Evidence map›Paper›PMID 16107701›Full record

ArticleMolecular and cellular biology2005

Human histone chaperone nucleophosmin enhances acetylation-dependent chromatin transcription.

V Swaminathan, A Hari Kishore, K K Febitha, Tapas K Kundu

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

76 citing papers in PubMed, 188 citations in OpenAlex.

  1. Trial
  2. Two Decades ofCancers · 2026
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  16. Article
  17. Article
  18. The Role of Nucleophosmin 1 (Life (Basel, Switzerland) · 2022
    Review
  19. Article
  20. Significance of NPM1 Gene Mutations in AML.International journal of molecular sciences · 2021
    Review

16 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

V SwaminathanTranscription and Disease Laboratory, Molecular Biology and Genetics Unit, Jawaharlal Nehru Center for Advanced Scientific Research, Jakkur, Bangalore, India.
A Hari Kishore
K K Febitha
Tapas K Kundu
Jawaharlal Nehru Centre for Advanced Scientific Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Histone chaperones are a group of proteins that aid in the dynamic chromatin organization during different cellular processes. Here, we report that the human histone chaperone nucleophosmin interacts with the core histones H3, H2B, and H4 but that this histone interaction is not sufficient to confer the chaperone activity. Significantly, nucleophosmin enhances the acetylation-dependent chromatin transcription and it becomes acetylated both in vitro and in vivo. Acetylation of nucleophosmin and the core histones was found to be essential for the enhancement of chromatin transcription. The acetylated NPM1 not only shows an increased affinity toward acetylated histones but also shows enhanced histone transfer ability. Presumably, nucleophosmin disrupts the nucleosomal structure in an acetylation-dependent manner, resulting in the transcriptional activation. These results establish nucleophosmin (NPM1) as a human histone chaperone that becomes acetylated, resulting in the enhancement of chromatin transcription.

Indexed as

Gene Expression RegulationAcetylationAmino Acid SequenceAnimalsChromatinHeLa CellsHistonesHumansMolecular ChaperonesMolecular Sequence DataNuclear ProteinsNucleophosminProtein BindingTranscription, GeneticTumor Suppressor Protein p53Xenopus laevisChromatinHistonesMolecular ChaperonesNPM1 protein, humanNuclear ProteinsNucleophosminTumor Suppressor Protein p53

Identifiers

PMID16107701
PMCPMC1190275
OpenAlexW2141702415

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.