Insights on the Role of PGRMC1 in Mitotic and Meiotic Cell Division
Valentina Lodde1, Rodrigo Garcia Barros1, Laura Terzaghi1
1Reproductive and Developmental Biology Laboratory, Department of Veterinary Medicine and Animal Sciences, Università degli Studi di Milano, 20122 Milano, Italy.
Abstract:
During mitosis, chromosome missegregation and cytokinesis defects have been recognized as hallmarks of cancer cells. Cytoskeletal elements composing the spindle and the contractile ring and their associated proteins play crucial roles in the faithful progression of mitotic cell division. The hypothesis that PGRMC1, most likely as a part of a yet-to-be-defined complex, is involved in the regulation of spindle function and, more broadly, the cytoskeletal machinery driving cell division is particularly appealing. Nevertheless, more than ten years after the preliminary observation that PGRMC1 changes its localization dynamically during meiotic and mitotic cell division, this field of research has remained a niche and needs to be fully explored. To encourage research in this fascinating field, in this review, we will recap the current knowledge on PGRMC1 function during mitotic and meiotic cell division, critically highlighting the strengths and limitations of the experimental approaches used so far. We will focus on known interacting partners as well as new putative associated proteins that have recently arisen in the literature and that might support current as well as new hypotheses of a role for PGRMC1 in specific spindle subcompartments, such as the centrosome, kinetochores, and the midzone/midbody.
Insights
Progesterone receptor membrane component 1 (PGRMC1) dynamically changes localization during cell division. This review explores its potential role in regulating spindle function and cytoskeletal dynamics, crucial for accurate cell division.
Area of Science:
- Cell Biology
- Molecular Biology
- Cancer Research
Background:
- Chromosome missegregation and cytokinesis defects are hallmarks of cancer cells.
- Cytoskeletal proteins are critical for accurate mitotic cell division.
- Progesterone receptor membrane component 1 (PGRMC1) localization changes dynamically during cell division.
Purpose of the Study:
- To review current knowledge on PGRMC1 function in mitotic and meiotic cell division.
- To highlight experimental strengths and limitations in PGRMC1 research.
- To explore PGRMC1's potential role in regulating spindle function and cytoskeletal machinery.
Main Methods:
- Literature review of existing studies on PGRMC1.
- Analysis of known and putative PGRMC1 interacting partners.
- Critical evaluation of experimental approaches used in PGRMC1 research.
Main Results:
- PGRMC1's dynamic localization suggests a role in cell division.
- Existing research on PGRMC1 in cell division is limited but growing.
- Potential roles in spindle subcompartments like centrosomes and kinetochores are emerging.
Conclusions:
- PGRMC1 may regulate spindle function and cytoskeletal dynamics during cell division.
- Further research is needed to fully elucidate PGRMC1's role and associated complexes.
- Understanding PGRMC1's function could offer insights into cancer cell division defects.
Related Concept Videos
M-Cdk Drives Transition Into Mitosis
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
Molecular Factors Affecting Cell Division
Several proteins function as internal regulators to ensure each cell cycle stage is completed faithfully before proceeding to the next. Regulator molecules may act directly or influence the activity or production of other...
Mitogens and the Cell Cycle
The Cell Cycle Control System
Cyclins and cyclin-dependent kinases (Cdks) are the primary cell cycle regulators and...
Negative Regulator Molecules
Meiosis vs. Mitosis
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...


