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Functions of Aurora kinase C in meiosis and cancer
Suzanne M Quartuccio1, Karen Schindler1
1Department of Genetics, Rutgers, The State University of New Jersey Piscataway, NJ, USA.
Abstract:
The mammalian genome encodes three Aurora kinase protein family members: A, B, and C. While Aurora kinase A (AURKA) and B (AURKB) are found in cells throughout the body, significant protein levels of Aurora kinase C (AURKC) are limited to cells that undergo meiosis (sperm and oocyte). Despite its discovery nearly 20 years ago, we know little about the function of AURKC compared to that of the other 2 Aurora kinases. This lack of understanding can be attributed to the high sequence homology between AURKB and AURKC preventing the use of standard approaches to understand non-overlapping and meiosis I (MI)-specific functions of the two kinases. Recent evidence has revealed distinct functions of AURKC in meiosis and may aid in our understanding of why chromosome segregation during MI often goes awry in oocytes. Many cancers aberrantly express AURKC, but because we do not fully understand AURKC function in its normal cellular context, it is difficult to predict the biological significance of this expression on the disease. Here, we consolidate and update what is known about AURKC signaling in meiotic cells to better understand why it has oncogenic potential.
Insights
Aurora kinase C (AURKC) plays a key role in meiosis, but its functions are poorly understood due to similarities with Aurora kinase B (AURKB). Research aims to clarify AURKC
Area of Science:
- Cell Biology
- Genetics
- Molecular Biology
Background:
- Mammalian genomes encode three Aurora kinases: A, B, and C.
- Aurora kinase A (AURKA) and B (AURKB) are ubiquitously expressed, while Aurora kinase C (AURKC) is primarily found in meiotic cells (sperm and oocytes).
- Despite its discovery 20 years ago, AURKC's function remains largely uncharacterized compared to AURKA and AURKB.
Purpose of the Study:
- To consolidate and update current knowledge on AURKC signaling in meiotic cells.
- To elucidate the distinct functions of AURKC in meiosis, particularly in meiosis I (MI).
- To understand the oncogenic potential of AURKC in the context of aberrant cancer expression.
Main Methods:
- Review and synthesis of existing literature on AURKC.
- Analysis of sequence homology between AURKB and AURKC to understand research challenges.
- Examination of recent evidence on AURKC's role in meiotic chromosome segregation.
Main Results:
- High sequence homology between AURKB and AURKC hinders the study of their non-overlapping functions.
- Emerging evidence suggests specific roles for AURKC in meiosis.
- Aberrant AURKC expression is observed in many cancers, but its significance is unclear due to limited understanding of its normal function.
Conclusions:
- Further research into AURKC's meiotic functions is crucial for understanding chromosome segregation errors, especially in oocytes.
- Clarifying AURKC's role in normal cellular contexts is essential for predicting its biological significance in cancer.
- Understanding AURKC signaling may reveal insights into its oncogenic potential.
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