Dynamic loading and redistribution of the Mcm2-7 helicase complex through the cell cycle.

Journal Article (Journal Article)

Eukaryotic replication origins are defined by the ORC-dependent loading of the Mcm2-7 helicase complex onto chromatin in G1. Paradoxically, there is a vast excess of Mcm2-7 relative to ORC assembled onto chromatin in G1. These excess Mcm2-7 complexes exhibit little co-localization with ORC or replication foci and can function as dormant origins. We dissected the mechanisms regulating the assembly and distribution of the Mcm2-7 complex in the Drosophila genome. We found that in the absence of cyclin E/Cdk2 activity, there was a 10-fold decrease in chromatin-associated Mcm2-7 relative to the levels found at the G1/S transition. The minimal amounts of Mcm2-7 loaded in the absence of cyclin E/Cdk2 activity were strictly localized to ORC binding sites. In contrast, cyclin E/Cdk2 activity was required for maximal loading of Mcm2-7 and a dramatic genome-wide reorganization of the distribution of Mcm2-7 that is shaped by active transcription. Thus, increasing cyclin E/Cdk2 activity over the course of G1 is not only critical for Mcm2-7 loading, but also for the distribution of the Mcm2-7 helicase prior to S-phase entry.

Full Text

Duke Authors

Cited Authors

  • Powell, SK; MacAlpine, HK; Prinz, JA; Li, Y; Belsky, JA; MacAlpine, DM

Published Date

  • February 12, 2015

Published In

Volume / Issue

  • 34 / 4

Start / End Page

  • 531 - 543

PubMed ID

  • 25555795

Pubmed Central ID

  • PMC4331006

Electronic International Standard Serial Number (EISSN)

  • 1460-2075

Digital Object Identifier (DOI)

  • 10.15252/embj.201488307


  • eng

Conference Location

  • England