Evidence map›Paper›PMID 30382773›Full record

ArticleCell cycle (Georgetown, Tex.)2018

Survivin regulates chromosome segregation by modulating the phosphorylation of Aurora B during porcine oocyte meiosis.

Li Chen, Tailang Yin, Zheng-Wen Nie, Tao Wang, Ying-Ying Gao, Shu-Yuan Yin, Li-Jun Huo, Xia Zhang, Jing Yang, Yi-Liang Miao

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

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  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Li Chena Institute of Stem Cell and Regenerative Biology, College of Animal Science and Veterinary Medicine , Huazhong Agricultural University , Wuhan , China.
Tailang Yinc Reproductive Medicine Center , Renmin Hospital of Wuhan University , Wuhan , China.
Zheng-Wen Niea Institute of Stem Cell and Regenerative Biology, College of Animal Science and Veterinary Medicine , Huazhong Agricultural University , Wuhan , China.
Tao Wanga Institute of Stem Cell and Regenerative Biology, College of Animal Science and Veterinary Medicine , Huazhong Agricultural University , Wuhan , China.
Ying-Ying Gaoa Institute of Stem Cell and Regenerative Biology, College of Animal Science and Veterinary Medicine , Huazhong Agricultural University , Wuhan , China.
Shu-Yuan Yina Institute of Stem Cell and Regenerative Biology, College of Animal Science and Veterinary Medicine , Huazhong Agricultural University , Wuhan , China.
Li-Jun Huob Key Laboratory of Agricultural Animal Genetics , Breeding and Reproduction (Huazhong Agricultural University), Ministry of Education , Wuhan , China.
Xia Zhanga Institute of Stem Cell and Regenerative Biology, College of Animal Science and Veterinary Medicine , Huazhong Agricultural University , Wuhan , China.
Jing Yangc Reproductive Medicine Center , Renmin Hospital of Wuhan University , Wuhan , China.
Yi-Liang Miaoa Institute of Stem Cell and Regenerative Biology, College of Animal Science and Veterinary Medicine , Huazhong Agricultural University , Wuhan , China.
Huazhong Agricultural University · CNRenmin Hospital of Wuhan University · CNWuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SURVIVIN is an essential chromosomal passenger complex (CPC) subunit and participates in cell division. In this study, we used porcine oocyte as a model to investigate the roles of Survivin during porcine oocyte maturation. Survivin was highly expressed in germinal vesicle (GV) and germinal vesicle breakdown (GVBD) stages oocytes, mainly localized in the GV at GV stage and on the chromosomes after GVBD. We have used RNA interference to specifically deplete Survivin in oocytes during in vitro maturation (IVM). Immunofluorescence assay showed that Survivin-depleted oocytes failed to produce polar body in meiosisⅠ (failed to complete cytokinesis), and they were arrested in metaphaseⅠwith misaligned chromosomes. The homologous chromosomes in Survivin-depleted oocytes could not be separated normally. Moreover, both the phosphorylation levels of Aurora B and the mRNA level of Mad2L1 related to spindle assembly checkpoint (SAC) was decreased in Survivin-depleted oocytes, which thus inhibited the degradation of Cyclin B1 (CCNB1) to complete meiosis. Taken together, we conclude that Survivin is an important mediator of centromere and midbody docking of Aurora-B as well as its activity and regulates SAC and MPF activity during meiosis in porcine oocytes.

Indexed as

Chromosome SegregationMeiosisAnimalsAurora Kinase BCells, CulturedFemaleGene Expression Regulation, DevelopmentalOocytesPhosphorylationSignal TransductionSpindle ApparatusSurvivinSus scrofaAurora Kinase BSurvivinchromosomesmetaphase Ioocytepigspindle assembly checkpointSurvivin

Identifiers

PMID30382773
PMCPMC6342075
OpenAlexW2898696337

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.