We previously cloned a rat cDNA encoding GAK, an association partner o
f cyclin G and CDK5. Here, we report the cloning of a cDNA encoding hu
man GAK (1311 amino acids) and show that all of the unique motifs that
characterize rat GAK, such as the presence of a Ser/Thr kinase domain
, a tensin/auxilin homologous domain, and a Tyr phosphorylation target
site, are conserved. The expression profiles of GAK and cyclin G duri
ng the synchronized HeLa cell cycle showed that GAK expression oscilla
tes slightly, peaking at G1 phase, although the histone H1 kinase acti
vity remains constant throughout the cell cycle. We also found that th
e kinase activity of immunoprecipitates of anti-cyclin G antibody fluc
tuates during the cell cycle with a peak at G1 phase, although the exp
ression level of cyclin G remains almost constant. Northern blot analy
sis showed that GAK is expressed ubiquitously, with the highest level
of expression being observed in the testis. Ey the FISH technique, we
assigned the chromosomal localization of GAK to 4p16. (C) 1997 Academi
c Press.