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Transcriptional Regulation Technology for Gene Perturbation in Fission Yeast

Isolation and introduction of genetic mutations is the primary approach to characterize gene functions in model yeasts. Although this approach has proven very powerful, it is not applicable to all genes in these organisms. For example, introducing defective mutations into essential genes causes leth...

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Detalles Bibliográficos
Autores principales: Ishikawa, Ken, Saitoh, Shigeaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135669/
https://www.ncbi.nlm.nih.gov/pubmed/37189462
http://dx.doi.org/10.3390/biom13040716
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author Ishikawa, Ken
Saitoh, Shigeaki
author_facet Ishikawa, Ken
Saitoh, Shigeaki
author_sort Ishikawa, Ken
collection PubMed
description Isolation and introduction of genetic mutations is the primary approach to characterize gene functions in model yeasts. Although this approach has proven very powerful, it is not applicable to all genes in these organisms. For example, introducing defective mutations into essential genes causes lethality upon loss of function. To circumvent this difficulty, conditional and partial repression of target transcription is possible. While transcriptional regulation techniques, such as promoter replacement and 3′ untranslated region (3′UTR) disruption, are available for yeast systems, CRISPR–Cas-based technologies have provided additional options. This review summarizes these gene perturbation technologies, including recent advances in methods based on CRISPR–Cas systems for Schizosaccharomyces pombe. We discuss how biological resources afforded by CRISPRi can promote fission yeast genetics.
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spelling pubmed-101356692023-04-28 Transcriptional Regulation Technology for Gene Perturbation in Fission Yeast Ishikawa, Ken Saitoh, Shigeaki Biomolecules Review Isolation and introduction of genetic mutations is the primary approach to characterize gene functions in model yeasts. Although this approach has proven very powerful, it is not applicable to all genes in these organisms. For example, introducing defective mutations into essential genes causes lethality upon loss of function. To circumvent this difficulty, conditional and partial repression of target transcription is possible. While transcriptional regulation techniques, such as promoter replacement and 3′ untranslated region (3′UTR) disruption, are available for yeast systems, CRISPR–Cas-based technologies have provided additional options. This review summarizes these gene perturbation technologies, including recent advances in methods based on CRISPR–Cas systems for Schizosaccharomyces pombe. We discuss how biological resources afforded by CRISPRi can promote fission yeast genetics. MDPI 2023-04-21 /pmc/articles/PMC10135669/ /pubmed/37189462 http://dx.doi.org/10.3390/biom13040716 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ishikawa, Ken
Saitoh, Shigeaki
Transcriptional Regulation Technology for Gene Perturbation in Fission Yeast
title Transcriptional Regulation Technology for Gene Perturbation in Fission Yeast
title_full Transcriptional Regulation Technology for Gene Perturbation in Fission Yeast
title_fullStr Transcriptional Regulation Technology for Gene Perturbation in Fission Yeast
title_full_unstemmed Transcriptional Regulation Technology for Gene Perturbation in Fission Yeast
title_short Transcriptional Regulation Technology for Gene Perturbation in Fission Yeast
title_sort transcriptional regulation technology for gene perturbation in fission yeast
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135669/
https://www.ncbi.nlm.nih.gov/pubmed/37189462
http://dx.doi.org/10.3390/biom13040716
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