Evidence map›Paper›PMID 29445069›Full record

ArticleThe Journal of reproduction and development2018

Expression and distribution of the zinc finger protein, SNAI3, in mouse ovaries and pre-implantation embryos.

Shujuan Guo, Xingyu Yan, Feifei Shi, Ke Ma, Zi-Jiang Chen, Cong Zhang

Open access · goldAbstract read
In one paragraph

Article in The Journal of reproduction and development, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Downregulation of decidual SKP2 is associated with human recurrent miscarriage.Reproductive biology and endocrinology : RB&E · 2021
    Article
  5. Review
  6. The Impact ofInternational journal of hypertension · 2021
    Article
  7. Melatonin protects against Epirubicin-induced ovarian damage.The Journal of reproduction and development · 2020
    Article
  8. Article
  9. Review
  10. Article
  11. 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 4 institutions in 1 country.

Shujuan GuoKey Laboratory of Animal Resistance Research, College of Life Science, Shandong Normal University, Ji'nan, Shandong 250014, China.
Xingyu YanHebei Medical University Nursing School, Shijiazhuang 050000, China.
Feifei ShiKey Laboratory of Animal Resistance Research, College of Life Science, Shandong Normal University, Ji'nan, Shandong 250014, China.
Ke MaKey Laboratory of Animal Resistance Research, College of Life Science, Shandong Normal University, Ji'nan, Shandong 250014, China.
Zi-Jiang ChenCenter for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200135, China.
Cong ZhangKey Laboratory of Animal Resistance Research, College of Life Science, Shandong Normal University, Ji'nan, Shandong 250014, China.
Shandong Normal University · CNHebei Medical University · CNRenji Hospital · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Snail gene family includes Snai1, Snai2, and Snai3 that encode zinc finger-containing transcriptional repressors in mammals. The expression and localization of SNAI1 and SNAI2 have been studied extensively during folliculogenesis, ovulation, luteinization, and embryogenesis in mice. However, the role of SNAI3 is unknown. In this study, we investigated the expression of SNAI3 during these processes. Our immunohistochemistry data showed that SNAI3 first appeared in oocytes by postnatal day (PD) 9. Following this, SNAI3 was found to be expressed consistently in theca and interstitial cells, along with oocytes. In gonadotropin-treated immature mice, the expression of SNAI3 did not change significantly during follicular development. The expression of SNAI3 was reduced during ovulation, after which it increased gradually during luteinization. Similar results were obtained from western blot analyses. Furthermore, real-time polymerase chain reaction (RT-PCR) analyses revealed varying mRNA levels of different Snail factors at a given time in gonadotropin-induced ovaries. During early embryo cleavage, SNAI3 was localized to the nucleus, except the nucleolus at the germinal vesicle and one-cell stages. From two- to eight-cell stages, SNAI3 was localized only to the nucleolus. Thereafter, SNAI3 was detected only in the cytoplasm, except during the blastocyst stage when it was localized to the nucleus of the trophectoderm and the inner cell mass. RT-PCR results showed that the expression of Snail superfamily genes was decreased during the blastocyst stage. From the eight-cell to morula stage, when compaction occurs that is a prerequisite for blastocyst formation, Snai3 mRNA was expressed at very low levels and was opposite to the highest expression level of the compaction-related gene, E-cadherin, at the eight-cell stage. Taken together, our results suggest that SNAI3 likely plays some roles during folliculogenesis, luteinization, and early embryonic development.

Indexed as

Embryonic DevelopmentGene Expression Regulation, DevelopmentalOvulationActive Transport, Cell NucleusAnimalsAnimals, NewbornBlastocystCell NucleolusCell NucleusFemaleImmunohistochemistryLuteinizationMiceMicroscopy, ConfocalMorulaOocytesRNA, MessengerSnai3 protein, mouseSnail Family Transcription FactorsE-cadherin-catenin complexMouseOvariesPre-implantation embryosSNAI3

Identifiers

PMID29445069
PMCPMC5902906
OpenAlexW2788087111

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.