Kinase Subfamily MOK
MOK is a primordial eukaryotic kinase, predicted to be in the last common ancestor of all eukaryotes. However, it has been lost from several lineages, including nematodes, insects, fungi, and higher plants. The single human member is called MOK (MAPK/MAK/MRK Overlapping Kinase), also known as RAGE1 (renal tumor antigen).
All MOK kinases have an N-terminal kinase domain and a variable length (~100-300 AA) C-terminal tail without any known domains.
MOK function is poorly understood. Its absence from organisms that have also lost motile cilia, and the association of the related MAK kinases to cilia suggests that it might be involved in motile cilia function. This is supported by LF4, the Chlamydomonas MOK. LF4 regulates flagellum growth and interacts genetically with LF2 (a CDK20 subfamily kinase) .
Human MOK transcript is expressed in testis, thyroid, retina, while mouse is largely expressed in testis and maybe in two stem cell lines BioGPS. Mouse MOK is selectively expressed in intestinal crypt cells, under the regulation of the Cdx2 homeodomain protein . The mouse gene was also reported as expressed mostly in testicular germ cells (Gopalan et al - no Medline citation but the direct link is http://onlinelibrary.wiley.com/doi/10.1002/(SICI)1098-2795(199901)52:1%3C9::AID-MRD2%3E3.0.CO;2-O/citedby ). Human MOK protein is localized to the cytoplasm and stained the Golgi in one cell line (http://proteinatlas.org).
MOK is also known as RAGE1 (Renal Tumor Antigen), as a tumor-associated antigen that is recognized by autologous cytolytic T cells . RAGE1 was isolated from a renal cell carcinoma, but was not expressed in other RCC samples, though it was reported in normal retina and in a variety of other tumors (e.g. [6, 7, 8]).