ReviewBioEssays : news and reviews in molecular, cellular and developmental biology2025
Compact Origins and Where to Find Them: ORC's Guide to Genome-Wide Licensing.
Review in BioEssays : news and reviews in molecular, cellular and developmental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Mechanisms of MCM2-7 helicase activation and initial DNA melting at near base-pair resolution.Nature communications · 2026Article
- Chromatin architecture sets origin licensing capacity.Research square · 2026Article
- Chromatin architecture sets origin licensing capacity.bioRxiv : the preprint server for biology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Origin licensing is the first step in the fundamental process of DNA replication, which ensures the accurate transmission of an organism's genetic information. Studies in budding yeast have provided crucial insights into replication origins, revealing sequence-specific features and structural DNA elements guiding helicase loading. Here, we review the recent advances in our understanding of DNA replication origin licensing, focusing on insights into origin architecture and advancements in high-resolution sequencing. Progress in the field demonstrates that origins are compact units that load an individual MCM2-7 double hexamer, which in turn causes steric occlusion of the origin recognition complex (ORC) binding site. We discuss why, in addition to the DNA sequence, DNA shape, DNA flexibility, and correct spacing of A- and B2-elements are crucial for efficient helicase loading. These recent findings provide a mechanistic explanation for the regulation of genome-wide origin licensing and reveal fundamental principles of MCM2-7 helicase loading.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.