Evidence map›Paper›PMID 28145526›Full record

ArticleScientific reports2017

ZP3 is Required for Germinal Vesicle Breakdown in Mouse Oocyte Meiosis.

Lei-Lei Gao, Chun-Xiang Zhou, Xiao-Lan Zhang, Peng Liu, Zhen Jin, Gang-Yi Zhu, Yang Ma, Jing Li, Zhi-Xia Yang, Dong Zhang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 35 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Lei-Lei GaoState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 211166, China.
Chun-Xiang ZhouState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 211166, China.
Xiao-Lan ZhangState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 211166, China.
Peng LiuState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 211166, China.
Zhen JinState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 211166, China.
Gang-Yi ZhuState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 211166, China.
Yang MaState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 211166, China.
Jing LiState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 211166, China.
Zhi-Xia YangState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 211166, China.
Dong ZhangState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 211166, China.
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ZP3 is a principal component of the zona pellucida (ZP) of mammalian oocytes and is essential for normal fertility, and knockout of ZP3 causes complete infertility. ZP3 promotes fertilization by recognizing sperm binding and activating the acrosome reaction; however, additional cellular roles for ZP3 in mammalian oocytes have not been yet reported. In the current study, we found that ZP3 was strongly expressed in the nucleus during prophase and gradually translocated to the ZP. Knockdown of ZP3 by a specific siRNA dramatically inhibited germinal vesicle breakdown (GVBD) (marking the beginning of meiosis), significantly reducing the percentage of MII oocytes. To investigate the ZP3-mediated mechanisms governing GVBD, we identified potential ZP3-interacting proteins by immunoprecipitation and mass spectrometry. We identified Protein tyrosine phosphatase, receptor type K (Ptprk), Aryl hydrocarbon receptor-interacting protein-like 1 (Aipl1), and Diaphanous related formin 2 (Diaph2) as potential candidates, and established a working model to explain how ZP3 affects GVBD. Finally, we provided preliminary evidence that ZP3 regulates Akt phosphorylation, lamin binding to the nuclear membrane via Aipl1, and organization of the actin cytoskeleton via Diaph2. These findings contribute to our understanding of a novel role played by ZP3 in GVBD.

Indexed as

MeiosisAdaptor Proteins, Signal TransducingAnimalsCarrier ProteinsCell DifferentiationCell NucleusFemaleLaminsMice, Inbred ICROocytesPhosphorylationProtein TransportProto-Oncogene Proteins c-aktSpindle ApparatusZona PellucidaZona Pellucida GlycoproteinsAdaptor Proteins, Signal TransducingAipl1 protein, mouseCarrier ProteinsLaminsProto-Oncogene Proteins c-aktZona Pellucida GlycoproteinsZp3 protein, mouse

Identifiers

PMID28145526
PMCPMC5286536
OpenAlexW2586024546

What OpenQuestion holds

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LicenceCC BY
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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.