Beltran-Sastre, VioletaBenisty, Hannah, 1986-Burnier, JuliaBerger, ImreSerrano Pubull, Luis, 1982-Kiel, Christina2023-06-272023-06-272015Beltran-Sastre V, Benisty H, Burnier J, Berger I, Serrano L, Kiel C. Tuneable endogenous mammalian target complementation via multiplexed plasmid-based recombineering. Sci Rep. 2015 Nov 27;5(1):17432. DOI: 10.1038/srep174322045-2322http://hdl.handle.net/10230/57357Includes supplementary materials for the online appendix.Understanding the quantitative functional consequences of human disease mutations requires silencing of endogenous genes and expression of mutants at close to physiological levels. Changing protein levels above or below these levels is also important for system perturbation and modelling. Fast design optimization demands flexible interchangeable cassettes for endogenous gene silencing and tuneable expression. Here, we introduce ‘TEMTAC’, a multigene recombineering and delivery system for simultaneous siRNA-based knockdown and regulated mutant (or other variant) expression with different dynamic ranges. We show its applicability by confirming known phenotypic effects for selected mutations for BRAF, HRAS and SHP2.application/pdfengThis work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/MalaltiesProteïnesAnomalies cromosòmiquesMutació (Biologia)info:eu-repo/semantics/articlehttp://dx.doi.org/10.1038/srep17432info:eu-repo/semantics/openAccess