Evidence map›Paper›PMID 27260975›Full record

ArticleCell cycle (Georgetown, Tex.)2016

PGRMC1 participates in late events of bovine granulosa cells mitosis and oocyte meiosis.

L Terzaghi, I Tessaro, F Raucci, V Merico, G Mazzini, S Garagna, M Zuccotti, F Franciosi, V Lodde

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

19 citing papers in PubMed, 50 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

L Terzaghia Reproductive and Developmental Biology Laboratory, Department of Health , Animal Science and Food Safety, University of Milan , Milan , Italy.
I Tessaroa Reproductive and Developmental Biology Laboratory, Department of Health , Animal Science and Food Safety, University of Milan , Milan , Italy.
F Rauccia Reproductive and Developmental Biology Laboratory, Department of Health , Animal Science and Food Safety, University of Milan , Milan , Italy.
V Mericob Dipartimento di Biologia e Biotecnologie "Lazzaro Spallanzani," University of Pavia , Pavia , Italy.
G Mazzinic Istituto di Genetica Molecolare - Consiglio Nazionale delle Ricerche , Pavia , Italy.
S Garagnab Dipartimento di Biologia e Biotecnologie "Lazzaro Spallanzani," University of Pavia , Pavia , Italy.
M Zuccottid Sezione di Anatomia, Istologia ed Embriologia, Dipartimento di Scienze Biomediche , Biotecnologiche e Traslazionali (S.Bi.Bi.T.), University of Parma , Italy.
F Franciosia Reproductive and Developmental Biology Laboratory, Department of Health , Animal Science and Food Safety, University of Milan , Milan , Italy.
V Loddea Reproductive and Developmental Biology Laboratory, Department of Health , Animal Science and Food Safety, University of Milan , Milan , Italy.
University of Milan · ITUniversity of Pavia · ITIstituto di Genetica Molecolare · ITUniversity of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progesterone Receptor Membrane Component 1 (PGRMC1) is expressed in both oocyte and ovarian somatic cells, where it is found in multiple cellular sub-compartments including the mitotic spindle apparatus. PGRMC1 localization in the maturing bovine oocytes mirrors its localization in mitotic cells, suggesting a possible common action in mitosis and meiosis. To test the hypothesis that altering PGRMC1 activity leads to similar defects in mitosis and meiosis, PGRMC1 function was perturbed in cultured bovine granulosa cells (bGC) and maturing oocytes and the effect on mitotic and meiotic progression assessed. RNA interference-mediated PGRMC1 silencing in bGC significantly reduced cell proliferation, with a concomitant increase in the percentage of cells arrested at G2/M phase, which is consistent with an arrested or prolonged M-phase. This observation was confirmed by time-lapse imaging that revealed defects in late karyokinesis. In agreement with a role during late mitotic events, a direct interaction between PGRMC1 and Aurora Kinase B (AURKB) was observed in the central spindle at of dividing cells. Similarly, treatment with the PGRMC1 inhibitor AG205 or PGRMC1 silencing in the oocyte impaired completion of meiosis I. Specifically the ability of the oocyte to extrude the first polar body was significantly impaired while meiotic figures aberration and chromatin scattering within the ooplasm increased. Finally, analysis of PGRMC1 and AURKB localization in AG205-treated oocytes confirmed an altered localization of both proteins when meiotic errors occur. The present findings demonstrate that PGRMC1 participates in late events of both mammalian mitosis and oocyte meiosis, consistent with PGRMC1's localization at the mid-zone and mid-body of the mitotic and meiotic spindle.

Indexed as

MeiosisMitosisAnimalsAurora Kinase BCattleCell Nucleus DivisionCell ProliferationFemaleGene SilencingGranulosa CellsOocytesPolar BodiesProtein BindingReceptors, ProgesteroneThiazolesTime-Lapse ImagingAG205Aurora Kinase BReceptors, ProgesteroneThiazolescytokinesisgranulosa cellsinfertilityKaryokinesismammalian oocytemeiosismitosisPGRMC1polar body

Identifiers

PMID27260975
PMCPMC4968956
OpenAlexW2412308920

What OpenQuestion holds

Textmetadata
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.