Evidence map›Paper›PMID 26060891›Full record

ArticleAutophagy2015

MYBL2 guides autophagy suppressor VDAC2 in the developing ovary to inhibit autophagy through a complex of VDAC2-BECN1-BCL2L1 in mammals.

Jia Yuan, Ying Zhang, Yue Sheng, Xiazhou Fu, Hanhua Cheng, Rongjia Zhou

Open access · hybridAbstract read
In one paragraph

Article in Autophagy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 2 pooled it
3.2field-weighted citation impact, top 8% 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

58 citing papers in PubMed, 2 syntheses or guidelines pooled it, 100 citations in OpenAlex.

  1. Endoplasmic reticulum in oocytes: spatiotemporal distribution and function.Journal of assisted reproduction and genetics · 2023
    Pooled it
  2. Guideline
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Spatiotemporal Distribution and Function of Mitochondria in Oocytes.Reproductive sciences (Thousand Oaks, Calif.) · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

6 authors at 1 institution in 1 country.

Jia Yuana Department of Genetics; College of Life Sciences; Wuhan University ; Wuhan , China.
Ying Zhang
Yue Sheng
Xiazhou Fu
Hanhua Cheng
Rongjia Zhou
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oogenesis is essential for female gamete production in mammals. The total number of ovarian follicles is determined early in life and production of ovarian oocytes is thought to stop during the lifetime. However, the molecular mechanisms underling oogenesis, particularly autophagy regulation in the ovary, remain largely unknown. Here, we reveal an important MYBL2-VDAC2-BECN1-BCL2L1 pathway linking autophagy suppression in the developing ovary. The transcription factors GATA1 and MYBL2 can bind to and activate the Vdac2 promoter. MYBL2 regulates the spatiotemporal expression of VDAC2 in the developing ovary. Strikingly, in the VDAC2 transgenic pigs (Sus scrofa/Ss), VDAC2 exerts its function by inhibiting autophagy in the ovary. In contrast, Vdac2 knockout promotes autophagy. Moreover, VDAC2-mediated autophagy suppression is dependent on its interactions with both BECN1 and BCL2L1 to stabilize the BECN1 and BCL2L1 complex, suggesting VDAC2 as an autophagy suppressor in the pathway. Our findings provide a functional connection among the VDAC2, MYBL2, the BECN1-BCL2L1 pathway and autophagy suppression in the developing ovary, which is implicated in improving female fecundity.

Indexed as

AutophagyAnimalsAnimals, Genetically ModifiedAnimals, NewbornApoptosis Regulatory ProteinsBase Sequencebcl-X ProteinChromatin ImmunoprecipitationDNA Mutational AnalysisElectrophoretic Mobility Shift AssayFemaleGATA1 Transcription FactorMammalsMiceMolecular Sequence DataOvaryApoptosis Regulatory Proteinsbcl-X ProteinGATA1 Transcription FactorTrans-ActivatorsVoltage-Dependent Anion Channel 2ATG12, autophagy-related 12ATG16L1, autophagy-related 16-like 1ATG5, autophagy-related 5BAK, BCL2-antagonist/killer 1BCL2, B-cell CLL/lymphoma 2BCL2L1, BCL2-like 1Beclin1BECN1, Beclin 1, autophagy relatedCDS, coding DNA sequenceDpp, days postpartumGATA1, GATA binding protein 1 (globin transcription factor 1)GATA2, GATA binding protein 2LC3B, microtubule-associated protein 1 light chain 3 betaMBS, MYBL2 binding siteMYBL2MYBL2, v-myb avian myeloblastosis viral oncogene homolog-like 2ovaryreproductionSP1, Sp1 transcription factortranscription regulationVDAC2VDAC, voltage-dependent anion channelwt, wild type

Identifiers

PMID26060891
PMCPMC4590641
OpenAlexW1553446143

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.