{"title":"编码翻译延伸因子 eEF3 的基因 YEF3 的功能在真菌中部分保守。","authors":"Giovanna Maldonado, Alejandra García, Saturnino Herrero, Irene Castaño, Michael Altmann, Reinhard Fischer, Greco Hernández","doi":"10.3389/fmicb.2024.1438900","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Translation is a fundamental process of life. In eukaryotes, the elongation step of translation is highly conserved and is driven by eukaryotic translation elongation factors (eEF)1A and eEF2. A significant variation of the elongation is the activity of eukaryotic elongation factor (eEF) 3 in <i>Saccharomyces cerevisiae</i> encoded by the gene yeast elongation factor (<i>YEF3</i>) with orthologs in all fungal species, a few algae, and some protists. In <i>S. cerevisiae, YEF3</i> is an essential gene and eEF3 plays a critical role in translation elongation, as it promotes binding of the ternary complex acylated-Transfer RNA (tRNA)-eEF1A-Guanosine-5'-triphosphate (GTP) to the aminoacyl (A) site of the ribosome, the release of uncharged tRNAs after peptide translocation, and ribosome recycling. Even though <i>YEF3</i> was discovered more than 40 years ago, eEF3 has been characterized almost exclusively in <i>S. cerevisiae</i>.</p><p><strong>Methods: </strong>We undertook an <i>in vivo</i> genetic approach to assess the functional conservation of <i>eEF3</i> across phylogenetically distant fungal species.</p><p><strong>Results: </strong>We found that <i>eEF3</i> from <i>Zygosaccharomyces rouxii</i> and <i>Candida glabrata</i> (both belonging to <i>phylum</i> Ascomycota), <i>Ustilago maydis</i> (<i>phylum</i> Basidiomycota), and <i>Gonapodya prolifera</i> (<i>phylum</i> Monoblepharomycota), but not <i>Aspergillus nidulans</i> (<i>phylum</i> Ascomycota), supported the growth of <i>S. cerevisiae</i> lacking the endogenous <i>YEF3</i> gene. We also proved that <i>eEF3</i> is an essential gene in the ascomycetes <i>C. glabrata</i> and <i>A. nidulans</i>.</p><p><strong>Discussion: </strong>Given that most existing knowledge on fungal translation has only been obtained from <i>S. cerevisiae</i>, our findings beyond this organism showed variability in the elongation process in Fungi. We also proved that <i>eEF3</i> is essential in pathogenic fungi, opening the possibility of using eEF3 as a target to fight candidiasis.</p>","PeriodicalId":12466,"journal":{"name":"Frontiers in Microbiology","volume":null,"pages":null},"PeriodicalIF":4.0000,"publicationDate":"2024-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11378755/pdf/","citationCount":"0","resultStr":"{\"title\":\"The gene <i>YEF3</i> function encoding translation elongation factor eEF3 is partially conserved across fungi.\",\"authors\":\"Giovanna Maldonado, Alejandra García, Saturnino Herrero, Irene Castaño, Michael Altmann, Reinhard Fischer, Greco Hernández\",\"doi\":\"10.3389/fmicb.2024.1438900\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Translation is a fundamental process of life. In eukaryotes, the elongation step of translation is highly conserved and is driven by eukaryotic translation elongation factors (eEF)1A and eEF2. A significant variation of the elongation is the activity of eukaryotic elongation factor (eEF) 3 in <i>Saccharomyces cerevisiae</i> encoded by the gene yeast elongation factor (<i>YEF3</i>) with orthologs in all fungal species, a few algae, and some protists. In <i>S. cerevisiae, YEF3</i> is an essential gene and eEF3 plays a critical role in translation elongation, as it promotes binding of the ternary complex acylated-Transfer RNA (tRNA)-eEF1A-Guanosine-5'-triphosphate (GTP) to the aminoacyl (A) site of the ribosome, the release of uncharged tRNAs after peptide translocation, and ribosome recycling. Even though <i>YEF3</i> was discovered more than 40 years ago, eEF3 has been characterized almost exclusively in <i>S. cerevisiae</i>.