Evidence map›Paper›PMID 27895110›Full record

ArticleGenome research2017

Nucleosome occupancy as a novel chromatin parameter for replication origin functions.

Jairo Rodriguez, Laura Lee, Bryony Lynch, Toshio Tsukiyama

Abstract read
In one paragraph

Article in Genome research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Investigation of the acetic acid stress response inMicrobial cell (Graz, Austria) · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The Protective Role of Dormant Origins in Response to Replicative Stress.International journal of molecular sciences · 2018
    Review
  18. Article
  19. Article
  20. Review
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

4 authors.

Jairo RodriguezBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
Laura LeeBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
Bryony LynchBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
Toshio TsukiyamaBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.

Funding

TRAINING IN MOLECULAR AND CELLULAR BIOLOGYT32GM007270 · NIGMS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2020
$21.0M
Mechanisms and functions of chromatin regulation for cell-cycle controlR01GM111428 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI TSUKIYAMA, TOSHIO · 2015 to 2020
$2.4M
NIGMS NIH HHS R01 GM111428NIGMS NIH HHS T32 GM007270
6 · The paper itself

Abstract

Eukaryotic DNA replication initiates from multiple discrete sites in the genome, termed origins of replication (origins). Prior to S phase, multiple origins are poised to initiate replication by recruitment of the pre-replicative complex (pre-RC). For proper replication to occur, origin activation must be tightly regulated. At the population level, each origin has a distinct firing time and frequency of activation within S phase. Many studies have shown that chromatin can strongly influence initiation of DNA replication. However, the chromatin parameters that affect properties of origins have not been thoroughly established. We found that nucleosome occupancy in G1 varies greatly around origins across the S. cerevisiae genome, and nucleosome occupancy around origins significantly correlates with the activation time and efficiency of origins, as well as pre-RC formation. We further demonstrate that nucleosome occupancy around origins in G1 is established during transition from G2/M to G1 in a pre-RC-dependent manner. Importantly, the diminished cell-cycle changes in nucleosome occupancy around origins in the orc1-161 mutant are associated with an abnormal global origin usage profile, suggesting that proper establishment of nucleosome occupancy around origins is a critical step for regulation of global origin activities. Our work thus establishes nucleosome occupancy as a novel and key chromatin parameter for proper origin regulation.

Indexed as

Cell CycleChromatinDNA ReplicationG2 Phase Cell Cycle CheckpointsMutant ProteinsNucleosomesOrigin Recognition ComplexReplication OriginSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsS PhaseChromatinMutant ProteinsNucleosomesORC1 protein, S cerevisiaeOrigin Recognition ComplexSaccharomyces cerevisiae Proteins

Identifiers

PMID27895110
PMCPMC5287232

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.