Evidence map›Paper›PMID 27579498›Full record

ReviewNucleus (Austin, Tex.)2016

Chromatin condensation during terminal erythropoiesis.

Baobing Zhao, Jing Yang, Peng Ji

Abstract readReview
In one paragraph

Review in Nucleus (Austin, Tex.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. ReducedInternational journal of molecular sciences · 2026
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  12. Analyses of erythropoiesis from embryonic stem cell-CD34Journal of cellular and molecular medicine · 2022
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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

3 authors.

Baobing Zhaoa Department of Pathology , Feinberg School of Medicine, Northwestern University , Chicago , IL , USA.
Jing Yanga Department of Pathology , Feinberg School of Medicine, Northwestern University , Chicago , IL , USA.
Peng Jia Department of Pathology , Feinberg School of Medicine, Northwestern University , Chicago , IL , USA.

Funding

The roles of pleckstrin-2 as a functional node in erythropoiesisR01DK102718 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JI, PENG · 2015 to 2019
$1.7M
NIDDK NIH HHS R01 DK102718
6 · The paper itself

Abstract

Mammalian terminal erythropoiesis involves gradual but dramatic chromatin condensation steps that are essential for cell differentiation. Chromatin and nuclear condensation is followed by a unique enucleation process, which is believed to liberate more spaces for hemoglobin enrichment and enable the generation of a physically flexible mature red blood cell. Although these processes have been known for decades, the mechanisms are still unclear. Our recent study reveals an unexpected nuclear opening formation during mouse terminal erythropoiesis that requires caspase-3 activity. Major histones, except H2AZ, are partially released from the opening, which is important for chromatin condensation. Block of the nuclear opening through caspase inhibitor or knockdown of caspase-3 inhibits chromatin condensation and enucleation. We also demonstrate that nuclear opening and histone release are cell cycle regulated. These studies reveal a novel mechanism for chromatin condensation in mammalia terminal erythropoiesis.

Indexed as

ErythropoiesisAnimalsCaspase 3Cell NucleusChromatinChromatin Assembly and DisassemblyHistonesHumansCaspase 3ChromatinHistonescaspase-3chromatin condensationenucleationerythropoiesishistone releasenuclear opening

Identifiers

PMID27579498
PMCPMC5120594

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.