基于基因组学鉴定脱氧核糖核酸(Deinococcus)中适应寒冷的支系。

IF 4.4 1区 生物学 Q1 BIOLOGY BMC Biology Pub Date : 2024-07-02 DOI:10.1186/s12915-024-01944-8
Liang Shen, Jiayu Hu, Luyao Zhang, Zirui Wu, Liangzhong Chen, Namita Paudel Adhikari, Mukan Ji, Shaoxing Chen, Fang Peng, Yongqin Liu
{"title":"基于基因组学鉴定脱氧核糖核酸(Deinococcus)中适应寒冷的支系。","authors":"Liang Shen, Jiayu Hu, Luyao Zhang, Zirui Wu, Liangzhong Chen, Namita Paudel Adhikari, Mukan Ji, Shaoxing Chen, Fang Peng, Yongqin Liu","doi":"10.1186/s12915-024-01944-8","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Microbes in the cold polar and alpine environments play a critical role in feedbacks that amplify the effects of climate change. Defining the cold adapted ecotype is one of the prerequisites for understanding the response of polar and alpine microbes to climate change.</p><p><strong>Results: </strong>Here, we analysed 85 high-quality, de-duplicated genomes of Deinococcus, which can survive in a variety of harsh environments. By leveraging genomic and phenotypic traits with reverse ecology, we defined a cold adapted clade from eight Deinococcus strains isolated from Arctic, Antarctic and high alpine environments. Genome-wide optimization in amino acid composition and regulation and signalling enable the cold adapted clade to produce CO<sub>2</sub> from organic matter and boost the bioavailability of mineral nitrogen.</p><p><strong>Conclusions: </strong>Based primarily on in silico genomic analysis, we defined a potential cold adapted clade in Deinococcus and provided an updated view of the genomic traits and metabolic potential of Deinococcus. Our study would facilitate the understanding of microbial processes in the cold polar and alpine environments.</p>","PeriodicalId":9339,"journal":{"name":"BMC Biology","volume":null,"pages":null},"PeriodicalIF":4.4000,"publicationDate":"2024-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11218099/pdf/","citationCount":"0","resultStr":"{\"title\":\"Genomics-based identification of a cold adapted clade in Deinococcus.\",\"authors\":\"Liang Shen, Jiayu Hu, Luyao Zhang, Zirui Wu, Liangzhong Chen, Namita Paudel Adhikari, Mukan Ji, Shaoxing Chen, Fang Peng, Yongqin Liu\",\"doi\":\"10.1186/s12915-024-01944-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Microbes in the cold polar and alpine environments play a critical role in feedbacks that amplify the effects of climate change. Defining the cold adapted ecotype is one of the prerequisites for understanding the response of polar and alpine microbes to climate change.</p><p><strong>Results: </strong>Here, we analysed 85 high-quality, de-duplicated genomes of Deinococcus, which can survive in a variety of harsh environments. By leveraging genomic and phenotypic traits with reverse ecology, we defined a cold adapted clade from eight Deinococcus strains isolated from Arctic, Antarctic and high alpine environments. Genome-wide optimization in amino acid composition and regulation and signalling enable the cold adapted clade to produce CO<sub>2</sub> from organic matter and boost the bioavailability of mineral nitrogen.</p><p><strong>Conclusions: </strong>Based primarily on in silico genomic analysis, we defined a potential cold adapted clade in Deinococcus and provided an updated view of the genomic traits and metabolic potential of Deinococcus. Our study would facilitate the understanding of microbial processes in the cold polar and alpine environments.</p>\",\"PeriodicalId\":9339,\"journal\":{\"name\":\"BMC Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2024-07-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11218099/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMC Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1186/s12915-024-01944-8\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12915-024-01944-8","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:极地和高山寒冷环境中的微生物在放大气候变化影响的反馈中发挥着关键作用。确定适应寒冷的生态型是了解极地和高山微生物对气候变化反应的先决条件之一:在这里,我们分析了 85 个高质量、去重复的 Deinococcus 基因组,它们可以在各种恶劣环境中生存。通过利用反向生态学的基因组和表型特征,我们从从北极、南极和高寒环境中分离出的8个Deinococcus菌株中定义了一个适应寒冷的支系。氨基酸组成、调控和信号传导方面的全基因组优化使冷适应支系能够从有机物中产生二氧化碳,并提高矿物氮的生物利用率:我们主要基于硅基因组学分析,定义了Deinococcus中一个潜在的寒冷适应支系,并提供了关于Deinococcus基因组特征和代谢潜力的最新观点。我们的研究将有助于了解寒冷极地和高山环境中的微生物过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Genomics-based identification of a cold adapted clade in Deinococcus.

Background: Microbes in the cold polar and alpine environments play a critical role in feedbacks that amplify the effects of climate change. Defining the cold adapted ecotype is one of the prerequisites for understanding the response of polar and alpine microbes to climate change.

Results: Here, we analysed 85 high-quality, de-duplicated genomes of Deinococcus, which can survive in a variety of harsh environments. By leveraging genomic and phenotypic traits with reverse ecology, we defined a cold adapted clade from eight Deinococcus strains isolated from Arctic, Antarctic and high alpine environments. Genome-wide optimization in amino acid composition and regulation and signalling enable the cold adapted clade to produce CO2 from organic matter and boost the bioavailability of mineral nitrogen.

Conclusions: Based primarily on in silico genomic analysis, we defined a potential cold adapted clade in Deinococcus and provided an updated view of the genomic traits and metabolic potential of Deinococcus. Our study would facilitate the understanding of microbial processes in the cold polar and alpine environments.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
期刊最新文献
Novel function of single-target regulator NorR involved in swarming motility and biofilm formation revealed in Vibrio alginolyticus. Hibernation reduces GABA signaling in the brainstem to enhance motor activity of breathing at cool temperatures. A powerful and versatile new fixation protocol for immunostaining and in situ hybridization that preserves delicate tissues. Bridging chemical structure and conceptual knowledge enables accurate prediction of compound-protein interaction. Evolutionary divergent clusters of transcribed extinct truncated retroposons drive low mRNA expression and developmental regulation in the protozoan Leishmania.
×
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:481959085
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