Nuclear localization of 68 kDa calmodulin-binding protein is associated with the onset of DNA replication

✍ Scribed by C. Subramanyam; Susan C. Honn; William C. Reed; G. Prem Veer Reddy

• Publisher: John Wiley and Sons
• Year: 1990
• Tongue: English
• Weight: 744 KB
• Volume: 144
• Category: Article
• ISSN: 0021-9541
• DOI: 10.1002/jcp.1041440309

✦ Synopsis

Abstract

In Chinese hamster embryo fibroblast cells, an increase in intracellular calmodulin levels coincided with the nuclear localization of a calmodulin‐binding protein of about 68 kDa as the cells progressed from G1 to S phase. When cells were limited from entering into S phase, by omitting insulin a defined medium, intracellular CaM levels did not increase and the 68 kDa calmodulin‐binding protein was completely absent from the nuclei. Corresponding to the nuclear localization of calmodulin and the 68 kDa calmodulin‐binding protein in S phase cells, there was a dramatic increase in DNA polymerase and thymidine kinase activities in the nuclei of S phase cells as compared to G1 phase cells. In addition, the 68 kDa calmodulin‐binding protein along with calmodulin, is observed to be an integral component of replitase complex responsible for nuclear DNA replication in S phase cells. These observations point to the association of calmodulin and calmodulin‐binding protein(s) with the replication machinery responsible for nuclear DNA replication during S phase. A possible regulatory role of these proteins in the onset of DNA replication and cell proliferation is discussed.