Evidence map›Paper›PMID 28236007›Full record

ReviewProtoplasma2017

Function of heterochromatin protein 1 during DNA repair.

Eva Bártová, Barbora Malyšková, Denisa Komůrková, Soňa Legartová, Jana Suchánková, Jana Krejčí, Stanislav Kozubek

Abstract readReview
PubMed Publisher
In one paragraph

Review in Protoplasma, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 23% of its field
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

17 citing papers in PubMed, 26 citations in OpenAlex.

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  17. Editorial.Protoplasma · 2017
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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

7 authors at 1 institution in 1 country.

Eva BártováInstitute of Biophysics of the Czech Academy of Sciences, v.v.i., Královopolská 135, 612 65, Brno, Czech Republic. bartova@ibp.cz.
Barbora MalyškováInstitute of Biophysics of the Czech Academy of Sciences, v.v.i., Královopolská 135, 612 65, Brno, Czech Republic.
Denisa KomůrkováInstitute of Biophysics of the Czech Academy of Sciences, v.v.i., Královopolská 135, 612 65, Brno, Czech Republic.
Soňa LegartováInstitute of Biophysics of the Czech Academy of Sciences, v.v.i., Královopolská 135, 612 65, Brno, Czech Republic.
Jana SuchánkováInstitute of Biophysics of the Czech Academy of Sciences, v.v.i., Královopolská 135, 612 65, Brno, Czech Republic.
Jana KrejčíInstitute of Biophysics of the Czech Academy of Sciences, v.v.i., Královopolská 135, 612 65, Brno, Czech Republic.
Stanislav KozubekInstitute of Biophysics of the Czech Academy of Sciences, v.v.i., Královopolská 135, 612 65, Brno, Czech Republic.
Czech Academy of Sciences, Institute of Biophysics · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This review focuses on the function of heterochromatin protein HP1 in response to DNA damage. We specifically outline the regulatory mechanisms in which HP1 and its interacting partners are involved. HP1 protein subtypes (HP1α, HP1β, and HP1γ) are the main components of constitutive heterochromatin, and HP1α and HP1β in particular are responsible for heterochromatin maintenance. The recruitment of these proteins to DNA lesions is also important from the perspective of proper DNA repair mechanisms. For example, HP1α is necessary for the binding of the main DNA damage-related protein 53BP1 at DNA repair foci, which are positive not only for the HP1α protein but also for the RAD51 protein, a component of DNA repair machinery. The HP1β protein also appears in monomeric form in DNA lesions together with the evolutionarily well-conserved protein called proliferating cell nuclear antigen (PCNA). The role of HP1 in DNA lesions is also mediated via the Kap1 transcription repressor. Taken together, these results indicate that the function of HP1 after DNA injury depends strongly on the kinetics of other DNA repair-related factors and their post-translational modifications, such as the phosphorylation of Kap-1.

Indexed as

ChromatinChromobox Protein Homolog 5Chromosomal Proteins, Non-HistoneDNA DamageDNA RepairHumansProliferating Cell Nuclear AntigenProtein Processing, Post-TranslationalRepressor ProteinsTripartite Motif-Containing Protein 28CBX1 protein, humanCBX5 protein, humanChromatinChromobox Protein Homolog 5Chromosomal Proteins, Non-HistoneProliferating Cell Nuclear AntigenRepressor ProteinsTRIM28 protein, humanTripartite Motif-Containing Protein 28DNA damage responseDNA repairHP1 protein

Identifiers

PMID28236007
OpenAlexW2590406372

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.