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Perfect duet: Dual recombinases improve genetic resolution

As a powerful genetic tool, site‐specific recombinases (SSRs) have been widely used in genomic manipulation to elucidate cell fate plasticity in vivo, advancing research in stem cell and regeneration medicine. However, the low resolution of conventional single‐recombinase‐mediated lineage tracing st...

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Detalles Bibliográficos
Autores principales: Li, Hongxin, Weng, Wendong, Zhou, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10212704/
https://www.ncbi.nlm.nih.gov/pubmed/37060165
http://dx.doi.org/10.1111/cpr.13446
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author Li, Hongxin
Weng, Wendong
Zhou, Bin
author_facet Li, Hongxin
Weng, Wendong
Zhou, Bin
author_sort Li, Hongxin
collection PubMed
description As a powerful genetic tool, site‐specific recombinases (SSRs) have been widely used in genomic manipulation to elucidate cell fate plasticity in vivo, advancing research in stem cell and regeneration medicine. However, the low resolution of conventional single‐recombinase‐mediated lineage tracing strategies, which rely heavily on the specificity of one marker gene, has led to controversial conclusions in many scientific questions. Therefore, different SSRs systems are combined to improve the accuracy of lineage tracing. Here we review the recent advances in dual‐recombinase‐mediated genetic approaches, including the development of novel genetic recombination technologies and their applications in cell differentiation, proliferation, and genetic manipulation. In comparison with the single‐recombinase system, we also discuss the advantages of dual‐genetic strategies in solving scientific issues as well as their technical limitations.
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spelling pubmed-102127042023-05-27 Perfect duet: Dual recombinases improve genetic resolution Li, Hongxin Weng, Wendong Zhou, Bin Cell Prolif Reviews As a powerful genetic tool, site‐specific recombinases (SSRs) have been widely used in genomic manipulation to elucidate cell fate plasticity in vivo, advancing research in stem cell and regeneration medicine. However, the low resolution of conventional single‐recombinase‐mediated lineage tracing strategies, which rely heavily on the specificity of one marker gene, has led to controversial conclusions in many scientific questions. Therefore, different SSRs systems are combined to improve the accuracy of lineage tracing. Here we review the recent advances in dual‐recombinase‐mediated genetic approaches, including the development of novel genetic recombination technologies and their applications in cell differentiation, proliferation, and genetic manipulation. In comparison with the single‐recombinase system, we also discuss the advantages of dual‐genetic strategies in solving scientific issues as well as their technical limitations. John Wiley and Sons Inc. 2023-04-14 /pmc/articles/PMC10212704/ /pubmed/37060165 http://dx.doi.org/10.1111/cpr.13446 Text en © 2023 The Authors. Cell Proliferation published by Beijing Institute for Stem Cell and Regenerative Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Li, Hongxin
Weng, Wendong
Zhou, Bin
Perfect duet: Dual recombinases improve genetic resolution
title Perfect duet: Dual recombinases improve genetic resolution
title_full Perfect duet: Dual recombinases improve genetic resolution
title_fullStr Perfect duet: Dual recombinases improve genetic resolution
title_full_unstemmed Perfect duet: Dual recombinases improve genetic resolution
title_short Perfect duet: Dual recombinases improve genetic resolution
title_sort perfect duet: dual recombinases improve genetic resolution
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10212704/
https://www.ncbi.nlm.nih.gov/pubmed/37060165
http://dx.doi.org/10.1111/cpr.13446
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