Keyword search (4,163 papers available)

"Greco BM" Authored Publications:

Title Authors PubMed ID
1 PARPAL: PARalog Protein Redistribution using Abundance and Localization in Yeast Database Greco BM; Zapata G; Dandage R; Papkov M; Pereira V; Lefebvre F; Bourque G; Parts L; Kuzmin E; 40580499
BIOLOGY
2 Single-cell imaging of protein dynamics of paralogs reveals sources of gene retention Dandage R; Papkov M; Greco BM; Pereira V; Fishman D; Friesen H; Wang K; Styles EB; Kraus O; Grys B; Zapata G; Lefebvre F; Bourque G; Boone C; Andrews BJ; Parts L; Kuzmin E; 40585364
BIOLOGY
3 A Humanized Yeast Model for Studying TRAPP Complex Mutations; Proof-of-Concept Using Variants from an Individual with a TRAPPC1-Associated Neurodevelopmental Syndrome Zykaj E; Abboud C; Asadi P; Warsame S; Almousa H; Milev MP; Greco BM; López-Sánchez M; Bratkovic D; Kachroo AH; Pérez-Jurado LA; Sacher M; 39273027
BIOLOGY
4 Single-cell imaging of protein dynamics of paralogs reveals mechanisms of gene retention Dandage R; Papkov M; Greco BM; Fishman D; Friesen H; Wang K; Styles E; Kraus O; Grys B; Boone C; Andrews B; Parts L; Kuzmin E; 38045359
BIOLOGY
5 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
6 Humanized yeast to model human biology, disease and evolution Kachroo AH; Vandeloo M; Greco BM; Abdullah M; 35661208
BIOLOGY

 

Title:Rapid, scalable, combinatorial genome engineering by marker-less enrichment and recombination of genetically engineered loci in yeast
Authors:Abdullah MGreco BMLaurent JMGarge RKBoutz DRVandeloo MMarcotte EMKachroo AH
Link:https://pubmed.ncbi.nlm.nih.gov/37323580/
DOI:10.1016/j.crmeth.2023.100464
Publication:Cell reports methods
Keywords:CRISPR-Cas9combinatorial genome editinggene drivehumanized proteasomehumanized yeast
PMID:37323580 Category: Date Added:2023-06-16
Dept Affiliation: BIOLOGY

Description:

A major challenge to rationally building multi-gene processes in yeast arises due to the combinatorics of combining all of the individual edits into the same strain. Here, we present a precise and multi-site genome editing approach that combines all edits without selection markers using CRISPR-Cas9. We demonstrate a highly efficient gene drive that selectively eliminates specific loci by integrating CRISPR-Cas9-mediated double-strand break (DSB) generation and homology-directed recombination with yeast sexual assortment. The method enables marker-less enrichment and recombination of genetically engineered loci (MERGE). We show that MERGE converts single heterologous loci to homozygous loci at ~100% efficiency, independent of chromosomal location. Furthermore, MERGE is equally efficient at converting and combining multiple loci, thus identifying compatible genotypes. Finally, we establish MERGE proficiency by engineering a fungal carotenoid biosynthesis pathway and most of the human a-proteasome core into yeast. Therefore, MERGE lays the foundation for scalable, combinatorial genome editing in yeast.





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