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      Human TopBP1 participates in cyclin E/CDK2 activation and preinitiation complex assembly during G1/S transition.

      The Journal of Biological Chemistry
      Carrier Proteins, metabolism, Cell Line, Chromatin, Cyclin E, Cyclin-Dependent Kinase 2, Cyclin-Dependent Kinase Inhibitor p27, DNA, biosynthesis, DNA Damage, DNA-Binding Proteins, G1 Phase, physiology, Humans, Multiprotein Complexes, Nuclear Proteins, Protein-Serine-Threonine Kinases, S Phase, p21-Activated Kinases

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          Abstract

          Human TopBP1 with eight BRCA1 C terminus domains has been mainly reported to be involved in DNA damage response pathways. Here we show that TopBP1 is also required for G(1) to S progression in a normal cell cycle. TopBP1 deficiency inhibited cells from entering S phase by up-regulating p21 and p27, resulting in down-regulation of cyclin E/CDK2. Although co-depletion of p21 and p27 with TopBP1 restored the cyclin E/CDK2 kinase activity, however, cells remained arrested at the G(1)/S boundary, showing defective chromatin-loading of replication components. Based on these results, we suggest a dual role of TopBP1 necessary for the G(1)/S transition: one for activating cyclin E/CDK2 kinase and the other for loading replication components onto chromatin to initiate DNA synthesis.

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