Nuclear PGK1 Alleviates ADP-Dependent Inhibition of CDC7 to Promote DNA Replication.

Abstract:

:DNA replication is initiated by assembly of the kinase cell division cycle 7 (CDC7) with its regulatory activation subunit, activator of S-phase kinase (ASK), to activate DNA helicase. However, the mechanism underlying regulation of CDC7-ASK complex is unclear. Here, we show that ADP generated from CDC7-mediated MCM phosphorylation binds to an allosteric region of CDC7, disrupts CDC7-ASK interaction, and inhibits CDC7-ASK activity in a feedback way. EGFR- and ERK-activated casein kinase 2α (CK2α) phosphorylates nuclear phosphoglycerate kinase (PGK) 1 at S256, resulting in interaction of PGK1 with CDC7. CDC7-bound PGK1 converts ADP to ATP, thereby abrogating the inhibitory effect of ADP on CDC7-ASK activity, promoting the recruitment of DNA helicase to replication origins, DNA replication, cell proliferation, and brain tumorigenesis. These findings reveal an instrumental self-regulatory mechanism of CDC7-ASK activity by its kinase reaction product ADP and a nonglycolytic role for PGK1 in abrogating this negative feedback in promoting tumor development.

journal_name

Mol Cell

journal_title

Molecular cell

authors

Li X,Qian X,Jiang H,Xia Y,Zheng Y,Li J,Huang BJ,Fang J,Qian CN,Jiang T,Zeng YX,Lu Z

doi

10.1016/j.molcel.2018.09.007

subject

Has Abstract

pub_date

2018-11-15 00:00:00

pages

650-660.e8

issue

4

eissn

1097-2765

issn

1097-4164

pii

S1097-2765(18)30754-8

journal_volume

72

pub_type

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