Evidence map›Paper›PMID 29067790›Full record

ArticleAging cell2018

Sirt2-BubR1 acetylation pathway mediates the effects of advanced maternal age on oocyte quality.

Danhong Qiu, Xiaojing Hou, Longsen Han, Xiaoyan Li, Juan Ge, Qiang Wang

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
10.6field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 51 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Ovarian aging: energy metabolism of oocytes.Journal of ovarian research · 2024
    Review
  9. A Molecular Perspective and Role of NADInternational journal of molecular sciences · 2024
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Insufficient HtrA2 causes meiotic defects in aging germinal vesicle oocytes.Reproductive biology and endocrinology : RB&E · 2022
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Sirtuins in female meiosis and in reproductive longevity.Molecular reproduction and development · 2020
    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

6 authors at 2 institutions in 1 country.

Danhong QiuState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Xiaojing HouState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Longsen HanState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Xiaoyan LiState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Juan GeState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Qiang WangState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Nanjing Medical University · CNNanjing Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The level of Sirt2 protein is reduced in oocytes from aged mice, while exogenous expression of Sirt2 could ameliorate the maternal age-associated meiotic defects. To date, the underlying mechanism remains unclear. Here, we confirmed that specific depletion of Sirt2 disrupts maturational progression and spindle/chromosome organization in mouse oocytes, with compromised kinetochore-microtubule attachments. Candidate screening revealed that acetylation state of lysine 243 on BubR1 (BubR1-K243, an integral part of the spindle assembly checkpoint complex) functions during oocyte meiosis, and acetylation-mimetic mutant BubR1-K243Q results in the very similar phenotypes as Sirt2-knockdown oocytes. Furthermore, we found that nonacetylatable-mimetic mutant BubR1-K243R partly prevents the meiotic deficits in oocytes depleted of Sirt2. Importantly, BubR1-K243R overexpression in oocytes derived from aged mice markedly suppresses spindle/chromosome anomalies and thereupon lowers the incidence of aneuploid eggs. In sum, our data suggest that Sirt2-dependent BubR1 deacetylation involves in the regulation of meiotic apparatus in normal oocytes and mediates the effects of advanced maternal age on oocyte quality.

Indexed as

Cell Cycle ProteinsMaternal AgeOocytesProtein Serine-Threonine KinasesSirtuin 2AcetylationAneuploidyAnimalsFemaleMeiosisMiceM Phase Cell Cycle CheckpointsBub1b protein, mouseCell Cycle ProteinsProtein Serine-Threonine KinasesSirt2 protein, mouseSirtuin 2aginganeuploidymeiosisoocytesirtuin

Identifiers

PMID29067790
PMCPMC5770883
OpenAlexW2766682035

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.