Cell-type specific, inducible and acute degradation of targeted protein in mice by two degron systems

Despite its broad application in in vitro studies, the application of targeted protein degradation (TPD) to animal models faces considerable challenges. Here, we develop inducible and cell-type specific TPD systems in mice using two degron systems: Oryza sativa TIR1<sup>F74G</sup> (OsTIR1)-auxin-inducible degron 2 (AID2) and human cereblon (hCRBN)-SALL4 degron (S4D). Efficient degradation of Satb1<sup>Venus</sup> protein by these systems recapitulates phenotypes observed in the Satb1-deficient mice. These TPD are successfully applied in both the fetal and neonatal stages. The OsTIR1-AID2 system proves to be effective for membrane proteins such as PD-1, emulating the effects of the anti-PD-1 antibody. Degradation of Bcl11b reveals a role of Bcl11b which was not characterized by the Cre-loxP system. Collectively, in vivo TPD technologies developed in this study enable inducible, temporal, and cell type-specific depletion of target proteins with high efficacy in mice. These technologies have a wide range of applications in the diverse fields of biological and medical research.

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Publication Details

Journal
Nature Communications
Published
2024-11-29
DOI
https://doi.org/10.1038/s41467-024-54308-9
Citations
14
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
3.27

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article

Cell-type specific, inducible and acute degradation of targeted protein in mice by two degron systems

Tetsuro Kobayashi, Aneela Nomura, Baihao Zhang, Tatsuya Sawasaki et al.
14 citations
Nature Communications
Protein Degradation and Inhibitors
3.27
article

Cell-type specific, inducible and acute degradation of targeted protein in mice by two degron systems

Tetsuro Kobayashi, Aneela Nomura, Baihao Zhang, Tatsuya Sawasaki, Masato T. Kanemaki, Sidonia Fagarasan, Satoshi Yamanaka, Jun Seita, Clive S. Barker, Koshi Imami, Chengcheng Zou, Motoi Yamashita, Yoichi Shinkai, Ken‐ichiro Hayashi, Kazuyo Moro, Fumiyuki Shirai, Chihiro Ogawa, Ichiro Taniuchi
article en
14 citations

Abstract

Despite its broad application in in vitro studies, the application of targeted protein degradation (TPD) to animal models faces considerable challenges. Here, we develop inducible and cell-type specific TPD systems in mice using two degron systems: Oryza sativa TIR1<sup>F74G</sup> (OsTIR1)-auxin-inducible degron 2 (AID2) and human cereblon (hCRBN)-SALL4 degron (S4D). Efficient degradation of Satb1<sup>Venus</sup> protein by these systems recapitulates phenotypes observed in the Satb1-deficient mice. These TPD are successfully applied in both the fetal and neonatal stages. The OsTIR1-AID2 system proves to be effective for membrane proteins such as PD-1, emulating the effects of the anti-PD-1 antibody. Degradation of Bcl11b reveals a role of Bcl11b which was not characterized by the Cre-loxP system. Collectively, in vivo TPD technologies developed in this study enable inducible, temporal, and cell type-specific depletion of target proteins with high efficacy in mice. These technologies have a wide range of applications in the diverse fields of biological and medical research.

Nature CommunicationsVol. 15(1)
National Institute of Genetics (JP), Okayama University of Science (JP), The Graduate University for Advanced Studies, SOKENDAI (JP), CellFree Sciences (Japan) (JP), RIKEN Center for Sustainable Resource Science (JP), RIKEN (JP), RIKEN Center for Integrative Medical Sciences (JP), Ehime University (JP), The University of Tokyo (JP)
Takeda Science Foundation, Japan Society for the Promotion of Science, RIKEN, Core Research for Evolutional Science and Technology
Openalex Percentile: Top 7%
Protein Degradation and Inhibitors
3.27
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