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极光激酶C在减数分裂和癌症中的作用。

Functions of Aurora kinase C in meiosis and cancer.

作者信息

Quartuccio Suzanne M, Schindler Karen

机构信息

Department of Genetics, Rutgers, The State University of New Jersey Piscataway, NJ, USA.

出版信息

Front Cell Dev Biol. 2015 Aug 20;3:50. doi: 10.3389/fcell.2015.00050. eCollection 2015.

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.

摘要

哺乳动物基因组编码三种极光激酶蛋白家族成员

A、B和C。极光激酶A(AURKA)和B(AURKB)在全身细胞中都有发现,而极光激酶C(AURKC)的显著蛋白水平仅限于经历减数分裂的细胞(精子和卵母细胞)。尽管AURKC在近20年前就已被发现,但与其他两种极光激酶相比,我们对其功能了解甚少。这种认识上的不足可归因于AURKB和AURKC之间的高序列同源性,这使得我们无法使用标准方法来了解这两种激酶的非重叠和减数分裂I(MI)特异性功能。最近的证据揭示了AURKC在减数分裂中的独特功能,这可能有助于我们理解为什么MI期间的染色体分离在卵母细胞中常常出错。许多癌症中AURKC异常表达,但由于我们尚未完全了解AURKC在其正常细胞环境中的功能,因此很难预测这种表达对疾病的生物学意义。在这里,我们整合并更新了关于减数分裂细胞中AURKC信号传导的已知信息,以便更好地理解它为何具有致癌潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2f1/4542505/9501646b5343/fcell-03-00050-g0001.jpg

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