TY - JOUR TI - Ubiquitin-Specific Protease 3 Deubiquitinates and Stabilizes Oct4 Protein in Human Embryonic Stem Cells AU - Rhie, Byung-Ho AU - Antao, Ainsley Mike AU - Karapurkar, Janardhan Keshav AU - Kim, Min-Seong AU - Jo, Won-Jun AU - Ramakrishna, Suresh AU - Kim, Kye-Seong T2 - International Journal of Molecular Sciences AB - Oct4 is an important mammalian POU family transcription factor expressed by early human embryonic stem cells (hESCs). The precise level of Oct4 governs the pluripotency and fate determination of hESCs. Several post-translational modifications (PTMs) of Oct4 including phosphorylation, ubiquitination, and SUMOylation have been reported to regulate its critical functions in hESCs. Ubiquitination and deubiquitination of Oct4 should be well balanced to maintain the pluripotency of hESCs. The protein turnover of Oct4 is regulated by several E3 ligases through ubiquitin-mediated degradation. However, reversal of ubiquitination by deubiquitinating enzymes (DUBs) has not been reported for Oct4. In this study, we generated a ubiquitin-specific protease 3 (USP3) gene knockout using the CRISPR/Cas9 system and demonstrated that USP3 acts as a protein stabilizer of Oct4 by deubiquitinating Oct4. USP3 interacts with endogenous Oct4 and co-localizes in the nucleus of hESCs. The depletion of USP3 leads to a decrease in Oct4 protein level and loss of pluripotent morphology in hESCs. Thus, our results show that USP3 plays an important role in controlling optimum protein level of Oct4 to retain pluripotency of hESCs. DA - 2021/01// PY - 2021 DO - 10.3390/ijms22115584 DP - www.mdpi.com VL - 22 IS - 11 SP - 5584 LA - en UR - https://www.mdpi.com/1422-0067/22/11/5584 Y2 - 2021/06/02/17:24:39 KW - 26S proteasome KW - CRISPR/Cas9 KW - embryonic carcinoma cells KW - gene knockout KW - post-translational modifications ER -