Keyword search (4,164 papers available)

"crispr" Keyword-tagged Publications:

Title Authors PubMed ID
1 Tri-Functional CRISPR Screen Reveals Overexpression of em QDR2 /em and em QDR3 /em Transporters Increase Fumaric Acid Production in em Kluyveromyces marxianus /em Thornbury M; Omran RP; Kumar L; Knoops A; Abushahin R; Whiteway M; Martin VJJ; 41277095
BIOLOGY
2 Sequencing of a Dairy Isolate Unlocks em Kluyveromyces marxianus /em as a Host for Lactose Valorization Thornbury M; Knoops A; Summerby-Murray I; Dhaliwal J; Johnson S; Utomo JC; Joshi J; Narcross L; Remondetto G; Pouliot M; Whiteway M; Martin VJJ; 40629255
BIOLOGY
3 Endogenous tagging using split mNeonGreen in human iPSCs for live imaging studies Husser MC; Pham NP; Law C; Araujo FRB; Martin VJJ; Piekny A; 38652106
BIOLOGY
4 CRISPR/Cas9 mediated gene editing of transcription factor ACE1 for enhanced cellulase production in thermophilic fungus Rasamsonia emersonii Singh V; Raheja Y; Basotra N; Sharma G; Tsang A; Chadha BS; 37658430
CSFG
5 CRAPS: Chromosomal-Repair-Assisted Pathway Shuffling in Yeast Dykstra CB; Pyne ME; Martin VJJ; 37584634
BIOLOGY
6 Rapid, scalable, combinatorial genome engineering by marker-less enrichment and recombination of genetically engineered loci in yeast Abdullah M; Greco BM; Laurent JM; Garge RK; Boutz DR; Vandeloo M; Marcotte EM; Kachroo AH; 37323580
BIOLOGY
7 Cytokinetic diversity in mammalian cells is revealed by the characterization of endogenous anillin, Ect2 and RhoA Husser MC; Ozugergin I; Resta T; Martin VJJ; Piekny AJ; 36416720
BIOLOGY
8 The MyLo CRISPR-Cas9 Toolkit: A Markerless Yeast Localization and Overexpression CRISPR-Cas9 Toolkit Bean BDM; Whiteway M; Martin VJJ; 35708612
BIOLOGY
9 The chimeric GaaR-XlnR transcription factor induces pectinolytic activities in the presence of D-xylose in Aspergillus niger Kun RS; Garrigues S; Di Falco M; Tsang A; de Vries RP; 34236481
CSFG
10 Identification of a Novel Biosynthetic Gene Cluster in Aspergillus niger Using Comparative Genomics Evdokias G; Semper C; Mora-Ochomogo M; Di Falco M; Nguyen TTM; Savchenko A; Tsang A; Benoit-Gelber I; 34064722
BIOLOGY
11 Using the endogenous CRISPR-Cas system of Heliobacterium modesticaldum to delete the photochemical reaction center core subunit gene. Baker PL, Orf GS, Kevershan K, Pyne ME, Bicer T, Redding KE 31540988
BIOLOGY
12 Single-step Precision Genome Editing in Yeast Using CRISPR-Cas9. Akhmetov A, Laurent JM, Gollihar J, Gardner EC, Garge RK, Ellington AD, Kachroo AH, Marcotte EM 29770349
BIOLOGY
13 A Highly Characterized Synthetic Landing Pad System for Precise Multicopy Gene Integration in Yeast. Bourgeois L, Pyne ME, Martin VJJ 30372609
BIOLOGY
14 Seamless site-directed mutagenesis of the Saccharomyces cerevisiae genome using CRISPR-Cas9. Biot-Pelletier D, Martin VJ 27134651
BIOLOGY
15 W361R mutation in GaaR, the regulator of D-galacturonic acid-responsive genes, leads to constitutive production of pectinases in Aspergillus niger. Alazi E, Niu J, Otto SB, Arentshorst M, Pham TTM, Tsang A, Ram AFJ 30298571
CSFG

 

Title:Seamless site-directed mutagenesis of the Saccharomyces cerevisiae genome using CRISPR-Cas9.
Authors:Biot-Pelletier DMartin VJ
Link:https://www.ncbi.nlm.nih.gov/pubmed/27134651?dopt=Abstract
DOI:10.1186/s13036-016-0028-1
Publication:Journal of biological engineering
Keywords:CRISPR-Cas9Genome editingSaccharomyces cerevisiaeSite-directed mutagenesis
PMID:27134651 Category:J Biol Eng Date Added:2019-06-07
Dept Affiliation: BIOLOGY
1 Department of Biology, Concordia University, 7141 Sherbrooke West, Montréal, QC H4B 1R6 Canada ; Centre for Structural and Functional Genomics, Concordia University, 7141 Sherbrooke West, Montréal, QC H4B 1R6 Canada.

Description:

Seamless site-directed mutagenesis of the Saccharomyces cerevisiae genome using CRISPR-Cas9.

J Biol Eng. 2016;10:6

Authors: Biot-Pelletier D, Martin VJ

Abstract

CRISPR assisted homology directed repair enables the introduction of virtually any modification to the Saccharomyces cerevisiae genome. Of obvious interest is the marker-free and seamless introduction of point mutations. To fulfill this promise, a strategy that effects single nucleotide changes while preventing repeated recognition and cutting by the gRNA/Cas9 complex is needed. We demonstrate a two-step method to introduce point mutations at 17 positions in the S. cerevisiae genome. We show the general applicability of the method, enabling the seamless introduction of single nucleotide changes at any location, including essential genes and non-coding regions. We also show a quantifiable phenotype for a point mutation introduced in gene GSH1. The ease and wide applicability of this general method, combined with the demonstration of its feasibility will enable genome editing at an unprecedented level of detail in yeast and other organisms.

PMID: 27134651 [PubMed]





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