</p><p><strong>Methods: </strong>We undertook an <i>in vivo</i> genetic approach to assess the functional conservation of <i>eEF3</i> across phylogenetically distant fungal species.</p><p><strong>Results: </strong>We found that <i>eEF3</i> from <i>Zygosaccharomyces rouxii</i> and <i>Candida glabrata</i> (both belonging to <i>phylum</i> Ascomycota), <i>Ustilago maydis</i> (<i>phylum</i> Basidiomycota), and <i>Gonapodya prolifera</i> (<i>phylum</i> Monoblepharomycota), but not <i>Aspergillus nidulans</i> (<i>phylum</i> Ascomycota), supported the growth of <i>S. cerevisiae</i> lacking the endogenous <i>YEF3</i> gene. We also proved that <i>eEF3</i> is an essential gene in the ascomycetes <i>C. glabrata</i> and <i>A. nidulans</i>.</p><p><strong>Discussion: </strong>Given that most existing knowledge on fungal translation has only been obtained from <i>S. cerevisiae</i>, our findings beyond this organism showed variability in the elongation process in Fungi. 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引用次数: 0
摘要
引言翻译是生命的基本过程。在真核生物中,翻译的延伸步骤是高度保守的,由真核翻译延伸因子(eEF)1A 和 eEF2 驱动。在酿酒酵母(Saccharomyces cerevisiae)中,由酵母伸长因子(YEF3)基因编码的真核生物伸长因子(eEF)3 的活性是伸长过程的一个重要变异,在所有真菌物种、少数藻类和一些原生生物中都有同源物。在酿酒酵母中,YEF3 是一个重要基因,eEF3 在翻译伸长过程中发挥着关键作用,因为它能促进酰化转运核糖核酸(tRNA)-eEF1A-鸟苷-5'-三磷酸(GTP)三元复合物与核糖体氨基酰(A)位点的结合、多肽转位后释放不带电的 tRNA 以及核糖体再循环。尽管 YEF3 早在 40 多年前就已被发现,但 eEF3 几乎只在 S. cerevisiae 中被描述:方法:我们采用体内遗传学方法来评估 eEF3 在系统发育遥远的真菌物种中的功能保护:结果:我们发现,来自胭脂虫(Zygosaccharomyces rouxii)和光滑念珠菌(Candida glabrata)(均属于子囊菌门)、Ustilago maydis(担子菌门)和Gonapodya prolifera(单双子叶菌门)的eEF3支持缺乏内源YEF3基因的麦角菌的生长,但不支持黑曲霉(Aspergillus nidulans)(子囊菌门)的生长。我们还证明,eEF3 是子囊菌 C. glabrata 和 A. nidulans 的必需基因:讨论:鉴于现有的关于真菌翻译的知识大多只来自于 S. cerevisiae,我们在该生物体之外的研究结果显示了真菌中延伸过程的可变性。我们还证明了 eEF3 在致病真菌中的重要性,这为利用 eEF3 作为抗击念珠菌病的靶标提供了可能性。
The gene YEF3 function encoding translation elongation factor eEF3 is partially conserved across fungi.
Introduction: Translation is a fundamental process of life. In eukaryotes, the elongation step of translation is highly conserved and is driven by eukaryotic translation elongation factors (eEF)1A and eEF2. A significant variation of the elongation is the activity of eukaryotic elongation factor (eEF) 3 in Saccharomyces cerevisiae encoded by the gene yeast elongation factor (YEF3) with orthologs in all fungal species, a few algae, and some protists. In S. cerevisiae, YEF3 is an essential gene and eEF3 plays a critical role in translation elongation, as it promotes binding of the ternary complex acylated-Transfer RNA (tRNA)-eEF1A-Guanosine-5'-triphosphate (GTP) to the aminoacyl (A) site of the ribosome, the release of uncharged tRNAs after peptide translocation, and ribosome recycling. Even though YEF3 was discovered more than 40 years ago, eEF3 has been characterized almost exclusively in S. cerevisiae.
Methods: We undertook an in vivo genetic approach to assess the functional conservation of eEF3 across phylogenetically distant fungal species.
Results: We found that eEF3 from Zygosaccharomyces rouxii and Candida glabrata (both belonging to phylum Ascomycota), Ustilago maydis (phylum Basidiomycota), and Gonapodya prolifera (phylum Monoblepharomycota), but not Aspergillus nidulans (phylum Ascomycota), supported the growth of S. cerevisiae lacking the endogenous YEF3 gene. We also proved that eEF3 is an essential gene in the ascomycetes C. glabrata and A. nidulans.
Discussion: Given that most existing knowledge on fungal translation has only been obtained from S. cerevisiae, our findings beyond this organism showed variability in the elongation process in Fungi. We also proved that eEF3 is essential in pathogenic fungi, opening the possibility of using eEF3 as a target to fight candidiasis.
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.