Evidence map›Paper›PMID 41111111›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

A Biochemical Assay to Monitor the Encounter Between Cohesin and DNA Replication.

Yasuto Murayama

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Yasuto MurayamaDepartment of Chromosome Science, National Institute of Genetics, Mishima, Japan. murayama.yasuto@nig.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In eukaryotes, newly duplicated chromatids are physically linked together until the onset of chromosome segregation. This physical connection, known as sister chromatid cohesion, is mediated by the cohesin complex, a multisubunit ATPase assembly with a closed-ring conformation that topologically entraps DNA. Cohesin is loaded onto chromatin with the help of regulatory proteins prior to DNA replication and then establishes cohesion when it encounters the replication machinery. This process involves the physical tethering of two replicated sister DNAs and the stabilization of cohesin through acetylation. Here, we describe a biochemical assay to assess the response of cohesin to DNA replication using the purified budding yeast proteins.

Indexed as

Cell Cycle ProteinsChromosomal Proteins, Non-HistoneDNA ReplicationChromatidsChromosome SegregationCohesinsDNA, FungalSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinsDNA, FungalSaccharomyces cerevisiae ProteinsBiochemical reconstitutionCohesinDNA replicationScc2-Scc4Sister chromatid cohesionTopological DNA entrapment

Identifiers

PMID41111111

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.