Evidence map›Paper›PMID 34493071›Full record

ReviewOpen biology2021

Recent insights into mechanisms preventing ectopic centromere formation.

Qianhua Dong, Jinpu Yang, Jinxin Gao, Fei Li

Open access · goldAbstract readReview
In one paragraph

Review in Open biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Cell cycle control of kinetochore assembly.Nucleus (Austin, Tex.) · 2022
    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 at 1 institution in 1 country.

Qianhua DongDepartment of Biology, New York University, New York, NY 10003-6688, USA.ORCID 0000-0002-7667-8323
Jinpu YangDepartment of Biology, New York University, New York, NY 10003-6688, USA.
Jinxin GaoDepartment of Biology, New York University, New York, NY 10003-6688, USA.ORCID 0000-0001-5429-7442
Fei LiDepartment of Biology, New York University, New York, NY 10003-6688, USA.ORCID 0000-0002-1206-9684
New York Proton Center · US

Funding

Molecular Basis of Centromere Specification and InheritanceR35GM134920 · NIGMS · NEW YORK UNIVERSITY · PI LI, FEI · 2020 to 2025
$4.2M
NIGMS NIH HHS R35 GM134920
6 · The paper itself

Abstract

The centromere is a specialized chromosomal structure essential for chromosome segregation. Centromere dysfunction leads to chromosome segregation errors and genome instability. In most eukaryotes, centromere identity is specified epigenetically by CENP-A, a centromere-specific histone H3 variant. CENP-A replaces histone H3 in centromeres, and nucleates the assembly of the kinetochore complex. Mislocalization of CENP-A to non-centromeric regions causes ectopic assembly of CENP-A chromatin, which has a devastating impact on chromosome segregation and has been linked to a variety of human cancers. How non-centromeric regions are protected from CENP-A misincorporation in normal cells is largely unexplored. Here, we review the most recent advances on the mechanisms underlying the prevention of ectopic centromere formation, and discuss the implications in human disease.

Indexed as

CentromereChromosome SegregationGenomic InstabilityAnimalsCentromere Protein AChromatinHistonesHumansNeoplasmsCentromere Protein AChromatinHistonesCENP-Achromosomes segregationectopic centromeresepigeneticskinetochoreneocentromere

Identifiers

PMID34493071
PMCPMC8424319
OpenAlexW3197536812

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.