Evidence map›Paper›PMID 28818972›Full record

ArticleScience (New York, N.Y.)2017

Fertile offspring from sterile sex chromosome trisomic mice.

Takayuki Hirota, Hiroshi Ohta, Benjamin E Powell, Shantha K Mahadevaiah, Obah A Ojarikre, Mitinori Saitou, James M A Turner

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.5field-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

23 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Generation of iPSC Cell Lines from Patients with Sex Chromosome Aneuploidies.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Frontiers in endocrinology · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Autonomous trisomic rescue of Down syndrome cells.Laboratory investigation; a journal of technical methods and pathology · 2019
    Article
  19. Article
  20. 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

7 authors at 2 institutions in 2 countries.

Takayuki HirotaSex Chromosome Biology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.ORCID 0000-0002-8145-3225
Hiroshi OhtaDepartment of Anatomy and Cell Biology, Graduate School of Medicine, Kyoto University, Kyoto, 606-8501, Japan.
Benjamin E PowellSex Chromosome Biology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.ORCID 0000-0003-2533-8262
Shantha K MahadevaiahSex Chromosome Biology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.ORCID 0000-0002-8925-0844
Obah A OjarikreSex Chromosome Biology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK.
Mitinori SaitouDepartment of Anatomy and Cell Biology, Graduate School of Medicine, Kyoto University, Kyoto, 606-8501, Japan. saitou@anat2.med.kyoto-u.ac.jp james.turner@crick.ac.uk.ORCID 0000-0002-2895-6798
James M A TurnerSex Chromosome Biology Laboratory, The Francis Crick Institute, London, NW1 1AT, UK. saitou@anat2.med.kyoto-u.ac.jp james.turner@crick.ac.uk.ORCID 0000-0003-1722-7677
The Francis Crick Institute · GBKyoto University · JP

Funding

Medical Research Council FC001193Wellcome Trust FC001193
6 · The paper itself

Abstract

Having the correct number of chromosomes is vital for normal development and health. Sex chromosome trisomy affects 0.1% of the human population and is associated with infertility. We show that during reprogramming to induced pluripotent stem cells (iPSCs), fibroblasts from sterile trisomic XXY and XYY mice lose the extra sex chromosome through a phenomenon we term trisomy-biased chromosome loss (TCL). Resulting euploid XY iPSCs can be differentiated into the male germ cell lineage and functional sperm that can be used in intracytoplasmic sperm injection to produce chromosomally normal, fertile offspring. Sex chromosome loss is comparatively infrequent during mouse XX and XY iPSC generation. TCL also applies to other chromosomes, generating euploid iPSCs from cells of a Down syndrome mouse model. It can also create euploid iPSCs from human trisomic patient fibroblasts. The findings have relevance to overcoming infertility and other trisomic phenotypes.

Indexed as

Cellular Reprogramming TechniquesAnimalsCellular ReprogrammingDisease Models, AnimalDown SyndromeFemaleFertilityFibroblastsHumansInduced Pluripotent Stem CellsInfertilityKlinefelter SyndromeMaleMiceMice, Inbred C57BLSex Chromosome Disorders

Identifiers

PMID28818972
PMCPMC5581950
OpenAlexW2750409364

What OpenQuestion holds

Textmetadata
LicenceTDM
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.