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Publication : Identification, characterization and chromosomal localization of the cognate human and murine DBF4 genes.

First Author  Lepke M Year  1999
Journal  Mol Gen Genet Volume  262
Issue  2 Pages  220-9
PubMed ID  10517317 Mgi Jnum  J:58256
Mgi Id  MGI:1347141 Doi  10.1007/s004380051078
Citation  Lepke M, et al. (1999) Identification, characterization and chromosomal localization of the cognate human and murine DBF4 genes. Mol Gen Genet 262(2):220-9
abstractText  The kinase Dbf4p/Cdc7p is required for the G1/S phase transition during the cell cycle and plays a direct role in the activation of individual origins of replication in Saccharomyces cerevisiae. Here, we report the identification and characterization of mouse and human cDNAs whose products are related in sequence to Saccharomyces cerevisiae DBF4 cDNA. Both mammalian Dbf4 proteins contain a putative site for phosphorylation by CDK, PEST protease cleavage sites, nuclear localization signals and a short-looped zinc finger-like domain. Transcription of MmDBF4 is suppressed in mouse NIH3T3 fibroblasts made quiescent by serum starvation. Upon replenishment of the medium, transcript levels increase during progression through G1, peaking as cells enter S phase. MmDbf4p interacts physically with Cdc7p and Mcm2p in vivo. Using fluorescence in situ hybridization (FISH), the human DBF4 gene was localized to chromosome 7 (q21.3), whereas FISH mapped the murine counterpart to band A2 on chromosome 5. The results of chromosome mapping indicate that in both mouse and human the gene is present as a single copy. The structural conservation between Dbf4-related proteins suggests that these proteins play a key role in the regulation of DNA replication during the cell cycle in all eukaryotes.
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