Mammalian homologues of the plant Tousled gene code for cell-cycle-regulated kinases with maximal activities linked to ongoing DNA replication

• Published in: The EMBO journal 1999-10, Vol.18 (20), p.5691-5702
• Main Authors: Silljé, H.H.W., Takahashi, K., Tanaka, K., Van Houwe, G., Nigg, E.A.
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Arabidopsis - enzymology; Arabidopsis - genetics; Base Sequence; Cell Cycle; Cell Nucleus - enzymology; Cloning; Deoxyribonucleic acid; development; DNA; DNA Damage; DNA Primers - genetics; DNA Replication; DNA, Complementary - genetics; DNA, Complementary - isolation & purification; Genes, Plant; HeLa Cells; Humans; Mammals; Mice; Molecular Sequence Data; protein kinase; Protein-Serine-Threonine Kinases - genetics; Protein-Serine-Threonine Kinases - metabolism; Recombinant Proteins - genetics; Recombinant Proteins - metabolism; S phase; Sequence Homology, Amino Acid; Species Specificity; Tousled
• ISSN: 0261-4189; 1460-2075; 1460-2075
• DOI: 10.1093/emboj/18.20.5691

The Tousled ( TSL ) gene of the plant Arabidopsis thaliana encodes a serine/threonine kinase that is essential for proper flower development. Here we report the cloning and characterization of two human putative homologues of the Arabidopsis TSL gene, termed TLK1 and TLK2 (Tousled‐like kinase). At the protein level, the two human Tlks share 84% sequence similarity with each other and almost 50% with Arabidopsis Tsl. Furthermore, nuclear localization signals and predicted coiled‐coil regions are conserved in the N‐terminal domains of all three kinases. The mammalian Tlks share several functional properties with plant Tsl, including a broad expression, a propensity to dimerize and autophosphorylate, and a preference for similar substrates. Most interestingly, human Tlks are cell‐cycle‐regulated enzymes, displaying maximal activities during S phase. Whereas protein levels are virtually constant throughout the cell cycle, both Tlks appear to be regulated by cell‐cycle‐dependent phosphorylation. Drug‐induced inhibition of DNA replication causes a rapid loss of Tlk activity, indicating that Tlk function is tightly linked to ongoing DNA replication. These findings provide the first biochemical clues as to the possible molecular functions of Tlks, a highly conserved family of kinases implicated in the development of multicellular organisms.