Literature DB >> 34709611

Design and Generation of a CRISPR Interference System for Genetic Repression and Essential Gene Analysis in the Fungal Pathogen Candida albicans.

Lauren Wensing1, Rebecca S Shapiro2.   

Abstract

Studying life-threatening fungal pathogens such as Candida albicans is of critical importance, yet progress can be hindered by challenges associated with manipulating these pathogens genetically. CRISPR-based technologies have significantly improved our ability to manipulate the genomes of countless organisms, including fungal pathogens such as C. albicans. CRISPR interference (CRISPRi) is a modified variation of CRISPR technology that enables the targeted genetic repression of specific genes of interest and can be used as a technique for studying essential genes. We recently developed tools to enable CRISPRi in C. albicans and the repression of essential genes in this fungus. Here, we describe a protocol for CRISPRi in C. albicans, including the design of the single-guide RNAs (sgRNAs) for targeting essential genes, the high-efficiency cloning of sgRNAs into C. albicans-optimized CRISPRi plasmids, transformation into fungal strains, and testing to monitor the repression capabilities of these constructs. Together, this protocol will illuminate efficient strategies for targeted genetic repression of essential genes in C. albicans using a novel CRISPRi platform.
© 2022. Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  CRISPR; CRISPRi; Candida albicans; Fungal genetics; Fungal pathogens; Genetic regulation; Genetic repression

Mesh:

Substances:

Year:  2022        PMID: 34709611     DOI: 10.1007/978-1-0716-1720-5_4

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  5 in total

Review 1.  New pathogens, new tricks: emerging, drug-resistant fungal pathogens and future prospects for antifungal therapeutics.

Authors:  Jennifer Geddes-McAlister; Rebecca S Shapiro
Journal:  Ann N Y Acad Sci       Date:  2018-05-15       Impact factor: 5.691

2.  An Efficient, Rapid, and Recyclable System for CRISPR-Mediated Genome Editing in Candida albicans.

Authors:  Namkha Nguyen; Morgan M F Quail; Aaron D Hernday
Journal:  mSphere       Date:  2017-04-26       Impact factor: 4.389

3.  EuPaGDT: a web tool tailored to design CRISPR guide RNAs for eukaryotic pathogens.

Authors:  Duo Peng; Rick Tarleton
Journal:  Microb Genom       Date:  2015-10-30

4.  Enabling genetic analysis of diverse bacteria with Mobile-CRISPRi.

Authors:  Jason M Peters; Byoung-Mo Koo; Ramiro Patino; Gary E Heussler; Cameron C Hearne; Jiuxin Qu; Yuki F Inclan; John S Hawkins; Candy H S Lu; Melanie R Silvis; M Michael Harden; Hendrik Osadnik; Joseph E Peters; Joanne N Engel; Rachel J Dutton; Alan D Grossman; Carol A Gross; Oren S Rosenberg
Journal:  Nat Microbiol       Date:  2019-01-07       Impact factor: 17.745

5.  Dramatic Improvement of CRISPR/Cas9 Editing in Candida albicans by Increased Single Guide RNA Expression.

Authors:  Henry Ng; Neta Dean
Journal:  mSphere       Date:  2017-04-19       Impact factor: 4.389

  5 in total

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