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Essential Genes Discovery in Microorganisms by Transposon-Directed Sequencing (Tn-Seq): Experimental Approaches, Major Goals, and Future Perspectives

dc.contributor.authorFernández García, Gemma 
dc.contributor.authorValdés Chiara, Paula 
dc.contributor.authorVillazán Gamonal, Patricia
dc.contributor.authorAlonso Fernández, Sergio 
dc.contributor.authorManteca Fernández, Ángel 
dc.date.accessioned2024-11-13T11:49:16Z
dc.date.available2024-11-13T11:49:16Z
dc.date.issued2024-10-21
dc.identifier.citationInternational Journal of Molceular Sciences, 25 (2024); doi:10.3390/ijms252011298
dc.identifier.urihttps://hdl.handle.net/10651/75599
dc.description.abstractEssential genes are crucial for microbial viability, playing key roles in both the primary and secondary metabolism. Since mutations in these genes can threaten organism viability, identifying them is challenging. Conditionally essential genes are required only under specific conditions and are important for functions such as virulence, immunity, stress survival, and antibiotic resistance. Transposon-directed sequencing (Tn-Seq) has emerged as a powerful method for identifying both essential and conditionally essential genes. In this review, we explored Tn-Seq workflows, focusing on eubacterial species and some yeast species. A comparison of 14 eubacteria species revealed 133 conserved essential genes, including those involved in cell division (e.g., ftsA, ftsZ), DNA replication (e.g., dnaA, dnaE), ribosomal function, cell wall synthesis (e.g., murB, murC), and amino acid synthesis (e.g., alaS, argS). Many other essential genes lack clear orthologues across different microorganisms, making them specific to each organism studied. Conditionally essential genes were identified in 18 bacterial species grown under various conditions, but their conservation was low, reflecting dependence on specific environments and microorganisms. Advances in Tn-Seq are expected to reveal more essential genes in the near future, deepening our understanding of microbial biology and enhancing our ability to manipulate microbial growth, as well as both the primary and secondary metabolism.spa
dc.description.sponsorshipThis research was funded by “Ministerio de Ciencia, Innovación Universidades/Agencia Estatal de Investigación/Fondo Europeo de Desarrollo Regional” (PID2021-122911OB-I00) and the “Consejería de Empleo, Industria y Turismo del Principado de Asturias” (SV-PA-21-AYUD/2021/51399). Sergio Alonso-Fernández was funded by a “Severo Ochoa” predoctoral grant (grant no. PA-20- PFBP19-006) from “Consejería de Ciencia, Innovación y Universidad del Principado de Asturias”. Paula Valdés-Chiara was supported by a predoctoral grant from the "Asociación Española Contra el Cáncer en Asturias" (grant no. PRDAS245960VALD)spa
dc.language.isoengspa
dc.publisherMarcello Tagliavia and Lucila Saavedraspa
dc.relation.ispartofInternational Journal of Molceular Sciences, 25spa
dc.rightsCC Reconocimiento 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectTn-Seq; transposon; essential genesspa
dc.titleEssential Genes Discovery in Microorganisms by Transposon-Directed Sequencing (Tn-Seq): Experimental Approaches, Major Goals, and Future Perspectivesspa
dc.typejournal articlespa
dc.identifier.doi10.3390/ijms252011298
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-122911OB-I00/ES/ACTIVACION DE RUTAS CRIPTICAS DE METABOLITOS SECUNDARIOS DE STREPTOMYCES MEDIANTE LA DIFERENCIACION DE LAS HIFAS Y LA HOMEOSTASIS DEL COBRE/
dc.relation.projectIDSV-PA-21-AYUD/2021/51399
dc.relation.projectIDPA-20-PFBP19-006
dc.relation.publisherversionhttps://doi.org/10.3390/ijms252011298
dc.rights.accessRightsopen accessspa
dc.type.hasVersionVoR


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