Evidence map›Paper›PMID 23472205›Full record

ArticlePloS one2013

Aberrant gene expression and sexually incompatible genomic imprinting in oocytes derived from XY mouse embryonic stem cells in vitro.

Mai Nitta, Masanori Imamura, Yu Inoue, Yasuo Kunitomo, Zachary Yu-Ching Lin, Takuya Ogawa, Keiichiro Yogo, Norihiro Ishida-Kitagawa, Noritaka Fukunaga, Hideyuki Okano and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. 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

13 authors at 5 institutions in 1 country.

Mai NittaGraduate School of Biological Sciences, Nara Institute of Science and Technology, Nara, Japan.
Masanori Imamura
Yu Inoue
Yasuo Kunitomo
Zachary Yu-Ching Lin
Takuya Ogawa
Keiichiro Yogo
Norihiro Ishida-Kitagawa
Noritaka Fukunaga
Hideyuki Okano
Eimei Sato
Tatsuo Takeya
Jun Miyoshi
Nara Institute of Science and Technology · JPKeio University · JPOsaka Medical Center for Cancer and Cardiovascular Diseases · JPTohoku University · JPShizuoka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mouse embryonic stem cells (ESCs) have the potential to differentiate into germ cells (GCs) in vivo and in vitro. Interestingly, XY ESCs can give rise to both male and female GCs in culture, irrespective of the genetic sex. Recent studies showed that ESC-derived primordial GCs contributed to functional gametogenesis in vivo; however, in vitro differentiation techniques have never succeeded in generating mature oocytes from ESCs due to cryptogenic growth arrest during the preantral follicle stages of development. To address this issue, a mouse ESC line, capable of producing follicle-like structures (FLSs) efficiently, was established to investigate their properties using conventional molecular biological methods. The results revealed that the ESC-derived FLSs were morphologically similar to ovarian primary-to-secondary follicles but never formed an antrum; instead, the FLSs eventually underwent abnormal development or cell death in culture, or formed teratomas when transplanted under the kidney capsule in mice. Gene expression analyses demonstrated that the FLSs lacked transcripts for genes essential to late folliculogenesis, including gonadotropin receptors and steroidogenic enzymes, whereas some other genes were overexpressed in FLSs compared to the adult ovary. The E-Cadherin protein, which is involved in cell-to-cell interactions, was also expressed ectopically. Remarkably, it was seen that oocyte-like cells in the FLSs exhibited androgenetic genomic imprinting, which is ordinarily indicative of male GCs. Although the FLSs did not express male GC marker genes, the DNA methyltransferase, Dnmt3L, was expressed at an abnormally high level. Furthermore, the expression of sex determination factors was ambiguous in FLSs as both male and female determinants were expressed weakly. These data suggest that the developmental dysfunction of the ESC-derived FLSs may be attributable to aberrant gene expression and genomic imprinting, possibly associated with uncertain sex determination in culture.

Indexed as

Gene Expression Regulation, DevelopmentalGenomic ImprintingAnimalsBone Morphogenetic Protein 4Bone Morphogenetic ProteinsCadherinsCulture Media, ConditionedDNA (Cytosine-5-)-MethyltransferasesEmbryonic Stem CellsFemaleGene Expression ProfilingGerm CellsKidneyMaleMiceMice, Inbred C57BLBmp4 protein, mouseBmp8b protein, mouseBone Morphogenetic Protein 4Bone Morphogenetic ProteinsCadherinsCulture Media, ConditionedDNA (Cytosine-5-)-MethyltransferasesDnmt3l protein, mouseReceptors, Gonadotropin

Identifiers

PMID23472205
PMCPMC3589367
OpenAlexW2160228479

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.