| Online-Ressource |
Verfasst von: | Buchmuller, Benjamin [VerfasserIn]  |
| Herbst, Konrad [VerfasserIn]  |
| Meurer, Matthias [VerfasserIn]  |
| Kirrmaier, Daniel [VerfasserIn]  |
| Sass, Ehud [VerfasserIn]  |
| Levy, Emmanuel D. [VerfasserIn]  |
| Knop, Michael [VerfasserIn]  |
Titel: | Pooled clone collections by multiplexed CRISPR/Cas12a-assisted gene tagging in yeast |
Verf.angabe: | Benjamin C. Buchmuller, Konrad Herbst, Matthias Meurer, Daniel Kirrmaier, Ehud Sass, Emmanuel D. Levy, Michael Knop |
E-Jahr: | 2018 |
Jahr: | November 22, 2018 |
Umfang: | 57 S. |
Fussnoten: | Gesehen am 16.05.2019 |
Titel Quelle: | Enthalten in: bioRxiv beta |
Ort Quelle: | Cold Spring Harbor : Cold Spring Harbor Laboratory, NY, 2013 |
Jahr Quelle: | 2018 |
Band/Heft Quelle: | (2018) Artikel-Nummer 476804, 57 Seiten |
Abstract: | Clone collections of modified strains (‘libraries’) are a major resource for systematic studies with the yeast <i>Saccharomyces cerevisiae</i>. Construction of such libraries is time-consuming, costly and confined to the genetic background of a specific yeast strain. To overcome these limitations, we developed CRISPR/Cas12a (Cpf1)-assisted tag library engineering (CASTLING) for multiplexed strain construction. CASTLING uses microarray-synthesized oligonucleotide pools and <i>in vitro</i> recombineering to program the genomic insertion of long DNA constructs via homologous recombination. One simple transformation yields pooled libraries with >90% of correctly tagged clones. Up to several hundred genes can be tagged in a single step and, on a genomic scale, approximately half of all genes are tagged with only ~10-fold oversampling. We report several parameters that affect tagging success and provide a quantitative targeted next-generation sequencing method to analyze such pooled collections. Thus, CASTLING unlocks new avenues for increased throughput in functional genomics and cell biology research. (max 150 words)</p> |
DOI: | doi:10.1101/476804 |
URL: | Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.
Volltext ; Verlag: https://doi.org/10.1101/476804 |
| Volltext: https://www.biorxiv.org/content/10.1101/476804v1 |
| DOI: https://doi.org/10.1101/476804 |
Datenträger: | Online-Ressource |
Sprache: | eng |
Bibliogr. Hinweis: | Forschungsdaten: Buchmuller, Benjamin, 1991 - : Pooled clone collections by multiplexed CRISPR-Cas12a-assisted gene tagging in yeast [dataset] |
K10plus-PPN: | 1665791055 |
Verknüpfungen: | → Sammelwerk |
Pooled clone collections by multiplexed CRISPR/Cas12a-assisted gene tagging in yeast / Buchmuller, Benjamin [VerfasserIn]; November 22, 2018 (Online-Ressource)