Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Antagonistic control of DDK binding to licensed replication origins by Mcm2 and Rad53

View through CrossRef
Eukaryotic replication origins are licensed by the loading of the replicative DNA helicase, Mcm2-7, in inactive double hexameric form around DNA. Subsequent origin activation is under control of multiple protein kinases that either promote or inhibit origin activation, which is important for genome maintenance. Using the reconstituted budding yeast DNA replication system, we find that the flexible N-terminal extension (NTE) of Mcm2 promotes the stable recruitment of Dbf4-dependent kinase (DDK) to Mcm2-7 double hexamers, which in turn promotes DDK phosphorylation of Mcm4 and −6 and subsequent origin activation. Conversely, we demonstrate that the checkpoint kinase, Rad53, inhibits DDK binding to Mcm2-7 double hexamers. Unexpectedly, this function is not dependent on Rad53 kinase activity, suggesting steric inhibition of DDK by activated Rad53. These findings identify critical determinants of the origin activation reaction and uncover a novel mechanism for checkpoint-dependent origin inhibition.
eLife Sciences Publications, Ltd
Title: Antagonistic control of DDK binding to licensed replication origins by Mcm2 and Rad53
Description:
Eukaryotic replication origins are licensed by the loading of the replicative DNA helicase, Mcm2-7, in inactive double hexameric form around DNA.
Subsequent origin activation is under control of multiple protein kinases that either promote or inhibit origin activation, which is important for genome maintenance.
Using the reconstituted budding yeast DNA replication system, we find that the flexible N-terminal extension (NTE) of Mcm2 promotes the stable recruitment of Dbf4-dependent kinase (DDK) to Mcm2-7 double hexamers, which in turn promotes DDK phosphorylation of Mcm4 and −6 and subsequent origin activation.
Conversely, we demonstrate that the checkpoint kinase, Rad53, inhibits DDK binding to Mcm2-7 double hexamers.
Unexpectedly, this function is not dependent on Rad53 kinase activity, suggesting steric inhibition of DDK by activated Rad53.
These findings identify critical determinants of the origin activation reaction and uncover a novel mechanism for checkpoint-dependent origin inhibition.

Related Results

Chromatin-dependent pre-replication complex positioning and activation in mammals
Chromatin-dependent pre-replication complex positioning and activation in mammals
Positionnement et activation du complexe de pré-réplication dépendant de la chromatine dans les mammifères Chaque division cellulaire requiert une duplication préci...
Rad53 checkpoint kinase regulation of DNA replication fork rate via Mrc1 phosphorylation
Rad53 checkpoint kinase regulation of DNA replication fork rate via Mrc1 phosphorylation
Summary The Rad53 DNA checkpoint protein kinase plays multiple roles in the budding yeast cell response to DNA replication stress. Key amongst th...
Sparse DDK: A Data-Driven Decorrelation Filter for GRACE Level-2 Products
Sparse DDK: A Data-Driven Decorrelation Filter for GRACE Level-2 Products
High-frequency and correlated noise filtering is one of the important preprocessing steps for GRACE level-2 products before calculating mass anomaly. Decorrelation and denoising ke...
DNA replication initiation and fidelity : a nanoscale view of the code of life
DNA replication initiation and fidelity : a nanoscale view of the code of life
<p dir="ltr">Every time a cell divides it needs to copy its entire genome. This is a fragile and challenging task, involving billions of DNA base pairs, tightly bound protein...
DNA replication initiation and fidelity : a nanoscale view of the code of life
DNA replication initiation and fidelity : a nanoscale view of the code of life
<p dir="ltr">Every time a cell divides it needs to copy its entire genome. This is a fragile and challenging task, involving billions of DNA base pairs, tightly bound protein...

Back to Top