Unknown

Dataset Information

0

MCM2-7 form double hexamers at licensed origins in Xenopus egg extract.


ABSTRACT: In late mitosis and G1, Mcm2-7 are assembled onto replication origins to license them for initiation in the upcoming S phase. After initiation, Mcm2-7 provide helicase activity to unwind DNA at the replication fork. Here we examine the structure of Mcm2-7 on chromatin in Xenopus egg extracts. We show that prior to replication initiation, Mcm2-7 is present at licensed replication origins in a complex with a molecular mass close to double that of the Mcm2-7 hexamer. This complex has approximately stoichiometric quantities of the 6 Mcm2-7 proteins and we conclude that it consists of a double heterohexamer. This provides a configuration potentially capable of initiating a pair of bidirectional replication forks in S phase. We also show that after initiation, Mcm2-7 associate with Cdc45 and GINS to form a relatively stable CMG (Cdc45-MCM-GINS) complex. The CMG proteins also associate less strongly with other replication proteins, consistent with the idea that a single CMG complex forms the core of the replisome.

SUBMITTER: Gambus A 

PROVIDER: S-EPMC3064236 | biostudies-literature | 2011 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

MCM2-7 form double hexamers at licensed origins in Xenopus egg extract.

Gambus Agnieszka A   Khoudoli Guennadi A GA   Jones Richard C RC   Blow J Julian JJ  

The Journal of biological chemistry 20110131 13


In late mitosis and G1, Mcm2-7 are assembled onto replication origins to license them for initiation in the upcoming S phase. After initiation, Mcm2-7 provide helicase activity to unwind DNA at the replication fork. Here we examine the structure of Mcm2-7 on chromatin in Xenopus egg extracts. We show that prior to replication initiation, Mcm2-7 is present at licensed replication origins in a complex with a molecular mass close to double that of the Mcm2-7 hexamer. This complex has approximately  ...[more]

Similar Datasets

| S-EPMC7398698 | biostudies-literature
| S-EPMC6926450 | biostudies-literature
| S-EPMC2804858 | biostudies-literature
| S-EPMC2113033 | biostudies-literature
| S-EPMC4133086 | biostudies-literature
| S-EPMC379274 | biostudies-literature
| S-EPMC4914968 | biostudies-literature
| S-EPMC6540748 | biostudies-literature
| S-EPMC9947420 | biostudies-literature
| EMPIAR-10691 | biostudies-other