4.7 Review

Deubiquitinating Enzymes: A Critical Regulator of Mitosis

Journal

Publisher

MDPI
DOI: 10.3390/ijms20235997

Keywords

mitosis; ubiquitination; deubiquitination; cancer

Funding

  1. National Research Foundation of Korea (NRF) - Ministry of Science and ICT [2019R1A2C2004052, 2017R1A2B3007224]
  2. R&D Convergence Program of NST (National Research Council of Science & Technology) of Republic of Korea [CAP-16-03-KRIBB]
  3. National Research Council of Science & Technology (NST), Republic of Korea [CAP-16-03-KRIBB] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  4. National Research Foundation of Korea [2019R1A2C2004052, 2017R1A2B3007224] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

Ask authors/readers for more resources

Mitosis is a complex and dynamic process that is tightly regulated by a large number of mitotic proteins. Dysregulation of these proteins can generate daughter cells that exhibit genomic instability and aneuploidy, and such cells can transform into tumorigenic cells. Thus, it is important for faithful mitotic progression to regulate mitotic proteins at specific locations in the cells at a given time in each phase of mitosis. Ubiquitin-dependent modifications play critical roles in this process by regulating the degradation, translocation, or signal transduction of mitotic proteins. Here, we review how ubiquitination and deubiquitination regulate the progression of mitosis. In addition, we summarize the substrates and roles of some deubiquitinating enzymes (DUBs) crucial for mitosis and describe how they contribute error correction during mitosis and control the transition between the mitotic phases.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available