Evidence map›Paper›PMID 27433972›Full record

ArticleCell cycle (Georgetown, Tex.)2016

RNA- binding protein Stau2 is important for spindle integrity and meiosis progression in mouse oocytes.

Yan Cao, Juan Du, Dandan Chen, Qian Wang, Nana Zhang, Xiaoyun Liu, Xiaoyu Liu, Jing Weng, Yuanjing Liang, Wei Ma

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 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 35% 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, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. E3 ubiquitin ligase Mindbomb 1 facilitates nuclear delivery of adenovirus genomes.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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  5. Review
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.

Yan Caoa Department of Histology and Embryology , School of Basic Medical Sciences, Capital Medical University , Beijing , China.
Juan Dua Department of Histology and Embryology , School of Basic Medical Sciences, Capital Medical University , Beijing , China.
Dandan Chena Department of Histology and Embryology , School of Basic Medical Sciences, Capital Medical University , Beijing , China.
Qian Wanga Department of Histology and Embryology , School of Basic Medical Sciences, Capital Medical University , Beijing , China.
Nana Zhanga Department of Histology and Embryology , School of Basic Medical Sciences, Capital Medical University , Beijing , China.
Xiaoyun Liua Department of Histology and Embryology , School of Basic Medical Sciences, Capital Medical University , Beijing , China.
Xiaoyu Liua Department of Histology and Embryology , School of Basic Medical Sciences, Capital Medical University , Beijing , China.
Jing Wengb Experimental Center for Basic Medical Teaching, School of Basic Medical Sciences, Capital Medical University , Beijing , China.
Yuanjing Lianga Department of Histology and Embryology , School of Basic Medical Sciences, Capital Medical University , Beijing , China.
Wei Maa Department of Histology and Embryology , School of Basic Medical Sciences, Capital Medical University , Beijing , China.
Capital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Staufen2 (Stau2) is a double-stranded RNA-binding protein involved in cell fate decision by regulating mRNA transport, mRNA stability, translation, and ribonucleoprotein assembly. Little is known about Stau2 expression and function in mammalian oocytes during meiosis. Herein we report the sub-cellular distribution and function of Stau2 in mouse oocyte meiosis. Western blot analysis revealed high and stable expression of Stau2 in oocytes from germinal vesicle (GV) to metaphase II (MII). Immunofluorescence showed that Stau2 was evenly distributed in oocytes at GV stage, and assembled as filaments after germinal vesicle breakdown (GVBD), particularly, colocalized with spindle at MI and MII. Stau2 was disassembled when microtubules were disrupted with nocodazole, on the other hand, when MTs were stabilized with taxol, Stau2 was not colocalized with the stabilized microtubules, but aggregated around the chromosomes array, indicating Stau2 assembly and colocalization with microtubules require both microtubule integrity and its normal dynamics. During interphase and mitosis of BHK and MEF cells, Stau2 was not distributed on microtubules, but colocalized with cis-Golgi marker GM130, implying its association with Golgi complex but not the spindle in fully differentiated somatic cells. Specific morpholino oligo-mediated Stau2 knockdown disrupted spindle formation, chromosome alignment and microtubule-kinetochore attachment in oocytes. The majority oocytes were arrested at MI stage, with bright MAD1 at kinetochores, indicating activation of spindle assembly checkpoint (SAC). Some oocytes were stranded at telophase I (TI), implying suppressed first polar body extrution. Together these data demonstrate that Stau2 is required for spindle formation and timely meiotic progression in mouse oocytes.

Indexed as

MeiosisAnimalsChromosomes, MammalianFemaleGene Knockdown TechniquesKinetochoresMice, Inbred BALB CMice, Inbred C57BLMicrotubulesMitosisM Phase Cell Cycle CheckpointsNerve Tissue ProteinsOocytesRNA-Binding ProteinsSpindle ApparatusSubcellular FractionsNerve Tissue ProteinsRNA-Binding Proteinsstau2 protein, mouse1st PBEmeiosis; mouseoocytespindle formationStau2

Identifiers

PMID27433972
PMCPMC5053582
OpenAlexW2500347194

What OpenQuestion holds

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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.