Evidence map›Paper›PMID 28223544›Full record

ArticleOncotarget2017

HDAC8 functions in spindle assembly during mouse oocyte meiosis.

Kemei Zhang, Yajuan Lu, Chaohua Jiang, Wei Liu, Jing Shu, Xueqin Chen, Yingjiao Shi, Ensheng Wang, Li Wang, Qinbo Hu and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Role of Obesity in Female Reproduction.International journal of medical sciences · 2023
    Review
  4. Review
  5. Review
  6. Chromosome Segregation in the Oocyte: What Goes Wrong during Aging.International journal of molecular sciences · 2022
    Review
  7. Article
  8. Article
  9. Mechanisms of Oocyte Maturation and Related Epigenetic Regulation.Frontiers in cell and developmental biology · 2021
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
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

12 authors at 2 institutions in 1 country.

Kemei ZhangReproductive Medicine Center, Ningbo First Hospital, Zhejiang 315010, China.
Yajuan LuCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Chaohua JiangCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Wei LiuCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Jing ShuReproductive Medicine Center, Ningbo First Hospital, Zhejiang 315010, China.
Xueqin ChenReproductive Medicine Center, Ningbo First Hospital, Zhejiang 315010, China.
Yingjiao ShiReproductive Medicine Center, Ningbo First Hospital, Zhejiang 315010, China.
Ensheng WangReproductive Medicine Center, Ningbo First Hospital, Zhejiang 315010, China.
Li WangReproductive Medicine Center, Ningbo First Hospital, Zhejiang 315010, China.
Qinbo HuReproductive Medicine Center, Ningbo First Hospital, Zhejiang 315010, China.
Yibo DaiReproductive Medicine Center, Ningbo First Hospital, Zhejiang 315010, China.
Bo XiongCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Ningbo First Hospital · CNNanjing Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HDAC8 is a class I histone deacetylase that functions in a variety of biological processes through its non-histone substrates. However, its roles during oocyte meiosis remain elusive. Here, we document that HDAC8 localizes at spindle poles and positively participates in the regulation of microtubule organization and spindle assembly in mouse oocytes. Depletion of HDAC8 by siRNA-based gene silencing results in various spindle defects and chromosome misalignment during oocyte meiotic maturation, accompanied by impaired kinetochore-microtubule attachments. Consequently, a higher incidence of aneuploidy is generated in HDAC8-depleted MII eggs. In addition, inhibition of HDAC8 activity with its selective inhibitor PCI-34051 phenocopies the spindle/chromosome defects resulting from HDAC8 depletion by siRNA injection. Finally, we find that HDAC8 is required for the correct localization of ϕ-tubulin to spindle poles. Collectively, these data reveal that HDAC8 plays a significant role in regulating spindle assembly and thus ensuring the euploidy in mouse eggs.

Indexed as

AneuploidyAnimalsCells, CulturedChromosome SegregationFemaleHistone DeacetylasesHydroxamic AcidsIndolesMeiosisMiceMice, Inbred ICROocytesSpindle ApparatusTubulinHDAC8 protein, mouseHistone DeacetylasesHydroxamic AcidsIndolesPCI 34051Tubulinaneuploid eggschromosome alignmentHDAC8kinetochore-microtubule attachmentspindle assembly

Identifiers

PMID28223544
PMCPMC5386746
OpenAlexW2590240788

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.