Evidence map›Paper›PMID 29845740›Full record

ArticleAging cell2018

SIRT4 is essential for metabolic control and meiotic structure during mouse oocyte maturation.

Juan Zeng, Manxi Jiang, Xinghan Wu, Feiyang Diao, Danhong Qiu, Xiaojing Hou, Haichao Wang, Ling Li, Chunling Li, Juan Ge and 3 more

Abstract 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 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Rhynchophylline rewires DLAT lipoylationActa pharmaceutica Sinica. B · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Lock out SIRT4.eLife · 2024
    Article
  11. Article
  12. Ovarian aging: energy metabolism of oocytes.Journal of ovarian research · 2024
    Review
  13. A Molecular Perspective and Role of NADInternational journal of molecular sciences · 2024
    Review
  14. The role of CoQ10 in embryonic development.Journal of assisted reproduction and genetics · 2024
    Review
  15. Can Nicotinamide Adenine Dinucleotide (NADAnimals : an open access journal from MDPI · 2024
    Review
  16. Article
  17. SIRT4 in ageing.Biogerontology · 2023
    Review
  18. Review
  19. Article
  20. Insufficient HtrA2 causes meiotic defects in aging germinal vesicle oocytes.Reproductive biology and endocrinology : RB&E · 2022
    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

13 authors.

Juan ZengState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Manxi JiangFertility Preservation Laboratory, Human Reproduction Medical Center, Guangdong Second Provincial General Hospital, Guangzhou, China.
Xinghan WuState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Feiyang DiaoState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Danhong QiuState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Xiaojing HouState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Haichao WangState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Ling LiState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Chunling LiState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Juan GeState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Jiayin LiuState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Xianghong OuFertility Preservation Laboratory, Human Reproduction Medical Center, Guangdong Second Provincial General Hospital, Guangzhou, China.
Qiang WangState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.ORCID 0000-0003-0000-9139

Funding

National Key R&D Program 2017YFC1001500National Natural Science Foundation 31571543National Natural Science Foundation 31601202National Natural Science Foundation 31771657National Natural Science Foundation 81471429National Natural Science Foundation 81730041
6 · The paper itself

Abstract

SIRT4 modulates energy homeostasis in multiple cell types and tissues. However, its role in meiotic oocytes remains unknown. Here, we report that mouse oocytes overexpressing SIRT4 are unable to completely progress through meiosis, showing the inadequate mitochondrial redistribution, lowered ATP content, elevated reactive oxygen species (ROS) level, with the severely disrupted spindle/chromosome organization. Moreover, we find that phosphorylation of Ser293-PDHE1α mediates the effects of SIRT4 overexpression on metabolic activity and meiotic events in oocytes by performing functional rescue experiments. By chance, we discover the SIRT4 upregulation in oocytes from aged mice; and importantly, the maternal age-associated deficient phenotypes in oocytes can be partly rescued through the knockdown of SIRT4. These findings reveal the critical role for SIRT4 in the control of energy metabolism and meiotic apparatus during oocyte maturation and indicate that SIRT4 is an essential factor determining oocyte quality.

Indexed as

MeiosisAnimalsCells, CulturedFemaleMiceMice, Inbred ICRMitochondrial ProteinsOocytesReactive Oxygen SpeciesSirtuinsMitochondrial ProteinsReactive Oxygen SpeciesSIRT4 protein, mouseSirtuinsagingmeiosismetabolismoocyteSIRT4

Identifiers

PMID29845740
PMCPMC6052465

What OpenQuestion holds

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Registered trials

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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.