Keyword search (4,163 papers available)

"CRISPR-Cas9" Keyword-tagged Publications:

Title Authors PubMed ID
1 CRAPS: Chromosomal-Repair-Assisted Pathway Shuffling in Yeast Dykstra CB; Pyne ME; Martin VJJ; 37584634
BIOLOGY
2 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
3 Seamless site-directed mutagenesis of the Saccharomyces cerevisiae genome using CRISPR-Cas9. Biot-Pelletier D, Martin VJ 27134651
BIOLOGY
4 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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