代谢和蛋白质加工中显著富集。两菌株的差异积累代谢物(DAMs)富集于甘油磷脂代谢、α -亚麻酸代谢、辅助因子的生物合成等方面,但各菌株的调节方式不同。SP3富集的KEGG通路有下调的趋势,而SP30富集的KEGG通路则相反。MAPK信号通路基因与SP3的甘油磷脂代谢相关,而与SP30无关。组学整合分析揭示了两个菌株不同的调控网络,并鉴定出完全不同的枢纽基因。讨论:我们的研究结果首次揭示了两个相容核的不同耐热机制,并为进一步的实验验证提供了候选代谢物、响应基因和调控途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
期刊最新文献
(-)-Epicatechin and inflammation: Unraveling the role of microbial metabolites and interindividual metabolic variability. Comparative study on the molecular mechanisms of Trichoderma, Cladosporium and Penicillium strains (Ascomycota) in positively regulating Festuca sinensis cv. Qinghai based on multi-omics. Eucommia polysaccharides alleviate experimental colitis by reshaping colonic microbiota composition, metabolites, and modulating the IL-17 signaling pathway. Comparative resistome from toilet waste in three different income areas, Bangkok, Thailand. Genomic and metabolomic insights into the enhancement of rare ginsenosides in Panax ginseng through solid-state fermentation by Aspergillus cristatus JH-5.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1