Abstract

Origin recognition complex (ORC) binds to replication origins in eukaryotic DNAs and plays an important role in replication. Although yeast ORC is known to sequence-specifically bind to a replication origin, how human ORC recognizes a replication origin remains unknown. Previous genome-wide studies revealed that guanine (G)-rich sequences, potentially forming G-quadruplex (G4) structures, are present in most replication origins in human cells. We previously suggested that the region comprising residues 413–511 of human ORC subunit 1, hORC1413–511, binds preferentially to G-rich DNAs, which form a G4 structure in the absence of hORC1413–511. Here, we investigated the interaction of hORC1413-511 with various G-rich DNAs derived from human c-myc promoter and telomere regions. Fluorescence anisotropy revealed that hORC1413–511 binds preferentially to DNAs that have G4 structures over ones having double-stranded structures. Importantly, circular dichroism (CD) and nuclear magnetic resonance (NMR) showed that those G-rich DNAs retain the G4 structures even after binding with hORC1413–511. NMR chemical shift perturbation analyses revealed that the external G-tetrad planes of the G4 structures are the primary binding sites for hORC1413–511. The present study suggests that human ORC1 may recognize replication origins through the G4 structure.

Highlights

  • DNA replication starts from multiple chromosomal loci called replication origins.Origin recognition complex (ORC) binds to a replication origin and recruits other replication factors [1]

  • We demonstrated that hORC1413–511 binds to artificial Grich DNAs that form a G4 structure [27]

  • We demonstrated for the first time that hORC1413–511 binds to naturally occurring G-rich DNAs, derived from c-myc promoter and telomere regions, which form G4 structures, either parallel- or (3+1)-type G4 structures (Figure 1)

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Summary

Introduction

DNA replication starts from multiple chromosomal loci called replication origins. Origin recognition complex (ORC) binds to a replication origin and recruits other replication factors [1]. The structures of yeast [8,9,10], fly [11,12], and human [13,14,15,16] ORCs in free and complex forms with either double-stranded DNAs (dsDNAs) or other replication factors were determined by X-ray crystallography, NMR spectroscopy, and cryo-electron microscopy. It was indicated that some of those G-rich sequences form G4 structures in a chromatin [25,26] These findings suggest that G4 structures in the promoter region may be used for binding by hORC for initiation of replication. Fluorescein (FAM) is attached to the 50 -end of each DNA except for dsDNA_2

Binding of hORC1413–511 to DNAs Having a G4 Structure
Structures
G4 structure eveneven in the
Effects of hORC1
O solution were recorded
Effects ofofhORC1 on 11HHNMR
Discussion
Protein Expression and Purification
Preparation of DNAs
CD Spectroscopy
NMR Spectroscopy
Full Text
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