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Flexible DNA Path in the MCM Double Hexamer Loaded on DNA.
- Source :
-
Biochemistry [Biochemistry] 2017 May 16; Vol. 56 (19), pp. 2435-2445. Date of Electronic Publication: 2017 May 01. - Publication Year :
- 2017
-
Abstract
- The formation of the pre-replicative complex (pre-RC) during the G1 phase, which is also called the licensing of DNA replication, is the initial and essential step of faithful DNA replication during the subsequent S phase. It is widely accepted that in the pre-RC, double-stranded DNA passes through the holes of two ring-shaped minichromosome maintenance (MCM) 2-7 hexamers; however, the spatial organization of the DNA and proteins involved in pre-RC formation is unclear. Here we reconstituted the pre-RC from purified DNA and proteins and visualized the complex using atomic force microscopy (AFM). AFM revealed that the MCM double hexamers formed elliptical particles on DNA. Analysis of the angle of binding of DNA to the MCM double hexamer suggests that the DNA does not completely pass through both holes of the MCM hexamers, possibly because the DNA exited from the gap between Mcm2 and Mcm5. A DNA loop fastened by the MCM double hexamer was detected in pre-RC samples reconstituted from purified proteins as well as those purified from yeast cells, suggesting a higher-order architecture of the loaded MCM hexamers and DNA strands.
- Subjects :
- DNA Replication
DNA, Fungal biosynthesis
DNA, Fungal chemistry
DNA, Fungal isolation & purification
DNA-Binding Proteins chemistry
DNA-Binding Proteins genetics
DNA-Binding Proteins metabolism
Microscopy, Atomic Force
Minichromosome Maintenance Proteins chemistry
Minichromosome Maintenance Proteins genetics
Minichromosome Maintenance Proteins isolation & purification
Minichromosome Maintenance Proteins metabolism
Nucleic Acid Conformation
Origin Recognition Complex chemistry
Origin Recognition Complex genetics
Origin Recognition Complex isolation & purification
Osmolar Concentration
Protein Multimerization
Recombinant Fusion Proteins chemistry
Recombinant Fusion Proteins metabolism
Recombinant Proteins chemistry
Recombinant Proteins metabolism
Saccharomyces cerevisiae Proteins chemistry
Saccharomyces cerevisiae Proteins genetics
Saccharomyces cerevisiae Proteins isolation & purification
Transcription Factors chemistry
Transcription Factors genetics
Transcription Factors metabolism
DNA, Fungal metabolism
Models, Molecular
Origin Recognition Complex metabolism
Saccharomyces cerevisiae metabolism
Saccharomyces cerevisiae Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4995
- Volume :
- 56
- Issue :
- 19
- Database :
- MEDLINE
- Journal :
- Biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 28459551
- Full Text :
- https://doi.org/10.1021/acs.biochem.6b00922