| Literature DB >> 32023363 |
José María Martín-Fernández1, Aarne Fleischer1,2, Sara Vallejo-Diez2, Esther Palomino2, Almudena Sánchez-Gilabert1,2, Raúl Ruiz2, Yazmine Bejarano2,3, Pere Llinàs2,4, Antoni Gayá5, Daniel Bachiller2.
Abstract
Genome editing has become one of the most powerful tools in present-day stem cell and regenerative medicine research, but despite its rapid acceptance and widespread use, some elements of the technology still need improvement. In this unit, we present data regarding the use of a new, more efficient type of transcription activator-like effector nuclease (TALEN) for gene editing. Our group has generated bicistronic genes in which classical TALEN coding sequences are linked by 2A elements to different reporter molecules, such as fluorochromes (TALEN-F) or membrane receptors (TALEN-M). This structure results in two proteins transcribed from the same transcript, of which the second (the reporter) can be used as the target for selection by fluorescence-assisted cell sorting (FACS) or magnetic-activated cell sorting (MACS). The application of these new TALEN genes allows a rapid enrichment of cells in which both members of the TALEN pair are active, thus eliminating the need for lengthy selection in culture and laborious characterization of a large number of clones.Entities:
Keywords: FACS selection; MACS selection; TALENs; bicistronic transcription activator-like effector nuclease; genome editing
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Year: 2020 PMID: 32023363 DOI: 10.1002/cpsc.104
Source DB: PubMed Journal: Curr Protoc Stem Cell Biol ISSN: 1938-8969